Salcaprozate sodium
CAS No. 203787-91-1
Salcaprozate sodium( SNAC )
Catalog No. M23911 CAS No. 203787-91-1
Salcaprozate sodium is an oral absorption promoter, and has the potential as a delivery agent for oral forms of heparin and insulin.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 33 | In Stock |
|
| 1G | 54 | In Stock |
|
Biological Information
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Product NameSalcaprozate sodium
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NoteResearch use only, not for human use.
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Brief DescriptionSalcaprozate sodium is an oral absorption promoter, and has the potential as a delivery agent for oral forms of heparin and insulin.
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DescriptionSalcaprozate sodium is an oral absorption promoter, and has the potential as a delivery agent for oral forms of heparin and insulin. It could increase passive transcellular permeation across small intestinal epithelia based on increased lipophilicity arising from non-covalent macromolecule complexation.
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In Vitro——
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In VivoAnimal Model:Sprague-Dawley rats (6-7 weeks)Dosage:2000 mg/kg/d Administration:Oral gavage for 13 weeks Result:Induced 20% and 50% mortality in males and females at the dose of 2000 mg/kg/d.
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SynonymsSNAC
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number203787-91-1
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Formula Weight301.32
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Molecular FormulaC15H20NNaO4
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Purity>98% (HPLC)
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SolubilityDMSO:100 mg/mL?(331.88 mM;?Need ultrasonic)
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SMILESC1=CC=C(C(=C1)C(=O)NCCCCCCCC(=O)[O-])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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Phellopterin
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1H-Purine-2,6-dione
TH5427 hydrochloride is a potent, selective NUDT5 inhibitor (IC50=29 nM). TH5427 hydrochloride shows an apparent 690-fold selectivity for NUDT5 over MTH1. TH5427 hydrochloride blocks progestin-dependent, PAR-derived nuclear ATP synthesis and subsequent chromatin remodeling, gene regulation and proliferation in breast cancer cells.
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