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Details

Stereochemistry RACEMIC
Molecular Formula C10H13NO2
Molecular Weight 179.2157
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TENAMFETAMINE

SMILES

CC(N)CC1=CC2=C(OCO2)C=C1

InChI

InChIKey=NGBBVGZWCFBOGO-UHFFFAOYSA-N
InChI=1S/C10H13NO2/c1-7(11)4-8-2-3-9-10(5-8)13-6-12-9/h2-3,5,7H,4,6,11H2,1H3

HIDE SMILES / InChI

Molecular Formula C10H13NO2
Molecular Weight 179.2157
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:03:05 UTC 2023
Edited
by admin
on Sat Dec 16 17:03:05 UTC 2023
Record UNII
XJZ28FJ27W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TENAMFETAMINE
INN   MART.   WHO-DD  
INN  
Official Name English
TENAMFETAMINE [MART.]
Common Name English
LOVE
Common Name English
(±)-.ALPHA.-METHYL-3,4-(METHYLENEDIOXY)PHENETHYLAMINE
Systematic Name English
Tenamfetamine [WHO-DD]
Common Name English
EA-1299
Code English
METHYLENE DIOXYAMPHETAMINE
Common Name English
MDA [MI]
Common Name English
MDA (PSYCHEDELIC)
Common Name English
MDA
MI  
Common Name English
tenamfetamine [INN]
Common Name English
3,4-METHYLENEDIOXYAMPHETAMINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C47795
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
DEA NO. 7400
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
WIKIPEDIA PiHKAL
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
Code System Code Type Description
MERCK INDEX
m7104
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
3,4-METHYLENEDIOXYAMPHETAMINE
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
INN
5875
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
FDA UNII
XJZ28FJ27W
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
DRUG BANK
DB01509
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
CAS
51497-09-7
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
SUPERSEDED
HSDB
7593
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
SMS_ID
100000082947
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
CAS
4764-17-4
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
ChEMBL
CHEMBL6731
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
EPA CompTox
DTXSID40859958
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
PUBCHEM
1614
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
NCI_THESAURUS
C80152
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
EVMPD
SUB10891MIG
Created by admin on Sat Dec 16 17:03:06 UTC 2023 , Edited by admin on Sat Dec 16 17:03:06 UTC 2023
PRIMARY
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ENANTIOMER -> RACEMATE
PRECURSOR->PARENT
PRECURSOR->PARENT
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ACTIVE MOIETY