ID: ALA3143852

Max Phase: Preclinical

Molecular Formula: C21H29N4O10PSe

Molecular Weight: 607.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cn([C@H]2C[C@H](OP(C)(=O)[Se]C[C@H]3O[C@@H](n4cc(C)c(=O)[nH]c4=O)C[C@@H]3O)[C@@H](CO)O2)c(=O)[nH]c1=O

Standard InChI:  InChI=1S/C21H29N4O10PSe/c1-10-6-24(20(30)22-18(10)28)16-4-12(27)15(34-16)9-37-36(3,32)35-13-5-17(33-14(13)8-26)25-7-11(2)19(29)23-21(25)31/h6-7,12-17,26-27H,4-5,8-9H2,1-3H3,(H,22,28,30)(H,23,29,31)/t12-,13-,14+,15+,16+,17+,36?/m0/s1

Standard InChI Key:  PSGXXZNLMQMEKU-HAVNGMDZSA-N

Associated Targets(Human)

ATH-8 cell line 300 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: 607.42Molecular Weight (Monoisotopic): 608.0787AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Wozniak LA, Sochacki M, Mitsuya H, Kageyama S, Stec WJ.  (1994)  A new class of dinucleotide analogues. The synthesis of 3-O-thymidylyl(5-deoxy-5-selene-thymidylyl)-Se-phosphoroselenolate, its O-methyl ester and methanephosphonate derivatives.,  (8): [10.1016/S0960-894X(01)80676-4]

Source