MACAMIDE 1

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C23H39NO
Molecular Weight	345.5619
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of MACAMIDE 1

Structure Search

SMILES

CCCCCCCCCCCCCCCC(=O)NCC1=CC=CC=C1

InChI

InChIKey=MLGPKWUKOQAAGI-UHFFFAOYSA-N

InChI=1S/C23H39NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-23(25)24-21-22-18-15-14-16-19-22/h14-16,18-19H,2-13,17,20-21H2,1H3,(H,24,25)

HIDE SMILES / InChI

Molecular Formula	C23H39NO
Molecular Weight	345.5619
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 20:02:06 UTC 2023` Edited by `admin` on `Fri Dec 15 20:02:06 UTC 2023`
Record UNII	1M5UVS8JUU
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

MACAMIDE 1

Common Name

English

N-(PHENYLMETHYL)-HEXADECANAMIDE

Systematic Name

English

N-BENZYLHEXADECANAMIDE

Systematic Name

English

HEXADECANAMIDE, N-BENZYL-

Systematic Name

English

N-BENZYLPALMITAMIDE

Systematic Name

English

Code System Code Type Description

CAS

74058-71-2

Created by admin on Fri Dec 15 20:02:06 UTC 2023 , Edited by admin on Fri Dec 15 20:02:06 UTC 2023

PRIMARY

FDA UNII

1M5UVS8JUU

Created by admin on Fri Dec 15 20:02:06 UTC 2023 , Edited by admin on Fri Dec 15 20:02:06 UTC 2023

PRIMARY

PUBCHEM

11198769

Created by admin on Fri Dec 15 20:02:06 UTC 2023 , Edited by admin on Fri Dec 15 20:02:06 UTC 2023

PRIMARY

EPA CompTox

DTXSID50458532

Created by admin on Fri Dec 15 20:02:06 UTC 2023 , Edited by admin on Fri Dec 15 20:02:06 UTC 2023

PRIMARY

CHEBI

140849

Created by admin on Fri Dec 15 20:02:06 UTC 2023 , Edited by admin on Fri Dec 15 20:02:06 UTC 2023

PRIMARY

Related Record Type Details


					HP7119212T

LEPIDIUM MEYENII ROOT

PARENT -> CONSTITUENT ALWAYS PRESENT

Comments:

The structure elucidation of the isolated compound was based primarily on 1D and 2D NMR spectroscopic analyses, including 1H1H COSY, 1H13C HMQC, 1H13C HMBC and 1H1H NOESY experiments, as well as from 1H15N NMR HMBC correlations.