Details
Stereochemistry | RACEMIC |
Molecular Formula | C12H14N2 |
Molecular Weight | 186.253 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1NCCC2=C1NC3=C2C=CC=C3
InChI
InChIKey=LPIJOZBIVDCQTE-UHFFFAOYSA-N
InChI=1S/C12H14N2/c1-8-12-10(6-7-13-8)9-4-2-3-5-11(9)14-12/h2-5,8,13-14H,6-7H2,1H3
Molecular Formula | C12H14N2 |
Molecular Weight | 186.253 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2367107 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12410545 |
PubMed
Title | Date | PubMed |
---|---|---|
Formation of tetrahydroharman (1-methyl-1,2,3,4-tetrahydro-beta-carboline) by Helicobacter pylori in the presence of ethanol and tryptamine. | 1996 |
|
Antimalarial activity of extracts and alkaloids isolated from six plants used in traditional medicine in Mali and Sao Tome. | 2002 Nov |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 12:49:27 GMT 2023
by
admin
on
Sat Dec 16 12:49:27 GMT 2023
|
Record UNII |
W6CLK26X7V
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID901027440
Created by
admin on Sat Dec 16 12:49:27 GMT 2023 , Edited by admin on Sat Dec 16 12:49:27 GMT 2023
|
PRIMARY | |||
|
W6CLK26X7V
Created by
admin on Sat Dec 16 12:49:27 GMT 2023 , Edited by admin on Sat Dec 16 12:49:27 GMT 2023
|
PRIMARY | |||
|
2506-10-7
Created by
admin on Sat Dec 16 12:49:27 GMT 2023 , Edited by admin on Sat Dec 16 12:49:27 GMT 2023
|
PRIMARY | |||
|
219-711-4
Created by
admin on Sat Dec 16 12:49:27 GMT 2023 , Edited by admin on Sat Dec 16 12:49:27 GMT 2023
|
PRIMARY | |||
|
92525
Created by
admin on Sat Dec 16 12:49:27 GMT 2023 , Edited by admin on Sat Dec 16 12:49:27 GMT 2023
|
PRIMARY | |||
|
91522
Created by
admin on Sat Dec 16 12:49:27 GMT 2023 , Edited by admin on Sat Dec 16 12:49:27 GMT 2023
|
PRIMARY |