ID: ALA5206155

Max Phase: Preclinical

Molecular Formula: C21H19N7O2

Molecular Weight: 401.43

Representations

Canonical SMILES:  Cn1c(=O)[nH]c(=O)c2c1nc(Cc1nc3ccc(N)cc3[nH]1)n2Cc1ccccc1

Standard InChI:  InChI=1S/C21H19N7O2/c1-27-19-18(20(29)26-21(27)30)28(11-12-5-3-2-4-6-12)17(25-19)10-16-23-14-8-7-13(22)9-15(14)24-16/h2-9H,10-11,22H2,1H3,(H,23,24)(H,26,29,30)

Standard InChI Key:  BSPOXIARAGAMSY-UHFFFAOYSA-N

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

Properties

Molecular Weight: 401.43

Molecular Weight (Monoisotopic): 401.1600

AlogP: 1.52

#Rotatable Bonds: 4

Polar Surface Area: 127.38

Molecular Species: NEUTRAL

HBA: 7

HBD: 3

#RO5 Violations: 0

HBA (Lipinski): 9

HBD (Lipinski): 4

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 9.26

CX Basic pKa: 6.28

CX LogP: 1.75

CX LogD: 1.71

Aromatic Rings: 5

Heavy Atoms: 30

QED Weighted: 0.39

Np Likeness Score: -1.51

References

1. Specker E, Matthes S, Wesolowski R, Schütz A, Grohmann M, Alenina N, Pleimes D, Mallow K, Neuenschwander M, Gogolin A, Weise M, Pfeifer J, Ziebart N, Heinemann U, von Kries JP, Nazaré M, Bader M..  (2022)  Structure-Based Design of Xanthine-Benzimidazole Derivatives as Novel and Potent Tryptophan Hydroxylase Inhibitors.,  65  (16.0): [PMID:35921615] [10.1021/acs.jmedchem.2c00598]

Source

Source(1):

• Scientific Literature