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7 alpha-thiospironolactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (1R,4R,9aR,11aS)-9a,11a-dimethyl-4-sulfanyl-3,3a,3b,4,5,8,9,9b,10,11-decahydro-2H-spiro[cyclopenta[a]phenanthrene-1,2'-oxolane]-5',7-dione

    Cas No: 38753-76-3

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  • Pregn-4-ene-21-carboxylicacid, 17-hydroxy-7-mercapto-3-oxo-, g-lactone, (7a,17a)-

    Cas No: 38753-76-3

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  • 38753-76-3 Structure
  • Basic information

    1. Product Name: 7 alpha-thiospironolactone
    2. Synonyms: 7 alpha-thiospironolactone;(7R,8R,9S,10R,13S,14S,17R)-10,13-dimethyl-7-sulfanyl-spiro[2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,5-tetrahydrofuran]-2,3-dione
    3. CAS NO:38753-76-3
    4. Molecular Formula: C22H30O3S
    5. Molecular Weight: 374.54
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38753-76-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 561.7°Cat760mmHg
    3. Flash Point: 457.3°C
    4. Appearance: /
    5. Density: 1.22g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: -20°C Freezer, Under Inert Atmosphere
    8. Solubility: Chloroform (Slightly), DMSO (Slightly)
    9. PKA: 10.18±0.60(Predicted)
    10. CAS DataBase Reference: 7 alpha-thiospironolactone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 7 alpha-thiospironolactone(38753-76-3)
    12. EPA Substance Registry System: 7 alpha-thiospironolactone(38753-76-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 38753-76-3(Hazardous Substances Data)

38753-76-3 Usage

Uses

A metabolite of Spironolactone.

Check Digit Verification of cas no

The CAS Registry Mumber 38753-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,5 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38753-76:
(7*3)+(6*8)+(5*7)+(4*5)+(3*3)+(2*7)+(1*6)=153
153 % 10 = 3
So 38753-76-3 is a valid CAS Registry Number.

38753-76-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-oxo-7α-thio-17β-hydroxy-4-androsten-17α-yl)propionic acid γ-lactone

1.2 Other means of identification

Product number -
Other names 3-oxo-17α-pregna-4-ene-7α-(thia)-21,17-carbolactone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38753-76-3 SDS

38753-76-3Upstream product

38753-76-3Relevant articles and documents

Fungal biotransformation of diuretic and antihypertensive drug spironolactone with Gibberella fujikuroi, Curvularia lunata, Fusarium lini, and Aspergillus alliaceus

Al-Aboudi, Amal,Kana'an, Belal Muneeb,Zarga, Musa Abu,Bano, Saira,Atia-tul-Wahab,Javed, Kulsoom,Choudhary, M. Iqbal

, p. 15 - 22 (2017/10/31)

Derivatives of spironolactone (1), a diuretic and antihypertensive drug, were synthesized by using fungal cells for the first time. Ten different fungi were screened for their ability to biotransform 1, four of which were able to produce metabolites 2–8. Gibberella fujikuroi produced canrenone (2), 1-dehydrocanrenone (3), Curvularia lunuta provided compound 2, and 7α-thio-spironolactone (4), Fusarium lini yielded compounds 2, 3, 1β-hydroxycanrenone (5), 1α-hydroxycanrenone (6), 1-dehydro-15α-hydroxycanrenone (7), and 15α-hydroxycanrenone (8), while Aspergillus alliaceus was able to produce all the seven metabolites. Metabolites 5, 6, and 7 were identified as new compounds. Their structures were elucidated by using different spectroscopic techniques. Substrate 1 and its metabolites 2, 3, and 5–8 were also evaluated for α-glucosidase inhibitory activity in vitro. Substrate 1 was found to be strongly active with IC50 = 335 ± 4.3 μM as compared to the standard drug acarbose IC50 = 840 ± 1.73 μM, whereas all of resulting metabolites were found to be inactive.

EX VIVO METHODS FOR PREDICTING AND CONFIRMING IN VIVO METABOLISM OF PHARMACEUTICALLY ACTIVE COMPOUNDS

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Page/Page column 36; 37; 38, (2015/06/25)

Methods and compositions for the catalytic oxidation of pharmaceutically active compounds, and more particularly to ex vivo methods for predicting in vivo metabolism of pharmaceutically active compounds, including predicting in vivo interaction between two or more pharmaceutically active compounds.

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