ChemicalBook--->CAS DataBase List--->108885-69-4

108885-69-4

108885-69-4 Structure

108885-69-4 Structure
IdentificationBack Directory
[Name]

Taccalonolide B
[CAS]

108885-69-4
[Synonyms]

Taccalonolide B
ETaccalonolide B
16,24-Cycloergost-22-en-26-oic acid, 1,11,12-tris(acetyloxy)-2,3-epoxy-7,15,23,25-tetrahydroxy-6-oxo-, γ-lactone, (1α,2α,3α,5α,7β,11α,12α,15α,16β,24β,25S)-
(1alpha,2alpha,3alpha,5alpha,7beta,11alpha,12alpha,15alpha,16beta,24beta,25S)-1,11,12-Tris(acetyloxy)-2,3-epoxy-7,15,23,25-tetrahydroxy-6-oxo-16,24-cycloergost-22-en-26-oic acid gamma-lactone
[Molecular Formula]

C34H44O13
[MDL Number]

MFCD30725005
[MOL File]

108885-69-4.mol
[Molecular Weight]

660.71
Chemical PropertiesBack Directory
[density ]

1.43±0.1 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

White to off-white
[InChIKey]

FFQOXBQSZPYHSA-MPOUNFKCSA-N
Hazard InformationBack Directory
[Uses]

Taccalonolide B is microtubule stabilizer isolated from Tacca plantaginea, with antitumor activity. Taccalonolide B is effective in vitro against cell lines that overexpress P-glycoprotein (Pgp) and multidrug-resistance protein (MRP7). Taccalonolide B inhibits growth of SK-OV-3 cells with an IC50 of 208 nM[1][2].
[storage]

Store at -20°C
[References]

[1] LiangChen Zhong, et al. Steroidal bitter principles from tacca plantaginea structures of taccalonolide A and B. Tetrahedron Letters. 1987, 28(15): 1673-1675.
[2] Risinger AL, et al. The taccalonolides: microtubule stabilizers that circumvent clinically relevant taxane resistance mechanisms. Cancer Res. 2008 Nov 1;68(21):8881-8. DOI:10.1158/0008-5472.CAN-08-2037
Spectrum DetailBack Directory
[Spectrum Detail]

Taccalonolide B(108885-69-4)1HNMR
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