CAS 1000995-47-0

Fórmula: C39H42O14

InChI: InChI=1S/C39H42O14/c1-15-7-27(42)51-14-37(47)22-8-19(22)34(3)23(37)10-18-17(13-50-26(41)6-5-25(40)49-12-15)32(44)52-38(18)24(34)11-36(46)21-9-20(21)35(4)30(36)29(38)28-16(2)31(43)53-39(28,48)33(35)45/h7,19-24,33,45-48H,5-6,8-14H2,1-4H3/b15-7+/t19-,20+,21-,22-,23+,24-,33+,34-,35-,36-,37-,38-,39-/m0/s1

Chave InChI: SHDVXCYXBYXGAR-SALMQSNDSA-N

SMILES: C/C/1=C\C(=O)OC[C@@]2([C@H]3C[C@@H]3[C@]4([C@H]2CC5=C(COC(=O)CCC(=O)OC1)C(=O)O[C@]56[C@H]4C[C@@]7([C@H]8C[C@H]8[C@]9(C7=C6C1=C(C(=O)O[C@@]1([C@@H]9O)O)C)C)O)C)O

Chloramultilide B

CAS: 1000995-47-0

Chloramultilide B exhibits moderate in vitro antifungal activity.

Fórmula: C₃₉H₄₂O₁₄

Pureza: 98%

Cor e Forma: Solid

Peso molecular: 734.751

Ref: TM-TN3637

Chloramultilide B

CAS: 1000995-47-0

Fórmula: C₃₉H₄₂O₁₄

Pureza: 95%~99%

Peso molecular: 734.751

Ref: BP-SBP03241

Chloramultilide B

CAS: 1000995-47-0

Chloramultilide B is a complex macrolide, which is a type of natural product characterized by a large macrocyclic lactone ring. It is derived from marine bacteria, specifically isolated from Streptomyces species known for their prolific production of bioactive secondary metabolites. The mode of action of Chloramultilide B involves targeting and disrupting bacterial cell wall synthesis. This is achieved through its interaction with specific bacterial enzymes, leading to the inhibition of cell growth and ultimately resulting in bacterial cell death.

Fórmula: C₃₉H₄₂O₁₄

Pureza: Min. 95%

Peso molecular: 734.7 g/mol

Ref: 3D-AQB99547

16H-1,24,17a,15-[1]Propanyliden[3]ylidyne-14H,17aH-cyclopropa[r]cyclopropa[1,2]furo[3',2':6,7]acenaphtho[4,5-u][1,5,10,15]tetraoxacyclodocosin-4,9,12,16,19(2H,7H)-pentone, 1,10,11,20a,21,21a,21b,22,22a,22b,23,23a,24,24a,25,25a-hexadecahydro-1,20a,21,22b-tetrahydroxy-6,18,21a,24-tetramethyl-, (1S,5E,17aR,20aS,21R,21aS,21bR,22aS,22bS,23aS,24S,24aR,25aS,26R)-

CAS: 1000995-47-0

Fórmula: C₃₉H₄₂O₁₄

Pureza: 96.0%

Peso molecular: 734.7424

Ref: IN-DA0000WX