| Aminoglutethimide |
125-84-8 |
Aminoglutethimide is an aromatase inhibitor with an IC50 of 20 µM.... |
| Anastrozole |
120511-73-1 |
Anastrozole is a potent and selective aromatase inhibitor with an IC50 value of 15 nM.... |
| Anastrozole |
120511-73-1 |
Anastrozole is a potent and selective aromatase inhibitor with an IC50 value of 15 nM.... |
| Anastrozole |
120511-73-1 |
Anastrozole is a potent and selective aromatase inhibitor with an IC50 value of 15 nM.... |
| Andarine (GTX-007) |
401900-40-1 |
Andarine is a selective non-steroidal androgen receptor modulator (SARM) with a Ki of 4 nM.... |
| AZD1981 |
802904-66-1 |
.... |
| Bicalutamide |
90357-06-5 |
Bicalutamide is a pure androgen receptor (AR) antagonist used in the treatment of prostate cancer and hirsutism.... |
| Bicalutamide |
90357-06-5 |
Bicalutamide is a pure androgen receptor (AR) antagonist used in the treatment of prostate cancer and hirsutism.... |
| Bicalutamide |
90357-06-5 |
Bicalutamide is a pure androgen receptor (AR) antagonist used in the treatment of prostate cancer and hirsutism.... |
| BX471 |
217645-70-0 |
BX471 is a potent nonpeptide CC chemokine receptor-1 (CCR1) antagonist.... |
| BX471 |
217645-70-0 |
BX471 is a potent nonpeptide CC chemokine receptor-1 (CCR1) antagonist.... |
| Candesartan |
139481-59-7 |
.... |
| Candesartan |
139481-59-7 |
.... |
| Clomifene citrate |
50-41-9 |
.... |
| Ctep |
871362-31-1 |
.... |
| Ctep |
871362-31-1 |
.... |
| Ctep |
871362-31-1 |
.... |
| Eplerenone |
107724-20-9 |
Eplerenone is a selective aldosterone receptor blocker.... |
| Eplerenone |
107724-20-9 |
Eplerenone is a selective aldosterone receptor blocker.... |
| Exemestane |
107868-30-4 |
.... |
| Exemestane |
107868-30-4 |
.... |
| Exemestane |
107868-30-4 |
.... |
| Exemestane |
107868-30-4 |
.... |
| GSK2578215A |
1285515-21-0 |
GSK2578215A is a potent and highly selective leucine-rich repeat kinase 2 (LRRK2) inhibitor.... |
| GSK2578215A |
1285515-21-0 |
GSK2578215A is a potent and highly selective leucine-rich repeat kinase 2 (LRRK2) inhibitor.... |
| GW9508 |
885101-89-3 |
GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner [1].... |
| GW9508 |
885101-89-3 |
GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner [1].... |
| H2L5186303 |
139262-76-3 |
H2L5186303 is a potent nonselective lysophosphatidic acid 2 (LPA2) and LPA3 antagonist.... |
| H2L5186303 |
139262-76-3 |
H2L5186303 is a potent nonselective lysophosphatidic acid 2 (LPA2) and LPA3 antagonist.... |
| ICI 182,780 |
129453-61-8 |
.... |
| ICI 182,780 |
129453-61-8 |
.... |
| ICI 182,780 |
129453-61-8 |
.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| Letrozole |
112809-51-5 |
Letrozole is a third generation potent and selective aromatase inhibitor.... |
| MDV3100 |
915087-33-1 |
MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM.... |
| MDV3100 |
915087-33-1 |
MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM.... |
| Exemestane |
107868-30-4 |
.... |
| Exemestane |
107868-30-4 |
.... |
| Exemestane |
107868-30-4 |
.... |
| GSK2578215A |
1285515-21-0 |
GSK2578215A is a potent and highly selective leucine-rich repeat kinase 2 (LRRK2) inhibitor.... |
| GSK2578215A |
1285515-21-0 |
GSK2578215A is a potent and highly selective leucine-rich repeat kinase 2 (LRRK2) inhibitor.... |
| GW9508 |
885101-89-3 |
GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner [1].... |
| GW9508 |
885101-89-3 |
GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner [1].... |
| H2L5186303 |
139262-76-3 |
H2L5186303 is a potent nonselective lysophosphatidic acid 2 (LPA2) and LPA3 antagonist.... |
| H2L5186303 |
139262-76-3 |
