9-(4-Chloro-buta-1,2-dienyl)-9H-purin-6-ylamine

ID: ALA135456

Chembl Id: CHEMBL135456

PubChem CID: 135512506

Max Phase: Preclinical

Molecular Formula: C9H8ClN5

Molecular Weight: 221.65

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Nc1ncnc2c1ncn2C=C=CCCl

Standard InChI:  InChI=1S/C9H8ClN5/c10-3-1-2-4-15-6-14-7-8(11)12-5-13-9(7)15/h1,4-6H,3H2,(H2,11,12,13)

Standard InChI Key:  ZVKCHPLRXYPLFB-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA135456

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Associated Targets(Human)

PO3 (17 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

L1210 (27553 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MC-38 (857 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

Calculated Properties

Molecular Weight: 221.65Molecular Weight (Monoisotopic): 221.0468AlogP: 1.27#Rotatable Bonds: 2
Polar Surface Area: 69.62Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 3.40CX LogP: 0.89CX LogD: 0.89
Aromatic Rings: 2Heavy Atoms: 15QED Weighted: 0.61Np Likeness Score: 0.00

References

1. Phadtare S, Kessel D, Corbett TH, Renis HE, Court BA, Zimlicka J..  (1991)  Unsaturated and carbocyclic nucleoside analogues: synthesis, antitumor, and antiviral activity.,  34  (1): [PMID:1992143] [10.1021/jm00105a064]

Source