2-((3S,6S,12S,17S)-17-carbamoyl-3-cyclohexyl-12-(3-guanidinopropyl)-7-methyl-2,5,8,11,14-pentaoxo-1,4,7,10,13-pentaazacycloheptadecan-6-yl)acetic acid

ID: ALA5221029

Chembl Id: CHEMBL5221029

PubChem CID: 168298756

Max Phase: Preclinical

Molecular Formula: C26H43N9O8

Molecular Weight: 609.69

Names and Identifiers

Canonical SMILES:  CN1C(=O)CNC(=O)[C@H](CCCNC(=N)N)NC(=O)CC[C@@H](C(N)=O)NC(=O)[C@H](C2CCCCC2)NC(=O)[C@@H]1CC(=O)O

Standard InChI:  InChI=1S/C26H43N9O8/c1-35-17(12-20(38)39)24(42)34-21(14-6-3-2-4-7-14)25(43)33-15(22(27)40)9-10-18(36)32-16(8-5-11-30-26(28)29)23(41)31-13-19(35)37/h14-17,21H,2-13H2,1H3,(H2,27,40)(H,31,41)(H,32,36)(H,33,43)(H,34,42)(H,38,39)(H4,28,29,30)/t15-,16-,17-,21-/m0/s1

Standard InChI Key:  UGZIVRDEXXWIIZ-IAGYGMIVSA-N

Alternative Forms

1. Parent:

   

   ALA5221029

   ---

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: 609.69

Molecular Weight (Monoisotopic): 609.3235

AlogP: -3.02

#Rotatable Bonds: 8

Polar Surface Area: 279.00

Molecular Species: ZWITTERION

HBA: 8

HBD: 9

#RO5 Violations: 2

HBA (Lipinski): 17

HBD (Lipinski): 11

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 4.05

CX Basic pKa: 11.90

CX LogP: -5.63

CX LogD: -5.63

Aromatic Rings: 0

Heavy Atoms: 43

QED Weighted: 0.08

Np Likeness Score: 0.63

References

1. Tomassi S, D'Amore VM, Di Leva FS, Vannini A, Quilici G, Weinmüller M, Reichart F, Amato J, Romano B, Izzo AA, Di Maro S, Novellino E, Musco G, Gianni T, Kessler H, Marinelli L..  (2021)  Halting the Spread of Herpes Simplex Virus-1: The Discovery of an Effective Dual αvβ6/αvβ8 Integrin Ligand.,  64  (10.0): [PMID:33961417] [10.1021/acs.jmedchem.1c00533]

Source

Source(1):

• Scientific Literature