(E)-(1-([1,1'-biphenyl]-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methyl 3-formyl 5-(5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl)pent-3-enoate

ID: ALA4170734

Chembl Id: CHEMBL4170734

PubChem CID: 145949153

Max Phase: Preclinical

Molecular Formula: C36H43N3O3

Molecular Weight: 565.76

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  C=C1CC[C@H]2C(C)(C)CCC[C@]2(C)C1C/C=C(/C=O)CC(=O)OCc1cn(Cc2ccccc2-c2ccccc2)nn1

Standard InChI:  InChI=1S/C36H43N3O3/c1-26-15-18-33-35(2,3)19-10-20-36(33,4)32(26)17-16-27(24-40)21-34(41)42-25-30-23-39(38-37-30)22-29-13-8-9-14-31(29)28-11-6-5-7-12-28/h5-9,11-14,16,23-24,32-33H,1,10,15,17-22,25H2,2-4H3/b27-16+/t32?,33-,36+/m0/s1

Standard InChI Key:  UMODJNYTULVTCJ-HGXJMCTDSA-N

Alternative Forms

1. Parent:

   

   ALA4170734

   ---

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: 565.76

Molecular Weight (Monoisotopic): 565.3304

AlogP: 7.74

#Rotatable Bonds: 10

Polar Surface Area: 74.08

Molecular Species: NEUTRAL

HBA: 6

HBD: ┄

#RO5 Violations: 2

HBA (Lipinski): 6

HBD (Lipinski): ┄

#RO5 Violations (Lipinski): 2

CX Acidic pKa: ┄

CX Basic pKa: ┄

CX LogP: 7.52

CX LogD: 7.52

Aromatic Rings: 3

Heavy Atoms: 42

QED Weighted: 0.11

Np Likeness Score: 0.91

References

1. Jalaja R, Leela SG, Valmiki PK, Salfeena CTF, Ashitha KT, Krishna Rao VRD, Nair MS, Gopalan RK, Somappa SB..  (2018)  Discovery of Natural Product Derived Labdane Appended Triazoles as Potent Pancreatic Lipase Inhibitors.,  9  (7): [PMID:30034597] [10.1021/acsmedchemlett.8b00109]

Source

Source(1):

• Scientific Literature