Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C17H25F2N3O5 |
Molecular Weight | 389.3943 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC(CCC)C(=O)NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)C2(F)F
InChI
InChIKey=MEOYFIHNRBNEPI-UXIGCNINSA-N
InChI=1S/C17H25F2N3O5/c1-3-5-10(6-4-2)14(25)20-12-7-8-22(16(26)21-12)15-17(18,19)13(24)11(9-23)27-15/h7-8,10-11,13,15,23-24H,3-6,9H2,1-2H3,(H,20,21,25,26)/t11-,13-,15-/m1/s1
DescriptionCurator's Comment: Description was created using several sources including:
https://www.ncbi.nlm.nih.gov/pubmed/19860433/|https://www.ncbi.nlm.nih.gov/pubmed/23325581
Curator's Comment: Description was created using several sources including:
https://www.ncbi.nlm.nih.gov/pubmed/19860433/|https://www.ncbi.nlm.nih.gov/pubmed/23325581
LY2334737 an orally active amide prodrug of gemcitabine, a nucleoside analog chemotherapeutic with a broad spectrum of anti-tumor activity against several human malignancies including pancreatic, ovarian, lung, breast, and bladder. LY2334737 was developed to be absorbed intact and cleaved in vivo, releasing gemcitabine and valproic acid to achieve prolonged systemic exposure, good efficacy with lower toxicity along with added flexibility of administration and greater patient convenience. The hydrolysis and pharmacokinetics of LY2334737 and its downstream metabolites was evaluated in preclinical in vitro and in vivo experiments in mice, rats, and dogs, which demonstrated the prodrug is absorbed largely intact across the intestinal epithelium and delivers LY2334737 to systemic circulation. The hydrolysis of LY2334737 is relatively slow, resulting in sustained release of gemcitabine in vivo. A major enzyme involved in the hydrolysis of LY2334737 is carboxylesterase 2 (CES2). The compound has entered clinical trials and is being evaluated as a potential new anticancer agent.
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19860433/
Curator's Comment: # Eli Lilly
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: P23921 Gene ID: 6240.0 Gene Symbol: RRM1 Target Organism: Homo sapiens (Human) |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Unknown Approved UseUnknown |
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Primary | GEMZAR Approved UseGemzar (gemcitabine HCl) is indicated as first-line treatment for patients with locally advanced (nonresectable Stage II or Stage III) or metastatic (Stage IV) adenocarcinoma of the pancreas. Gemzar is indicated for patients previously treated with 5-FU. Launch Date1998 |
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Primary | GEMZAR Approved UseGemzar (gemcitabine HCl) is indicated in combination with cisplatin for the
first-line treatment of patients with inoperable, locally advanced (Stage IIIA or IIIB) or
metastatic (Stage IV) non-small cell lung cancer. Launch Date1998 |
PubMed
Title | Date | PubMed |
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Phase I study of Oral gemcitabine prodrug (LY2334737) alone and in combination with erlotinib in patients with advanced solid tumors. | 2011 Sep 15 |
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Novel agents and new combination treatments on phase I studies on solid tumors and pancreatic cancer. | 2012 Jul 10 |
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Low-dose metronomic oral dosing of a prodrug of gemcitabine (LY2334737) causes antitumor effects in the absence of inhibition of systemic vasculogenesis. | 2012 Mar |
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Efficacy of low-dose oral metronomic dosing of the prodrug of gemcitabine, LY2334737, in human tumor xenografts. | 2013 Apr |
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High sensitive assay employing column switching chromatography to enable simultaneous quantification of an amide prodrug of gemcitabine (LY2334737), gemcitabine, and its metabolite dFdU in human plasma by LC-MS/MS. | 2013 Aug 1 |
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Phase I study of oral gemcitabine prodrug (LY2334737) in Japanese patients with advanced solid tumors. | 2013 Jun |
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Human carboxylesterase-2 hydrolyzes the prodrug of gemcitabine (LY2334737) and confers prodrug sensitivity to cancer cells. | 2013 Mar 1 |
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Preclinical absorption, distribution, metabolism, and excretion of an oral amide prodrug of gemcitabine designed to deliver prolonged systemic exposure. | 2013 May 8 |
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Novel developments in the use of antimetabolites. | 2014 |
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Phase 1 dose escalation and pharmacokinetic evaluation of oral gemcitabine prodrug (LY2334737) in combination with docetaxel in patients with advanced solid tumors. | 2014 Jun |
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Phase 1b study of the oral gemcitabine 'Pro-drug' LY2334737 in combination with capecitabine in patients with advanced solid tumors. | 2015 Apr |
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Phase I dose escalation and pharmacokinetic evaluation of two different schedules of LY2334737, an oral gemcitabine prodrug, in patients with advanced solid tumors. | 2015 Dec |
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Design, synthesis, and structure-activity relationship study of glycyrrhetinic acid derivatives as potent and selective inhibitors against human carboxylesterase 2. | 2016 Apr 13 |
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Enhanced Antitumor Activity of Monophosphate Ester Prodrugs of Gemcitabine: In Vitro and In Vivo Evaluation. | 2016 Sep |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26377590
Patients with advanced/metastatic solid tumors received escalating doses of LY2334737 either every other day for 21 days followed by 7 days-drug-free period (QoD) or once daily for 7 days every other week (QD). The 28 days-cycles were repeated until disease progression or unacceptable toxicity. Standard 3 plus 3 dose-escalation was succeeded by a dose-confirmation phase Forty-one patients received QoD- (40-100 mg) and 32 QD-dosing (40-90 mg).
Route of Administration:
Oral
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300000041400
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YLR364XYSA
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11646777
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892128-60-8
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DTXSID001025742
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DB12906
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C102856
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METABOLITE ACTIVE (PRODRUG)
SUBSTANCE RECORD