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Goitrin
CAS No. 13190-34-6
Goitrin( —— )
Catalog No. M17945 CAS No. 13190-34-6
Goitrin is a potent antithyroid compound found naturally in crucifers. Goitrin is responsible for the induction of glutathione S-transferases.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 51 | In Stock |
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| 5MG | 56 | In Stock |
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| 10MG | 92 | In Stock |
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| 25MG | 155 | In Stock |
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| 50MG | 226 | In Stock |
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| 100MG | 334 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameGoitrin
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NoteResearch use only, not for human use.
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Brief DescriptionGoitrin is a potent antithyroid compound found naturally in crucifers. Goitrin is responsible for the induction of glutathione S-transferases.
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DescriptionGoitrin is a potent antithyroid compound found naturally in crucifers. Goitrin is responsible for the induction of glutathione S-transferases.Goitrin is a moderate inhibitor of purified bovine adrenal dopamine beta-hydroxylase, leads to a depression of brain norepinephrine and to an elevation of heart and adrenal dopamine.
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In VitroThe active ingredients according to the report table Spring is the anti-influenza virus, according to the spring report not only without the active, more reported having certain toxicity.
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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 Number13190-34-6
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Formula Weight129.17
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Molecular FormulaC5H7NOS
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (774.11 mM)
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SMILESC=CC1CNC(=S)O1
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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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ML089
ML089 (CID-22416235) is an orally available and potent, selective inhibitor of phosphomannose isomerase (PMI), with potential inhibition of other PMI immediate homologs.
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PLpro inhibitor
PLpro inhibitor is a potent papain-like protease (PLpro) inhibitor(IC50 of 2.6 uM).
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CALP1
Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site; produces CaM-dependent activation of phosphodiesterase. Also binds to cytoplasmic sites on other Ca2+ channels, including NMDA and HIV-1 gp120-activated channels, inhibiting Ca2+-mediated cytotoxicity and apoptosis (IC50 = 52 μM). Shown to protect pancreatic acinar cells from gossypol induced necrosis. Inhibits VLA-5-mediated adhesion of mast cells to fibronectin in vitro and attenuates inflammatory cell influx in guinea pig lung in vivo.
