What is the 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid?

3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is , while it's Molecular Formula is C19H29NO3. Used in Medicinal Chemistry and Pharmacology: 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is utilized as a research compound for the development of novel pharmaceutical agents, particularly those aimed at androgen receptors. Its unique structure and potential biological activity make it a promising candidate for the treatment of various medical conditions. Used in Hormonal Imbalance Treatment: In the field of endocrinology, 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is used as a potential therapeutic agent for the treatment of hormonal imbalances. Its interaction with androgen receptors may help regulate hormone levels and alleviate symptoms associated with such imbalances. Used in Oncology Research: 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is employed as a research tool in oncology, with a focus on the development of targeted therapies for certain types of cancer. Its specific binding to androgen receptors may offer new avenues for cancer treatment, particularly for malignancies that are influenced by hormonal regulation. Used in Drug Development: In the pharmaceutical industry, 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid serves as a key component in the design and synthesis of new drugs. Its unique properties and potential therapeutic effects are being investigated to create medications with improved efficacy and safety profiles for various diseases.

What is 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid (103335-55-3) used for?

3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is a synthetic androstane steroid compound derived from the hormone testosterone, featuring a unique structure with a nitrogen atom substitution. This modification endows it with distinct biological activities and pharmacological properties, positioning it as a candidate for the development of innovative pharmaceutical agents targeting androgen receptors.InChI:InChI=1/C19H29NO3/c1-18-9-7-13-11(12(18)4-5-14(18)17(22)23)3-6-15-19(13,2)10-8-16(21)20-15/h11-15H,3-10H2,1-2H3,(H,20,21)(H,22,23)/t11-,12-,13-,14+,15+,18-,19+/m0/s1

What is the 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid?

3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is , while it's Molecular Formula is C19H29NO3. Used in Medicinal Chemistry and Pharmacology: 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is utilized as a research compound for the development of novel pharmaceutical agents, particularly those aimed at androgen receptors. Its unique structure and potential biological activity make it a promising candidate for the treatment of various medical conditions. Used in Hormonal Imbalance Treatment: In the field of endocrinology, 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is used as a potential therapeutic agent for the treatment of hormonal imbalances. Its interaction with androgen receptors may help regulate hormone levels and alleviate symptoms associated with such imbalances. Used in Oncology Research: 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is employed as a research tool in oncology, with a focus on the development of targeted therapies for certain types of cancer. Its specific binding to androgen receptors may offer new avenues for cancer treatment, particularly for malignancies that are influenced by hormonal regulation. Used in Drug Development: In the pharmaceutical industry, 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid serves as a key component in the design and synthesis of new drugs. Its unique properties and potential therapeutic effects are being investigated to create medications with improved efficacy and safety profiles for various diseases.

What is 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid (103335-55-3) used for?

3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is a synthetic androstane steroid compound derived from the hormone testosterone, featuring a unique structure with a nitrogen atom substitution. This modification endows it with distinct biological activities and pharmacological properties, positioning it as a candidate for the development of innovative pharmaceutical agents targeting androgen receptors.InChI:InChI=1/C19H29NO3/c1-18-9-7-13-11(12(18)4-5-14(18)17(22)23)3-6-15-19(13,2)10-8-16(21)20-15/h11-15H,3-10H2,1-2H3,(H,20,21)(H,22,23)/t11-,12-,13-,14+,15+,18-,19+/m0/s1

Product classification

Hormones and steriods major pro

Medroxyprogesterone acetate intermediates

Progesterone intermediate

Cyproterone acetate intermediate

Deflazacort intermediate

Desogestrel intermediate

Finasteride intermediate

Steroid & Hormone Products
Major Products

Rocuronium bromide intermediate

Ubrogepant intermediate

Rimegepant intermediate

Indacaterol intermedaite

Dapagliflozin intermediate

Pharmaceutical Products

Other
Others

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103335-55-3

Q: What is the CAS number for 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid?

The CAS number of 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is 103335-55-3.

