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

Details

Stereochemistry ABSOLUTE
Molecular Formula C27H41NO6
Molecular Weight 475.6175
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYDROCORTAMATE

SMILES

CCN(CC)CC(=O)OCC(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12C

InChI

InChIKey=FWFVLWGEFDIZMJ-FOMYWIRZSA-N
InChI=1S/C27H41NO6/c1-5-28(6-2)15-23(32)34-16-22(31)27(33)12-10-20-19-8-7-17-13-18(29)9-11-25(17,3)24(19)21(30)14-26(20,27)4/h13,19-21,24,30,33H,5-12,14-16H2,1-4H3/t19-,20-,21-,24+,25-,26-,27-/m0/s1

HIDE SMILES / InChI

Molecular Formula C27H41NO6
Molecular Weight 475.6175
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Hydrocortamate is a synthetic glucocorticoid possessing anti-inflammatory properties and acting as a glucocorticoid receptor agonist. Hydrocortamate was used under the brand name Magnacor to treat inflammation due to corticosteroid-responsive dermatoses btut that usage has been discontinued.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: CHEMBL2034
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
MAGNACORT

Approved Use

Unknown
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer
Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
yes
PubMed

PubMed

TitleDatePubMed
[On the topical use of a new pharmacological association of enzymes, neomycin and hydrocortamate. Clinical contribution].
1965-11
Hydrocortamate (magnacort) and neomycin-hydrocortamate (neo-magnacort) ointment in dermatology.
1959-01
Patents

Patents

Sample Use Guides

Unknown
Route of Administration: Irrigation
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:29:05 GMT 2025
Edited
by admin
on Mon Mar 31 18:29:05 GMT 2025
Record UNII
Y3N00BK5WK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
11.BETA.,17.ALPHA.,21-TRIHYDROXYPREGN-4-ENE-3,20-DIONE 21-DIETHYLAMINOACETATE
Preferred Name English
HYDROCORTAMATE
INN   MI  
INN  
Official Name English
Hydrocortamate [WHO-DD]
Common Name English
HYDROCORTAMATE [MI]
Common Name English
hydrocortamate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C521
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
Code System Code Type Description
EVMPD
SUB08064MIG
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
INN
686
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-963-9
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
FDA UNII
Y3N00BK5WK
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID1057824
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
SMS_ID
100000084195
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
WIKIPEDIA
Hydrocortamate
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
MERCK INDEX
m1187
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY Merck Index
CHEBI
50851
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
DRUG BANK
DB00769
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
PUBCHEM
84088
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
NCI_THESAURUS
C65862
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
CAS
76-47-1
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
DRUG CENTRAL
1387
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
ChEMBL
CHEMBL1201263
Created by admin on Mon Mar 31 18:29:05 GMT 2025 , Edited by admin on Mon Mar 31 18:29:05 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY