Molecule

(3S,4S,6R,9R,10R,16R,18S)-9-(carbamoyloxy)-10-hydroxy-3,6,16-trimethyl-18-[(1E,3E)-2-methylnona-1,3-dien-1-yl]-2-oxo-1-oxacyclooctadec-13-en-4-yl carbamate

AlkaPlorer ID: AK105129

Synonym: None

IUPAC Name: [(3R,4R,6S,9S,10S,13E,16R,18S)-4-carbamoyloxy-10-hydroxy-3,6,16-trimethyl-18-[(1E,3E)-2-methylnona-1,3-dienyl]-2-oxo-1-oxacyclooctadec-13-en-9-yl] carbamate

Structure

SMILES: CCCCC/C=C/C(C)=C/[C@@H]1C[C@H](C)C/C=C/CC[C@H](O)[C@@H](OC(N)=O)CC[C@H](C)C[C@@H](OC(N)=O)[C@@H](C)C(=O)O1

InChI: InChI=1S/C32H54N2O7/c1-6-7-8-9-11-14-22(2)19-26-20-23(3)15-12-10-13-16-27(35)28(40-31(33)37)18-17-24(4)21-29(41-32(34)38)25(5)30(36)39-26/h10-12,14,19,23-29,35H,6-9,13,15-18,20-21H2,1-5H3,(H2,33,37)(H2,34,38)/b12-10+,14-11+,22-19+/t23-,24+,25-,26-,27+,28+,29-/m1/s1

InChIKey: LVJVVBKSVCMFFS-YPLUWHBUSA-N

Reference

Isolation and Characterization of New 16-Membered Macrolides from the <i>aveA3</i> Gene Replacement Mutant Strain <i>Streptomyces avermitilis</i> TM24 with Acaricidal and Nematicidal Activities

HIGH-PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD FOR THE DETERMINATION OF OCCUPATIONAL EXPOSURE TO THE PESTICIDE ABAMECTIN

SAV4189, a MarR-Family Regulator in Streptomyces avermitilis, Activates Avermectin Biosynthesis

Direct production of ivermectin-like drugs after domain exchange in the avermectin polyketide synthase of Streptomyces avermitilis ATCC31272

Engineered biosynthesis of milbemycins in the avermectin high-producing strain Streptomyces avermitilis

Construction of ivermectin producer by domain swaps of avermectin polyketide synthase in Streptomyces avermitilis

PubChem CID: 101468445

SuperNatural Ⅲ: SN0216444-03

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain

Properties Information

Molecule Weight: 578.7910000000004

TPSA？: 151.17

MolLogP？: 6.478500000000006

Number of H-Donors: 3

Number of H-Acceptors: 7

RingCount: 1

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi

Metabolism Information