Orcinol gentiobioside
CAS No. 164991-86-0
Orcinol gentiobioside( —— )
Catalog No. M18106 CAS No. 164991-86-0
Orcinol gentiobioside (compound 4) is a natural product isolated from the rhizomes of C. breviscapa.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 77 | In Stock |
|
| 10MG | 111 | In Stock |
|
| 25MG | 178 | In Stock |
|
| 50MG | 265 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameOrcinol gentiobioside
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NoteResearch use only, not for human use.
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Brief DescriptionOrcinol gentiobioside (compound 4) is a natural product isolated from the rhizomes of C. breviscapa.
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DescriptionOrcinol gentiobioside (compound 4) is a natural product isolated from the rhizomes of C. breviscapa.
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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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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number164991-86-0
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Formula Weight448.42
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Molecular FormulaC19H28O12
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Purity>98% (HPLC)
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Solubility——
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SMILESCC1=CC(=CC(=C1)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O)O
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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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Stepharine
Alkaloids.
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γ-2-MSH (41-58), ami...
Melanocortin (MC) 3-MSH (Melanocyte-Stimulating Hormone) is believed to signal through the MC 3 receptor. It induces a sustained increase in intracellular free calcium levels ([Ca2+]i) in a subpopulation of pituitary cells. Most of the cells responding to 3-MSH express more than one pituitary hormone mRNA. The effect of 3-MSH is blocked by SHU9119, a MC3R and MC4R antagonist, in only 50% of the responsive cells, suggesting that in half of these cells the mediating receptor is not the MC3R. Low picomolar doses of 3-MSH increase [Ca2+]i in the growth hormone (GH)- and prolactin (PRL)-secreting GH3 cell line.
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Boc-MLF
Antagonist of formyl peptide receptor 1 (FPR1). Reduces superoxide production induced by fMLF with an EC50 of 0.63 μM. Almost completely blocks fMLF-stimulated primary granule exocytosis.
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