Physicochemical Properties
Molecular Formula | C18H20CLN3O3 |
Molecular Weight | 361.83 |
Exact Mass | 361.119 |
CAS # | 799247-52-2 |
PubChem CID | 11577870 |
Appearance | Off-white to light yellow solid powder |
Density | 1.221g/cm3 |
Index of Refraction | 1.57 |
LogP | 4.044 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 7 |
Heavy Atom Count | 25 |
Complexity | 461 |
Defined Atom Stereocenter Count | 0 |
SMILES | C(/C1C=CC(Cl)=C(CNC(=O)OC)C=1)(\C)=N\OCC1C=CC=C(C)N=1 |
InChi Key | CRFYLQMIDWBKRT-LPYMAVHISA-N |
InChi Code | InChI=1S/C18H20ClN3O3/c1-12-5-4-6-16(21-12)11-25-22-13(2)14-7-8-17(19)15(9-14)10-20-18(23)24-3/h4-9H,10-11H2,1-3H3,(H,20,23)/b22-13+ |
Chemical Name | methyl N-[[2-chloro-5-[(E)-C-methyl-N-[(6-methylpyridin-2-yl)methoxy]carbonimidoyl]phenyl]methyl]carbamate |
HS Tariff Code | 2934.99.9001 |
Storage |
Powder-20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
Shipping Condition | Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs) |
Biological Activity
ln Vitro | Pyribencarb is an effective inhibitor of the decylubiquinol-cytochrome c reductase (UCR) activity of B. cinerea and Corynespora cassiicola, as well as the succinate cytochrome c reductase (SCR) activity of B. cinerea and Corynespora cassiicola. cinerea. Pyribencarb prevents B's UCR function. cinerea, with an estimated substrate-dependent inhibition constant of 13 nM, in a non-competitive manner [1]. |
References | [1]. Satoshi Kataoka, et al. Mechanism of action and selectivity of a novel fungicide, pyribencarb. J Pestic Sci, 35(2), 99-106 (2010). |
Additional Infomation | Pyribencarb is a carbamate ester that is the methyl ester of (2-chloro-5-{(1E)-N-[(6-methylpyridin-2-yl)methoxy]ethanimidoyl}benzyl)carbamic acid. A fungicide having excellent activity against a wide range of plant pathogenic fungi, especially gray mould diseases caused by Botrytis cinerea. It has a role as a mitochondrial cytochrome-bc1 complex inhibitor and an antifungal agrochemical. It is a carbamate fungicide and a methyl (2-chloro-5-{N-[(6-methylpyridin-2-yl)methoxy]ethanimidoyl}benzyl)carbamate. |
Solubility Data
Solubility (In Vitro) | DMSO : 100 mg/mL (276.37 mM) |
Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.5 mg/mL (6.91 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 2: ≥ 2.5 mg/mL (6.91 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. Solubility in Formulation 3: ≥ 2.5 mg/mL (6.91 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.  (Please use freshly prepared in vivo formulations for optimal results.) |
Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
1 mM | 2.7637 mL | 13.8186 mL | 27.6373 mL | |
5 mM | 0.5527 mL | 2.7637 mL | 5.5275 mL | |
10 mM | 0.2764 mL | 1.3819 mL | 2.7637 mL |