ID: ALA278293

Max Phase: Preclinical

Molecular Formula: C27H22N2O5

Molecular Weight: 454.48

Molecule Type: Small molecule

Representations

Canonical SMILES:  N#Cc1cc(-c2ccoc2)c2ccc(OCc3cccc(C4(O)CC5COC(C4)O5)n3)cc2c1

Standard InChI:  InChI=1S/C27H22N2O5/c28-13-17-8-19-10-21(4-5-23(19)24(9-17)18-6-7-31-14-18)32-15-20-2-1-3-25(29-20)27(30)11-22-16-33-26(12-27)34-22/h1-10,14,22,26,30H,11-12,15-16H2

Standard InChI Key:  LBKHEHIDDIEBSX-UHFFFAOYSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 454.48

Molecular Weight (Monoisotopic): 454.1529

AlogP: 4.67

#Rotatable Bonds: 5

Polar Surface Area: 97.74

Molecular Species: NEUTRAL

HBA: 7

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 7

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 13.19

CX Basic pKa: 3.15

CX LogP: 3.92

CX LogD: 3.92

Aromatic Rings: 4

Heavy Atoms: 34

QED Weighted: 0.47

Np Likeness Score: -0.03

References

1. Dubé D, Blouin M, Brideau C, Chan CC, Desmarais S, Ethier D, Falgueyret JP, Friesen RW, Girard M, Girard Y, Guay J, Riendeau D, Tagari P, Young RN..  (1998)  Quinolines as potent 5-lipoxygenase inhibitors: synthesis and biological profile of L-746,530.,  8  (10): [PMID:9871745] [10.1016/s0960-894x(98)00201-7]

2. Hamel P, Riendeau D, Brideau C, Chan CC, Desmarais S, Delorme D, Dubé D, Ducharme Y, Ethier D, Grimm E, Falgueyret JP, Guay J, Jones TR, Kwong E, McAuliffe M, McFarlane CS, Piechuta H, Roumi M, Tagari P, Young RN, Girard Y..  (1997)  Substituted (pyridylmethoxy)naphthalenes as potent and orally active 5-lipoxygenase inhibitors; synthesis, biological profile, and pharmacokinetics of L-739,010.,  40  (18): [PMID:9288168] [10.1021/jm970046b]

3. Wu YJ, Meanwell NA..  (2021)  Geminal Diheteroatomic Motifs: Some Applications of Acetals, Ketals, and Their Sulfur and Nitrogen Homologues in Medicinal Chemistry and Drug Design.,  64  (14.0): [PMID:34213340] [10.1021/acs.jmedchem.1c00790]

Source

Source(1):

• Scientific Literature