Product Name：3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid(M3 acid)
Molecular Formula：C₁₉H₂₉NO₃
Purity：99%
Molecular Weight：319.444

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Product Details;

CasNo： 103335-55-3

Molecular Formula： C₁₉H₂₉NO₃

High quality purity >99% 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid(M3 acid) 103335-55-3 for sale

Molecular Formula:C19H29NO3
Molecular Weight:319.444
Vapor Pressure:0mmHg at 25°C
Melting Point:>308 °C(Solv: acetone (67-64-1))
Refractive Index:1.534
Boiling Point:518.189 °C at 760 mmHg
PKA:4.81±0.60(Predicted)
Flash Point:267.191 °C
PSA：66.40000
Density:1.145 g/cm³
LogP:3.53720

3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid(Cas 103335-55-3) Usage

General Description

3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid is a synthetic chemical compound that belongs to the class of androstane steroids. It is derived from the hormone testosterone and possesses a modified structure with a substituted nitrogen atom. 3-Oxo-4-aza-5-alpha-androstane-17-beta-carboxylic acid has potential applications in the field of medicinal chemistry and pharmacology, particularly in the development of novel pharmaceutical agents targeting androgen receptors. Its specific biological activity and pharmacological properties are the subject of ongoing research and may hold promise for the treatment of various medical conditions, including hormonal imbalances and certain types of cancer. However, further studies are needed to fully elucidate its potential therapeutic effects and safety profile.

InChI:InChI=1/C19H29NO3/c1-18-9-7-13-11(12(18)4-5-14(18)17(22)23)3-6-15-19(13,2)10-8-16(21)20-15/h11-15H,3-10H2,1-2H3,(H,20,21)(H,22,23)/t11-,12-,13-,14+,15+,18-,19+/m0/s1

103335-55-3 Relevant articles

A synthetic 3-carbonyl-4-nitrogen mixed male steroid -17 β derivative method

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Paragraph 0056-0065, (2017/01/26)

The invention discloses a method for syn...

Impurities in finasteride: Identification, synthesis, characterization and control of potential carry-over impurities from reagents used for the process

Mohanty, Sandeep,Kumar, B. Pavan,Karmakar, Arun Chandra

, p. 4375 - 4380 (2014/08/05)

An assessment of the impurity profile of...

PROCESS FOR THE SYNTHESIS OF (5α,17β)-N-[(2,5-BIS(TRIFLUOROMETHYL)-PHENYL]-3-OXO-4-AZA-5-ANDROST-1-ENE-17-CARBOXAMIDE

-

, (2013/03/26)

The synthesis consists of reaction steps...

Process for preparing 3-oxo-4-aza-5-alpha-androstane-17-carboxylic acid

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Page/Page column 4, (2008/06/13)

A process for preparing the compound 3-o...

103335-55-3 Process route

: 103335-54-2
(4aR,4bS,6aS,7S,9aS,9bS)-4a,6a-dimethyl-2-oxo-2,3,4,4a,4b,5,6,6a,7,8,9,9a,9b,10-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid

: 103335-55-3,1430804-94-6
3-oxo-4-aza-5α-androstane-17β-carboxylic acid

Conditions

Conditions	Yield
With formic acid; zinc; In ethylene glycol; at 100 - 120 ℃; for 8h;	81%
With hydrogen; acetic acid; platinum(IV) oxide; at 60 ℃; for 3h; under 2068.6 Torr;	125 g

: 73711-89-4
3,20-dioxo-4-aza-5α-pregnane

: 103335-55-3,1430804-94-6
3-oxo-4-aza-5α-androstane-17β-carboxylic acid

Conditions

Conditions	Yield
3,20-dioxo-4-aza-5α-pregnane; With bromine; sodium hydroxide; In 1,4-dioxane; water; at 5 - 7 ℃; for 3h; With hydrogenchloride; In water; Temperature; Time;	94.5%

103335-55-3 Upstream products

103335-54-2
(4aR,4bS,6aS,7S,9aS,9bS)-4a,6a-dimethyl-2-oxo-2,3,4,4a,4b,5,6,6a,7,8,9,9a,9b,10-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid
20283-95-8
3,20-dioxo-4-aza-pregnan-5-ene
1416955-23-1
C₂₀H₃₁NO₃
73711-89-4
3,20-dioxo-4-aza-5α-pregnane