2α,7β,13α-Triacetoxy-5α-cinnamoyloxy-9β-hydroxy-2(3→20)abeotaxa-4(20),11-dien-10-one

95%

Reagent Code: #241387
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CAS Number 322471-42-1

science Other reagents with same CAS 322471-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 622.702 g/mol
Formula C₃₅H₄₂O₁₀
thermostat Physical Properties
Boiling Point 706.7±60.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.3±0.1g/ml
Storage 2-8℃

description Product Description

Used in research as a semi-synthetic derivative of taxane natural products, this compound is investigated for its potential anticancer properties. It interacts with microtubule dynamics, potentially inhibiting cell division, which makes it relevant in oncology drug development. Its ester and hydroxy modifications enhance cell membrane permeability and may improve bioavailability compared to parent compounds. Currently, it serves primarily as a tool compound in mechanistic studies of tubulin polymerization and cytotoxicity in tumor cell lines.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿42,840.00

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2α,7β,13α-Triacetoxy-5α-cinnamoyloxy-9β-hydroxy-2(3→20)abeotaxa-4(20),11-dien-10-one
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Used in research as a semi-synthetic derivative of taxane natural products, this compound is investigated for its potential anticancer properties. It interacts with microtubule dynamics, potentially inhibiting cell division, which makes it relevant in oncology drug development. Its ester and hydroxy modifications enhance cell membrane permeability and may improve bioavailability compared to parent compounds. Currently, it serves primarily as a tool compound in mechanistic studies of tubulin polymerizatio

Used in research as a semi-synthetic derivative of taxane natural products, this compound is investigated for its potential anticancer properties. It interacts with microtubule dynamics, potentially inhibiting cell division, which makes it relevant in oncology drug development. Its ester and hydroxy modifications enhance cell membrane permeability and may improve bioavailability compared to parent compounds. Currently, it serves primarily as a tool compound in mechanistic studies of tubulin polymerization and cytotoxicity in tumor cell lines.

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