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Details

Stereochemistry ABSOLUTE
Molecular Formula C38H59FO6
Molecular Weight 630.8699
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEXAMETHASONE PALMITATE

SMILES

[H][C@@]12C[C@@H](C)[C@](O)(C(=O)COC(=O)CCCCCCCCCCCCCCC)[C@@]1(C)C[C@H](O)[C@@]3(F)[C@@]2([H])CCC4=CC(=O)C=C[C@]34C

InChI

InChIKey=WDPYZTKOEFDTCU-WDJQFAPHSA-N
InChI=1S/C38H59FO6/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-34(43)45-26-33(42)38(44)27(2)23-31-30-20-19-28-24-29(40)21-22-35(28,3)37(30,39)32(41)25-36(31,38)4/h21-22,24,27,30-32,41,44H,5-20,23,25-26H2,1-4H3/t27-,30+,31+,32+,35+,36+,37+,38+/m1/s1

HIDE SMILES / InChI

Molecular Formula C38H59FO6
Molecular Weight 630.8699
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Dexamethasone palmitate (a derivative of Dexamethasone), anti-inflammatory, antirheumatic, glucocorticoid receptor agonist, is reported as an ingredient of Limethason in Japan and Lipotalon in Germany. Limethason (Dexamethasone palmitate) inhibits the function of leukocytes and tissue macrophages. It restricts the migration of leukocytes in the area of inflammation. Limethason (Dexamethasone palmitate) decreases capillary permeability caused by histamine release. It inhibits the activity of fibroblasts and collagen formation. Limethason inhibits the activity of phospholipase A2, which leads to suppression of the synthesis of prostaglandins and leukotrienes. Limethason (Dexamethasone palmitate) is indicated for rheumatoid arthritis.

Originator

Sources: Arzneimittel-Forschung (1960), 10, 886-90.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Macrophage viability and migration
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Limethason

Approved Use

Indications: rheumatoid arthritis

Launch Date

1988
PubMed

PubMed

TitleDatePubMed
Acute Treatment of Facet Syndrome by CT-Guided Injection of Dexamethasone-21-Palmitate Alone and in Combination with Mepivacaine.
2004
Patents

Sample Use Guides

0.25mg/kg, intravenous
Route of Administration: Intravenous
DEXAMETHASONE PALMITATE decreased the viability of RAW 264.7 cells by 75% at a concentration of 10 uM
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:03:15 GMT 2023
Edited
by admin
on Sat Dec 16 02:03:15 GMT 2023
Record UNII
601XWN7060
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEXAMETHASONE PALMITATE
JAN   WHO-DD  
Common Name English
9-FLUORO-11,17-DIHYDROXY-16-METHYL-21-((1- OXOHEXADECYL)OXY)PREGNA-1,4-DIENE-3,20-DIONE (11.BETA.,16.ALPHA.)-
Common Name English
DEXAMETHASONE PALMITATE [JAN]
Common Name English
NOVA63035
Code English
DEXAMETHASONE 21-PALMITATE
Common Name English
NOVA-63035
Common Name English
Dexamethasone palmitate [WHO-DD]
Common Name English
Code System Code Type Description
DRUG CENTRAL
828
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY
MESH
C035081
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY
ChEMBL
CHEMBL384467
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY
FDA UNII
601XWN7060
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY
EVMPD
SUB01611MIG
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY
CAS
14899-36-6
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY
PUBCHEM
63044
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID8022903
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY
SMS_ID
100000092376
Created by admin on Sat Dec 16 02:03:15 GMT 2023 , Edited by admin on Sat Dec 16 02:03:15 GMT 2023
PRIMARY