Pholiol D

ID: ALA5193607

Chembl Id: CHEMBL5193607

PubChem CID: 168285353

Max Phase: Preclinical

Molecular Formula: C39H62O10

Molecular Weight: 690.92

Names and Identifiers

Canonical SMILES:  COC(=O)C[C@@](C)(O)CC(=O)O[C@@H]1C[C@]2(C)C3=C(CC[C@H]2C(C)(C)[C@H]1OC(C)=O)[C@]1(C)CC[C@H]([C@H](C)CCC(=O)C(C)(C)O)[C@@]1(C)[C@H](O)C3

Standard InChI:  InChI=1S/C39H62O10/c1-22(12-15-29(41)35(5,6)45)24-16-17-38(9)25-13-14-28-34(3,4)33(48-23(2)40)27(49-32(44)21-36(7,46)20-31(43)47-11)19-37(28,8)26(25)18-30(42)39(24,38)10/h22,24,27-28,30,33,42,45-46H,12-21H2,1-11H3/t22-,24-,27-,28+,30-,33+,36-,37-,38+,39+/m1/s1

Standard InChI Key:  RDCKZLUVIJMANP-INNIYDRTSA-N

Alternative Forms

1. Parent:

   

   ALA5193607

   ---

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: 690.92

Molecular Weight (Monoisotopic): 690.4343

AlogP: 5.62

#Rotatable Bonds: 11

Polar Surface Area: 156.66

Molecular Species: NEUTRAL

HBA: 10

HBD: 3

#RO5 Violations: 2

HBA (Lipinski): 10

HBD (Lipinski): 3

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 13.50

CX Basic pKa:

CX LogP: 4.33

CX LogD: 4.33

Aromatic Rings: 0

Heavy Atoms: 49

QED Weighted: 0.14

Np Likeness Score: 2.74

References

1. Yazdani M, Béni Z, Dékány M, Szemerédi N, Spengler G, Hohmann J, Ványolós A..  (2022)  Triterpenes from Pholiota populnea as Cytotoxic Agents and Chemosensitizers to Overcome Multidrug Resistance of Cancer Cells.,  85  (4.0): [PMID:35293752] [10.1021/acs.jnatprod.1c01024]

Source

Source(1):

• Scientific Literature