Imazalil sulfate
CAS No. 58594-72-2
Imazalil sulfate( —— )
Catalog No. M24577 CAS No. 58594-72-2
Imazalil sulfate is a fungicide containing imidazole group, is extensively used for the prevention and treatment of fungal diseases in plants.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 29 | In Stock |
|
| 100MG | 29 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | 60 | In Stock |
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| 1G | 91 | In Stock |
|
Biological Information
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Product NameImazalil sulfate
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NoteResearch use only, not for human use.
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Brief DescriptionImazalil sulfate is a fungicide containing imidazole group, is extensively used for the prevention and treatment of fungal diseases in plants.
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DescriptionImazalil sulfate is a fungicide containing imidazole group, is extensively used for the prevention and treatment of fungal diseases in plants.
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In VitroRT-PCR Cell Line:EL4 cells Concentration:3, 10, 30 μM Incubation Time:6 h Result:Significantly suppressed IL-17 mRNAs.
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In VivoAnimal Model:IMZ Male C57BL/6N mice Dosage:25, 50, 75, 100 mg/kg Administration:Intraperitoneally; single dose Result:Significantly increased hepatic Cyp3a11 mRNA levels in a dose-dependent manner.
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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 Number58594-72-2
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Formula Weight395.23
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Molecular FormulaC14H14Cl2N2O.H2O4S
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Purity>98% (HPLC)
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Solubility——
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SMILESC=CCOC(C1=CC=C(Cl)C=C1Cl)CN2C=CN=C2.O=S(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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2-(2,4-Dihydroxyphen...
2-(2,4-Dihydroxyphenyl)-5,6-methylenedioxybenzofuran (ABF).
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Tilomisole
Tilomisole (Wy 18251) is an orally available benzimidazole thiazole with anti-inflammatory activity and immunomodulatory activity.Tilomisole is used in the study of cancer and inflammation.
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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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