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Details

Stereochemistry ACHIRAL
Molecular Formula C15H22Cl2N2
Molecular Weight 301.255
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BD-1008

SMILES

CN(CCN1CCCC1)CCC2=CC(Cl)=C(Cl)C=C2

InChI

InChIKey=ASGIQUHBAVIOTI-UHFFFAOYSA-N
InChI=1S/C15H22Cl2N2/c1-18(10-11-19-7-2-3-8-19)9-6-13-4-5-14(16)15(17)12-13/h4-5,12H,2-3,6-11H2,1H3

HIDE SMILES / InChI

Molecular Formula C15H22Cl2N2
Molecular Weight 301.255
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q99720|||Q7Z653
Gene ID: 10280.0
Gene Symbol: SIGMAR1
Target Organism: Homo sapiens (Human)
0.34 nM [Ki]
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:57:18 GMT 2023
Edited
by admin
on Sat Dec 16 16:57:18 GMT 2023
Record UNII
JCY43QE7FQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BD-1008
Code English
[2-(3,4-Dichloro-phenyl)-ethyl]-methyl-(2-pyrrolidin-1-yl-ethyl)-amine
Systematic Name English
2-(3,4-Dichlorophenyl)-N-methyl-N-(2-pyrrolidin-1-ylethyl)ethanamine
Systematic Name English
BD1008
Code English
N-[2-(3,4-Dichlorophenyl)ethyl]-N-methyl-1-pyrrolidineethanamine
Systematic Name English
1-Pyrrolidineethanamine, N-[2-(3,4-dichlorophenyl)ethyl]-N-methyl-
Systematic Name English
Code System Code Type Description
CAS
138356-08-8
Created by admin on Sat Dec 16 16:57:18 GMT 2023 , Edited by admin on Sat Dec 16 16:57:18 GMT 2023
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FDA UNII
JCY43QE7FQ
Created by admin on Sat Dec 16 16:57:18 GMT 2023 , Edited by admin on Sat Dec 16 16:57:18 GMT 2023
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PUBCHEM
126388
Created by admin on Sat Dec 16 16:57:18 GMT 2023 , Edited by admin on Sat Dec 16 16:57:18 GMT 2023
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WIKIPEDIA
BD1008
Created by admin on Sat Dec 16 16:57:18 GMT 2023 , Edited by admin on Sat Dec 16 16:57:18 GMT 2023
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EPA CompTox
DTXSID60160639
Created by admin on Sat Dec 16 16:57:18 GMT 2023 , Edited by admin on Sat Dec 16 16:57:18 GMT 2023
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