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T-900607

Catalog No. T68147   CAS 261944-52-9

T-900607 is a novel microtubule protein active agent that disrupts microtubule polymerization through a unique mechanism of action. t-900607 is cardiotoxic.

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T-900607 Chemical Structure
T-900607, CAS 261944-52-9
Pack Size Availability Price/USD Quantity
1 mg In stock $ 195.00
5 mg In stock $ 430.00
10 mg In stock $ 636.00
25 mg In stock $ 987.00
50 mg In stock $ 1,360.00
100 mg In stock $ 1,830.00
500 mg In stock $ 3,680.00
1 mL * 10 mM (in DMSO) In stock $ 478.00
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Biological Description
Chemical Properties
Storage & Solubility Information
Description T-900607 is a novel microtubule protein active agent that disrupts microtubule polymerization through a unique mechanism of action. t-900607 is cardiotoxic.
Targets&IC50 HeLa cells:< 5 μM, MCF-7/ADR cells:< 5 μM
In vitro t-900607 (compound 5 or VI) showed total growth inhibition for HeLa and MCF-7/ADR cells at<5 μM.[2]
In vivo t-900607 (15 to 270 mg/m; administered intravenously; advanced and/or metastatic solid malignancies patients; over 30 minutes every 21 days) no DLTs were seen until 270 mg/m, the sixth dose level. The dose was decreased to 180 mg/m with increased cardiac monitoring and at this dose 3/4 of patients experienced cardiac toxicity. The study was reopened at 130 mg/m of 6 enrolled patients, 1 had grade 3 drug-related lethargy considered to be a DLT and this dose was considered the RP2D. No objective responses were seen but stable disease was reported on 7/20. The recommended phase II dose for t-900607 is 130 mg/m given as an intravenous infusion over 60 minutes on a 21-day cycle. Cardiac toxicity was seen with this schedule.[1]
Molecular Weight 411.3
Formula C14H10F5N3O4S
CAS No. 261944-52-9

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 4.11 mg/mL (10 mM), Sonication is recommended.

TargetMolReferences and Literature

1. Gelmon KA, et al. A phase I study of T900607 given once every 3 weeks in patients with advanced refractory cancers; National Cancer Institute of Canada Clinical Trials Group (NCIC-CTG) IND 130. Invest New Drugs. 2005;23(5):445-453. 2. Houze, et al. Preparation of arylsulfonanilide ureas as antiproliferative agents. WO2000017159 A1.

Related compound libraries

This product is contained In the following compound libraries:
Microtubule-Targeted Compound Library Bioactive Compound Library Bioactive Compounds Library Max

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Keywords

T-900607 261944-52-9 Cytoskeletal Signaling Microtubule Associated inhibitor inhibit

 

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