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Cevipabulin fumarate (Synonyms: TTI-237 fumarate)

Katalog-Nr.GC35659

Cevipabulinfumarat (TTI-237-Fumarat) ist eine orale, Mikrotubuli-aktive Antitumorverbindung und hemmt die Bindung von [3H]NSC 49842 an Tubulin mit einem IC50-Wert von 18-40 nM fÜr ZytotoxizitÄt in menschlichen Tumorzelllinien.

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Cevipabulin fumarate Chemische Struktur

Cas No.: 849550-67-0

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10mM (in 1mL DMSO)
101,00 $
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5mg
79,00 $
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10mg
135,00 $
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50mg
454,00 $
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100mg
725,00 $
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Sample solution is provided at 25 µL, 10mM.

Description of Cevipabulin fumarate

Cevipabulin fumarate (TTI-237 fumarate) is an oral, microtubule-active, antitumor compound and inhibits the binding of [3H] vinblastine to tubulin, with an IC50 of 18-40 nM for cytotoxicity in human tumor cell line[1][2]. IC50: 18-40 nM (microtubule in human tumor cells)[1].

Cevipabulin (0-50 nM, 72 hours) shows good activity (between 18 and 40 nM IC50 values) on cell lines from ovarian, breast, prostate, and cervical tumors[1].Flow cytometry experiments reveal that, Cevipabulin (TTI-237) at low concentrations (20-40 nM) produces sub-G1 nuclei and, at concentrations above 50 nM, it causes a strong G2-M block[1]. Cell Cytotoxicity Assay[1] Cell Line: Human cancer cell lines (SK-OV-3, MDA-MB-435, MDA-MB-468, LnCaP, and Hela cells).

Cevipabulin (TTI-2370)( 5, 10, 15, and 20 mg/kg, every 4 days for 4 cycles, in mice) is active by i.v. and p.o. administration against human tumor xenografts, showing dose-dependent effects, with good antitumor activity at 20 and 15 mg/kg[1]. Animal Model: Athymic nu/nu female mice implanted s.c. in the flank with 1×107 LoVo human colon adenocarcinoma cells[1].

[1]. Beyer CF, et al. TTI-237: a novel microtubule-active compound with in vivo antitumor activity. Cancer Res. 2008 Apr 1;68(7):2292-300. [2]. Beyer CF, et al. The microtubule-active antitumor compound TTI-237 has both DB01229-like and Leurocristine-like properties. Cancer Chemother Pharmacol. 2009 Sep;64(4):681-9.

Chemical Properties of Cevipabulin fumarate

Cas No. 849550-67-0 SDF
Überlieferungen TTI-237 fumarate
Canonical SMILES C[C@@H](C(F)(F)F)NC1=C(C2=C(F)C=C(OCCCNC)C=C2F)C(Cl)=NC3=NC=NN13.O=C(O)/C=C/C(O)=O
Formula C22H22ClF5N6O5 M.Wt 580.89
Löslichkeit DMSO: 50 mg/mL (86.07 mM) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Cevipabulin fumarate

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 1.7215 mL 8.6075 mL 17.215 mL
5 mM 344.3 μL 1.7215 mL 3.443 mL
10 mM 172.1 μL 860.7 μL 1.7215 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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3. All of the above co-solvents are available for purchase on the GlpBio website.

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