156294-36-9

156294-36-9 structure
156294-36-9 structure
  • Name: Larotaxel
  • Chemical Name: (3ξ,5β,7β,10β)-4,10-Diacetoxy-1-hydroxy-13-{[(3S)-2-hydroxy-3-({[ (2-methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoyl]oxy}-9 -oxo-5,20-epoxy-7,19-cyclotax-11-en-2-yl benzoate
  • CAS Number: 156294-36-9
  • Molecular Formula: C45H53NO14
  • Molecular Weight: 831.901
  • Catalog: Signaling Pathways Apoptosis Apoptosis
  • Create Date: 2016-08-18 22:03:56
  • Modify Date: 2024-01-12 18:19:57
  • Larotaxel (XRP9881) is a taxane analogue with preclinical activity against taxane-resistant breast cancer. Larotaxel (XRP9881) exerts its cytotoxic effect by promoting tubulin assembly and stabilizing microtubules, ultimately leading to cell death by apoptosis. It presents the ability to cross the blood brain barrier and has a much lower affinity for P-glycoprotein 1 than Docetaxel[1][2][3].

Name (3ξ,5β,7β,10β)-4,10-Diacetoxy-1-hydroxy-13-{[(3S)-2-hydroxy-3-({[ (2-methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoyl]oxy}-9 -oxo-5,20-epoxy-7,19-cyclotax-11-en-2-yl benzoate
Synonyms acetylcyclopropyl docetaxel
Valiolamine hydrate
Benzenepropanoic acid, β-[[(1,1-dimethylethoxy)carbonyl]amino]-α-hydroxy-, (1S,2S,4S,7R,8aR,9aS,10aR,12aS,12bR)-7,12a-bis(acetyloxy)-1-(benzoyloxy)-1,3,4,7,8,9,9a,10,10a,12,12a,12b-dodecahydro- 2-hydroxy-5,13,13-trimethyl-8-oxo-2,6-methano-2H-cyclodeca[3,4]cyclopropa[4,5]benz[1,2-b]oxet-4-yl ester, (αR,βS)-
Valinolamine
valiolamine
acetocyclopropyl taxotere
(2α,5β,7β,10β,13α)-4,10-Diacetoxy-1-hydroxy-13-{[(2R,3S)-2-hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoyl]oxy}-9-oxo-5,20-epoxy-7,19-cyclotax-11-en-2-yl benzo 
ate
Description Larotaxel (XRP9881) is a taxane analogue with preclinical activity against taxane-resistant breast cancer. Larotaxel (XRP9881) exerts its cytotoxic effect by promoting tubulin assembly and stabilizing microtubules, ultimately leading to cell death by apoptosis. It presents the ability to cross the blood brain barrier and has a much lower affinity for P-glycoprotein 1 than Docetaxel[1][2][3].
Related Catalog
References

[1]. Diéras V, et al. Phase II multicenter study of larotaxel (XRP9881), a novel taxoid, in patients with metastatic breast cancer who previously received taxane-based therapy. Ann Oncol. 2008 Jul;19(7):1255-60.

[2]. Morris PG, et al. Novel anti-tubulin cytotoxic agents for breast cancer. Expert Rev Anticancer Ther. 2009 Feb;9(2):175-85.

[3]. Zatloukal P, et al. Randomized multicenter phase II study of larotaxel (XRP9881) in combination with cisplatin or gemcitabine as first-line chemotherapy in nonirradiable stage IIIB or stage IV non-small cell lung cancer. J Thorac Oncol. 2008 Aug;3(8):894-901.

Density 1.4±0.1 g/cm3
Boiling Point 889.3±65.0 °C at 760 mmHg
Molecular Formula C45H53NO14
Molecular Weight 831.901
Flash Point 491.7±34.3 °C
Exact Mass 831.346619
PSA 213.78000
LogP 7.06
Vapour Pressure 0.0±0.3 mmHg at 25°C
Index of Refraction 1.613

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156294-36-9 structure

156294-36-9

Literature: US2012/149925 A1, ; Page/Page column 17 ;

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156294-36-9 structure

156294-36-9

Literature: US2012/149925 A1, ;

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156294-36-9 structure

156294-36-9

Literature: US2012/149925 A1, ;

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156294-36-9 structure

156294-36-9

Literature: US2012/149925 A1, ;
Precursor  3

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