| 10058-F4 |
403811-55-2 |
.... |
| 17-AAG |
75747-14-7 |
17-AAG is a potent Hsp90 inhibitor.... |
| 17-AAG |
75747-14-7 |
17-AAG is a potent Hsp90 inhibitor.... |
| 17-AAG |
75747-14-7 |
17-AAG is a potent Hsp90 inhibitor.... |
| 17-DMAG |
467214-20-6 |
17-DMAG is a potent HSP90 inhibitor.... |
| 17-DMAG |
467214-20-6 |
17-DMAG is a potent HSP90 inhibitor.... |
| 17-DMAG |
467214-20-6 |
17-DMAG is a potent HSP90 inhibitor.... |
| 5-fluorouracil |
51-21-8 |
5-fluorouracil is a thymidylate synthase inhibitor.... |
| 5-fluorouracil |
51-21-8 |
5-fluorouracil is a thymidylate synthase inhibitor.... |
| 6-Mercaptopurine |
50-44-2 |
6-Mercaptopurine is a cytotoxic drug and a purine antagonist.... |
| ABR215062 |
248281-84-7 |
.... |
| ABR215062 |
248281-84-7 |
.... |
| ABT-199 |
1257044-40-8 |
ABT-199 is a potent and selective BCL-2 inhibitor.... |
| ABT-199 |
1257044-40-8 |
ABT-199 is a potent and selective BCL-2 inhibitor.... |
| ABT-737 |
852808-04-9 |
ABT-737 is a small molecule that occupies the pro-apoptotic Bcl-2 homology domain (BH3) binding groove of anti-apoptotic Bcl-2 family members, and, thereby, strongly and selectively inhibits Bcl-2, Bcl-XL, and Bcl-w with high affinity (Ki< 1 nM) but binds weakly (Ki>460 nM) to other antiapoptotic BCL-2 family members, including MCL-1 and BFL-1.... |
| ABT-737 |
852808-04-9 |
ABT-737 is a small molecule that occupies the pro-apoptotic Bcl-2 homology domain (BH3) binding groove of anti-apoptotic Bcl-2 family members, and, thereby, strongly and selectively inhibits Bcl-2, Bcl-XL, and Bcl-w with high affinity (Ki< 1 nM) but binds weakly (Ki>460 nM) to other antiapoptotic BCL-2 family members, including MCL-1 and BFL-1.... |
| ABT-737 |
852808-04-9 |
ABT-737 is a small molecule that occupies the pro-apoptotic Bcl-2 homology domain (BH3) binding groove of anti-apoptotic Bcl-2 family members, and, thereby, strongly and selectively inhibits Bcl-2, Bcl-XL, and Bcl-w with high affinity (Ki< 1 nM) but binds weakly (Ki>460 nM) to other antiapoptotic BCL-2 family members, including MCL-1 and BFL-1.... |
| ABT-737 |
852808-04-9 |
ABT-737 is a small molecule that occupies the pro-apoptotic Bcl-2 homology domain (BH3) binding groove of anti-apoptotic Bcl-2 family members, and, thereby, strongly and selectively inhibits Bcl-2, Bcl-XL, and Bcl-w with high affinity (Ki< 1 nM) but binds weakly (Ki>460 nM) to other antiapoptotic BCL-2 family members, including MCL-1 and BFL-1.... |
| ABT-751 |
141430-65-1 |
ABT-751 is a novel sulfonamide antimitotic agent.... |
| ABT-751 |
141430-65-1 |
ABT-751 is a novel sulfonamide antimitotic agent.... |
| ABT-751 |
141430-65-1 |
ABT-751 is a novel sulfonamide antimitotic agent.... |
| Acetaminophen |
103-90-2 |
Acetaminophen is a selective cyclooxygenase-2 (COX-2) inhibitor used as a nonsteroidal anti-inflammatory drugs for the relief of headaches and other minor aches and pains.... |
| Acetaminophen |
103-90-2 |
Acetaminophen is a selective cyclooxygenase-2 (COX-2) inhibitor used as a nonsteroidal anti-inflammatory drugs for the relief of headaches and other minor aches and pains.... |
| Actron |
22071-15-4 |
Ketoprofen is a potent nonsteroidal anti-inflammatory drug.... |
| ADL5859 HCl |
850173-95-4 |
.... |
| ADL5859 HCl |
850173-95-4 |
.... |
| Adriamycin |
25316-40-9 |
Adriamycin is an antibiotic anthracycline that inhibits DNA topoisomerase II (TOP2).... |
| Adriamycin |
25316-40-9 |
Adriamycin is an antibiotic anthracycline that inhibits DNA topoisomerase II (TOP2).... |
| Adriamycin |
25316-40-9 |
Adriamycin is an antibiotic anthracycline that inhibits DNA topoisomerase II (TOP2).... |
| Aminophylline |
317-34-0 |
Aminophylline is a bronchodilator.... |
| Aminophylline |
317-34-0 |
Aminophylline is a bronchodilator.... |
| AR42 |
935881-37-1 |
.... |
| ARRY-380 |
937265-83-3 |
ARRY-380 is a potent and selective HER2 (also known as ErbB2) inhibitor.... |
| ARRY-380 |
937265-83-3 |
ARRY-380 is a potent and selective HER2 (also known as ErbB2) inhibitor.... |
| ARRY-380 |
937265-83-3 |
ARRY-380 is a potent and selective HER2 (also known as ErbB2) inhibitor.... |
| ARRY-380 |
937265-83-3 |
ARRY-380 is a potent and selective HER2 (also known as ErbB2) inhibitor.... |
| ARRY-380 |
937265-83-3 |
ARRY-380 is a potent and selective HER2 (also known as ErbB2) inhibitor.... |
| ARRY-380 |
937265-83-3 |
ARRY-380 is a potent and selective HER2 (also known as ErbB2) inhibitor.... |
| ARRY-380 |
937265-83-3 |
ARRY-380 is a potent and selective HER2 (also known as ErbB2) inhibitor.... |
| ARRY520 trifluoroacetate |
885060-09-3 |