H2L5186303 is a potent nonselective lysophosphatidic acid 2 (LPA2) and LPA3 antagonist.... |
| ICI 182,780 |
129453-61-8 |
.... |
| ICI 182,780 |
129453-61-8 |
.... |
| ICI 182,780 |
129453-61-8 |
.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| JNJ-26481585 |
875320-29-9 |
JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor.... |
| Letrozole |
112809-51-5 |
Letrozole is a third generation potent and selective aromatase inhibitor.... |
| MDV3100 |
915087-33-1 |
MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM.... |
| MDV3100 |
915087-33-1 |
MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM.... |
| MDV3100 |
915087-33-1 |
MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM.... |
| Mifepristone |
84371-65-3 |
Mifepristone is a selective antagonist at progesterone (PR) and glucocorticoid (GR) receptors with IC50 values of 307 and 100 nM, respectively.... |
| NS6180 |
353262-04-1 |
NS6180 is a novel class of KCa3.1 channel inhibitors.... |
| NS6180 |
353262-04-1 |
NS6180 is a novel class of KCa3.1 channel inhibitors.... |
| Ostarine |
841205-47-8 |
Ostarine is a selective androgen receptor modulator (SARM) with Ki of 3.8 nM.... |
| Ostarine |
841205-47-8 |
Ostarine is a selective androgen receptor modulator (SARM) with Ki of 3.8 nM.... |
| Ostarine |
841205-47-8 |
Ostarine is a selective androgen receptor modulator (SARM) with Ki of 3.8 nM.... |
| Ostarine |
841205-47-8 |
Ostarine is a selective androgen receptor modulator (SARM) with Ki of 3.8 nM.... |
| PD 123319 ditrifluoroacetate |
130663-39-7 |
.... |
| Raloxifene HCl |
82640-04-8 |
Raloxifene HCl is a hydrochloride salt form of raloxifene which is an oral selective estrogen receptor modulator.... |
| Raloxifene HCl |
82640-04-8 |
Raloxifene HCl is a hydrochloride salt form of raloxifene which is an oral selective estrogen receptor modulator.... |
| SCH 563705 |
473728-58-4 |
SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively.... |
| SCH 563705 |
473728-58-4 |
SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively.... |
| SCH 563705 |
473728-58-4 |
SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively.... |
| SCH 563705 |
473728-58-4 |
SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively.... |
| SYN-115 |
870070-55-6 |
SYN-115 is a selective and potent adenosine A(2A) receptor antagonist.... |
| SYN-115 |
870070-55-6 |
SYN-115 is a selective and potent adenosine A(2A) receptor antagonist.... |
| SYN-115 |
870070-55-6 |
SYN-115 is a selective and potent adenosine A(2A) receptor antagonist.... |
| SYN-115 |
870070-55-6 |
SYN-115 is a selective and potent adenosine A(2A) receptor antagonist.... |
| TAK438 |
1260141-27-2 |
.... |
| Taltirelin |
103300-74-9 |
Taltirelin is a thyrotropin-releasing hormone (TRH) analog.... |
| Taltirelin |
103300-74-9 |
Taltirelin is a thyrotropin-releasing hormone (TRH) analog.... |
| Tamoxifen |
54965-24-1 |
Tamoxifen is a tissue-selective estrogen receptor modulator (SERM).... |
| Toremifene Citrate |
89778-27-8 |
Toremifene Citrate is an estrogen agonist/antagonist indicated for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors [1].... |
| Torin 1 |
1222998-36-8 |
.... |
| Torin 1 |
1222998-36-8 |
.... |
| Trilostane |
13647-35-3 |
Trilostane is an inhibitor of 3 β-hydroxysteroid dehydrogenase with an IC50 value of 1 µM.... |
| Trilostane |
13647-35-3 |
Trilostane is an inhibitor of 3 β-hydroxysteroid dehydrogenase with an IC50 value of 1 µM.... |
| Trilostane |
13647-35-3 |
Trilostane is an inhibitor of 3 β-hydroxysteroid dehydrogenase with an IC50 value of 1 µM.... |
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