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Key Documents

A7755

Sigma-Aldrich

5α-Androstane-3α,17β-diol

Sinonimo/i:

3α,17β-Dihydroxy-5α-androstane, Dihydroandrosterone

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About This Item

Formula empirica (notazione di Hill):
C19H32O2
Numero CAS:
Peso molecolare:
292.46
Numero CE:
Numero MDL:
Codice UNSPSC:
51111800
ID PubChem:
NACRES:
NA.77

Saggio

≥98% (TLC)

Livello qualitativo

Forma fisica

powder

Controllo stupefacenti

USDEA Schedule III; Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada

tecniche

toxicology assay: suitable

Solubilità

methanol: 19.60-20.40 mg/mL, clear, colorless

Temperatura di conservazione

room temp

Stringa SMILE

[H][C@@]12CC[C@@]3([H])[C@]4([H])CC[C@H](O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@@H](O)C2

InChI

1S/C19H32O2/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/h12-17,20-21H,3-11H2,1-2H3/t12-,13+,14-,15-,16-,17-,18-,19-/m0/s1
CBMYJHIOYJEBSB-KHOSGYARSA-N

Informazioni sul gene

rat ... Ar(24208)

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Applicazioni

5α-Androstane-3α,17β-diol (dihydroandrosterone) is a testosterone metabolite. Dihyroandrosterone inhibited the cell growth of seven cancer cell lines while showing weak toxicity on normal cell lines.

Azioni biochim/fisiol

Dihydroandrosterone is a testosterone metabolite; affects sperm maturation and survival.

Pittogrammi

Health hazard

Avvertenze

Danger

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Carc. 2 - Repr. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


Certificati d'analisi (COA)

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Wei Liu et al.
Journal of chromatography. A, 1233, 1-7 (2012-03-06)
In this paper, a convenient and self-assembled hollow fiber solvent-stir bar microextraction (HF-SSBME) device was developed, which could stir by itself. In the extraction process, the proposed device made the solvent "bar" not floating at the sample solution and exposing
Hajer Jegham et al.
Anti-cancer drugs, 23(8), 803-814 (2012-03-01)
This study investigated the antineoplasic potential of a new family of aminosteroids. The antiproliferative activity of seven 5α-androstane-3α,17β-diol derivatives selected from a screening study was measured on nine cancerous cell lines (HL-60, K-562, LNCaP, PC-3, Shionogi, MCF-7, MDA-MB-231, BT-20, and
J P Deslypere et al.
The Journal of clinical endocrinology and metabolism, 53(2), 430-434 (1981-08-01)
Testosterone, 5 alpha-androstane-17 beta-ol-3-one (DHT) and 5 alpha-androstane-3 alpha,17 beta-diol (Adiol) concentrations were measured in postmortem tissues (pubic skin, scrotal skin, thigh skin, and striated muscle) from 24 males, aged 20-82 yr. Androgen concentrations were highest in scrotal skin, followed
Cheryl A Frye
Pharmacology, biochemistry, and behavior, 86(2), 354-367 (2006-11-23)
The abuse of anabolic-androgenic steroids (AS) is a growing problem; however, the effects and mechanisms underlying their addictive effects are not well understood. Research findings regarding androgen abuse in people and hedonic effects of androgens in laboratory rats are reviewed.
D H Garnier et al.
General and comparative endocrinology, 116(2), 281-290 (1999-11-24)
Concentrations of testosterone, progesterone, Delta4-androstenedione, dihydrotestosterone, 11-ketotestosterone, estrone, estradiol-17beta, 5alpha-androstane, 3alpha, 17beta-diol, and 17alpha-hydroxy, 20beta-dihydroprogesterone were determined by radioimmunoassays in the blood plasma and testicular homogenates of Scyliorhinus canicula. Samples were collected almost every month for 27 months. The weights

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