ARRY520 trifluoroacetate is a potent and selective inhibitor of kinesin spindle protein (KSP).... |
| ASP-3026 |
1097917-15-1 |
ASP-3026 is a potent and selective inhibitor of ALK kinase.... |
| ASP-3026 |
1097917-15-1 |
ASP-3026 is a potent and selective inhibitor of ALK kinase.... |
| ASP-3026 |
1097917-15-1 |
ASP-3026 is a potent and selective inhibitor of ALK kinase.... |
| ASP-3026 |
1097917-15-1 |
ASP-3026 is a potent and selective inhibitor of ALK kinase.... |
| AT-7519 |
902135-91-5 |
AT-7519 is an inhibitor of multiple cyclin-dependent kinases (CDKs).... |
| AT-7519 |
902135-91-5 |
AT-7519 is an inhibitor of multiple cyclin-dependent kinases (CDKs).... |
| AT-7519 |
902135-91-5 |
AT-7519 is an inhibitor of multiple cyclin-dependent kinases (CDKs).... |
| AT-7519 |
902135-91-5 |
AT-7519 is an inhibitor of multiple cyclin-dependent kinases (CDKs).... |
| AT101 |
90141-22-3 |
.... |
| AT101 |
90141-22-3 |
.... |
| AUY922 |
747412-49-3 |
NVP-AUY922 is a potent and selective heat shock protein 90 (HSP90) inhibitor with Kd of 1.7 nM.... |
| AUY922 |
747412-49-3 |
NVP-AUY922 is a potent and selective heat shock protein 90 (HSP90) inhibitor with Kd of 1.7 nM.... |
| AUY922 |
747412-49-3 |
NVP-AUY922 is a potent and selective heat shock protein 90 (HSP90) inhibitor with Kd of 1.7 nM.... |
| AUY922 |
747412-49-3 |
NVP-AUY922 is a potent and selective heat shock protein 90 (HSP90) inhibitor with Kd of 1.7 nM.... |
| Avanafil |
330784-47-9 |
Avanafil is a PDE5 inhibitor approved for erectile dysfunction by FDA[1].... |
| Avanafil |
330784-47-9 |
Avanafil is a PDE5 inhibitor approved for erectile dysfunction by FDA[1].... |
| AZ3146 |
1124329-14-1 |
AZ3146 is a potent and selective Mps1 inhibitor.... |
| AZ3146 |
1124329-14-1 |
AZ3146 is a potent and selective Mps1 inhibitor.... |
| AZ3146 |
1124329-14-1 |
AZ3146 is a potent and selective Mps1 inhibitor.... |
| AZ3146 |
1124329-14-1 |
AZ3146 is a potent and selective Mps1 inhibitor.... |
| AZ3146 |
1124329-14-1 |
AZ3146 is a potent and selective Mps1 inhibitor.... |
| AZD-3514 |
1240299-33-5 |
AZD-3514 is an a small-molecule androgen receptor(AR) inhibitor.... |
| AZD-3514 |
1240299-33-5 |
AZD-3514 is an a small-molecule androgen receptor(AR) inhibitor.... |
| AZD-3514 |
1240299-33-5 |
AZD-3514 is an a small-molecule androgen receptor(AR) inhibitor.... |
| AZD-3514 |
1240299-33-5 |
AZD-3514 is an a small-molecule androgen receptor(AR) inhibitor.... |
| AZD-5363 |
1143532-39-1 |
AZD-5363 is a potent and selective inhibitor of AKT.... |
| AZD-5363 |
1143532-39-1 |
AZD-5363 is a potent and selective inhibitor of AKT.... |
| AZD5438 |
602306-29-6 |
AZD5438 is a potent oral inhibitor of cyclin-dependent kinase (CDK) 1, CDK 2, and CDK 9.... |
| AZD5438 |
602306-29-6 |
AZD5438 is a potent oral inhibitor of cyclin-dependent kinase (CDK) 1, CDK 2, and CDK 9.... |
| AZD5438 |
602306-29-6 |
AZD5438 is a potent oral inhibitor of cyclin-dependent kinase (CDK) 1, CDK 2, and CDK 9.... |
| AZD7762 |
860352-01-8 |
AZD7762 is a novel ATP-competitive and selective checkpoint kinase inhibitor with IC50 values of 5 and < 10 nM for checkpoint kinases 1 (CHK1) and checkpoint kinases 2 (CHK2), respectively.... |
| AZD7762 |
860352-01-8 |
AZD7762 is a novel ATP-competitive and selective checkpoint kinase inhibitor with IC50 values of 5 and < 10 nM for checkpoint kinases 1 (CHK1) and checkpoint kinases 2 (CHK2), respectively.... |
| AZD7762 |
860352-01-8 |
AZD7762 is a novel ATP-competitive and selective checkpoint kinase inhibitor with IC50 values of 5 and < 10 nM for checkpoint kinases 1 (CHK1) and checkpoint kinases 2 (CHK2), respectively.... |
| AZD7762 |
860352-01-8 |
AZD7762 is a novel ATP-competitive and selective checkpoint kinase inhibitor with IC50 values of 5 and < 10 nM for checkpoint kinases 1 (CHK1) and checkpoint kinases 2 (CHK2), respectively.... |
| Bay 11-7082 |
19542-67-7 |
Bay 11-7082 is an inhibitor of NF-κB.... |
| Bay 11-7082 |
19542-67-7 |
Bay 11-7082 is an inhibitor of NF-κB.... |
| BAY 59-7939 |
366789-02-8 |
BAY 59-7939 is a direct inhibitor of factor Xa.... |
| Bay 60-7550 |
439083-90-6 |
Bay 60-7550 is a potent and selective PDE2 inhibitor.... |
| bay 73-6691 |
794568-92-6 |
BAY 73-6691 is a potent and selective inhibitor of phosphodiesterase 9(PDE9).... |
| Beta-Lapachone |
4707-32-8 |
.... |
| BI 2536 |
755038-02-9 |
BI 2536 is a novel, potent, and highly specific inhibitor of polo-like kinase (Plk1), which has an essential role in the regulation of mitotic progression.... |
| BI 2536 |
755038-02-9 |
