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Details

Stereochemistry ACHIRAL
Molecular Formula C17H27NO3
Molecular Weight 293.4012
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NORDIHYDROCAPSAICIN

SMILES

COC1=CC(CNC(=O)CCCCCC(C)C)=CC=C1O

InChI

InChIKey=VQEONGKQWIFHMN-UHFFFAOYSA-N
InChI=1S/C17H27NO3/c1-13(2)7-5-4-6-8-17(20)18-12-14-9-10-15(19)16(11-14)21-3/h9-11,13,19H,4-8,12H2,1-3H3,(H,18,20)

HIDE SMILES / InChI

Molecular Formula C17H27NO3
Molecular Weight 293.4012
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of topical application of capsaicin and its related compounds on dermal insulin-like growth factor-I levels in mice and on facial skin elasticity in humans.
2007 Apr
Capsaicinoids, chloropicrin and sulfur mustard: possibilities for exposure biomarkers.
2010
Glycosylation of capsaicinoids with Panax ginseng stimulated by salicylic acid.
2010 Dec
Effect of oral intake of capsaicinoid beadlets on catecholamine secretion and blood markers of lipolysis in healthy adults: a randomized, placebo controlled, double-blind, cross-over study.
2010 Jul 15
Effects of dihydrocapsiate on adaptive and diet-induced thermogenesis with a high protein very low calorie diet: a randomized control trial.
2010 Oct 6
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:16:25 GMT 2025
Edited
by admin
on Mon Mar 31 18:16:25 GMT 2025
Record UNII
RF657P8DA8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NORDIHYDROCAPSAICIN (CONSTITUENT OF CAPSICUM) [DSC]
Preferred Name English
NORDIHYDROCAPSAICIN
Common Name English
NORHYDROCAPSAICIN
Common Name English
OCTANAMIDE, 7-METHYL-N-VANILLYL-
Systematic Name English
OCTANAMIDE, N-((4-HYDROXY-3-METHOXYPHENYL)METHYL)-7-METHYL-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 70707
Created by admin on Mon Mar 31 18:16:25 GMT 2025 , Edited by admin on Mon Mar 31 18:16:25 GMT 2025
Code System Code Type Description
MESH
C517386
Created by admin on Mon Mar 31 18:16:25 GMT 2025 , Edited by admin on Mon Mar 31 18:16:25 GMT 2025
PRIMARY
WIKIPEDIA
NORDIHYDROCAPSAICIN
Created by admin on Mon Mar 31 18:16:25 GMT 2025 , Edited by admin on Mon Mar 31 18:16:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID3042217
Created by admin on Mon Mar 31 18:16:25 GMT 2025 , Edited by admin on Mon Mar 31 18:16:25 GMT 2025
PRIMARY
CAS
28789-35-7
Created by admin on Mon Mar 31 18:16:25 GMT 2025 , Edited by admin on Mon Mar 31 18:16:25 GMT 2025
PRIMARY
PUBCHEM
168836
Created by admin on Mon Mar 31 18:16:25 GMT 2025 , Edited by admin on Mon Mar 31 18:16:25 GMT 2025
PRIMARY
FDA UNII
RF657P8DA8
Created by admin on Mon Mar 31 18:16:25 GMT 2025 , Edited by admin on Mon Mar 31 18:16:25 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST
9,100,000 Scoville units
PARENT -> CONSTITUENT ALWAYS PRESENT
7.4% of Capsaicinoid components.
PARENT -> CONSTITUENT ALWAYS PRESENT
7.4% of Capsaicinoid components.
PARENT -> CONSTITUENT ALWAYS PRESENT
7.4% of Capsaicinoid components.
PARENT -> CONSTITUENT ALWAYS PRESENT
7.4% of Capsaicinoid components.
PARENT -> CONSTITUENT ALWAYS PRESENT
7.4% of Capsaicinoid components.