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Moenomycin Complex

CAT: 0931-T36990-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0931-T36990-01Size:5 mg
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CAS Number
11015-37-5
Target
Antibacterial, Antibiotic
Related Pathways
Microbiology/Virology
Bioactivity
Moenomycin complex is a mixture of moenomycins A, A12, C1, C3 and C4, which are antibiotics isolated from several strains of Streptomyces that directly inhibit bacterial peptidoglycan glycosyltransferases. The minimal inhibitory concentration of moenomycin A against various Gram-positive bacteria ranges from 1-100 nM.
Smiles
C[C@@H]1O[C@H](O[C@@H]2[C@@H](O)[C@H](NC(C)=O)[C@@H](O[C@@H]3[C@H](OP(O)(=O)OC[C@H](OC\C=C(\C)CC\C=C/C(C)(C)CCC(=C)C\C=C(/C)CCC=C(C)C)C(O)=O)O[C@@H](C(N)=O)[C@](C)(O)[C@H]3OC(C)=O)O[C@H]2COC(=O)CO)[C@@H](NC(C)=O)[C@H](O)[C@H]1O[C@H]1O[C@H]([C@@H](O)[C@@H](O)[C@@H]1O)C(=O)NC1=C(O)CCC1=O
Molecular Formula
C66H101N4O31P
Molecular Weight
1477.505
Shipping Conditions
Ice Packs
Storage Temperature
-20°C

Chemical Information

Flavomycin

Bambermycin is a glycophospholipid antibiotic compound with the lipid portion conjugated to a pentasaccharide fraction via a phosphate linkage. It has a role as an antimicrobial agent.

CAS Number11015-37-5
PubChem CID11953887
IUPAC Name(2S,3S,4R,5R,6R)-5-[(2S,3R,4R,5S,6R)-3-acetamido-5-[(2S,3R,4R,5S,6R)-3-acetamido-4-hydroxy-6-methyl-5-[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-[(2-hydroxy-5-oxocyclopenten-1-yl)carbamoyl]oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-4-carbamoyloxy-6-[[(2R)-2-carboxy-2-[(2E,6E,13E)-3,8,8,14,18-pentamethyl-11-methylidenenonadeca-2,6,13,17-tetraenoxy]ethoxy]-hydroxyphosphoryl]oxy-3-hydroxy-3-methyloxane-2-carboxylic acid
Molecular FormulaC69H107N4O35P
Molecular Weight1583.6
XLogP-0.7
Topological Polar Surface Area602
Hydrogen Bond Donor Count18
Hydrogen Bond Acceptor Count35
Rotatable Bond Count38
Heavy Atom Count109
Formal Charge0
Complexity3370
SMILES
C[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)NC(=O)C)O[C@@H]3[C@H]([C@]([C@H](O[C@@H]3OP(=O)(O)OC[C@H](C(=O)O)OC/C=C(\C)/CC/C=C/C(C)(C)CCC(=C)C/C=C(\C)/CCC=C(C)C)C(=O)O)(C)O)OC(=O)N)CO[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)NC(=O)C)O)O[C@H]5[C@@H]([C@H]([C@H]([C@H](O5)C(=O)NC6=C(CCC6=O)O)O)O)O
InChI
InChI=1S/C69H107N4O35P/c1-30(2)15-14-17-31(3)18-19-33(5)22-25-68(9,10)24-13-12-16-32(4)23-26-96-41(60(88)89)29-98-109(94,95)108-66-56(57(107-67(70)92)69(11,93)58(106-66)61(90)91)105-63-44(72-36(8)76)47(81)54(40(101-63)28-97-64-51(85)48(82)45(79)39(27-74)100-64)103-62-43(71-35(7)75)46(80)53(34(6)99-62)102-65-52(86)49(83)50(84)55(104-65)59(87)73-42-37(77)20-21-38(42)78/h13,15,18,23-24,34,39-41,43-58,62-66,74,77,79-86,93H,5,12,14,16-17,19-22,25-29H2,1-4,6-11H3,(H2,70,92)(H,71,75)(H,72,76)(H,73,87)(H,88,89)(H,90,91)(H,94,95)/b24-13+,31-18+,32-23+/t34-,39-,40-,41-,43-,44-,45-,46-,47-,48+,49+,50-,51-,52-,53-,54-,55+,56-,57-,58-,62+,63+,64-,65-,66-,69+/m1/s1
InChIKey
PERZMHJGZKHNGU-JGYWJTCASA-N
Chemical Structure
2D Structure
2D structure of Flavomycin
CAS: 11015-37-5
CID: 11953887
Formula: C69H107N4O35P
MW: 1583.6
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight1583.6
XLogP3-0.7
Hydrogen Bond Donor Count18
Hydrogen Bond Acceptor Count35
Rotatable Bond Count38
Exact Mass1582.6453481
Monoisotopic Mass1582.6453481
Topological Polar Surface Area602 Ų
Heavy Atom Count109
Formal Charge0
Complexity3370
Isotope Atom Count0
Defined Atom Stereocenter Count26
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count3
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes