ID: ALA5087883

Max Phase: Preclinical

Molecular Formula: C62H89ClF2N6O13

Molecular Weight: 1199.87

Molecule Type: Unknown

Associated Items:

Representations

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

Associated Targets(Human)

Keratinocyte 44 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 1199.87Molecular Weight (Monoisotopic): 1198.6144AlogP: #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. 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