BI 2536 is a novel, potent, and highly specific inhibitor of polo-like kinase 1 (Plk1), which has an essential role in the regulation of mitotic progression.... |
| BI 2536 |
755038-02-9 |
BI 2536 is a novel, potent, and highly specific inhibitor of polo-like kinase (Plk1), which has an essential role in the regulation of mitotic progression.... |
| BI 2536 |
755038-02-9 |
BI 2536 is a novel, potent, and highly specific inhibitor of polo-like kinase(Plk1), which has an essential role in the regulation of mitotic progression.... |
| BI6727 |
755038-65-4 |
BI6727 is a potent and selective cell-cycle kinase inhibitor that induces mitotic arrest and apoptosis by targeting Polo-like kinase (Plk).... |
| BI6727 |
755038-65-4 |
BI6727 is a potent and selective cell-cycle kinase inhibitor that induces mitotic arrest and apoptosis by targeting Polo-like kinase (Plk).... |
| BI6727 |
755038-65-4 |
BI6727 is a potent and selective cell-cycle kinase inhibitor that induces mitotic arrest and apoptosis by targeting Polo-like kinase (Plk).... |
| BIBR 1532 |
321674-73-1 |
BIBR 1532 is a potent and selective telomerase inhibitor with an IC50 of 100 nM.... |
| BIIB021 |
848695-25-0 |
.... |
| BIIB021 |
848695-25-0 |
.... |
| BMN673 |
1207456-01-6 |
.... |
| BMS-265246 |
582315-72-8 |
BMS-265246 is a selective Cyclin-dependent kinase 1/2 (CDK1/2) inhibitor.... |
| BMS-740808 |
280118-23-2 |
BMS-740808 is an orally bioavailable, highly potent, and selective inhibitor of Factor Xa with a Ki value of 30 pM.... |
| BMS-754807 |
1001350-96-4 |
BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR.... |
| BMS-754807 |
1001350-96-4 |
BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR.... |
| BMS-754807 |
1001350-96-4 |
BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR.... |
| BMS-754807 |
1001350-96-4 |
BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR.... |
| BRL-50481 |
433695-36-4 |
BRL 50481 is a novel and selective inhibitor of phosphodiesterase (PDE) 7.... |
| BS-181 |
1092443-52-1 |
BS-181 is a potent and selective CDK inhibitor.... |
| BS-181 |
1092443-52-1 |
BS-181 is a potent and selective CDK inhibitor.... |
| Cabazitaxel |
183133-96-2 |
Cabazitaxel is a semi-synthetic derivative of a natural taxoid.... |
| Cabazitaxel |
183133-96-2 |
Cabazitaxel is a semi-synthetic derivative of a natural taxoid.... |
| Cabazitaxel |
183133-96-2 |
Cabazitaxel is a semi-synthetic derivative of a natural taxoid.... |
| Cabazitaxel |
183133-96-2 |
Cabazitaxel is a semi-synthetic derivative of a natural taxoid.... |
| Carboplatin |
41575-94-4 |
Carboplatin is an active agent for acute myeloid leukemia.... |
| Carboplatin |
41575-94-4 |
Carboplatin is an active agent for acute myeloid leukemia.... |
| Carboplatin |
41575-94-4 |
Carboplatin is an active agent for acute myeloid leukemia.... |
| Cataflam |
15307-86-5 |
Cataflam is a non steroidal anti-inflammatory drug (NSAID).... |
| CB7630 |
154229-18-2 |
.... |
| Celecoxib |
169590-42-5 |
Celecoxib is a sulfa non-steroidal anti-inflammatory drug and selective COX-2 inhibitor with an IC50 of 40 nM.... |
| Celecoxib |
169590-42-5 |
Celecoxib is a sulfa non-steroidal anti-inflammatory drug and selective COX-2 inhibitor with an IC50 of 40 nM.... |
| CHIR-124 |
405168-58-3 |
CHIR-124 is a potent, selective human checkpoint kinase 1 (Chk1) inhibitor.... |
| CHS828 |
200484-11-3 |
CHS-828 is a competitive inhibitor of NAMPT and an inhibitor of NF-ΚB pathway activity as well, with anti-tumor activity in vitro and in vivo.... |
| Cilomilast |
153259-65-5 |
.... |
| Cilostazol |
73963-72-1 |
Cilostazol is a phosphodiesterase 3 inhibitor with antiplatelet and antithrombotic properties.... |
| Cilostazol |
73963-72-1 |
Cilostazol is a phosphodiesterase 3 inhibitor with antiplatelet and antithrombotic properties.... |
| Ciproxifan |
184025-18-1 |
.... |
| Ciproxifan |
184025-18-1 |
.... |
| CNX2006 |
1375465-09-0 |
.... |
| CNX2006 |
1375465-09-0 |
.... |
| CX-5461 |
1138549-36-6 |
CX-5461 is a potent small-molecule inhibitor of rRNA synthesis.... |
| CX-5461 |
1138549-36-6 |
CX-5461 is a potent small-molecule inhibitor of rRNA synthesis.... |
| CX-5461 |
1138549-36-6 |
CX-5461 is a potent small-molecule inhibitor of rRNA synthesis.... |
| CX-5461 |
1138549-36-6 |
CX-5461 is a potent small-molecule inhibitor of rRNA synthesis.... |
| CYC116 |
693228-63-6 |
.... |
| CYC202 |
186692-46-6 |
CYC202 is a potent inhibitor of recombinant cyclin dependent kinase (CDK)-2/cyclin E kinase.... |
| CYC202 |
186692-46-6 |
CYC202 is a potent inhibitor of recombinant cyclin dependent kinase (CDK)-2/cyclin E kinase.... |
| CYC202 |
186692-46-6 |
