Minodronic acid
CAS No. 180064-38-4
Minodronic acid( —— )
Catalog No. M37531 CAS No. 180064-38-4
Minodronic acid(YM-529) is a P2X2/3 receptor antagonist with anticancer activity, directly or indirectly inhibiting the proliferation of cancer cells and inducing apoptosis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 38 | Get Quote |
|
| 25MG | 59 | Get Quote |
|
| 50MG | 86 | Get Quote |
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| 100MG | 116 | Get Quote |
|
| 500MG | 293 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameMinodronic acid
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NoteResearch use only, not for human use.
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Brief DescriptionMinodronic acid(YM-529) is a P2X2/3 receptor antagonist with anticancer activity, directly or indirectly inhibiting the proliferation of cancer cells and inducing apoptosis.
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DescriptionMinodronic acid (YM-529) is a third-generation bisphosphonate that directly and indirectly prevents proliferation, induces apoptosis, and inhibits metastasis of various types of cancer cells. Minodronic acid (YM-529) is an antagonist of purinergic P2X2/3 receptors involved in pain.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayMembrane Transporter/Ion Channel
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TargetP2X Receptor
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RecptorP2X Receptor | Apoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number180064-38-4
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Formula Weight322.15
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Molecular FormulaC9H12N2O7P2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 5 mg/mL (15.52 mM) DMSO : < 1 mg/mL (insoluble or slightly soluble)
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SMILESOC(Cc1cnc2ccccn12)(P(O)(O)=O)P(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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PPADS tetrasodium
PPADS tetrasodiuma is a potent P2X receptor antagonist and inhibitor of the inverse mode of Na/Ca2? exchange in guinea pig airway smooth muscle and is neuroprotective against glutamate/NMDA toxicity.PPADS tetrasodiuma inhibits P2X1, P2X-2, P2X-3, and P2X- 5. 5.
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Sivopixant
Sivopixant (S-600918) is a potent and selective P2X3 receptor antagonist (P2X3 IC 50 =4.2 nM; P2X2/3 IC 50 =1100 nM). Sivopixant shows strong analgesic effect .
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AZD-9056
A potent, selective, orally bioavailable P2X7 receptor antagonist; inhibits release of pro-inflammatory mediators from isolated human peripheral monocytes (IL-1β and IL-18) and human alveolar macrophages (IL-1β) with IC50 values of 10-13 nM.
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