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

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H25ClO5
Molecular Weight 392.873
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOPREDNOL

SMILES

C[C@]12C[C@H](O)[C@H]3[C@@H](C=C(Cl)C4=CC(=O)C=C[C@]34C)[C@@H]1CC[C@]2(O)C(=O)CO

InChI

InChIKey=YTJIBEDMAQUYSZ-FDNPDPBUSA-N
InChI=1S/C21H25ClO5/c1-19-5-3-11(24)7-14(19)15(22)8-12-13-4-6-21(27,17(26)10-23)20(13,2)9-16(25)18(12)19/h3,5,7-8,12-13,16,18,23,25,27H,4,6,9-10H2,1-2H3/t12-,13-,16-,18+,19-,20-,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H25ClO5
Molecular Weight 392.873
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Cloprednol is a steroid, which was used for the treatment of asthma. The exact mechanism of cloprednol action is unknown. The drug was marketed under several names, including Syntestan and Cloradryn, however, its current marketing status is unknown and supposed to be discontinued.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
SYNTESTAN

Approved Use

Asthma.
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
41.3 ng/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CLOPREDNOL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
426 ng/mL
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CLOPREDNOL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
126 ng × h/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CLOPREDNOL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.87 h
2.5 mg single, oral
dose: 2.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CLOPREDNOL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
16%
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CLOPREDNOL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
12.5 mg 1 times / day multiple, oral
Highest studied dose
Dose: 12.5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 12.5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Comparison of cloprednol and prednisolone in chronic asthmatic patients.
1978-07
Patents

Sample Use Guides

Cloprednol is given as a single morning dose of 5-12.5 mg orally.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:57:07 GMT 2025
Edited
by admin
on Wed Apr 02 09:57:07 GMT 2025
Record UNII
SYP56O3GJG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLORADRYN
Preferred Name English
CLOPREDNOL
INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
CLOPREDNOL [MI]
Common Name English
6-Chloro-11?,17,21-trihydroxypregna-1,4,6-triene-3,20-dione
Systematic Name English
RS-4691
Code English
PREGNA-1,4,6-TRIENE-3,20-DIONE, 6-CHLORO-11,17,21-TRIHYDROXY-, (11.BETA.)-
Systematic Name English
Cloprednol [WHO-DD]
Common Name English
CLOPREDNOL [USAN]
Common Name English
cloprednol [INN]
Common Name English
CLOPREDNOL [MART.]
Common Name English
Classification Tree Code System Code
WHO-VATC QH02AB14
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
WHO-ATC H02AB14
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
NCI_THESAURUS C521
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
Code System Code Type Description
DRUG CENTRAL
709
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
DRUG BANK
DB13843
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
SMS_ID
100000084000
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
ChEMBL
CHEMBL1697832
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
RXCUI
21285
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY RxNorm
FDA UNII
SYP56O3GJG
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
CAS
5251-34-3
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
MERCK INDEX
m3657
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY Merck Index
INN
3566
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
WIKIPEDIA
Cloprednol
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
MESH
C011731
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
PUBCHEM
5284535
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
ECHA (EC/EINECS)
226-052-6
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
NCI_THESAURUS
C80809
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
EVMPD
SUB06744MIG
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID1022849
Created by admin on Wed Apr 02 09:57:07 GMT 2025 , Edited by admin on Wed Apr 02 09:57:07 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY