U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C5H9N3
Molecular Weight 111.1451
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HISTAMINE

SMILES

NCCC1=CNC=N1

InChI

InChIKey=NTYJJOPFIAHURM-UHFFFAOYSA-N
InChI=1S/C5H9N3/c6-2-1-5-3-7-4-8-5/h3-4H,1-2,6H2,(H,7,8)

HIDE SMILES / InChI

Molecular Formula C5H9N3
Molecular Weight 111.1451
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 15:10:56 UTC 2023
Edited
by admin
on Fri Dec 15 15:10:56 UTC 2023
Record UNII
820484N8I3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HISTAMINE
HSDB   MART.   MI   VANDF   WHO-DD  
Systematic Name English
ERGOTIDINE
Common Name English
ERGAMINE
Common Name English
NSC-33792
Code English
Histamine [WHO-DD]
Common Name English
HISTAMINE [MI]
Common Name English
5-IMIDAZOLEETHYLAMINE
Systematic Name English
HISTAMINE [MART.]
Common Name English
1H-IMIDAZOLE-4-ETHANAMINE
Systematic Name English
HISTAMINE [VANDF]
Common Name English
.BETA.-AMINOETHYLGLYOXALINE
Common Name English
4-IMIDAZOLEETHYLAMINE
Systematic Name English
.BETA.-AMINOETHYLIMIDAZOLE
Systematic Name English
2-(4-IMIDAZOLYL)ETHYLAMINE
Systematic Name English
HISTAMINE [HSDB]
Common Name English
Classification Tree Code System Code
LOINC 34316-0
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 33290-8
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 25439-1
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 2417-4
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 34317-8
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
NCI_THESAURUS C687
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
FDA ORPHAN DRUG 127199
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 2416-6
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
FDA ORPHAN DRUG 127399
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 13755-4
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 13756-2
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 9410-2
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 2415-8
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 25925-9
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
WHO-ATC L03AX14
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
NCI_THESAURUS C2139
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 35260-9
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 43577-6
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
LOINC 44371-3
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C73238
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
NSC
33792
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
FDA UNII
820484N8I3
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
DRUG BANK
DB05381
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-100-6
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
CAS
51-45-6
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
WIKIPEDIA
HISTAMINE
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
MESH
D006632
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
DRUG CENTRAL
1375
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
MERCK INDEX
m6026
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY Merck Index
PUBCHEM
774
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
CHEBI
18295
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
CHEBI
58432
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
EPA CompTox
DTXSID4023125
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
HSDB
3338
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
SMS_ID
100000089506
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
DAILYMED
820484N8I3
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
RXCUI
5333
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY RxNorm
EVMPD
SUB14107MIG
Created by admin on Fri Dec 15 15:10:56 UTC 2023 , Edited by admin on Fri Dec 15 15:10:56 UTC 2023
PRIMARY
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CHO-H1 cells, histamine stimulation resulted in a concentration-dependent increase in [Ca2+]i with an EC50 of 170±30 nM.
EC50
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TRANSPORTER -> INHIBITOR
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