CYC202 is a potent inhibitor of recombinant cyclin dependent kinase (CDK)-2/cyclin E kinase.... |
| Dipyridamole |
58-32-2 |
Dipyridamole is a phosphodiesterase inhibitor.... |
| Docetaxel |
114977-28-5 |
Docetaxel is a anti-cancer agent, reversibly binds to microtubules, such as β- tubulin, mainly for the treatment of breast, ovarian, prostate, and non-small cell lung cancer.... |
| Docetaxel |
114977-28-5 |
Docetaxel is a anti-cancer agent, reversibly binds to microtubules, such as β- tubulin, mainly for the treatment of breast, ovarian, prostate, and non-small cell lung cancer.... |
| Edoxaban |
0480449-70-5 |
Edoxaban is an oral and direct factor Xa inhibitor.... |
| Epothilone B |
152044-54-7 |
Epothilone B is a highly potent non-taxane microtubule stabilizing agent with a Ki of 0.75 µM.... |
| Epothilone B |
152044-54-7 |
Epothilone B is a highly potent non-taxane microtubule stabilizing agent with a Ki of 0.75 µM.... |
| Epothilone B |
152044-54-7 |
Epothilone B is a highly potent non-taxane microtubule stabilizing agent with a Ki of 0.75 µM.... |
| Epothilone B |
152044-54-7 |
Epothilone B is a highly potent non-taxane microtubule stabilizing agent with a Ki of 0.75 µM.... |
| EPZ-6438 |
1403254-99-8 |
EPZ-6438 is a potent and selective inhibitor of EZH2.... |
| EPZ-6438 |
1403254-99-8 |
EPZ-6438 is a potent and selective inhibitor of EZH2.... |
| EPZ-6438 |
1403254-99-8 |
EPZ-6438 is a potent and selective inhibitor of EZH2.... |
| EPZ-6438 |
1403254-99-8 |
EPZ-6438 is a potent and selective inhibitor of EZH2.... |
| Etodolac |
41340-25-4 |
Etodolac is a highly cyclooxygenase-2 (COX-2)-selective inhibitor.... |
| Exatecan |
171335-80-1 |
.... |
| Firocoxib |
189954-96-9 |
Firocoxib is a non-steroidal anti-inflammatory drug of the cyclooxygenase(COX)-2 inhibitor.... |
| FK866 |
658084-64-1 |
FK866 is a highly specific noncompetitive inhibition of nicotinamide phosphoribosyltransferase (NAPRT).... |
| Flavopiridol |
146426-40-6 |
Flavopiridol is a potent CDK inhibitor with IC50 values of 30, 170, 100, 170, 80 and 20 nM for CDK1, CDK2, CDK4, CDK5, CDK6 and CDK9, respectively.... |
| Flavopiridol |
146426-40-6 |
Flavopiridol is a potent CDK inhibitor with IC50 values of 30, 170, 100, 170, 80 and 20 nM for CDK1, CDK2, CDK4, CDK5, CDK6 and CDK9, respectively.... |
| Flavopiridol |
146426-40-6 |
Flavopiridol is a potent CDK inhibitor with IC50 values of 30, 170, 100, 170, 80 and 20 nM for CDK1, CDK2, CDK4, CDK5, CDK6 and CDK9, respectively.... |
| Flavopiridol |
146426-40-6 |
Flavopiridol is a potent CDK inhibitor with IC50 values of 30, 170, 100, 170, 80 and 20 nM for CDK1, CDK2, CDK4, CDK5, CDK6 and CDK9, respectively.... |
| Flavopiridol |
146426-40-6 |
Flavopiridol is a potent CDK inhibitor with IC50 values of 30, 170, 100, 170, 80 and 20 nM for CDK1, CDK2, CDK4, CDK5, CDK6 and CDK9, respectively.... |
| Fostamatinib |
901119-35-5 |
.... |
| Fostamatinib |
901119-35-5 |
.... |
| Fostamatinib |
901119-35-5 |
.... |
| Ganetespib |
888216-25-9 |
Ganetespib is a novel small molecule heat shock protein 90 (Hsp90) inhibitor with an IC50 of 4 nM in osteosarcoma (OSA) 8 cells.... |
| Ganetespib |
888216-25-9 |
Ganetespib is a novel small molecule heat shock protein 90 (Hsp90) inhibitor with an IC50 of 4 nM in osteosarcoma (OSA) 8 cells.... |
| Ganetespib |
888216-25-9 |
Ganetespib is a novel small molecule heat shock protein 90 (Hsp90) inhibitor with an IC50 of 4 nM in osteosarcoma (OSA) 8 cells.... |
| Ganetespib |
888216-25-9 |
Ganetespib is a novel small molecule heat shock protein 90 (Hsp90) inhibitor with an IC50 of 4 nM in osteosarcoma (OSA) 8 cells.... |
| GRI977143 |
325850-81-5 |
GRI977143 is a specific agonist of the LPA2 receptor.... |
| GRI977143 |
325850-81-5 |
GRI977143 is a specific agonist of the LPA2 receptor.... |
| GSK 1210151A (I-BET151) |
1300031-49-5 |
GSK1210151A is a novel and selective inhibitor of the bromodomain and extra terminal (BET) family proteins.... |
| GSK 1210151A (I-BET151) |
1300031-49-5 |
GSK1210151A is a novel and selective inhibitor of the bromodomain and extra terminal (BET) family proteins.... |
| GSK 1210151A (I-BET151) |
1300031-49-5 |
GSK1210151A is a novel and selective inhibitor of the bromodomain and extra terminal (BET) family proteins.... |
| GSK 1210151A (I-BET151) |
1300031-49-5 |
GSK1210151A is a novel and selective inhibitor of the bromodomain and extra terminal (BET) family proteins.... |
| GW5074 |
220904-83-6 |
GW5074 is a potent and specific inhibitor of c-Raf.... |
| GW5074 |
220904-83-6 |
GW5074 is a potent and specific inhibitor of c-Raf.... |
| H-89 |
