MedChemExpress MCE - Products
MedChemExpress (MCE) offers a wide range of high-quality research chemicals and biochemicals (novel life-science reagents, reference compounds and natural compounds) for scientific use.
| Product | Description | |
|---|---|---|
| PF-8380 | PF-8380 is a potent autotaxin inhibitor with an IC 50 of 2.8 nM in isolated enzyme assay and 101 nM in human whole blood. Uses: Scientific research. Group: Signaling pathways. CAS No. 1144035-53-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13344. |  |
| PF-8380 hydrochloride | PF-8380 hydrochloride is a potent autotaxin inhibitor with an IC 50 of 2.8 nM in isolated enzyme assay and 101 nM in human whole blood. Uses: Scientific research. Group: Signaling pathways. CAS No. 2070015-01-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13344A. | |
| PF-9363 | PF-9363 (CTx-648) is a first-in-class potent and high selective KAT6A/KAT6B inhibitor. PF-9363 can be used for the research of cancer[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CTx-648. CAS No. 2569009-58-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-132283. | |
| PF-9366 | PF-9366 is a human methionine adenosyltransferase 2A (Mat2A) inhibitor, with an IC50 of 420 nM and a Kd of 170 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 72882-78-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107778. | |
| PFB-FDGlu | PFB-FDGlu is a selective lysosomal Glucocerebrosidase (GCase) substrate, which is metabolised by GCase to yield fluorescein. PFB-FDGlu is cell permeable and can be used with a flow cytometer to measure GCase activity in living cells on a single-cell basis[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 209540-62-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139452. | |
| PfDHODH-IN-1 | PfDHODH-IN-1 is an analogue of the active metabolite of Leflunomide. PfDHODH-IN-1 is a Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH) inhibitor. PfDHODH-IN-1 has antimalarial activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 183945-55-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-135648. | |
| PFI-2 hydrochloride | PFI-2 ((R)-PFI-2 hydrochloride) hydrochloride is a potent and selective SET domain containing lysine methyltransferase 7 (SETD7) inhibitor. (R)-PFI-2 shows high inhibiting activity with IC 50 value of 2.0??nM and (S)-PFI-2 shows inhibiting activity with IC 50 ?value of?1.0??μM. PFI-2 hydrochloride can be used for the research of chronic kidney disease and inflammation response in the development of renal fibrosis [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (R)-PFI-2 hydrochloride. CAS No. 1627607-87-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-18627A. | |
| PFI-3 | PFI-3 is a selective, potent and cell-permeable SMARCA2/4 bromodomain inhibitor with a Kd of 89 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 1819363-80-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-12409. | |
| PFI-90 | PFI-90 is a selective inhibitor of histone demethylase (KDM3B) that inhibits PAX3-FOXO1 action. PFI-90 induces apoptosis and myogenic differentiation, resulting in the cell death increased. PFI-90 has the potential for the antitumor activity. (patent WO2021101929A1). Uses: Scientific research. Group: Signaling pathways. CAS No. 53995-62-3. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-139348. | |
| PFK-015 | PFK-015, a derivative of 3PO, is a specific PFKFB3 inhibitor. PFK-015 inhibits recombinant PFKFB3 with an IC50 value of 110 nM and inhibits PFKFB3 activity in cancer cells with an IC50 value of 20 nM. PFK-015 can be used for the research of multiple cancers such as lung cancer, stomach cancer, colon cancer and esophageal squamous cell carcinoma (ESCC)[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 4382-63-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12204. | |
| PFK-158 | PFK-158 is a potent and selective PFKFB3 inhibitor with an IC50 value 137 nM. PFK-158 reduces glucose uptake, ATP production, lactate release, and induces apoptosis and autophagy in cancer cells. PFK-158 has broad anti-tumor activity. PFK-158 can also enhance Colistin's resistance to bacteria[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1462249-75-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12203. | |
| PFM01 | PFM01, N-alkylated Mirin derivative, is a MRE11 endonuclease inhibitor. PFM01 can regulate double-strand break repair (DSBR) by nonhomologous end-joining (NHEJ) versus homologous recombination (HR)[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1558598-41-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-116770. | |
| PFM03 | PFM03 is a MRE11 Endonuclease inhibitor. PFM03 regulates DNA double-strand break repair (DSBR) by nonhomologous end-joining (NHEJ)[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1558598-48-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-148078. | |
| PFM39 | PFM39, a Mirin analog, is a potent and selective MRE11 exonuclease inhibitor. PFM39 inhibits phosphate rotation for dsDNA exonuclease activity. PFM39 does not inhibit TmMre11 or human MRE11/MRN endonuclease activity[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1310744-67-2. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120951. | |
| PG 34 | PG 34 is a weak O-GlcNAc transferase ( OGT ) inhibitor ( IC 50 =68 μM), and a close structural analog of OSMI-1 (HY-119738) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1681056-62-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148113. | |
| PG-931 | PG-931, an analog of SHU 9119 (HY-P0227), is a potent melanocortin 4 (MC4) receptor ( IC 50 =0.58 nM) agonist and is more selective than for the hMC3R ( IC 50 =55 nM) or the hMC5R ( IC 50 =2.4 nM). PG-931 can reverse haemorrhagic shock and prevent multiple organ damage in vivo [2]. Uses: Scientific research. Group: Peptides. CAS No. 667430-81-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1208. | |
