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hydroxy alpha sanshool(Q900922)

From Wikidata

chemical compound

hydroxy-alpha-sanshool

Language	Label	Description	Also known as
default for all languages	No label defined
English	hydroxy alpha sanshool	chemical compound	hydroxy-alpha-sanshool

Statements

type of chemical entity

0 references

fatty acid amide

0 references

chemical structure

Hydroxy-alpha-sanshool.svg
780 × 425; 11 KB

0 references

chemical formula

C₁₆H₂₅NO₂

2 references

imported from Wikimedia project

English Wikipedia

canonical SMILES

CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O

2 references

imported from Wikimedia project

English Wikipedia

isomeric SMILES

C(/C=C/CC/C=C\C=C\C=C\C)(=O)NCC(C)(C)O

0 references

Zanthoxylum bungeanum

7 references

Distribution of unsaturated aliphatic acid amides in japanese Zanthoxylum species

New polyunsaturated fatty acid amides isolated from the seeds of Zanthoxylum piperitum

Pungent qualities of sanshool-related compounds evaluated by a sensory test and activation of rat TRPV1.

Aroma constituents and alkylamides of red and green huajiao (Zanthoxylum bungeanum and Zanthoxylum schinifolium).

Amides from huajiao, pericarps of Zanthoxylum bungeanum MAXIM.

Alkylamides that produce tingling paresthesia activate tactile and thermal trigeminal neurons

A 'toothache tree' alkylamide inhibits Aδ mechanonociceptors to alleviate mechanical pain.

Zanthoxylum piperitum

2 references

Quantitative analysis of sanshool compounds in Japanese pepper (Xanthoxylum piperitum DC.) and their pungent characteristics

Human acyl-CoA: cholesterol acyltransferase inhibitory activities of aliphatic acid amides from Zanthoxylum piperitum DC

Zanthoxylum schinifolium

1 reference

Characterization and Comparison of the Pungent Components in Commercial Zanthoxylum bungeanum Oil and Zanthoxylum schinifolium Oil

263.18852904dalton

1 reference

based on heuristic

inferred from SMILES

Identifiers

InChI=1S/C16H25NO2/c1-4-5-6-7-8-9-10-11-12-13-15(18)17-14-16(2,3)19/h4-9,12-13,19H,10-11,14H2,1-3H3,(H,17,18)/b5-4+,7-6+,9-8-,13-12+

1 reference

LHFKHAVGGJJQFF-UEOYEZOQSA-N

1 reference

CAS Registry Number

1 reference

LHFKHAVGGJJQFF-UEOYEZOQSA-N

CAS Common Chemistry

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=83883-10-7

1 reference

imported from Wikimedia project

English Wikipedia

2 references

imported from Wikimedia project

English Wikipedia

matched by identifier from

LHFKHAVGGJJQFF-UEOYEZOQSA-N

mapping relation type

2 references

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI=1S/C16H25NO2/c1-4-5-6-7-8-9-10-11-12-13-15(18)17-14-16(2,3)19/h4-9,12-13,19H,10-11,14H2,1-3H3,(H,17,18)/b5-4+,7-6+,9-8-,13-12+

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

LHFKHAVGGJJQFF-UEOYEZOQSA-N

UniChem compound ID

1 reference

DSSTox substance ID

1 reference

matched by identifier from

LHFKHAVGGJJQFF-UEOYEZOQSA-N

DSSTOX compound identifier

0 references

Probes And Drugs ID

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

15 January 2022

LHFKHAVGGJJQFF-UEOYEZOQSA-N

1 reference

Freebase Data Dumps

publication date

28 October 2013

Microsoft Academic ID

0 references

Sitelinks

Wikipedia(11 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q900922&oldid=2425734828"

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