3-O-Descladinosyl-3-keto-6-O-methylerythromycin A E-9-O-[3-(5'-pyrimidyl)-2-propargyl]oxime 11,12-cyclic carbonate

ID: ALA2316674

PubChem CID: 71570652

Max Phase: Preclinical

Molecular Formula: C38H56N4O11

Molecular Weight: 744.88

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(OC)C[C@@H](C)/C(=N\OCC#Cc2cncnc2)[C@H](C)[C@H]2OC(=O)O[C@@]21C

Standard InChI:  InChI=1S/C38H56N4O11/c1-12-28-38(8)33(52-36(46)53-38)23(4)29(41-48-15-13-14-26-18-39-20-40-19-26)21(2)17-37(7,47-11)32(24(5)30(43)25(6)34(45)50-28)51-35-31(44)27(42(9)10)16-22(3)49-35/h18-25,27-28,31-33,35,44H,12,15-17H2,1-11H3/b41-29+/t21-,22-,23+,24+,25-,27+,28-,31-,32-,33-,35+,37-,38-/m1/s1

Standard InChI Key:  MVADRHURRVRRCU-QKIZNIJLSA-N

Molfile:  

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M  END

Associated Targets(non-human)

Staphylococcus hominis (482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus epidermidis (22802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus haemolyticus (1695 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus pyogenes (16140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus dysgalactiae (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus pneumoniae (31063 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: 744.88Molecular Weight (Monoisotopic): 744.3946AlogP: 3.55#Rotatable Bonds: 7
Polar Surface Area: 177.43Molecular Species: NEUTRALHBA: 15HBD: 1
#RO5 Violations: 2HBA (Lipinski): 15HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 8.93CX Basic pKa: 8.27CX LogP: 4.81CX LogD: 4.20
Aromatic Rings: 1Heavy Atoms: 53QED Weighted: 0.14Np Likeness Score: 1.04

References

1. Liang JH, An K, Lv W, Cushman M, Wang H, Xu YC..  (2013)  Synthesis, antibacterial activity and docking of 14-membered 9-O-(3-arylalkyl) oxime 11,12-cyclic carbonate ketolides.,  59  [PMID:23202851] [10.1016/j.ejmech.2012.10.054]

Source