| PGP-4008 | PGP-4008 is a specific P-glycoprotein ( Pgp ) inhibitor. PGP-4008 inhibits tumor growth in a murine syngeneic Pgp-mediated multiple agent resistance (MDR) solid tumor model when given in combination with Doxorubicin [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 365565-02-2. Pack Sizes: 10 mM * 1 mL; 500 μg; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119823. | |
| P-gp inhibitor 1 | P-gp inhibitor 1 is a novel inhibitor reversing P-glycoprotein -mediated multidrug resistance. Uses: Scientific research. Group: Signaling pathways. CAS No. 2050747-49-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101791. | |
| PH-797804 | PH-797804 is a ATP-competitive, selective p38?/p38? inhibitor (IC50=26 nM and Ki=5.8 nM for p38?; Ki=40 nM for p38?) and does not inhibit JNK2. Uses: Scientific research. Group: Signaling pathways. CAS No. 586379-66-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10403. | |
| PHA-543613 | PHA-543613 is a potent, orally active, brain-penetrant and selective α7 nAChR agonist with a K i of 8.8 nM. PHA-543613 displays selectivity for α7-nAChR over α3β4, α1β1γδ, α4β2 and 5-HT3 receptors [1]. PHA-543613 can be used for the cognitive deficits of Alzheimer's disease and schizophrenia research [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 478149-53-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105670. | |
| PHA 568487 free base | PHA 568487 free base is a selective alpha 7 nicotinic acetylcholine receptor ( α-7 nAchR ) agonist. PHA 568487 free base reduces neuroinflammation [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 527680-56-4. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-129674. | |
| PHA-665752 | PHA-665752 is a selective, ATP-competitive, and active-site inhibitor of the catalytic activity of c-Met kinase ( K i=4 nM; IC 50=9 nM). PHA-665752 exhibits >50-fold selectivity for c-Met compared with a panel of diverse tyrosine and serine-threonine kinases. PHA-665752 induces apoptosis and cell cycle arrest, and exhibits cytoreductive antitumor activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 477575-56-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-11107. | |
| PHA-767491 | PHA-767491 is a dual Cdc7/Cdk9 inhibitor, with IC50s of 10 nM and 34 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CAY10572. CAS No. 845714-00-3. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-13461. | |
| PHA-767491 hydrochloride | PHA-767491 hydrochloride is a dual Cdc7/Cdk9 inhibitor, with IC50s of 10 nM and 34 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CAY-10572 hydrochloride. CAS No. 942425-68-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13461A. | |
| PHA-793887 | PHA-793887 is a potent, ATP-competitive CDK inhibitor, can inhibit Cdk2, Cdk1, Cdk4, and Cdk9 with IC50s of 8 nM, 60 nM, 62 nM and 138 nM, respectively, and also inhibits glycogen synthase kinase 3? with an IC50 of 79 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 718630-59-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-11001. | |
| Phaclofen | Phaclofen is a selective GABA B receptor antagonist. Phaclofen is a peripheral and central baclofen antagonist. Phaclofen maybe a potential compound in determining the physiological significance of central and peripheral bicuculline-insensitive receptors with which GABA and (-)-baclofen interact [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 114012-12-3. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-100798. | |
| Phallacidin | Phallacidin is a member of the phallotoxin family of mushroom toxins. Phallacidin binds F-actin [1]. Uses: Scientific research. Group: Peptides. CAS No. 26645-35-2. Pack Sizes: 1 mg. Product ID: HY-P2031. | |
| Phalloidin | Phalloidin is a mushroom-derived toxin which can be used to label F-actin of the cytoskeleton with fluorochrome [1]. Uses: Scientific research. Group: Peptides. CAS No. 17466-45-4. Pack Sizes: 1 mg. Product ID: HY-P0028. | |
| PHCCC | PHCCC is a Group I mGluR antagonist with an IC 50 of 3 μM. PHCCC is a selective positive modulator of mGlu4 receptor. Antiparkinsonian effect [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 179068-02-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100409. | |
| Phe-Gly | Phe-Gly hydrate is a Glycine (HY-Y0966) derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 721-90-4. Pack Sizes: 50 mg; 100 mg. Product ID: HY-W141936. | |
| Phe-Met-Arg-Phe amide trifluoroacetate | Phe-Met-Arg-Phe amide trifluoroacetate is an activator of K + current, with ED 50 of 23 nM in the peptidergic caudodorsal neurons. Uses: Scientific research. Group: Peptides. CAS No. 159237-99-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P0249A. | |
| Phenacetin | Phenacetin (Acetophenetidin) is a non-opioid analgesic/antipyretic agent. Phenacetin is a selective COX-3 inhibitor. Phenacetin is used as probe of cytochrome P450 enzymes CYP1A2 in human liver microsomes and in rats [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Acetophenetidin. CAS No. 62-44-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0476. | |
| Phenacetin (Standard) | Phenacetin (Standard) is the analytical standard of Phenacetin. This product is intended for research and analytical applications. Phenacetin (Acetophenetidin) is a non-opioid analgesic/antipyretic agent. Phenacetin is a selective COX-3 inhibitor. Phenacetin is used as probe of cytochrome P450 enzymes CYP1A2 in human liver microsomes and in rats [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Acetophenetidin (Standard). CAS No. 62-44-2. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-B0476R. | |
| