(2S)-2-amino-4-[[4-amino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-2-oxo-pyrimidin-5-yl]methyl-[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl]amino]butanoic acid

ID: ALA5192832

Chembl Id: CHEMBL5192832

PubChem CID: 156564607

Max Phase: Preclinical

Molecular Formula: C24H34N10O9

Molecular Weight: 606.60

Names and Identifiers

Canonical SMILES:  Nc1nc(=O)n([C@H]2C[C@H](O)[C@@H](CO)O2)cc1CN(CC[C@H](N)C(=O)O)C[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O

Standard InChI:  InChI=1S/C24H34N10O9/c25-11(23(39)40)1-2-32(4-10-5-33(24(41)31-19(10)26)15-3-12(36)14(7-35)42-15)6-13-17(37)18(38)22(43-13)34-9-30-16-20(27)28-8-29-21(16)34/h5,8-9,11-15,17-18,22,35-38H,1-4,6-7,25H2,(H,39,40)(H2,26,31,41)(H2,27,28,29)/t11-,12-,13+,14+,15+,17+,18+,22+/m0/s1

Standard InChI Key:  PLBYMBRPNYRBIZ-RGGOSWGQSA-N

Alternative Forms

1. Parent:

   

   ALA5192832

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 606.60

Molecular Weight (Monoisotopic): 606.2510

AlogP: -3.89

#Rotatable Bonds: 11

Polar Surface Area: 296.47

Molecular Species: ZWITTERION

HBA: 18

HBD: 8

#RO5 Violations: 3

HBA (Lipinski): 19

HBD (Lipinski): 11

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 1.82

CX Basic pKa: 9.19

CX LogP: -6.97

CX LogD: -6.97

Aromatic Rings: 3

Heavy Atoms: 43

QED Weighted: 0.10

Np Likeness Score: 0.70

References

1. Lamiable-Oulaidi F, Harijan RK, Shaffer KJ, Crump DR, Sun Y, Du Q, Gulab SA, Khan AA, Luxenburger A, Woolhouse AD, Sidoli S, Tyler PC, Schramm VL..  (2022)  Synthesis and Characterization of Transition-State Analogue Inhibitors against Human DNA Methyltransferase 1.,  65  (7.0): [PMID:35324190] [10.1021/acs.jmedchem.1c01869]

Source

Source(1):

• Scientific Literature