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(11alpha,15alpha)-11,15-dihydroxypregn-4-ene-3,20-dione is a steroid hormone and a derivative of progesterone. It is a natural hormone produced in the body and plays a crucial role in the menstrual cycle and maintaining pregnancy. Its molecular structure consists of a steroid backbone with hydroxyl groups at the 11th and 15th positions and a keto group at the 3rd position.

640-33-5

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640-33-5 Usage

Uses

Used in Medical Applications:
(11alpha,15alpha)-11,15-dihydroxypregn-4-ene-3,20-dione is used as a medication for preventing miscarriage and treating certain hormone-related conditions such as endometriosis and certain types of cancer. It helps regulate hormone levels and supports the normal functioning of the reproductive system.
Used in Pharmaceutical Industry:
(11alpha,15alpha)-11,15-dihydroxypregn-4-ene-3,20-dione is used as an intermediate in the synthesis of other steroid hormones. It plays a key role in the production of various medications used to treat hormonal imbalances and other related conditions.
Used in Research and Laboratory Settings:
(11alpha,15alpha)-11,15-dihydroxypregn-4-ene-3,20-dione is used as a research compound to study hormone function and regulation. It helps scientists understand the complex mechanisms of hormone action and develop new treatments for hormone-related disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 640-33-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 640-33:
(5*6)+(4*4)+(3*0)+(2*3)+(1*3)=55
55 % 10 = 5
So 640-33-5 is a valid CAS Registry Number.

640-33-5SDS

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 11a,15a-Dihydroxyprogesterone

1.2 Other means of identification

Product number -
Other names -

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:640-33-5 SDS

640-33-5Downstream Products

640-33-5Relevant academic research and scientific papers

Microbial hydroxylation of hydroxyprogesterones and α-glucosidase inhibition activity of their metabolites

Choudhary, Muhammad Iqbal,Nasir, Muhammad,Khan, Shamsun N.,Atif, Muhammad,Ali, Rahat A.,Khalil, Syed M.,Atta-ur-Rahman

, p. 593 - 599 (2007/10/03)

Microbial transformation of 11α-hydroxyprogesterone (1) with Cunninghamella elegans, Gibberella fujikuroi, Fusarium lini, and Candida albicans yielded 11α,15α,16α-trihydroxypregn-4-ene-3,20-dione (3), 11α-hydroxy-5α-pregnane-3,20-dione (4), 6β,11α- dihydroxypregn-4-ene-3,20-dione(5), 11α-hydroxypregna-1,4-diene-3,20-dione (6), 11α,17β-dihydroxyandrost-4-en-3-one (7), and 11α,15α-dihydroxypregn-4-ene-3,20-dione (8). On the other hand, microbial transformation of 17α-hydroxyprogesterone (2) with Cunninghamella elegans and Fusarium Uni yielded 11α,17α- dihydroxypregn-4-ene-3,20-dione (9), and 17α-hydroxypregna-1,4-diene-3,20- dione (10). The structures of the metabolites 3-10 were deduced on the basis of spectroscopic methods. Compound 3 was identified as a new metabolite, which exhibited a promising inhibitory activity against the α-glucosidase enzyme.

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