127243-85-0 |
H-89 is a specific cyclic AMP-dependent protein kinase A (protein kinase A) inhibitor.... |
| HA14-1 |
65673-63-4 |
HA14-1 is a B-cell lymphoma 2 (Bcl-2) antagonist.... |
| HKI357 |
848133-17-5 |
HKI357 is a dual inhibitor of EGFR and ERBB2.... |
| HKI357 |
848133-17-5 |
HKI357 is a dual inhibitor of EGFR and ERBB2.... |
| HMN-214 |
173529-46-9 |
HMN-214 (IVX-214) is a potent inhibitor of Polo-like kinase (Plk)1 with IC50 of 118 nM.HMN-214 is an oral prodrug of HMN-176.... |
| HMN-214 |
173529-46-9 |
HMN-214 (IVX-214) is a potent inhibitor of Polo-like kinase (Plk)1 with IC50 of 118 nM.HMN-214 is an oral prodrug of HMN-176.... |
| HMN-214 |
173529-46-9 |
HMN-214 (IVX-214) is a potent inhibitor of Polo-like kinase (Plk)1 with IC50 of 118 nM.HMN-214 is an oral prodrug of HMN-176.... |
| HMN-214 |
173529-46-9 |
HMN-214 (IVX-214) is a potent inhibitor of Polo-like kinase (Plk)1 with IC50 of 118 nM.HMN-214 is an oral prodrug of HMN-176.... |
| HSP-990 |
934343-74-5 |
HSP-990 is an potent inhibitor of human heat-shock protein 90 (Hsp90).... |
| HSP-990 |
934343-74-5 |
HSP-990 is an potent inhibitor of human heat-shock protein 90 (Hsp90).... |
| Hydroxyurea |
127-07-1 |
Hydroxyurea is a M2 specific inhibitor that binds to the free radical and inactivates the enzyme ribonucleotide reductase.... |
| IEM1754 dihydrobromide |
162831-31-4 |
.... |
| Indisulam |
165668-41-7 |
Indisulam is a potent carbonic anhydrase inhbitor and tubulin polymerization inhibitor.... |
| Indometacin |
53-86-1 |
Indometacin is a nonselective inhibitor of cyclooxygenase (COX) 1 and 2.... |
| INH1 |
313553-47-8 |
.... |
| Ispinesib |
336113-53-2 |
Ispinesib is a potent allosteric small-molecule inhibitor of kinesin spindle protein (KSP, also known as HsEg5).... |
| Ispinesib |
336113-53-2 |
Ispinesib is a potent allosteric small-molecule inhibitor of kinesin spindle protein (KSP, also known as HsEg5).... |
| Ispinesib |
336113-53-2 |
Ispinesib is a potent allosteric small-molecule inhibitor of kinesin spindle protein (KSP, also known as HsEg5).... |
| JNJ-7706621 |
443797-96-4 |
JNJ-7706621 is a dual inhibitor of cyclin-dependent kinases (CDKs) and aurora kinases.... |
| Kenpaullone |
142273-20-9 |
Kenpaullone is a potent ATP-competitive GSK3-β and CDK inhibitor.... |
| KW-2478 |
819812-04-9 |
KW-2478 is a novel heat shock protein 90 (Hsp90) inhibitor.... |
| KW-2478 |
819812-04-9 |
KW-2478 is a novel heat shock protein 90 (Hsp90) inhibitor.... |
| KW-2478 |
819812-04-9 |
KW-2478 is a novel heat shock protein 90 (Hsp90) inhibitor.... |
| KW-2478 |
819812-04-9 |
KW-2478 is a novel heat shock protein 90 (Hsp90) inhibitor.... |
| lcl161 |
1005342-46-0 |
LCL161 is a small molecule mimetic of the second mitochondria-derived activator of caspases (SMAC) that is an inhibitor of inhibitors of apoptosis (IAP).... |
| LEE011 |
1211441-98-3 |
.... |
| LLL12 |
1260247-42-4 |
LLL12 is a novel signal transducer and activator of transcription 3 (STAT3) inhibitor.... |
| LY-2874455 |
1254473-64-7 |
LY2874455 is a potent FGF/FGFR inhibitor.... |
| LY-2874455 |
1254473-64-7 |
LY2874455 is a potent FGF/FGFR inhibitor.... |
| LY-2874455 |
1254473-64-7 |
LY2874455 is a potent FGF/FGFR inhibitor.... |
| LY-2874455 |
1254473-64-7 |
LY2874455 is a potent FGF/FGFR inhibitor.... |
| LY-2874455 |
1254473-64-7 |
LY2874455 is a potent FGF/FGFR inhibitor.... |
| LY-2874455 |
1254473-64-7 |
LY2874455 is a potent FGF/FGFR inhibitor.... |
| LY-2874455 |
1254473-64-7 |
LY2874455 is a potent FGF/FGFR inhibitor.... |
| LY2603618 |
911222-45-2 |
LY2603618 is a selective inhibitor of Chk1.... |
| LY2603618 |
911222-45-2 |
LY2603618 is a selective inhibitor of Chk1.... |
| LY2603618 |
911222-45-2 |
LY2603618 is a selective inhibitor of Chk1.... |
| LY411575 |
209984-57-6 |
.... |
| LY411575 |
209984-57-6 |
.... |
| LY411575 |
209984-57-6 |
.... |
| LY411575 |
209984-57-6 |
.... |
| MK-1775 |
955365-80-7 |
MK-1775 is a potent and selective small molecule inhibitor of Wee1 kinase with an IC50 of 5.2 nM.... |
| MK-1775 |
955365-80-7 |
MK-1775 is a potent and selective small molecule inhibitor of Wee1 kinase with an IC50 of 5.2 nM.... |
| MK-1775 |
955365-80-7 |
MK-1775 is a potent and selective small molecule inhibitor of Wee1 kinase with an IC50 of 5.2 nM.... |
| MK-1775 |
955365-80-7 |
MK-1775 is a potent and selective small molecule inhibitor of Wee1 kinase with an IC50 of 5.2 nM.... |
| MK0752 |
471905-41-6 |
.... |
| MK8745 |
885325-71-3 |
.... |
| ML167 |
1285702-20-6 |
.... |
| ML167 |
1285702-20-6 |
.... |
| ML167 |
1285702-20-6 |
.... |
| ML167 |
