ML400
CAS No. 1908414-42-5
ML400( —— )
Catalog No. M34104 CAS No. 1908414-42-5
ML400 (CID73050863) is an allosteric inhibitor of LMPTP with an EC50 of 1μM. ML400 displays good cell-based activity and rodent pharmacokinetics.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 235 | In Stock |
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| 5MG | 181 | In Stock |
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| 10MG | 297 | In Stock |
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| 25MG | 472 | In Stock |
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| 50MG | 639 | In Stock |
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| 100MG | 882 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | 1758 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameML400
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NoteResearch use only, not for human use.
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Brief DescriptionML400 (CID73050863) is an allosteric inhibitor of LMPTP with an EC50 of 1μM. ML400 displays good cell-based activity and rodent pharmacokinetics.
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DescriptionML 400 is a potent and selective LMPTP inhibitor with an IC50 value of 1680 nM. ML 400 inhibits adipogenesis.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayMetabolic Enzyme/Protease
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TargetPhosphatase
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RecptorPhosphatase
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Research Area——
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Indication——
Chemical Information
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CAS Number1908414-42-5
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Formula Weight375.51
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Molecular FormulaC24H29N3O
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Purity>98% (HPLC)
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Solubility——
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SMILESN(CCCN1CCCCC1)C=2C3=C(N=C(C2)C4=CC=C(OC)C=C4)C=CC=C3
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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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Vutiglabridin
Vutiglabridin (HSG4112) is a novel and safe modulator of PON2, a racemic compound. vutiglabridin is an optimized structural analogue of Glabridin and is superior to Glabridin in terms of weight loss and chemical stability.
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BCI hydrochloride
BCI hydrochloride ((E)-BCI hydrochloride) is a selective dual-specificity phosphatase 6 (DUSP6) inhibitor that inhibits RANKL-mediated osteoclastogenesis and attenuates oophorectomy-induced bone loss.
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Raphin1 acetate
Raphin1 acetate is a selective and orally bioavailable regulatory phosphatase PPP1R15B (R15B) inhibitor.Raphin1, a selective inhibitor of R15B.?In cells, Raphin1 caused a rapid and transient accumulation of its phosphorylated substrate, resulting in a transient attenuation of protein synthesis.?
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