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Gemcitabine monophosphate sodium salt hydrate
Gemcitabine monophosphate sodium salt hydrate
CAS No. 1638288-31-9
Gemcitabine monophosphate sodium salt hydrate( —— )
Catalog No. M18102 CAS No. 1638288-31-9
Gemcitabine monophosphate disodium salt is a monophosphate derivative of Gemcitabine.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 178 | In Stock |
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| 25MG | 340 | In Stock |
|
| 50MG | 567 | In Stock |
|
| 100MG | 956 | In Stock |
|
| 200MG | 1474 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameGemcitabine monophosphate sodium salt hydrate
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NoteResearch use only, not for human use.
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Brief DescriptionGemcitabine monophosphate disodium salt is a monophosphate derivative of Gemcitabine.
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DescriptionGemcitabine monophosphate disodium salt is a monophosphate derivative of Gemcitabine.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayGPCR/G Protein
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TargetDopamine Receptor
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RecptorAutophagy| DNA| Thymidylate synthase| UMP-CMP kinase
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Research Area——
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Indication——
Chemical Information
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CAS Number1638288-31-9
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Formula Weight405.16
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Molecular FormulaC9H12F2N3Na2O8P
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Purity>98% (HPLC)
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Solubility——
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SMILESO=c1nc(N)ccn1[C@@H]1O[C@H](COP(=O)([O-])[O-])[C@@H](O)C1(F)F.[Na+].O.[Na+]
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Bromopride
Bromopride is a dopamine antagonist with prokinetic properties closely related to metoclopramide, and is widely used as an antiemetic.
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ONC206
ONC206 is an analogue of TRAIL inducer ONC201 and is a selective antagonist of the D2-like dopamine receptors (DRD2/3/4) at nanomolar concentrations. ONC206 also has broad-spectrum anti-tumor activity. ONC206 (Oncoceutics) is an imipiridone with nanomolar potency and analogue of ONC201, a selective dopamine receptor D2 (DRD2) antagonist currently being investigated in phase II clinical trials for serous endometrial cancer (SEC).??
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Dexpramipexole
A partial/full agonist of dopamine receptor with Ki of 3.9/2.2/0.5/5.1 nM for D2S/D2L/D3/D4, respeectively.
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