Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5087883
Max Phase: Preclinical
Molecular Formula: C62H89ClF2N6O13
Molecular Weight: 1199.87
Molecule Type: Unknown
Associated Items:
ID: ALA5087883
Max Phase: Preclinical
Molecular Formula: C62H89ClF2N6O13
Molecular Weight: 1199.87
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CO[C@]1(C)C[C@H](O[C@H]2[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@H](N(C)C)[C@H]3O)[C@](C)(O)C[C@@H](C)CN(C)C(=O)C[C@@H](Cc3ccc(NC(=O)[C@H](Cc4ccccc4Cl)NC(=O)C(F)(F)c4ccccc4)cc3)NC(=O)[C@H](C(C)C)NC(=O)[C@@H]2C)O[C@@H](C)[C@@H]1O
Standard InChI: InChI=1S/C62H89ClF2N6O13/c1-34(2)50-57(77)67-44(28-40-23-25-43(26-24-40)66-56(76)46(29-41-19-17-18-22-45(41)63)68-59(78)62(64,65)42-20-15-14-16-21-42)30-48(72)71(12)33-35(3)31-60(8,79)54(84-58-51(73)47(70(10)11)27-36(4)81-58)37(5)52(38(6)55(75)69-50)83-49-32-61(9,80-13)53(74)39(7)82-49/h14-26,34-39,44,46-47,49-54,58,73-74,79H,27-33H2,1-13H3,(H,66,76)(H,67,77)(H,68,78)(H,69,75)/t35-,36-,37+,38-,39+,44-,46+,47+,49+,50+,51-,52+,53+,54-,58+,60-,61-/m1/s1
Standard InChI Key: PTUMYUHOOAMOQY-SBAMXTJPSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 1199.87 | Molecular Weight (Monoisotopic): 1198.6144 | 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. Koštrun S, Fajdetić A, Pešić D, Brajša K, Bencetić Mihaljević V, Jelić D, Petrinić Grba A, Elenkov I, Rupčić R, Kapić S, Ozimec Landek I, Butković K, Grgičević A, Žiher D, Čikoš A, Padovan J, Saxty G, Dack K, Bladh H, Skak-Nielsen T, Feldbaek Nielsen S, Lambert M, Stahlhut M.. (2021) Macrolide Inspired Macrocycles as Modulators of the IL-17A/IL-17RA Interaction., 64 (12.0): [PMID:34100601] [10.1021/acs.jmedchem.1c00327] |
Source(1):