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Details

Stereochemistry ABSOLUTE
Molecular Formula C32H44O7
Molecular Weight 540.6876
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CICLESONIDE

SMILES

[H][C@@]12C[C@H]3O[C@H](O[C@@]3(C(=O)COC(=O)C(C)C)[C@@]1(C)C[C@H](O)[C@@]4([H])[C@@]2([H])CCC5=CC(=O)C=C[C@]45C)C6CCCCC6

InChI

InChIKey=LUKZNWIVRBCLON-GXOBDPJESA-N
InChI=1S/C32H44O7/c1-18(2)28(36)37-17-25(35)32-26(38-29(39-32)19-8-6-5-7-9-19)15-23-22-11-10-20-14-21(33)12-13-30(20,3)27(22)24(34)16-31(23,32)4/h12-14,18-19,22-24,26-27,29,34H,5-11,15-17H2,1-4H3/t22-,23-,24-,26+,27+,29+,30-,31-,32+/m0/s1

HIDE SMILES / InChI

Molecular Formula C32H44O7
Molecular Weight 540.6876
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:28:15 UTC 2023
Edited
by admin
on Fri Dec 15 16:28:15 UTC 2023
Record UNII
S59502J185
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CICLESONIDE
INN   JAN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
CICLESONIDE [EP MONOGRAPH]
Common Name English
ciclesonide [INN]
Common Name English
CICLESONIDE [MI]
Common Name English
CICLESONIDE [MART.]
Common Name English
(11β,16α)-16,17-[[(R)-Cyclohexylmethylene]bis(oxy)]-11-hydroxy-21-(2-methyl-1-oxopropoxy)pregna-1,4-diene-3,20-dione
Systematic Name English
OMNARIS
Brand Name English
PREGNA-1,4-DIENE-3,20-DIONE, 16,17-(((R)-CYCLOHEXYLMETHYLENE)BIS(OXY))-11-HYDROXY-21-(2-METHYL-1-OXOPROPOXY)-, (11.BETA.,16.ALPHA.)
Common Name English
CICLESONIDE [ORANGE BOOK]
Common Name English
BI54903
Code English
CICLESONIDE [VANDF]
Common Name English
ZETONNA
Brand Name English
RPR-251526
Code English
CICLESONIDE [JAN]
Common Name English
Ciclesonide [WHO-DD]
Common Name English
RPR251526
Code English
CICLESONIDE [USAN]
Common Name English
ALVESCO
Brand Name English
Classification Tree Code System Code
WHO-ATC R03BA08
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
WHO-ATC R01AD13
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
NCI_THESAURUS C521
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
WHO-VATC QR03BA08
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
WHO-VATC QR01AD13
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
Code System Code Type Description
USAN
PP-61
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
DAILYMED
S59502J185
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
MERCK INDEX
m3536
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL2040682
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
DRUG CENTRAL
633
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
WIKIPEDIA
CICLESONIDE
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
INN
6546
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
NCI_THESAURUS
C65326
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
CAS
126544-47-6
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
PUBCHEM
6918155
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
FDA UNII
S59502J185
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
EVMPD
SUB06236MIG
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
MESH
C120481
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
LACTMED
Ciclesonide
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID9046659
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
SMS_ID
100000081904
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
DRUG BANK
DB01410
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
CAS
141845-82-1
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
ALTERNATIVE
IUPHAR
7469
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY
RXCUI
274964
Created by admin on Fri Dec 15 16:28:15 UTC 2023 , Edited by admin on Fri Dec 15 16:28:15 UTC 2023
PRIMARY RxNorm
Related Record Type Details
TARGET -> AGONIST
BINDER->LIGAND
BINDING
METABOLIC ENZYME -> SUBSTRATE
MAJOR
METABOLIC ENZYME -> SUBSTRATE
MINOR
Related Record Type Details
METABOLITE ACTIVE -> PRODRUG
Des-ciclesonide has anti-inflammatory activity with affinity for the glucocorticoid receptor that is 120 times higher than the parent compound.
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC INTRAVENOUS ADMINISTRATION

ORAL BIOAVAILABILITY PHARMACOKINETIC