propyl 1-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino)benzoyl)piperidine-4-carboxylate

ID: ALA5205559

Chembl Id: CHEMBL5205559

PubChem CID: 168297592

Max Phase: Preclinical

Molecular Formula: C24H30N8O3

Molecular Weight: 478.56

Names and Identifiers

Canonical SMILES:  CCCOC(=O)C1CCN(C(=O)c2ccc(N(C)Cc3cnc4nc(N)nc(N)c4n3)cc2)CC1

Standard InChI:  InChI=1S/C24H30N8O3/c1-3-12-35-23(34)16-8-10-32(11-9-16)22(33)15-4-6-18(7-5-15)31(2)14-17-13-27-21-19(28-17)20(25)29-24(26)30-21/h4-7,13,16H,3,8-12,14H2,1-2H3,(H4,25,26,27,29,30)

Standard InChI Key:  AMDVLSYFJVONRJ-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA5205559

   ---

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: 478.56

Molecular Weight (Monoisotopic): 478.2441

AlogP: 2.03

#Rotatable Bonds: 7

Polar Surface Area: 153.45

Molecular Species: NEUTRAL

HBA: 10

HBD: 2

#RO5 Violations: ┄

HBA (Lipinski): 11

HBD (Lipinski): 4

#RO5 Violations (Lipinski): 1

CX Acidic pKa: ┄

CX Basic pKa: 3.00

CX LogP: 1.63

CX LogD: 1.63

Aromatic Rings: 3

Heavy Atoms: 35

QED Weighted: 0.48

Np Likeness Score: -1.15

References

1. Pöhner I, Quotadamo A, Panecka-Hofman J, Luciani R, Santucci M, Linciano P, Landi G, Di Pisa F, Dello Iacono L, Pozzi C, Mangani S, Gul S, Witt G, Ellinger B, Kuzikov M, Santarem N, Cordeiro-da-Silva A, Costi MP, Venturelli A, Wade RC..  (2022)  Multitarget, Selective Compound Design Yields Potent Inhibitors of a Kinetoplastid Pteridine Reductase 1.,  65  (13.0): [PMID:35675511] [10.1021/acs.jmedchem.2c00232]

Source

Source(1):

• Scientific Literature