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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
Structure of TETRAHYDROHARMANE

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

HIDE SMILES / InChI
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

Unknown
149124
Targets

Targets

Primary TargetPharmacologyConditionPotency
Inhibitor
8504
PubMed

PubMed

TitleDatePubMed
Direct infusion ESI-IT-MSn alkaloid profile and isolation of tetrahydroharman and other alkaloids from Bocageopsis pleiosperma maas (Annonaceae).
2014-10-17
Antimalarial activity of extracts and alkaloids isolated from six plants used in traditional medicine in Mali and Sao Tome.
2002-11
Formation of tetrahydroharman (1-methyl-1,2,3,4-tetrahydro-beta-carboline) by Helicobacter pylori in the presence of ethanol and tryptamine.
1996
Substance Class Chemical
Created
by admin
on Tue Apr 01 19:50:01 GMT 2025
Edited
by admin
on Tue Apr 01 19:50:01 GMT 2025
Record UNII
W6CLK26X7V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TETRAHYDROHARMANE
Common Name English
NSC-92525
Preferred Name English
2,3,4,9-TETRAHYDRO-1-METHYL-1H-PYRIDO(3,4-B)INDOLE
Systematic Name English
(±)-TETRAHYDROHARMAN
Common Name English
1-METHYL-2,3,4,9-TETRAHYDRO-1H-PYRIDO(3,4-B)INDOLE
Systematic Name English
(±)-TETRAHYDROHARMANE
Common Name English
TETRAHYDROHARMAN
Common Name English
CALLIGONINE
Common Name English
ELEAGNINE
Common Name English
1H-PYRIDO(3,4-B)INDOLE, 2,3,4,9-TETRAHYDRO-1-METHYL-
Systematic Name English
(±)-1-METHYL-1,2,3,4-TETRAHYDRO-.BETA.-CARBOLINE
Common Name English
1,2,3,4-TETRAHYDROHARMANE
Common Name English
1-METHYL-1,2,3,4-TETRAHYDRO-.BETA.-CARBOLINE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID901027440
Created by admin on Tue Apr 01 19:50:01 GMT 2025 , Edited by admin on Tue Apr 01 19:50:01 GMT 2025
PRIMARY
FDA UNII
W6CLK26X7V
Created by admin on Tue Apr 01 19:50:01 GMT 2025 , Edited by admin on Tue Apr 01 19:50:01 GMT 2025
PRIMARY
CAS
2506-10-7
Created by admin on Tue Apr 01 19:50:01 GMT 2025 , Edited by admin on Tue Apr 01 19:50:01 GMT 2025
PRIMARY
ECHA (EC/EINECS)
219-711-4
Created by admin on Tue Apr 01 19:50:01 GMT 2025 , Edited by admin on Tue Apr 01 19:50:01 GMT 2025
PRIMARY
NSC
92525
Created by admin on Tue Apr 01 19:50:01 GMT 2025 , Edited by admin on Tue Apr 01 19:50:01 GMT 2025
PRIMARY
PUBCHEM
91522
Created by admin on Tue Apr 01 19:50:01 GMT 2025 , Edited by admin on Tue Apr 01 19:50:01 GMT 2025
PRIMARY
NIH
NCATS
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