NA

ID: ALA4476528

PubChem CID: 155538183

Max Phase: Preclinical

Molecular Formula: C68H103N21O22S4

Molecular Weight: 1694.97

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CC(C)C[C@@H]1NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](CCCCC(=O)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H]2CSSC[C@H](NC(=O)CN)C(=O)N[C@@H](CSSC[C@@H](C(N)=O)NC1=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)N2

Standard InChI:  InChI=1S/C68H103N21O22S4/c1-32(2)18-39-58(101)84-44(54(70)97)26-112-114-29-47-63(106)82-42(24-90)59(102)81-41(20-36-23-72-31-74-36)68(111)88-16-8-11-48(88)64(107)75-34(5)55(98)85-46(28-115-113-27-45(61(104)86-47)76-50(92)21-69)62(105)83-43(25-91)60(103)87-53(33(3)4)66(109)78-37(10-6-7-13-51(93)94)56(99)80-40(19-35-22-71-30-73-35)67(110)89-17-9-12-49(89)65(108)77-38(57(100)79-39)14-15-52(95)96/h22-23,30-34,37-49,53,90-91H,6-21,24-29,69H2,1-5H3,(H2,70,97)(H,71,73)(H,72,74)(H,75,107)(H,76,92)(H,77,108)(H,78,109)(H,79,100)(H,80,99)(H,81,102)(H,82,106)(H,83,105)(H,84,101)(H,85,98)(H,86,104)(H,87,103)(H,93,94)(H,95,96)/t34-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48-,49-,53-/m0/s1

Standard InChI Key:  QQODMJRPCBCHDU-PCZBOVPISA-N

Molfile:  

 
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M  END

Alternative Forms

1. Parent:

   

   ALA4476528

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 1694.97

Molecular Weight (Monoisotopic): 1693.6469

AlogP: ┄

#Rotatable Bonds: ┄

Polar Surface Area: ┄

Molecular Species: ┄

HBA: ┄

HBD: ┄

#RO5 Violations: ┄

HBA (Lipinski): ┄

HBD (Lipinski): ┄

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: ┄

CX LogP: ┄

CX LogD: ┄

Aromatic Rings: ┄

Heavy Atoms: ┄

QED Weighted: ┄

Np Likeness Score: ┄

References

1. Hone AJ, Fisher F, Christensen S, Gajewiak J, Larkin D, Whiteaker P, McIntosh JM..  (2019)  PeIA-5466: A Novel Peptide Antagonist Containing Non-natural Amino Acids That Selectively Targets α3β2 Nicotinic Acetylcholine Receptors.,  62  (13): [PMID:31194549] [10.1021/acs.jmedchem.9b00566]

2. Hone AJ, Kaas Q, Kearns I, Hararah F, Gajewiak J, Christensen S, Craik DJ, McIntosh JM..  (2021)  Computational and Functional Mapping of Human and Rat α6β4 Nicotinic Acetylcholine Receptors Reveals Species-Specific Ligand-Binding Motifs.,  64  (3.0): [PMID:33523678] [10.1021/acs.jmedchem.0c01973]

Source

Source(1):

• Scientific Literature