ID: ALA5281783

Max Phase: Preclinical

Molecular Formula: C32H48N2O2

Molecular Weight: 492.75

Representations

Canonical SMILES:  CC(=O)C1CCN(CCCOc2ccc3c(c2)CC[C@@H]2[C@@H]3CC[C@]3(C)[C@@H](N4CCCC4)CC[C@@H]23)CC1

Standard InChI:  InChI=1S/C32H48N2O2/c1-23(35)24-13-19-33(20-14-24)16-5-21-36-26-7-9-27-25(22-26)6-8-29-28(27)12-15-32(2)30(29)10-11-31(32)34-17-3-4-18-34/h7,9,22,24,28-31H,3-6,8,10-21H2,1-2H3/t28-,29-,30+,31+,32+/m1/s1

Standard InChI Key:  JZHDMAKZPRQFAR-KQLGDFJMSA-N

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

Properties

Molecular Weight: 492.75

Molecular Weight (Monoisotopic): 492.3716

AlogP: 6.08

#Rotatable Bonds: 7

Polar Surface Area: 32.78

Molecular Species: BASE

HBA: 4

HBD: 0

#RO5 Violations: 1

HBA (Lipinski): 4

HBD (Lipinski): 0

#RO5 Violations (Lipinski): 1

CX Acidic pKa:

CX Basic pKa: 10.69

CX LogP: 5.49

CX LogD: 1.32

Aromatic Rings: 1

Heavy Atoms: 36

QED Weighted: 0.43

Np Likeness Score: 0.43

References

1. Ledneczki I, Tapolcsányi P, Gábor E, Éles J, Greiner I, Schmidt É, Némethy Z, Kedves RS, Balázs O, Román V, Lévay G, Mahó S..  (2017)  Discovery of novel steroidal histamine H₃ receptor antagonists/inverse agonists.,  27  (19): [PMID:28888822] [10.1016/j.bmcl.2017.08.060]

Source

Source(1):

• Scientific Literature