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

Details

Stereochemistry EPIMERIC
Molecular Formula C31H37NO7
Molecular Weight 535.628
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 8
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of NICOCORTONIDE

SMILES

[H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])[C@@H](O)C[C@]4(C)[C@]5(CC[C@@]24OC(O5)\C=C/C)C(=O)COC(=O)C6=CC=NC=C6

InChI

InChIKey=LZHLAFIPUJPCBN-ZTOAAZPKSA-N
InChI=1S/C31H37NO7/c1-4-5-25-38-30-12-13-31(39-25,24(35)18-37-27(36)19-9-14-32-15-10-19)29(30,3)17-23(34)26-22(30)7-6-20-16-21(33)8-11-28(20,26)2/h4-5,9-10,14-16,22-23,25-26,34H,6-8,11-13,17-18H2,1-3H3/b5-4-/t22-,23+,25?,26-,28+,29+,30-,31+/m1/s1

HIDE SMILES / InChI

Molecular Formula C31H37NO7
Molecular Weight 535.628
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 6 / 8
E/Z Centers 1
Optical Activity UNSPECIFIED

PubMed

PubMed

TitleDatePubMed
Effect of five anti-inflammatory steroids on collagen and glycoaminoglycan synthessis in vitro.
1980 Aug

Sample Use Guides

In Vitro Use Guide
At concentration 10(-9) M nicocortonide inhibited synthesis of hyaluronic acid by 23%. An inhibition of collagen synthesis was obtained with nicocortonide only at the highest studied concentration: 1 x 10(-4) M. The synthesis of sulphated glycosaminoglycans was inhibited (by 30- 35%) at the highest steroid concentration tested (1 x 10(-5) M).
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:28:18 GMT 2023
Edited
by admin
on Fri Dec 15 16:28:18 GMT 2023
Record UNII
341BNG318Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NICOCORTONIDE
INN  
INN  
Official Name English
nicocortonide [INN]
Common Name English
11.BETA.,14,17,21-TETRAHYDROXYPREGN-4-ENE-3,20-DIONE CYCLIC 14,17-ACETAL WITH CROTONALDEHYDE, 21-ISONICOTINATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C521
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
Code System Code Type Description
EVMPD
SUB09234MIG
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
SMS_ID
100000084170
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
FDA UNII
341BNG318Y
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID901024353
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
WIKIPEDIA
Nicocortonide
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
INN
4490
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
NCI_THESAURUS
C84009
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
PUBCHEM
6436148
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
CAS
65415-41-0
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
265-754-7
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106447
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
MESH
C027263
Created by admin on Fri Dec 15 16:28:18 GMT 2023 , Edited by admin on Fri Dec 15 16:28:18 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY