(23R,24S)-24-O-beta-D-fucopyranosyloxy-16beta,23-dihydroxy-6-oxo-5alpha-cholestan-3beta-yl-O-beta-D-glucopyranosyl-(1->6)-beta-D-glucopyranoside

ID: ALA2088134

PubChem CID: 66553816

Max Phase: Preclinical

Molecular Formula: C45H76O19

Molecular Weight: 921.08

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Synonyms: 6-dehydrochamaeliroside B | 6-dehydrochamaeliroside B|CHEMBL2088134

Canonical SMILES:  CC(C)[C@H](O[C@@H]1O[C@H](C)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)C[C@@H](C)[C@H]1[C@@H](O)C[C@H]2[C@@H]3CC(=O)[C@H]4C[C@@H](O[C@@H]5O[C@H](CO[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@@H](O)[C@H](O)[C@H]5O)CC[C@]4(C)[C@H]3CC[C@]12C

Standard InChI:  InChI=1S/C45H76O19/c1-17(2)40(64-42-38(57)34(53)31(50)19(4)60-42)27(49)11-18(3)30-26(48)14-23-21-13-25(47)24-12-20(7-9-44(24,5)22(21)8-10-45(23,30)6)61-43-39(58)36(55)33(52)29(63-43)16-59-41-37(56)35(54)32(51)28(15-46)62-41/h17-24,26-43,46,48-58H,7-16H2,1-6H3/t18-,19-,20+,21-,22+,23+,24-,26+,27-,28-,29-,30+,31+,32-,33-,34+,35+,36+,37-,38-,39-,40+,41-,42+,43-,44-,45+/m1/s1

Standard InChI Key:  BYQBLXOEOJKCOU-RUNVMKEQSA-N

Molfile:  

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M  END

Alternative Forms

  1. Parent:

Associated Targets(Human)

NFF (353 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MM96L (154 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 921.08Molecular Weight (Monoisotopic): 920.4981AlogP: -1.94#Rotatable Bonds: 13
Polar Surface Area: 315.21Molecular Species: NEUTRALHBA: 19HBD: 12
#RO5 Violations: 3HBA (Lipinski): 19HBD (Lipinski): 12#RO5 Violations (Lipinski): 3
CX Acidic pKa: 11.80CX Basic pKa: CX LogP: -1.36CX LogD: -1.36
Aromatic Rings: Heavy Atoms: 64QED Weighted: 0.09Np Likeness Score: 2.15

References

1. Challinor VL, Stuthe JM, Parsons PG, Lambert LK, Lehmann RP, Kitching W, De Voss JJ..  (2012)  Structure and bioactivity of steroidal saponins isolated from the roots of Chamaelirium luteum (false unicorn).,  75  (8): [PMID:22880631] [10.1021/np300393y]

Source