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MedKoo product information:

GPX150

MedKoo Code#:  201450

Name:  GPX150

CAS#:  236095-29-7

 

Synonym:   GPX150;5-imino-13-deoxydoxorubicin. (8R,10S)-10-((2S,5R,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-6,8,11-trihydroxy-8-(2-hydroxyethyl)-12-imino-1-methoxy-7,8,9,10-tetrahydrotetracen-5(12H)-one.

 

IUPAC/Chemical name: 

(8R,10S)-10-(((2S,4S,5R,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-6,8,11-trihydroxy-8-(2-hydroxyethyl)-12-imino-1-methoxy-7,8,9,10-tetrahydrotetracen-5(12H)-one.

 

Chemical structure Theoretical analysis

 

 

 

Chemical Formula: C27H32N2O9

Exact Mass: 528.21078

Molecular Weight: 528.55

m/z: 528.21078 (100.0%), 529.21414 (29.2%), 530.21749 (4.1%), 530.21503 (1.8%)

Elemental Analysis: C, 61.35; H, 6.10; N, 5.30; O, 27.24

 

 

Availability and price:

This agent is not in stock, which may be available through custom synthesis.

 

To inquire quotation and lead time or to ask questions, please send email to sales@medkoo.com to describe your needs. A representative will respond your email shortly. We offer big discount for orders of bulk quantities.

 

 

Information about this agent

GPX-150 is a synthetic non-cardiotoxic analogue of the anthracycline antibiotic doxorubicin with potential antineoplastic activity. Anthracycline analogue GPX-150 intercalates DNA and impedes the activity of topoisomerase II, inducing single and double-stranded breaks in DNA; inhibiting DNA replication and/or repair, transcription, and protein synthesis; and activating tumor cell apoptosis. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus).

 

As of August 2010, GPX-150 is under Phase I clinical trials sponsored by Coronado Biosciences, Inc. This is a Phase 1 safety and dose escalation study to define the maximum tolerated dose (MTD) and identify the dose limiting toxicities (DLT) following IV administration of GPX-150 once every 3 weeks. Escalating doses starting at the dose of 14 mg/m2 and increasing to the dose of 265 mg/m2 will be administered IV once every 3 weeks for up to 8 cycles of treatment. Patients who have previously received an anthracycline are limited to 4 cycles of treatment. (source: http://clinicaltrials.gov/ct2/show/NCT00710125).

 

Current developer:  Gem Pharmaceuticals, Inc and ACCESS Oncology, Inc.

 

References

1. Zhang; Xini (Hoover, AL), Olson; Richard D. (Nampa, ID) 5-imino-13-deoxy anthracycline derivatives, their uses, and processes for preparing them, United States Patent 5942605.

 

 

Contact MedKoo:

Email: sales@medkoo.com

 

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