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Picolinafen
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Catalog No. T211625Cas No. 137641-05-5
Alias AC 900001
Picolinafen is a pyridine herbicide that functions as an inhibitor of phytoene desaturase (PDS) and is utilized for its ability to manage the growth of broadleaf weeds by disrupting carotenoid biosynthesis. It exhibits cytotoxicity towards porcine trophoblast cells (pTr) and porcine luminal epithelial cells (pLE). By inducing the accumulation of reactive oxygen species (ROS), depleting calcium, and activating MAPK and PI3K signaling pathways, Picolinafen leads to reduced cell viability, increased apoptosis, impaired migration abilities, and altered expression of implantation-related genes, ultimately affecting the implantation capability of pTr cells. The LD50 value of Picolinafen for mammals is 2.7 mg/kg, and it is 7 μg/L for fish. Additionally, Picolinafen shows toxic effects during zebrafish embryonic development.
Picolinafen
😃Good
Catalog No. T211625Alias AC 900001Cas No. 137641-05-5
Picolinafen is a pyridine herbicide that functions as an inhibitor of phytoene desaturase (PDS) and is utilized for its ability to manage the growth of broadleaf weeds by disrupting carotenoid biosynthesis. It exhibits cytotoxicity towards porcine trophoblast cells (pTr) and porcine luminal epithelial cells (pLE). By inducing the accumulation of reactive oxygen species (ROS), depleting calcium, and activating MAPK and PI3K signaling pathways, Picolinafen leads to reduced cell viability, increased apoptosis, impaired migration abilities, and altered expression of implantation-related genes, ultimately affecting the implantation capability of pTr cells. The LD50 value of Picolinafen for mammals is 2.7 mg/kg, and it is 7 μg/L for fish. Additionally, Picolinafen shows toxic effects during zebrafish embryonic development.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
| Description | Picolinafen is a pyridine herbicide that functions as an inhibitor of phytoene desaturase (PDS) and is utilized for its ability to manage the growth of broadleaf weeds by disrupting carotenoid biosynthesis. It exhibits cytotoxicity towards porcine trophoblast cells (pTr) and porcine luminal epithelial cells (pLE). By inducing the accumulation of reactive oxygen species (ROS), depleting calcium, and activating MAPK and PI3K signaling pathways, Picolinafen leads to reduced cell viability, increased apoptosis, impaired migration abilities, and altered expression of implantation-related genes, ultimately affecting the implantation capability of pTr cells. The LD50 value of Picolinafen for mammals is 2.7 mg/kg, and it is 7 μg/L for fish. Additionally, Picolinafen shows toxic effects during zebrafish embryonic development. |
| In vitro | Picolinafen, at concentrations of 0.2-6 μM over 48 hours, reduces the viability of porcine trophectoderm cells (pTr) and uterine luminal epithelial cells (pLE), while altering their cell cycle. At 1-4 μM for the same duration, it induces apoptosis in these cells, disrupts their spheroid self-assembly ability, and impairs mitochondrial integrity and calcium homeostasis. Additionally, exposure to 1-4 μM for 2-48 hours leads to ROS accumulation and disturbance of intracellular Ca²⁺ regulation in pTr and pLE cells. At 4 μM over 15-24 hours, picolinafen inhibits migration of pTr cells and modifies transcriptional regulation of genes involved in apoptosis and implantation. Furthermore, within 3 hours at 1-4 μM, it activates the MAPK and PI3K/AKT signaling pathways in pTr and pLE cells. |
| In vivo | Picolinafen, when incubated at concentrations between 0.1-100 μM for 0-5 days, has an LC50 of 10 μM at 3 days and 5 μM at 5 days in zebrafish embryos. Additionally, Picolinafen, at concentrations of 1-10 μM and incubated for 24-72 hours, exhibits toxic effects during zebrafish embryo development. |
| Synonyms | AC 900001 |
| Molecular Weight | 376.30 |
| Formula | C19H12F4N2O2 |
| Cas No. | 137641-05-5 |
| Smiles | O=C(NC1=CC=C(F)C=C1)C2=NC(OC3=CC=CC(=C3)C(F)(F)F)=CC=C2 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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