Compound Summary


  Compound Information
 charantoside II

Compound Name:

charantoside II

Compound CID:

23626168

Synonyms:

charantoside II

CHEMBL255021







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Iupac Name:

(2R,3S,4R,5R,6R)-2-(hydroxymethyl)-6-[[(1R,4S,5S,8R,9R,12S,13S,16S,19R)-19-methoxy-8-[(2R,4R)-4-methoxy-6-methylhept-5-en-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-yl]oxy]oxane-3,4,5-triol

InChI:

InChI=1S/C38H62O9/c1-21(2)18-23(43-8)19-22(3)24-12-14-36(7)26-13-15-38-27(37(26,33(44-9)47-38)17-16-35(24,36)6)10-11-28(34(38,4)5)46-32-31(42)30(41)29(40)25(20-39)45-32/h13,15,18,22-33,39-42H,10-12,14,16-17,19-20H2,1-9H3/t22-,23+,24-,25-,26+,27+,28+,29-,30-,31-,32+,33-,35-,36+,37+,38-/m1/s1

InChIKey:

YDOSNHSZOCLBFE-HGJRUNHKSA-N

Canonical Smiles:

CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC34C2C=CC5(C3CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)OC4OC)C)C

Isomeric Smiles:

C[C@H](C[C@H](C=C(C)C)OC)[C@H]1CC[C@@]2([C@@]1(CC[C@]34[C@H]2C=C[C@]5([C@H]3CC[C@@H](C5(C)C)O[C@H]6[C@@H]([C@@H]([C@@H]([C@H](O6)CO)O)O)O)O[C@H]4OC)C)C

Molecular Weight:

662.9

Molecular Formula:

C38H62O9

  Compound Structure
 2D Structure:
 3D Structure:
  Computed Properties
 charantoside II

Molecular Weight:

662.9

Molecular Formula:

C38H62O9

Hydrogen Bond Donor Count:

4

Hydrogen Bond Acceptor Count:

9

Rotatable Bond Count:

9

Heavy Atom Count:

47

Complexity:

1220

  Synonyms
 charantoside II

charantoside II charantoside II

charantoside II

CHEMBL255021

  Experimental Data
 charantoside II

Species Dosage Unit CG Lifespan(AVG/MED days) TG Lifespan(AVG/MED days) Lifespan Change(AVG/MED%) CG Lifespan(MAX days) TG Lifespan(MAX days) Lifespan Change(MAX%) Significant Strain Gender PubMed Active Label
Saccharomyces cerevisiae 3 umol/L 7.7 9.73 0.26 S K6001 29765490 Active
Saccharomyces cerevisiae 1 umol/L 7.7 9.63 0.25 S K6001 29765490 Active
  Experimental Data Visualization
 charantoside II

  Statistics Data
 charantoside II

Species Lifespan Change(AVG/MED%) Lifespan Change(MAX%) Count Reference Count Data point
Saccharomyces cerevisiae 0.26 1 2
  Statistics Data Visualization
 charantoside II