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Details

Stereochemistry ABSOLUTE
Molecular Formula C33H47NO
Molecular Weight 473.7324
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of MOCTAMIDE

SMILES

CCCCC\C=C/C\C=C/CCCCCCCC(=O)N[C@@H](CC1=CC=C(C)C=C1)C2=CC=CC=C2

InChI

InChIKey=GSPPFJJUCULBDC-FOCYRBLYSA-N
InChI=1S/C33H47NO/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-20-23-33(35)34-32(31-21-18-17-19-22-31)28-30-26-24-29(2)25-27-30/h7-8,10-11,17-19,21-22,24-27,32H,3-6,9,12-16,20,23,28H2,1-2H3,(H,34,35)/b8-7-,11-10-/t32-/m0/s1

HIDE SMILES / InChI

Molecular Formula C33H47NO
Molecular Weight 473.7324
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 2
Optical Activity UNSPECIFIED

Moctamide is a synthetic linoleamide derivative patented by major Japanese chemical company Sumitomo Chemical Co., Ltd. as hypocholesterolemic agent useful as prophylactics against arteriosclerosis. Administration of Moctamide significantly lowered serum and liver cholesterol and significantly prevented formation of aortic atheromatous changes in animal models.

Approval Year

PubMed

PubMed

TitleDatePubMed
The effect of (--)N-(alpha-phenyl-beta-(p-tolyl)ethyl) linoleamide on experimental atherosclerosis in rabbits.
1970 Sep-Oct
Patents

Patents

Sample Use Guides

rabbit: 5–10 mg/day/animal
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:13:17 GMT 2023
Edited
by admin
on Fri Dec 15 16:13:17 GMT 2023
Record UNII
TN4C52M5ZT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MOCTAMIDE
INN  
INN  
Official Name English
NSC-309468
Code English
MOCTAMIDE [JAN]
Common Name English
moctamide [INN]
Common Name English
(-)-N-(P-METHYL-.ALPHA.-PHENYLPHENETHYL)LINOLEAMIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29703
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
Code System Code Type Description
CAS
29619-86-1
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
EVMPD
SUB09025MIG
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
NSC
309468
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
FDA UNII
TN4C52M5ZT
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
SMS_ID
100000080348
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
INN
3609
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
PUBCHEM
6436044
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID001043374
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
NCI_THESAURUS
C66174
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
MESH
C008537
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105100
Created by admin on Fri Dec 15 16:13:17 GMT 2023 , Edited by admin on Fri Dec 15 16:13:17 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY