S-(2-aminoethyl) Isothiourea (dihydrobromide)
CAS No. 56-10-0
S-(2-aminoethyl) Isothiourea (dihydrobromide)( —— )
Catalog No. M20857 CAS No. 56-10-0
S-(2-aminoethyl) Isothiourea (dihydrobromide) is a non-selective inhibitor of all NOS isoforms. For human nNOS eNOS and iNOS the Ki values are 1.8 2.1 and 0.59 μM respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 48 | Get Quote |
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| 10MG | 68 | Get Quote |
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| 25MG | 115 | Get Quote |
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| 50MG | 173 | Get Quote |
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| 100MG | 258 | Get Quote |
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| 200MG | 388 | Get Quote |
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| 500MG | 642 | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameS-(2-aminoethyl) Isothiourea (dihydrobromide)
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NoteResearch use only, not for human use.
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Brief DescriptionS-(2-aminoethyl) Isothiourea (dihydrobromide) is a non-selective inhibitor of all NOS isoforms. For human nNOS eNOS and iNOS the Ki values are 1.8 2.1 and 0.59 μM respectively.
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DescriptionS-(2-aminoethyl) Isothiourea (dihydrobromide) is a non-selective inhibitor of all NOS isoforms. For human nNOS eNOS and iNOS the Ki values are 1.8 2.1 and 0.59 μM respectively.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayImmunology/Inflammation
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TargetNOS
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RecptorNOS
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Research Area——
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Indication——
Chemical Information
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CAS Number56-10-0
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Formula Weight281.02
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Molecular FormulaC3H11Br2N3S
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Purity>98% (HPLC)
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Solubility——
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SMILESBr.Br.N=C(N)SCCN
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Chemical NameCarbamimidothioic acid 2-aminoethyl ester dihydrobromide
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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Anhydronotoptol
Anhydronotoptol (4-{[(2E,5E)-3,7-dimethylocta-2,5,7-trien-1-yl]oxy}-7H-furo[3,2-g]chromen-7-one), a natural compound extracted from the umbelliferae plant Qiangwu, is a potent inhibitor of nitric oxide production, inhibiting LPS-induced NO production in RAW 264.7 cells with an IC50 value of 36.6 μM.
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ETHYL CAFFEATE b
In vitro ECF suppressed the differentiation of naive CD4+ T cells into Th1. Furthermore ECF intensely blocked the transcriptional expression in interferon-γ-related signaling including IFN-γ T-bet STAT1 and STAT4.?
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AR-C102222
AR-C102222 is a potent, selective iNOS inhibitor with IC50 of 35 nM, dislapys 3,000-fold and 20-fold selectivity over eNOS and nNOS respectively; reduces inflammation produced by the application of arachidonic acid to the ear, attenuates FCA-induced mechanical hyperalgesia, and attenuates acetic acid-induced writhing in mice.Rheumatoid ArthritisDiscontinued
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