Compound Summary
Compound Name: | L-750,667 trihydrochloride |
Compound CID: | 11957592 |
Synonyms: | L-750,667 trihydrochloride 1021868-80-3 3-4-(4-Iodophenyl)piperazin-1-ylmethyl-1H-pyrrolo2,3-bpyridine trihydrochloride NCGC00094070-01 EU-0100722 More... |
Iupac Name: | 3-[[4-(4-iodophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine;trihydrochloride |
InChI: | InChI=1S/C18H19IN4.3ClH/c19-15-3-5-16(6-4-15)23-10-8-22(9-11-23)13-14-12-21-18-17(14)2-1-7-20-18;;;/h1-7,12H,8-11,13H2,(H,20,21);3*1H |
InChIKey: | YOURSPNOEWYAKO-UHFFFAOYSA-N |
Canonical Smiles: | C1CN(CCN1CC2=CNC3=C2C=CC=N3)C4=CC=C(C=C4)I.Cl.Cl.Cl |
Isomeric Smiles: | C1CN(CCN1CC2=CNC3=C2C=CC=N3)C4=CC=C(C=C4)I.Cl.Cl.Cl |
Molecular Weight: | 527.7 |
Molecular Formula: | C18H22Cl3IN4 |
Molecular Weight: | 527.7 |
Molecular Formula: | C18H22Cl3IN4 |
Hydrogen Bond Donor Count: | 4 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 3 |
Heavy Atom Count: | 26 |
Complexity: | 377 |
L-750,667 trihydrochloride | L-750,667 trihydrochloride |
---|---|
L-750,667 trihydrochloride |
1021868-80-3 |
3-4-(4-Iodophenyl)piperazin-1-ylmethyl-1H-pyrrolo2,3-bpyridine trihydrochloride |
NCGC00094070-01 |
EU-0100722 |
CHEMBL1496166 |
DTXSID10474692 |
L-750,667 trihydrochloride, solid |
LP00722 |
L-133 |
SR-01000075972 |
L750,667 |
SR-01000075972-1 |
L 750,667 |
( inverted question mark)-3-4-Iodophenyl)-1-piperazyl methylpyrrolo 2,3-b pyrimidine |
3-4-(4-iodophenyl)piperazin-1-ylmethyl-1H-pyrrolo2,3-bpyridine;trihydrochloride |
Species | Dose | Unit | Control(Avg days) | Treatment(Avg days) | Avg/Med Lifespan Change(%) | Control(Max days) | Treatment(Max days) | Max Lifespan Change(%) | Significant | Strain | Gender | PubMed | Avg/Med Lifespan Change tab |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Caenorhabditis elegans | 33.000000000000000 | umol/L | -43.000000000000000 | NS | N2 | 24134630 | Inactive |
Species | Avg/Med Lifespan Change(%) | Max Lifespan Change(%) | Count Reference | Count Data point |
---|---|---|---|---|
Caenorhabditis elegans | -43.000000000000000 | 1 | 1 |