1285702-20-6 |
.... |
| MLN0905 |
1228960-69-7 |
.... |
| Naproxen sodium |
26159-34-2 |
Naproxen sodium is a non-steroidal anti-inflammatory drug (NSAID).... |
| Navitoclax |
923564-51-6 |
Navitoclax is a potent and highly selective inhibitor of anti-apoptotic members of the Bcl-2 family, with binding affinities (Ki’s) <1 nM for Bcl-2, Bcl-xL, and Bcl-w, but Ki of 550 nM for Mcl-1.... |
| Navitoclax |
923564-51-6 |
Navitoclax is a potent and highly selective inhibitor of anti-apoptotic members of the Bcl-2 family, with binding affinities (Ki’s) <1 nM for Bcl-2, Bcl-xL, and Bcl-w, but Ki of 550 nM for Mcl-1.... |
| Navitoclax |
923564-51-6 |
Navitoclax is a potent and highly selective inhibitor of anti-apoptotic members of the Bcl-2 family, with binding affinities (Ki’s) <1 nM for Bcl-2, Bcl-xL, and Bcl-w, but Ki of 550 nM for Mcl-1.... |
| Navitoclax |
923564-51-6 |
Navitoclax is a potent and highly selective inhibitor of anti-apoptotic members of the Bcl-2 family, with binding affinities (Ki’s) <1 nM for Bcl-2, Bcl-xL, and Bcl-w, but Ki of 550 nM for Mcl-1.... |
| Nepafenac |
78281-72-8 |
Nepafenac is a selective cyclooxygenase–2 (COX–2) inhibitor.... |
| Nepafenac |
78281-72-8 |
Nepafenac is a selective cyclooxygenase–2 (COX–2) inhibitor.... |
| Nepafenac |
78281-72-8 |
Nepafenac is a selective cyclooxygenase–2 (COX–2) inhibitor.... |
| NS398 |
123653-11-2 |
NS-398 is a novel anti-inflammatory and analgesic agent.... |
| NSC-207895 (XI-006) |
58131-57-0 |
NSC-207895 is a MDM2-related protein suppressor that leads to activation of p53.... |
| NSC632839 |
157654-67-6 |
NSC632839 is a pan-specific ubiquitin and ubiquitin-like isopeptidase inhibitor.... |
| NSC632839 |
157654-67-6 |
NSC632839 is a pan-specific ubiquitin and ubiquitin-like isopeptidase inhibitor.... |
| NU7441 (KU-57788) |
503468-95-9 |
NU7441(KU-57788) is a highly potent and selective DNA-PK inhibitor.... |
| NUTLIN 3A |
675576-98-4 |
.... |
| NUTLIN 3B |
675576-97-3 |
.... |
| Nutlin-3 |
890090-75-2 |
Nutlin-3 is a novel small-molecule murine double minute 2 (MDM2) antagonist.... |
| Nutlin-3 |
890090-75-2 |
Nutlin-3 is a novel small-molecule murine double minute 2 (MDM2) antagonist.... |
| Nutlin-3 |
890090-75-2 |
Nutlin-3 is a novel small-molecule murine double minute 2 (MDM2) antagonist.... |
| Nutlin-3 |
890090-75-2 |
Nutlin-3 is a novel small-molecule murine double minute 2 (MDM2) antagonist.... |
| NVP-BEP800 |
847559-80-2 |
.... |
| NVP-TNKS656 |
1419949-20-4 |
NVP-TNKS656 is a potent tankyrase inhibitor.... |
| Obatoclax |
803712-79-0 |
Obatoclax is an inhibitor of Bcl-2 with a Ki of 220 nM.... |
| Obatoclax |
803712-79-0 |
Obatoclax is an inhibitor of Bcl-2 with a Ki of 220 nM.... |
| Obatoclax |
803712-79-0 |
Obatoclax is an inhibitor of Bcl-2 with a Ki of 220 nM.... |
| Oxaliplatin |
61825-94-3 |
.... |
| Oxaliplatin |
61825-94-3 |
.... |
| Oxaliplatin |
61825-94-3 |
.... |
| P22077 |
1247819-59-5 |
P22077 is an ubiquitin-specific protease 7 (USP7) inhibitor.... |
| P22077 |
1247819-59-5 |
P22077 is an ubiquitin-specific protease 7 (USP7) inhibitor.... |
| P5091(P005091) |
882257-11-6 |
P5091 is an inhibitor of ubiquitin specific protease 7 (USP7).... |
| P5091(P005091) |
882257-11-6 |
P5091 is an inhibitor of ubiquitin specific protease 7 (USP7).... |
| Palbociclib Isethionate |
571190-30-2 |
.... |
| PD0332991 |
827022-32-2 |
PD 0332991 specifically inhibits cyclin-dependent kinase 4 (Cdk4)/cyclin D1 and (cyclin-dependent kinase 6) Cdk6/cyclin D2 with IC50 values of 11 and 16 nM, respectively.... |
| PD0332991 |
827022-32-2 |
PD 0332991 specifically inhibits cyclin-dependent kinase 4 (Cdk4)/cyclin D1 and (cyclin-dependent kinase 6) Cdk6/cyclin D2 with IC50 values of 11 and 16 nM, respectively.... |
| PD0332991 |
827022-32-2 |
PD 0332991 specifically inhibits cyclin-dependent kinase 4 (Cdk4)/cyclin D1 and (cyclin-dependent kinase 6) Cdk6/cyclin D2 with IC50 values of 11 and 16 nM, respectively.... |
| PF-03814735 |
942487-16-3 |
.... |
| PF-2545920 |
1292799-56-4 |
PF-2545920 is a specific phosphodiesterase-10A (PDE10A) inhibitor.... |
| PF-2545920 |
1292799-56-4 |
PF-2545920 is a specific phosphodiesterase-10A (PDE10A) inhibitor.... |
| PF-2545920 |
1292799-56-4 |
PF-2545920 is a specific phosphodiesterase-10A (PDE10A) inhibitor.... |
| PF-2545920 |
1292799-56-4 |
PF-2545920 is a specific phosphodiesterase-10A (PDE10A) inhibitor.... |
| PF-3758309 |
898044-15-0 |
PF-3758309 is a potent and reversible ATP-competitive inhibitor of PAK4.... |
| PF-3758309 |
898044-15-0 |
PF-3758309 is a potent and reversible ATP-competitive inhibitor of PAK4.... |
