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Details

Stereochemistry ACHIRAL
Molecular Formula C14H26O2
Molecular Weight 226.355
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LOXANAST

SMILES

CC(C)CCC[C@H]1CC[C@](C)(CC1)C(O)=O

InChI

InChIKey=HARNFRANZLWZKO-XBXGTLAGSA-N
InChI=1S/C14H26O2/c1-11(2)5-4-6-12-7-9-14(3,10-8-12)13(15)16/h11-12H,4-10H2,1-3H3,(H,15,16)/t12-,14+

HIDE SMILES / InChI

Molecular Formula C14H26O2
Molecular Weight 226.355
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Cis-isomer of loxanast (IG-10) or 1-methyl-4-isohexylcyclohexane carboxylic acid has been reported as an inhibitor of delayed hypersensitivity reaction in animal models. It inhibited macrophage chemotaxis.

Approval Year

PubMed

PubMed

TitleDatePubMed
Immunopharmacological studies on experimental glomerulonephritis.
1983
Inhibition of delayed hypersensitivity reactions by a new agent, cis-1-methyl-4-isohexylcyclohexane carboxylic acid (IG-10).
1985
Inhibition of delayed hypersensitivity reactions by a new agent, cis-1-methyl-4-isohexylcyclohexane carboxylic acid (IG-10)--II. The mechanism regarding the action on lymphokines.
1987

Sample Use Guides

In Vitro Use Guide
In vitro, loxanast (0.1 -10 ug/ml) did not inhibit the generation of O2- from macrophages. The agent (0.1 -1 ug/ml) significantly inhibited the activity of MIF and this inhibition was not due to the facilitation of normal migration. For macrophage chemotaxis, loxanast (0.01 -1 ug/ml) significantly inhibited MCF-induced chemotaxis.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:11:30 GMT 2023
Edited
by admin
on Fri Dec 15 16:11:30 GMT 2023
Record UNII
746YWK1B07
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LOXANAST
INN  
INN  
Official Name English
loxanast [INN]
Common Name English
CIS-4-ISOHEXYL-1-METHYLCYCLOHEXANECARBOXYLIC ACID
Common Name English
LOXANAST [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C574
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2106814
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
SMS_ID
100000082266
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID801024455
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
PUBCHEM
68890
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
NCI_THESAURUS
C81164
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
INN
5069
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
CAS
69915-62-4
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
FDA UNII
746YWK1B07
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
EVMPD
SUB08606MIG
Created by admin on Fri Dec 15 16:11:30 GMT 2023 , Edited by admin on Fri Dec 15 16:11:30 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY