ID: ALA458939

Max Phase: Preclinical

Molecular Formula: C25H28N3O8P

Molecular Weight: 529.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@H](NP(=O)(OC[C@H]1O[C@@H](n2cccnc2=O)C[C@@H]1O)Oc1ccccc1)C(=O)OCc1ccccc1

Standard InChI:  InChI=1S/C25H28N3O8P/c1-18(24(30)33-16-19-9-4-2-5-10-19)27-37(32,36-20-11-6-3-7-12-20)34-17-22-21(29)15-23(35-22)28-14-8-13-26-25(28)31/h2-14,18,21-23,29H,15-17H2,1H3,(H,27,32)/t18-,21-,22+,23+,37?/m0/s1

Standard InChI Key:  PYZMMVJUIASJSA-FXNXOIJDSA-N

Associated Targets(Human)

CFPAC-1 421 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

T-24 2342 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: 529.49Molecular Weight (Monoisotopic): 529.1614AlogP: 2.82#Rotatable Bonds: 11
Polar Surface Area: 138.21Molecular Species: NEUTRALHBA: 10HBD: 2
#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.24CX Basic pKa: CX LogP: 2.17CX LogD: 2.17
Aromatic Rings: 3Heavy Atoms: 37QED Weighted: 0.28Np Likeness Score: 0.08

References

1. Yoo CB, Valente R, Congiatu C, Gavazza F, Angel A, Siddiqui MA, Jones PA, McGuigan C, Marquez VE..  (2008)  Activation of p16 gene silenced by DNA methylation in cancer cells by phosphoramidate derivatives of 2'-deoxyzebularine.,  51  (23): [PMID:19006382] [10.1021/jm8005965]

Source