ID: ALA4081435
PubChem CID: 137647644
Max Phase: Preclinical
Molecular Formula: C57H88N18O20S5
Molecular Weight: 1505.77
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CSCCC[C@@H]1NC(=O)[C@H](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)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H]3CCCN3C(=O)[C@H](CO)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)C)C(=O)N2
Standard InChI: InChI=1S/C57H88N18O20S5/c1-26(2)43-55(93)72-38-24-100-98-22-36(63-41(79)16-58)50(88)71-37(51(89)68-33(19-77)49(87)66-31(14-28-17-60-25-61-28)56(94)74-11-6-10-40(74)54(92)73-43)23-99-97-21-35(44(59)82)70-47(85)30(15-42(80)81)65-53(91)39-9-5-12-75(39)57(95)34(20-78)69-46(84)29(8-7-13-96-4)64-45(83)27(3)62-48(86)32(18-76)67-52(38)90/h17,25-27,29-40,43,76-78H,5-16,18-24,58H2,1-4H3,(H2,59,82)(H,60,61)(H,62,86)(H,63,79)(H,64,83)(H,65,91)(H,66,87)(H,67,90)(H,68,89)(H,69,84)(H,70,85)(H,71,88)(H,72,93)(H,73,92)(H,80,81)/t27-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-,40-,43-/m0/s1
Standard InChI Key: KWNFSJLIQMJIHN-PMIOLOJASA-N
Molfile:
RDKit 2D
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M END| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| 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 |
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| Molecular Weight: 1505.77 | Molecular Weight (Monoisotopic): 1504.5026 | 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: ┄ |
| 1. Wu Y, Zhangsun D, Zhu X, Kaas Q, Zhangsun M, Harvey PJ, Craik DJ, McIntosh JM, Luo S.. (2017) α-Conotoxin [S9A]TxID Potently Discriminates between α3β4 and α6/α3β4 Nicotinic Acetylcholine Receptors., 60 (13): [PMID:28603989] [10.1021/acs.jmedchem.7b00546] |
Source(1):