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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
59 Results for "
HPPD
" in MedChemExpress (MCE) Product Catalog:
Products (59)
59 Results for "HPPD" in MCE Product Catalog:
Cat. No.: HY-187378
CAS No.: 3124322-98-8
HPPD-IN-12 is an inhibitor of Arabidopsis thaliana 4-hydroxyphenylpyruvate dioxygenase (AtHPPD), with an IC50 of 27.8 μM and a Kd of 1.535 μM. HPPD-IN-12 binds to AtHPPD via Fe 2+ coordination, π-π interactions and hydrogen bonds. HPPD-IN-12 can be used in herbicide-related research .
Cat. No.: HY-187374
HPPD-IN-11 is an inhibitor of Arabidopsis thaliana 4-hydroxyphenylpyruvate dioxygenase (AtHPPD), with a Ki value of 0.016 μM, and exhibits herbicidal activity. HPPD-IN-11 enhances π-π interactions with Phe360 and Phe403 in the active site of AtHPPD, thereby strengthening its enzyme-binding ability. HPPD-IN-11 can be used in studies related to weed damage .
Cat. No.: HY-189092
CAS No.: 2776994-70-6
HPPD-IN-14 is an inhibitor of Arabidopsis thaliana 4-hydroxyphenylpyruvate dioxygenase (AtHPPD), with an IC50 of 0.188 μM and a Ki of 0.0077 μM. HPPD-IN-14 forms a stable complex through coordination with the active-site metal ion and multiple non-covalent interactions, thereby inhibiting the growth of target weeds, and exhibits high safety to wheat. HPPD-IN-14 can be used in herbicide-related research .
Cat. No.: HY-RS16336
Target:
Research Areas:
HPPD Human Pre-designed siRNA Set A contains three designed siRNAs for HPPD gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
Cat. No.: HY-W1115537
CAS No.: 2428458-82-4
Flusulfinam is a HPPD inhibitor and herbicide, with an IC50 of 0.0181 μM against Arabidopsis thaliana HPPD. Flusulfinam inhibits the catalytic activity of recombinant Arabidopsis thaliana HPPD. Flusulfinam exhibits potent herbicidal activity against barnyard grass (Echinochloa crus-galli). Flusulfinam inhibits the growth of Digitaria sanguinalis .
Cat. No.: HY-P70024
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HPD; HPPD; PPD; 4-Hydroxyphenylpyruvic Acid Oxidase; 4HPPD; Glyoxalase Domain Containing 3; 4-HPPD; HPPDASE; GLOD3; HPPDase; 4-Hydroxyphenylpyruvate Dioxygenase; P-Hydroxyphenylpyruvate Dioxygenase; rHu4-hydroxyphenylpyruvate dioxygenase /HPD, His; 4HPPD
Species:
Human
Source:
E. coli
Cat. No.: HY-W753209
CAS No.: 1101132-67-5
Tolpyralate is a selective post-emergence herbicide and corn Herbicide. Tolpyralate inhibits 4-HPPD. Tolpyralate exhibits herbicidal activity against a variety of weeds, including the glyphosate-resistant weed Amaranthus tuberculatus .
Cat. No.: HY-W727532
CAS No.: 1992017-55-6
Fenpyrazone is a 4-hydroxyphenylpyruvate dioxygenase (HPPD) inhibitor as well as a post-emergence herbicide. By inhibiting the activity of HPPD, Fenpyrazone indirectly blocks carotenoid biosynthesis in plants, causing bleaching of new tissues in sensitive plants, followed by necrosis and eventual death. Fenpyrazone is used in studies on controlling annual monocotyledonous and dicotyledonous weeds in summer maize fields .
Cat. No.: HY-W753723
CAS No.: 1622908-18-2
Biscarfentrazone is a HPPD-inhibiting herbicide for wheat fields, which can effectively control ALS-resistant broadleaf weeds and is safe to wheat .
Cat. No.: HY-189054
CAS No.: 3132207-16-7
Research Areas:
Herbicide safener-6 is a herbicide safener that competitively binds to the target HPPD. By competing with herbicides for binding to the HPPD target, Herbicide safener-6 stimulates endogenous GSH synthesis in rice and enhances the activities of multiple detoxification enzymes, thereby promoting the metabolic detoxification of herbicides and alleviating oxidative stress damage. Herbicide safener-6 can be used in studies related to Benzobicyclon-induced phytotoxicity in indica rice .
Cat. No.: HY-P83297A
Synonyms: 4-hydroxyphenylpyruvate dioxygenase like; GLOXD1; 4-HPPD-L
Cat. No.: HY-W705486
CAS No.: 143701-75-1
RPA 202248 is a p-hydroxy phenyl pyruvate dioxygenase (HPPD) inhibitor and degradation product of Isoxaflutole (HY-116139). RPA 202248 demonstrates environmental persistence and undergoes transport through soil matrix and macropores to subsurface drain flow in agricultural field settings .
Cat. No.: HY-B0871R
CAS No.: 84087-01-4
Research Areas:
Quinclorac (Standard) is the analytical standard of Quinclorac (HY-B0871). This product is intended for research and analytical applications. Quinclorac is a highly selective quinoline carboxylic acid synthetic auxin herbicide. Quinclorac weakly inhibits HPPD, accompanied by a transient decrease in carotenoids. Quinclorac upregulates ACC synthase (ACS), leading to the co-accumulation of ethylene and cyanide, while increasing the ABA/IAA ratio, which induces ROS burst, membrane lipid peroxidation (MDA) and lethal growth inhibition. Residual Quinclorac in soil can cause abnormal growth of subsequent tobacco crops. In calli of Phaseolus vulgaris, Quinclorac induces oxidative stress (increased MDA and decreased RGR), but cells after stepwise pressurized acclimation acquire a constitutive antioxidant state, which remains stable after de-acclimation and tolerates oxidative damage caused by Quinclorac. Quinclorac can be used in studies related to herbicide action mechanisms, bioremediation of soil residues, and adaptive responses of plant cells to oxidative stress .
Cat. No.: HY-B0871S
Research Areas:
Quinclorac- 13C is the 13C-labeled Quinclorac (HY-B0871). Quinclorac is a highly selective quinoline carboxylic acid synthetic auxin herbicide. Quinclorac weakly inhibits HPPD, accompanied by a transient decrease in carotenoids. Quinclorac upregulates ACC synthase (ACS), leading to the co-accumulation of ethylene and cyanide, while increasing the ABA/IAA ratio, which induces ROS burst, membrane lipid peroxidation (MDA) and lethal growth inhibition. Residual Quinclorac in soil can cause abnormal growth of subsequent tobacco crops. In calli of Phaseolus vulgaris, Quinclorac induces oxidative stress (increased MDA and decreased RGR), but cells after stepwise pressurized acclimation acquire a constitutive antioxidant state, which remains stable after de-acclimation and tolerates oxidative damage caused by Quinclorac. Quinclorac can be used in studies related to herbicide action mechanisms, bioremediation of soil residues, and adaptive responses of plant cells to oxidative stress .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
