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Pyribencarb
CAS No. 799247-52-2
Pyribencarb ( ZINC43065336 )
Catalog No. M28112 CAS No. 799247-52-2
Pyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 87 | Get Quote |
|
| 10MG | 147 | Get Quote |
|
| 25MG | 290 | Get Quote |
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| 50MG | 447 | Get Quote |
|
| 100MG | 651 | Get Quote |
|
| 500MG | 1368 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NamePyribencarb
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NoteResearch use only, not for human use.
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Brief DescriptionPyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi.
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DescriptionPyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi. Pyribencarb is a potent Qo inhibitor of cytochrome b. Pyribencarb is especially active against Botrytis cinerea and Sclerotinia sclerotirum.(In Vitro):Pyribencarb potently inhibits succinate-cytochrome c reductase (SCR) activities of Botrytis cinerea (cucumber gray mold), Corynespora cassiicola (leaf spot) and decylubiquinol-cytochrome c reductase (UCR) activity of B. cinerea. Pyribencarb inhibits the UCR of B. cinerea in an uncompetitive manner, and the substrate-dependent inhibition constant is found from calculation to be 13 nM. The target site of Pyribencarb is cytochrome b of complex III in the electron transport system of the respiratory chain. The inhibitory potency of pyribencarb on SCR activities of plants, rats and carp is relatively weak compared with that of strobilurin fungicides.
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SynonymsZINC43065336
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number799247-52-2
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Formula Weight361.8
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Molecular FormulaC18H20ClN3O3
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Purity>98% (HPLC)
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Solubility——
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SMILESC(=N\OCC=1N=C(C)C=CC1)(\C)/C2=CC(CNC(OC)=O)=C(Cl)C=C2
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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
1.Pribylova M, et al. Paclitaxel conjugation with the analog of the gonadotropin-releasing hormone as a targeting moiety. Int J Pharm. 2011 Aug 30;415(1-2):175-80.
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