[Ala10] Polymyxin B3

ID: ALA1091291

PubChem CID: 25231942

Max Phase: Preclinical

Molecular Formula: C54H94N16O12

Molecular Weight: 1159.45

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCCCCC(=O)N[C@@H](CCN)C(=O)N[C@H](C(=O)N[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)[C@H](C)NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CCN)NC1=O)[C@@H](C)O

Standard InChI:  InChI=1S/C54H94N16O12/c1-6-7-8-9-13-16-43(72)62-35(17-23-55)51(79)70-44(33(5)71)54(82)67-39(21-27-59)48(76)66-40-22-28-60-45(73)32(4)61-46(74)36(18-24-56)63-47(75)37(19-25-57)65-52(80)41(29-31(2)3)68-53(81)42(30-34-14-11-10-12-15-34)69-49(77)38(20-26-58)64-50(40)78/h10-12,14-15,31-33,35-42,44,71H,6-9,13,16-30,55-59H2,1-5H3,(H,60,73)(H,61,74)(H,62,72)(H,63,75)(H,64,78)(H,65,80)(H,66,76)(H,67,82)(H,68,81)(H,69,77)(H,70,79)/t32-,33+,35-,36-,37-,38-,39-,40-,41-,42+,44-/m0/s1

Standard InChI Key:  VMJRKKZSPJEFBH-YNVBWGHWSA-N

Molfile:  

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M  END

Associated Targets(non-human)

Lipopolysaccharide (LPS) (376 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Salmonella enterica (1497 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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

Calculated Properties

Molecular Weight: 1159.45Molecular Weight (Monoisotopic): 1158.7237AlogP: #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. Velkov T, Thompson PE, Nation RL, Li J..  (2010)  Structure--activity relationships of polymyxin antibiotics.,  53  (5): [PMID:19874036] [10.1021/jm900999h]
2. Mark Wenlock and Nicholas Tomkinson. Experimental in vitro DMPK and physicochemical data on a set of publicly disclosed compounds,  [10.6019/CHEMBL3301361]