grade
purum
assay
≥98.0% (HPLC)
optical activity
[α]20/D +189±2°, c = 1% in ethanol
drug control
USDEA Schedule IIIN; regulated under CDSA - not available from Sigma-Aldrich Canada
mp
170-173 °C
SMILES string
[H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)C(=O)CC[C@@]24[H]
InChI
1S/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-16H,3-10H2,1-2H3/t14-,15-,16-,18-,19-/m0/s1
InChI key
AEMFNILZOJDQLW-QAGGRKNESA-N
Biochem/physiol Actions
睾酮前体和具有雄激素活性的代谢物。
睾酮前体和具有雄激素活性的代谢物;可增大前列腺癌或胰腺癌的风险。
Other Notes
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法规信息
新产品
此项目有
Margarida M D S Cepa et al.
Journal of medicinal chemistry, 48(20), 6379-6385 (2005-09-30)
Inhibition of aromatase is an efficient approach for the prevention and treatment of breast cancer. New A,D-ring modified steroid analogues of formestane and testolactone were designed and synthesized and their biochemical activity was investigated in vitro in an attempt to
Béatrice Tchédam Ngatcha et al.
Journal of medicinal chemistry, 48(16), 5257-5268 (2005-08-05)
Type 3 17beta-hydroxysteroid dehydrogenase (17beta-HSD) is involved in the biosynthesis of androgen testosterone. To produce potent inhibitors of this key steroidogenic enzyme, we prepared a series of androsterone (ADT) derivatives by adding a variety of substituents at position 3. The
Patrick Bydal et al.
European journal of medicinal chemistry, 44(2), 632-644 (2008-05-13)
Androgens are well known to play a predominant role in prostate cancer and other androgen-dependent diseases. To decrease the level of androgen testosterone in the prostate, we are interested in developing inhibitors of 17beta-hydroxysteroid dehydrogenase type 5 (17beta-HSD5). This enzyme
Artem Cherkasov et al.
Journal of medicinal chemistry, 51(7), 2047-2056 (2008-03-12)
A benchmark data set of steroids with known affinity for sex hormone-binding globulin (SHBG) has been widely used to validate popular molecular field-based QSAR techniques. We have expanded the data set by adding a number of nonsteroidal SHBG ligands identified
Gustav Ahlin et al.
Journal of medicinal chemistry, 51(19), 5932-5942 (2008-09-16)
The liver-specific organic cation transport protein (OCT1; SLC22A1) transports several cationic drugs including the antidiabetic drug metformin and the anticancer agents oxaliplatin and imatinib. In this study, we explored the chemical space of registered oral drugs with the aim of
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 278785-50G | 04061837837005 |
| 278785-10G | 04061837836992 |
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