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Hosenkol B-3-O-β-D-glucopyranosyl(2-1)-β-D-glucopypyranosyl-28-O-β-D-glucopyranoside
Hosenkol B-3-O-β-D-glucopyranosyl(2-1)-β-D-glucopypyranosyl-28-O-β-D-glucopyranoside
CAS No. ———
Hosenkol B-3-O-β-D-glucopyranosyl(2-1)-β-D-glucopypyranosyl-28-O-β-D-glucopyranoside( ——— )
Catalog No. M38428 CAS No. ———
Hosenkol B-3-O-β-D-glucopyranosyl(2→1)-β-D-glucopypyranosyl-28-O-β-D-glucopyranoside
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | Get Quote | Get Quote |
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| 50MG | Get Quote | Get Quote |
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| 100MG | Get Quote | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameHosenkol B-3-O-β-D-glucopyranosyl(2-1)-β-D-glucopypyranosyl-28-O-β-D-glucopyranoside
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NoteResearch use only, not for human use.
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Brief DescriptionHosenkol B-3-O-β-D-glucopyranosyl(2→1)-β-D-glucopypyranosyl-28-O-β-D-glucopyranoside
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DescriptionHosenkol B-3-O-β-D-glucopyranosyl(2→1)-β-D-glucopypyranosyl-28-O-β-D-glucopyranoside
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In Vitro———
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In Vivo———
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Synonyms———
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PathwayOthers
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TargetOther Targets
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Recptor———
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Research Area———
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Indication———
Chemical Information
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CAS Number———
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Formula Weight———
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Molecular Formula———
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Purity>98% (HPLC)
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Solubility———
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SMILES———
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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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Silybin B
Silybin B is an effective inhibitor of raloxifene 4 '- and 6-glucosalylation, an effective anti-fibrinogenic and anti-oligomeric component of Silymarin, with free radical scavenging activity of 1, 1-diphenyl-2-pyridinyl hydrazine (DPPH), and a protective effect against cisplatin-induced neurotoxicity by alleviating DNA damage and apoptosis.
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Shield-1
Shield-1 is a specific, high-affinity and cell-permeant ligand of FK506-binding protein-12 (FKBP), and reverses the instability by binding to mutated FKBP (mtFKBP), allowing conditional expression of mtFKBP-fused proteins. Shield-1 can stabilize the entire fusion protein.
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CFI-402257
CFI-402257 is a orally active, and potent highly selective small-molecule inhibitor of Mps1 with Ki of 0.09 ± 0.02 nM.
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