Citreamicin θ A

AlkaPlorer ID: AK033112

Synonym: None

IUPAC Name: (7S,10R)-3,18,19,23-tetrahydroxy-7-(hydroxymethyl)-24-methoxy-7,10-dimethyl-9,28-dioxa-6-azaheptacyclo[15.12.0.02,14.04,12.06,10.020,29.022,27]nonacosa-1(17),2,4(12),13,18,20(29),22(27),23,25-nonaene-5,8,21-trione

Structure

SMILES: COC1=CC=C2OC3=C4C(=C(O)C(O)=C3C(=O)C2=C1O)CCC1=CC2=C(C(=O)N3[C@@](C)(C2)OC(=O)[C@]3(C)CO)C(O)=C14

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InChI: InChI=1S/C30H25NO11/c1-29(10-32)28(39)42-30(2)9-12-8-11-4-5-13-18(16(11)23(35)17(12)27(38)31(29)30)26-20(25(37)21(13)33)24(36)19-14(41-26)6-7-15(40-3)22(19)34/h6-8,32-35,37H,4-5,9-10H2,1-3H3/t29-,30+/m0/s1

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InChIKey: CELAFVAJJRUNHZ-XZWHSSHBSA-N

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Source

Properties Information

Molecule Weight: 575.5260000000004

TPSA: 187.2

MolLogP: 2.565100000000002

Number of H-Donors: 5

Number of H-Acceptors: 11

RingCount: 7

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Bacillus subtilis Bacillus subtilis MIC 1.0 ug.mL-1 10.1021/acs.jnatprod.6b00235
Staphylococcus aureus Staphylococcus aureus MIC 1.0 ug.mL-1 10.1021/acs.jnatprod.6b00235
Staphylococcus haemolyticus Staphylococcus haemolyticus MIC 1.0 ug.mL-1 10.1021/acs.jnatprod.6b00235

Metabolism Information