4-(4-methoxyphenyl)-6-(3,4,5-trimethoxyphenyl)-3,4-dihydropyrimidine-2(1H)-thione

ID: ALA2262110

Chembl Id: CHEMBL2262110

PubChem CID: 76312181

Max Phase: Preclinical

Molecular Formula: C20H22N2O4S

Molecular Weight: 386.47

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  COc1ccc(C2C=C(c3cc(OC)c(OC)c(OC)c3)NC(=S)N2)cc1

Standard InChI:  InChI=1S/C20H22N2O4S/c1-23-14-7-5-12(6-8-14)15-11-16(22-20(27)21-15)13-9-17(24-2)19(26-4)18(10-13)25-3/h5-11,15H,1-4H3,(H2,21,22,27)

Standard InChI Key:  LCVIXCCSXDDQAT-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA2262110

   4-(4-methoxyphenyl)-6-(3,4,5-trimethoxyphenyl)-3,4-dihydro-1H-pyrimidine-2-thione

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

Calculated Properties

Molecular Weight: 386.47

Molecular Weight (Monoisotopic): 386.1300

AlogP: 3.28

#Rotatable Bonds: 6

Polar Surface Area: 60.98

Molecular Species: NEUTRAL

HBA: 5

HBD: 2

#RO5 Violations: ┄

HBA (Lipinski): 6

HBD (Lipinski): 2

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 10.89

CX Basic pKa: ┄

CX LogP: 2.70

CX LogD: 2.70

Aromatic Rings: 2

Heavy Atoms: 27

QED Weighted: 0.74

Np Likeness Score: -0.11

References

1. Desta D, Sjoholm R, Lee L, Lee M, Dittenhafer K, Canche S, Babu B, Chavda S, Dewar C, Yanow S, Best AA, Lee M.  (2011)  Synthesis and antiprotozoal activity of 1,2,3,4-tetrahydro-2-thioxopyrimidine analogs of combretastatin A-4,  20  (3): [10.1007/s00044-010-9334-1]

2. El-Meligie S, Taher AT, Kamal AM, Youssef A..  (2017)  Design, synthesis and cytotoxic activity of certain novel chalcone analogous compounds.,  126  [PMID:27744186] [10.1016/j.ejmech.2016.09.099]

Source

Source(1):

• Scientific Literature