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Parishin C
CAS No. 174972-80-6
Parishin C ( —— )
Catalog No. M20723 CAS No. 174972-80-6
Parishin C is a phenolic glycoside and a major component of G. elata have antioxidant property.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 107 | In Stock |
|
| 10MG | 159 | In Stock |
|
| 25MG | 266 | In Stock |
|
| 50MG | 393 | In Stock |
|
| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameParishin C
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NoteResearch use only not for human use.
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Brief DescriptionParishin C is a phenolic glycoside and a major component of G. elata have antioxidant property.
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DescriptionParishin C is a phenolic glycoside and a major component of G. elata have antioxidant property.
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Synonyms——
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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 Number174972-80-6
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Formula Weight728.6
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Molecular FormulaC32H40O19
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Purity>98% (HPLC)
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Solubility——
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SMILESOC[C@H]1O[C@@H](Oc2ccc(COC(=O)CC(O)(CC(=O)OCc3ccc(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)cc3)C(O)=O)cc2)[C@H](O)[C@@H](O)[C@@H]1O
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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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CAY10781
CAY10781 is an inhibitor of the protein-protein interaction between neuropilin-1 (NRP-1) and VEGF-A.1It inhibits the interaction by 43% when used at a concentration of 12.5 μM. CAY10781 also inhibits VEGF-A-induced phosphorylation of VEGFR2 in catecholamine A-differentiated (CAD) cells when used at the same concentration.
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DL-Arabinose
D-Arabinose also known as (+/-)-arabinose or aloe sugar belongs to the class of organic compounds known as pentoses. D-Arabinose has been primarily detected in feces.
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WEHL-04
WEHL-04 is an intermediate used to prepare (isoquinolinylsulfonyl)benzoic acids as inhibitors of type 5 71-β-hydroxysteroid dehydrogenase AKR1C3. It is also used in the synthesis of 2-aminooctahydrocyclopentalene-3a-carboxamides as potent CCR2 antagonists.
