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Methoxatin disodium salt
CAS No. 122628-50-6
Methoxatin disodium salt( Pyrroloquinoline quinone disodium salt )
Catalog No. M20383 CAS No. 122628-50-6
Methoxatin disodium salt an aromatic tricyclic o-quinone is a redox cofactor for bacterial dehydrogenases. It is an efficient electron transfer catalyst from a number of organic substrates to molecular oxygen (O2) constructing quinoprotein model reactions.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 48 | In Stock |
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| 50MG | 130 | In Stock |
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| 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 NameMethoxatin disodium salt
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NoteResearch use only, not for human use.
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Brief DescriptionMethoxatin disodium salt an aromatic tricyclic o-quinone is a redox cofactor for bacterial dehydrogenases. It is an efficient electron transfer catalyst from a number of organic substrates to molecular oxygen (O2) constructing quinoprotein model reactions.
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DescriptionMethoxatin disodium salt an aromatic tricyclic o-quinone is a redox cofactor for bacterial dehydrogenases. It is an efficient electron transfer catalyst from a number of organic substrates to molecular oxygen (O2) constructing quinoprotein model reactions.
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In Vitro——
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In Vivo——
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SynonymsPyrroloquinoline quinone disodium salt
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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 Number122628-50-6
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Formula Weight374.17
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Molecular FormulaC14H4N2Na2O8
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Purity>98% (HPLC)
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SolubilityH2O:6.16 mg/mL (16.46 mM; Need ultrasonic and warming);H2O:5 mg/mL (13.36 mM; Need ultrasonic)
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SMILES[Na+].[Na+].OC(=O)c1cc(nc2C(=O)C(=O)c3cc([nH]c3-c12)C([O-])=O)C([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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ML-180
ML-180 is a potent orphan nuclear receptor liver receptor homolog 1 (LRH-1; NR5A2) inverse agonist (IC50 of 3.7 μM) .ML-180 (0.5-5 μM; 24 hours) shows a significant inhibition of cyclin-D1 and cyclin-E1 expression in hepatic cells, but has little effect on repression in SK-OV-3 cells[2]. ML-180 (5 μM; 24 hours) leads to a rapid decrease of LRH-1 expression and efficiently represses endogenous LRH-1 signaling.
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Zinc bacitracin
Bacitracin Zinc is a dephosphorylation of the C55-isoprenyl pyrophosphate interference for inhibition of cleavage of Tyr from Met-enkephalin with IC50 of 10 μM.
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(1R,2R)-2-PCCA hydro...
(1R,2R)-2-PCCA hydrochloride is a potent, selective, and blood-brain-barrier-crossing GPR88 receptor agonist with an EC50 value of 1140 n in striatal membranes of WT mice; it can be used to study the central nervous system.
