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Details

Stereochemistry ABSOLUTE
Molecular Formula C29H42O6
Molecular Weight 486.6402
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYDROCORTISONE CYPIONATE

SMILES

[H][C@@]12CC[C@](O)(C(=O)COC(=O)CCC3CCCC3)[C@@]1(C)C[C@H](O)[C@@]4([H])[C@@]2([H])CCC5=CC(=O)CC[C@]45C

InChI

InChIKey=DLVOSEUFIRPIRM-KAQKJVHQSA-N
InChI=1S/C29H42O6/c1-27-13-11-20(30)15-19(27)8-9-21-22-12-14-29(34,28(22,2)16-23(31)26(21)27)24(32)17-35-25(33)10-7-18-5-3-4-6-18/h15,18,21-23,26,31,34H,3-14,16-17H2,1-2H3/t21-,22-,23-,26+,27-,28-,29-/m0/s1

HIDE SMILES / InChI

Molecular Formula C29H42O6
Molecular Weight 486.6402
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:21:24 UTC 2023
Edited
by admin
on Fri Dec 15 16:21:24 UTC 2023
Record UNII
4XDY25L70B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYDROCORTISONE CYPIONATE
ORANGE BOOK   USP-RS   VANDF  
Common Name English
NSC-10721
Code English
Hydrocortisone cipionate [WHO-DD]
Common Name English
PREGN-4-ENE-3,20-DIONE, 21-(3-CYCLOPENTYL-1-OXOPROPOXY)-11,17-DIHYDROXY-, (11.BETA.)-
Systematic Name English
HYDROCORTISONE CYPIONATE [VANDF]
Common Name English
Cortisol 21-cyclopentanepropionate
Common Name English
HYDROCORTISONE CIPIONATE
MART.   WHO-DD  
Common Name English
HYDROCORTISONE CYPIONATE [ORANGE BOOK]
Common Name English
HYDROCORTISONE CIPIONATE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C555
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID90872930
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
WIKIPEDIA
Hydrocortisone cypionate
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
NSC
10721
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
CAS
508-99-6
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
ECHA (EC/EINECS)
208-091-0
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
EVMPD
SUB20610
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
SMS_ID
100000086187
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
ChEMBL
CHEMBL1549
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
RXCUI
163524
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY RxNorm
DRUG CENTRAL
1390
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
PUBCHEM
223253
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
MESH
C029109
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
DRUG BANK
DB14541
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
NCI_THESAURUS
C65864
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
FDA UNII
4XDY25L70B
Created by admin on Fri Dec 15 16:21:24 UTC 2023 , Edited by admin on Fri Dec 15 16:21:24 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY