(8S,14R)-8,14-diisopropyl-2,2,4,4,10,10,12,12-octamethyl-7-((4-methylbenzyl)oxy)-4,8,12,14-tetrahydrochromeno[2,3-a]xanthene-1,3,9,11(2H,10H)-tetraone

ID: ALA5195066

Chembl Id: CHEMBL5195066

PubChem CID: 168287565

Max Phase: Preclinical

Molecular Formula: C42H50O7

Molecular Weight: 666.86

Names and Identifiers

Canonical SMILES:  Cc1ccc(COc2cc3c(c4c2[C@H](C(C)C)C2=C(O4)C(C)(C)C(=O)C(C)(C)C2=O)[C@@H](C(C)C)C2=C(O3)C(C)(C)C(=O)C(C)(C)C2=O)cc1

Standard InChI:  InChI=1S/C42H50O7/c1-20(2)26-28-24(47-19-23-16-14-22(5)15-17-23)18-25-29(32(28)49-36-31(26)34(44)40(8,9)38(46)42(36,12)13)27(21(3)4)30-33(43)39(6,7)37(45)41(10,11)35(30)48-25/h14-18,20-21,26-27H,19H2,1-13H3/t26-,27+/m0/s1

Standard InChI Key:  CBUQFPPVYYOSAE-RRPNLBNLSA-N

Alternative Forms

1. Parent:

   

   ALA5195066

   ---

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: 666.86

Molecular Weight (Monoisotopic): 666.3557

AlogP: 8.75

#Rotatable Bonds: 5

Polar Surface Area: 95.97

Molecular Species: NEUTRAL

HBA: 7

HBD: ┄

#RO5 Violations: 2

HBA (Lipinski): 7

HBD (Lipinski): ┄

#RO5 Violations (Lipinski): 2

CX Acidic pKa: ┄

CX Basic pKa: ┄

CX LogP: 10.45

CX LogD: 10.45

Aromatic Rings: 2

Heavy Atoms: 49

QED Weighted: 0.29

Np Likeness Score: 0.79

References

1. Zhang Y, Yang H, Wang FT, Peng X, Liu HY, Li QJ, An LK..  (2022)  Discovery, enantioselective synthesis of myrtucommulone E analogues as tyrosyl-DNA phosphodiesterase 2 inhibitors and their biological activities.,  238  [PMID:35580424] [10.1016/j.ejmech.2022.114445]

Source

Source(1):

• Scientific Literature