69381-94-8 Usage
Description
Fenprostalene is a synthetic analog of Prostaglandin F2α, which is structurally related to Prostalene. It is known for its luteolytic properties, making it a significant compound in certain medical and veterinary applications.
Uses
Used in Veterinary Medicine:
Fenprostalene is used as a luteolytic agent for the synchronization of estrus in animals, particularly in the veterinary industry. It helps in the regulation of the estrous cycle, which is crucial for breeding management and overall reproductive health in animals.
Used in Pharmaceutical Applications:
Fenprostalene is also used as a pharmaceutical agent for its Prostaglandin F2α-like properties. It can be employed in the development of medications targeting various health conditions that benefit from the modulation of prostaglandin levels.
Brand Name:
One of the brand names for fenprostalene is Synchrocept B, which is specifically used in the veterinary industry for estrus synchronization.
Check Digit Verification of cas no
The CAS Registry Mumber 69381-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,8 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69381-94:
(7*6)+(6*9)+(5*3)+(4*8)+(3*1)+(2*9)+(1*4)=168
168 % 10 = 8
So 69381-94-8 is a valid CAS Registry Number.
InChI:InChI=1/C23H30O6/c1-28-23(27)12-8-3-2-7-11-19-20(22(26)15-21(19)25)14-13-17(24)16-29-18-9-5-4-6-10-18/h3-7,9-10,13-14,17,19-22,24-26H,8,11-12,15-16H2,1H3/b14-13+/t2?,17-,19-,20?,21+,22-/m1/s1
69381-94-8Relevant articles and documents
16-Phenoxy and 16-substituted phenoxy-prostatrienoic acid derivatives
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, (2008/06/13)
Novel racemic and 8R-antimeric 16-phenoxy- and 16-(o, m or p)-substituted phenoxy derivatives of 9α, 11α,15-trihydroxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acids, which may be further substituted at C-15 by a methyl or ethyl group, the pharmaceutically acceptable, non-toxic lower alkyl esters and salts thereof and processes for the production of such compounds. dl 9α,11α,15α-trihydroxy-16-m-trifluoromethylphenoxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acid and dl 9α,11α,15 -trihydroxy-15 -methyl-16-m-trifluoromethylphenoxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acid are representative compounds of the class. These compounds possess prostaglandin-like activities and thus are useful in the treatment of mammals where prostaglandins are indicated. They are particularly useful as luteolytic agents in female mammals.