U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C29H38ClFO8
Molecular Weight 569.059
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FORMOCORTAL

SMILES

CC(=O)OCC(=O)[C@@]12OC(C)(C)O[C@@H]1C[C@H]3[C@@H]4CC(C=O)=C5C=C(CC[C@]5(C)[C@@]4(F)[C@@H](O)C[C@]23C)OCCCl

InChI

InChIKey=QNXUUBBKHBYRFW-QWAPGEGQSA-N
InChI=1S/C29H38ClFO8/c1-16(33)37-15-23(35)29-24(38-25(2,3)39-29)12-20-21-10-17(14-32)19-11-18(36-9-8-30)6-7-26(19,4)28(21,31)22(34)13-27(20,29)5/h11,14,20-22,24,34H,6-10,12-13,15H2,1-5H3/t20-,21-,22-,24+,26-,27-,28-,29+/m0/s1

HIDE SMILES / InChI
FORMOCORTAL is a corticosteroid used in ophthalmology and in dermatology.

Approval Year

PubMed

PubMed

TitleDatePubMed
Evaluation of spontaneous contamination of ocular medications.
2001-06-16
Name Type Language
DEFLAMENE
Preferred Name English
FORMOCORTAL
INN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
formocortal [INN]
Common Name English
FORMOCORTAL [MI]
Common Name English
PREGNA-3,5-DIENE-6-CARBOXALDEHYDE, 21-(ACETYLOXY)-3-(2-CHLOROETHOXY)-9-FLUORO-11-HYDROXY-16,17-((1-METHYLETHYLIDENE)BIS(OXY))-20-OXO-, (11.BETA.,16.ALPHA.)-
Common Name English
NSC-150527
Code English
3-(2-Chloroethoxy)-9-fluoro-11?,16?,17,21-tetrahydroxy-20-oxo-pregna-3,5-diene-6-carboxaldehyde, cyclic 16,17-acetal with acetone, 21-acetate
Common Name English
FORMOCORTAL [USAN]
Common Name English
Formocortal [WHO-DD]
Common Name English
FORMOCORTAL [MART.]
Common Name English
FLUDERMA
Brand Name English
Classification Tree Code System Code
WHO-VATC QS01BA12
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
WHO-ATC S01BA12
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL1989587
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
MERCK INDEX
m1174
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY Merck Index
PUBCHEM
289085
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
NCI_THESAURUS
C175064
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
NSC
150527
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
SMS_ID
100000080435
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
FDA UNII
8E21R0Z4M5
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
DRUG CENTRAL
3245
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
WIKIPEDIA
FORMOCORTAL
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
ECHA (EC/EINECS)
220-584-2
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
EVMPD
SUB07787MIG
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
CAS
2825-60-7
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID00895059
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
INN
2289
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY
DRUG BANK
DB13664
Created by admin on Mon Mar 31 17:54:42 GMT 2025 , Edited by admin on Mon Mar 31 17:54:42 GMT 2025
PRIMARY