ID: ALA86963

Max Phase: Preclinical

Molecular Formula: C10H15N5S

Molecular Weight: 237.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCNc1ccc(/C=N/N=C(/N)S)nc1

Standard InChI:  InChI=1S/C10H15N5S/c1-2-5-12-8-3-4-9(13-6-8)7-14-15-10(11)16/h3-4,6-7,12H,2,5H2,1H3,(H3,11,15,16)/b14-7+

Standard InChI Key:  QKRCJKBFPOAADI-VGOFMYFVSA-N

Associated Targets(Human)

Ribonucleoside-diphosphate reductase M2 chain 14 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

L1210 27553 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 237.33Molecular Weight (Monoisotopic): 237.1048AlogP: 1.48#Rotatable Bonds: 5
Polar Surface Area: 75.66Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.66CX Basic pKa: 3.64CX LogP: 1.58CX LogD: 0.91
Aromatic Rings: 1Heavy Atoms: 16QED Weighted: 0.31Np Likeness Score: -1.69

References

1. Liu MC, Lin TS, Cory JG, Cory AH, Sartorelli AC..  (1996)  Synthesis and biological activity of 3- and 5-amino derivatives of pyridine-2-carboxaldehyde thiosemicarbazone.,  39  (13): [PMID:8691457] [10.1021/jm9600454]

Source