| PF-3758309 |
898044-15-0 |
PF-3758309 is a potent and reversible ATP-competitive inhibitor of PAK4.... |
| PF477736 |
952021-60-2 |
.... |
| PF477736 |
952021-60-2 |
.... |
| PF477736 |
952021-60-2 |
.... |
| PF562271 |
717907-75-0 |
.... |
| PF562271 |
717907-75-0 |
.... |
| Piroxicam |
36322-90-4 |
Piroxicam is a highly selective inhibitor of COX-1.... |
| PJ34 |
344458-19-1 |
.... |
| PJ34 |
344458-19-1 |
.... |
| PJ34 |
344458-19-1 |
.... |
| PX-478 |
685898-44-6 |
PX-478 is a hypoxia-inducible factor-1 (HIF-1)α inhibitor.... |
| Raltitrexed |
112887-68-0 |
Raltitrexed is an inhibitor of thymidylate synthase with a Ki of approximately 60 nM.... |
| Raltitrexed |
112887-68-0 |
Raltitrexed is an inhibitor of thymidylate synthase with a Ki of approximately 60 nM.... |
| RGFP966 |
1396841-57-8 |
RGFP966 is a potent HDAC3 inhibitor with an IC50 of 80 nM.... |
| RGFP966 |
1396841-57-8 |
RGFP966 is a potent HDAC3 inhibitor with an IC50 of 80 nM.... |
| RKI1447 |
1342278-01-6 |
.... |
| RKI1447 |
1342278-01-6 |
.... |
| RO3280 |
1062243-51-9 |
.... |
| RO3280 |
1062243-51-9 |
.... |
| RO4929097 |
847925-91-1 |
.... |
| RO4929097 |
847925-91-1 |
.... |
| RO4929097 |
847925-91-1 |
.... |
| Rolipram |
61413-54-5 |
Rolipram is a potent and selective type IV-specific phosphodiesterase inhibitor.... |
| Rolipram |
61413-54-5 |
Rolipram is a potent and selective type IV-specific phosphodiesterase inhibitor.... |
| Rolipram |
61413-54-5 |
Rolipram is a potent and selective type IV-specific phosphodiesterase inhibitor.... |
| S3I-201 |
501919-59-1 |
S3I-201 is a chemical probe inhibitor of signal transducer and activator of transcription 3 (STAT3), which effectively inhibits HCC cell growth.... |
| S3I-201 |
501919-59-1 |
S3I-201 is a chemical probe inhibitor of signal transducer and activator of transcription 3 (STAT3), which effectively inhibits HCC cell growth.... |
| S3I-201 |
501919-59-1 |
S3I-201 is a chemical probe inhibitor of signal transducer and activator of transcription 3 (STAT3), which effectively inhibits HCC cell growth.... |
| SB743921 |
940929-33-9 |
SB743921 is a second generation kinesin spindle protein (KSP) inhibitor.... |
| SB743921 |
940929-33-9 |
SB743921 is a second generation kinesin spindle protein (KSP) inhibitor.... |
| SB743921 |
940929-33-9 |
SB743921 is a second generation kinesin spindle protein (KSP) inhibitor.... |
| SB743921 |
940929-33-9 |
SB743921 is a second generation kinesin spindle protein (KSP) inhibitor.... |
| SB743921 |
940929-33-9 |
SB743921 is a second generation kinesin spindle protein (KSP) inhibitor.... |
| SB743921 |
940929-33-9 |
SB743921 is a second generation kinesin spindle protein (KSP) inhibitor.... |
| SC-514 |
354812-17-2 |
SC-514 is an IΚB kinase-β (IKK-β) inhibitor.... |
| SC-514 |
354812-17-2 |
SC-514 is an IΚB kinase-β (IKK-β) inhibitor.... |
| SCH772984 |
942183-80-4 |
SCH772984 is an extracellular signal-regulated kinase 1/2 (ERK1/2) inhibitor.... |
| Sildenafil citrate |
171599-83-0 |
Sildenafil citrate is a citrate salt form of sildenafil.... |
| Sildenafil citrate |
171599-83-0 |
Sildenafil citrate is a citrate salt form of sildenafil.... |
| Sildenafil citrate |
171599-83-0 |
Sildenafil citrate is a citrate salt form of sildenafil.... |
| SNS-032 |
345627-80-7 |
SNS-032 is a potent and selective cyclin-dependent kinase (CDK) inhibitor of CDK1, CDK2, CDK4, CDK7 and CDK9 with IC50 values of 480, 38, 925, 62 and 4 nM, respectively.... |
| SNS-032 |
345627-80-7 |
SNS-032 is a potent and selective cyclin-dependent kinase (CDK) inhibitor of CDK1, CDK2, CDK4, CDK7 and CDK9 with IC50 values of 480, 38, 925, 62 and 4 nM, respectively.... |
| SNS-032 |
345627-80-7 |
SNS-032 is a potent and selective cyclin-dependent kinase (CDK) inhibitor of CDK1, CDK2, CDK4, CDK7 and CDK9 with IC50 values of 480, 38, 925, 62 and 4 nM, respectively.... |
| SNS-032 |
345627-80-7 |
SNS-032 is a potent and selective cyclin-dependent kinase (CDK) inhibitor of CDK1, CDK2, CDK4, CDK7 and CDK9 with IC50 values of 480, 38, 925, 62 and 4 nM, respectively.... |
| SNX2112 |
908112-43-6 |
.... |
| Sulindac |
38194-50-2 |
Sulindac is a non-steroidal anti-inflammatory drug of the arylalkanoic acid class.... |
| Tadalafil |
171596-29-5 |
Tadalafil is a selective phosphodiesterase-5 (PDE-5) inhibitor.... |
| Tadalafil |
171596-29-5 |
Tadalafil is a selective phosphodiesterase-5 (PDE-5) inhibitor.... |
| Tadalafil |
171596-29-5 |
Tadalafil is a selective phosphodiesterase-5 (PDE-5) inhibitor.... |
| TAK-960 |
1137868-52-0 |
TAK-960 is a novel, potent and selective Polo-like kinase 1 (PLK1) inhibitor.... |
