What is the 5a-Androstanedione?

5a-Androstanedione is , while it's Molecular Formula is C19H28O2. 5a-Androstanedione is a metabolite of Androstendione (A637550). 5a-Androstanedione is an important intermediate in the conversion of Androstenedione to Androstanolone (A637540).

What is the CAS number for 5a-Androstanedione?

The CAS number of 5a-Androstanedione is 846-46-8.

What is 5a-Androstanedione (846-46-8) used for?

5a-Androstanedione, also known as 5a-AD, is a steroidal ketone and a key metabolite in the biosynthesis of androgens. It plays a crucial role in the conversion of Androstenedione to Androstanolone, which are essential for various physiological functions in the human body.InChI:InChI=1/C19H28O2/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/h12,14-16H,3-11H2,1-2H3/t12-,14?,15?,16?,18?,19?/m0/s1

What is the 5a-Androstanedione?

5a-Androstanedione is , while it's Molecular Formula is C19H28O2. 5α-Androstanedione is a metabolite of Androstendione (A637550). 5α-Androstanedione is an important intermediate in the conversion of Androstenedione to Androstanolone (A637540).

What is the CAS number for 5a-Androstanedione?

The CAS number of 5a-Androstanedione is 846-46-8.

What is 5a-Androstanedione (846-46-8) used for?

5α-Androstanedione, also known as 5α-AD, is a steroidal ketone and a key metabolite in the biosynthesis of androgens. It plays a crucial role in the conversion of Androstenedione to Androstanolone, which are essential for various physiological functions in the human body.InChI:InChI=1/C19H28O2/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/h12,14-16H,3-11H2,1-2H3/t12-,14?,15?,16?,18?,19?/m0/s1

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5a-Androstanedione

Product Name 5a-Androstanedione
cas 846-46-8
purity 99%

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Molecular Formula: C19H28O2
Molecular Weight: 288.43
Vapor Pressure: 5.68E-07mmHg at 25°C
Melting Point: 142°C
Refractive Index: 1.526
Boiling Point: 411.2 °C at 760 mmHg
Flash Point: 153.9 °C
PSA： 34.14000
Density: 1.079 g/cm³
LogP: 4.16730

5a-Androstanedione(Cas 846-46-8) Usage

Definition

ChEBI: The 5alpha-stereoisomer of androstane-3,17-dione.

InChI:InChI=1/C19H28O2/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/h12,14-16H,3-11H2,1-2H3/t12-,14?,15?,16?,18?,19?/m0/s1

846-46-8 Relevant articles

Thermodynamic analysis of remote substrate binding energy in 3α-hydroxysteroid dehydrogenase/carbonyl reductase catalysis

Hwang, Chi-Ching,Chang, Pei-Ru,Hsieh, Chia-Lin,Chou, Yun-Hao,Wang, Tzu-Pin

, p. 183 - 189 (2019)

The binding energy of enzyme and substra...

Kinetic analysis of androstenedione 5α-reductase in epithelium and stroma of human prostate

Weisser, Heike,Krieg, Michael

, p. 589 - 594 (1997)

In the human prostate, various androgen-...

-

Marker,Lawson

, p. 2928,2930 (1938)

Preparation method 5α- androstane -3,17- diketone (by machine translation)

-

, (2020/03/17)

The preparation method 5α - of, androsta...

Unified Total Synthesis of Five Bufadienolides

Hagiwara, Koichi,Inoue, Masayuki,Itoh, Hiroaki,Shimizu, Shinsuke

supporting information, (2020/11/13)

We report a unified total synthesis of f...

A sodium trifluoromethanesulfinate-mediated photocatalytic strategy for aerobic oxidation of alcohols

Zhu, Xianjin,Liu, Can,Liu, Yong,Yang, Haijun,Fu, Hua

, p. 12443 - 12446 (2020/10/30)

A sodium trifluoromethanesulfinate-media...

Photochemical Transformations with Iodine Azide after Release from an Ion-Exchange Resin

Dr?ger, Gerald,K?sel, Teresa,Kirschning, Andreas,Schulz, G?ran

supporting information, p. 12376 - 12380 (2020/05/08)

This report discloses the photochemical ...

846-46-8 Process route

: 53-43-0
dehydroepiandrosterone

: 521-17-5,1963-03-7,4593-57-1,4593-58-2,14504-94-0,16895-59-3,47122-33-8,64162-67-0,75767-22-5,139973-51-6,151284-19-4
5-androstenediol

: 846-46-8
androstanedione

: 2487-48-1,7522-54-5,62357-03-3,53-00-9
3β,7α-dihydroxyandrost-5-ene-17-one

: 20120-08-5
3β-hydroxyandrostan-17-one

: 39663-17-7
3β,11α-dihydroxyandrost-5-en-17-one

Conditions

Conditions	Yield
With Azadirachta indica A_. Juss_. cell suspension culture; at 25 ℃; for 120h; Enzymatic reaction;	7.23% 8.67% 7.9% 2.4% 3.2%

: 521-18-6
Stanolone

: 481-29-8
Epiandrosterone

: 53-41-8
cis-androsterone

: 846-46-8
androstanedione

: 571-20-0
5-androgen-3,17-diol

Conditions

Conditions	Yield
for 504h; Rhodotorula mucilaginosa;	5% 33% 33% 21%

846-46-8 Upstream products

571-20-0
(3S,5S,10S,13S)-10,13-Dimethyl-hexadecahydro-cyclopenta[a]phenanthrene-3,17-diol
53-41-8
epiandrosterone
53-41-8
androsterone
63-05-8
4-androstene-3,17-dione