| Sildenafil citrate |
171599-83-0 |
Sildenafil citrate is a citrate salt form of sildenafil.... |
| Sildenafil citrate |
171599-83-0 |
Sildenafil citrate is a citrate salt form of sildenafil.... |
| Sildenafil citrate |
171599-83-0 |
Sildenafil citrate is a citrate salt form of sildenafil.... |
| SNS-032 |
345627-80-7 |
SNS-032 is a potent and selective cyclin-dependent kinase (CDK) inhibitor of CDK1, CDK2, CDK4, CDK7 and CDK9 with IC50 values of 480, 38, 925, 62 and 4 nM, respectively.... |
| SNS-032 |
345627-80-7 |
SNS-032 is a potent and selective cyclin-dependent kinase (CDK) inhibitor of CDK1, CDK2, CDK4, CDK7 and CDK9 with IC50 values of 480, 38, 925, 62 and 4 nM, respectively.... |
| SNS-032 |
345627-80-7 |
SNS-032 is a potent and selective cyclin-dependent kinase (CDK) inhibitor of CDK1, CDK2, CDK4, CDK7 and CDK9 with IC50 values of 480, 38, 925, 62 and 4 nM, respectively.... |
| SNS-032 |
345627-80-7 |
SNS-032 is a potent and selective cyclin-dependent kinase (CDK) inhibitor of CDK1, CDK2, CDK4, CDK7 and CDK9 with IC50 values of 480, 38, 925, 62 and 4 nM, respectively.... |
| SNX2112 |
908112-43-6 |
.... |
| Sulindac |
38194-50-2 |
Sulindac is a non-steroidal anti-inflammatory drug of the arylalkanoic acid class.... |
| Tadalafil |
171596-29-5 |
Tadalafil is a selective phosphodiesterase-5 (PDE-5) inhibitor.... |
| Tadalafil |
171596-29-5 |
Tadalafil is a selective phosphodiesterase-5 (PDE-5) inhibitor.... |
| Tadalafil |
171596-29-5 |
Tadalafil is a selective phosphodiesterase-5 (PDE-5) inhibitor.... |
| TAK-960 |
1137868-52-0 |
TAK-960 is a novel, potent and selective Polo-like kinase 1 (PLK1) inhibitor.... |
| TAK-960 |
1137868-52-0 |
TAK-960 is a novel, potent and selective Polo-like kinase 1 (PLK1) inhibitor.... |
| TAK901 |
934541-31-8 |
.... |
| TAK901 |
934541-31-8 |
.... |
| TAK901 |
934541-31-8 |
.... |
| TAK901 |
934541-31-8 |
.... |
| TG 100801 |
867331-82-6 |
TG 100801 is a VEGFR2 targeting prodrug currently in a clinical trial.... |
| TL-32711 |
1260251-31-7 |
TL32711 is a mimic of Smac, natural inhibitor of IAPs.... |
| TL-32711 |
1260251-31-7 |
TL32711 is a mimic of Smac, natural inhibitor of IAPs.... |
| Topotecan |
119413-54-6 |
Topotecan is a topoisomerase I inhibitor.... |
| Topotecan |
119413-54-6 |
Topotecan is a topoisomerase I inhibitor.... |
| Topotecan Hydrochloride |
119413-54-6 |
.... |
| Topotecan Hydrochloride |
119413-54-6 |
.... |
| TRC102 |
593-56-6 |
TRC102 is a small molecule inhibitor of base-excision repair (BER).... |
| Tropisetron |
89565-68-4 |
.... |
| Tropisetron |
89565-68-4 |
.... |
| VE-822 |
1232416-25-9 |
VE-822 is a highly selective and potent derivative of ATR inhibitor.... |
| VE-822 |
1232416-25-9 |
VE-822 is a highly selective and potent derivative of ATR inhibitor.... |
| VE-822 |
1232416-25-9 |
VE-822 is a highly selective and potent derivative of ATR inhibitor.... |
| VE-822 |
1232416-25-9 |
VE-822 is a highly selective and potent derivative of ATR inhibitor.... |
| VE-822 |
1232416-25-9 |
VE-822 is a highly selective and potent derivative of ATR inhibitor.... |
| Vioxx |
162011-90-7 |
Vioxx is a highly selective inhibitor of cyclooxygenase-2 (COX-2).... |
| Voreloxin |
1174207-12-5 |
Voreloxin is a first-in-class topoisomerase II inhibitor.... |
| VP-16 |
33419-42-0 |
Etoposide is known as an inhibitor of the enzyme topoisomerase II that controls and alters the topologic states of DNA during transcription.... |
| VP-16 |
33419-42-0 |
Etoposide is known as an inhibitor of the enzyme topoisomerase II that controls and alters the topologic states of DNA during transcription.... |
| WAY100635 |
146714-97-8 |
.... |
| WP1130 |
856243-80-6 |
.... |
| WP1130 |
856243-80-6 |
.... |
| WP1130 |
856243-80-6 |
.... |
| Y-27632 |
146986-50-7 |
Y-27632 is a potent, highly specific, cell-permeable inhibitor of Rho kinase (ROCK) with Ki of 140 nM.... |
| Y-27632 |
146986-50-7 |
Y-27632 is a potent, highly specific, cell-permeable inhibitor of Rho kinase (ROCK) with Ki of 140 nM.... |
| Y-27632 |
146986-50-7 |
Y-27632 is a potent, highly specific, cell-permeable inhibitor of Rho kinase (ROCK) with Ki of 140 nM.... |
| Y-27632 |
146986-50-7 |
Y-27632 is a potent, highly specific, cell-permeable inhibitor of Rho kinase (ROCK) with Ki of 140 nM.... |
| Y27632 2HCl |
129830-38-2 |
.... |
| Y27632 2HCl |
129830-38-2 |
.... |
| Y27632 2HCl |
129830-38-2 |
.... |
| Y27632 2HCl |
129830-38-2 |
.... |
| （+）-JQ1 |
1268524-71-5 |
.... |
| （+）-JQ1 |
1268524-71-5 |
.... |
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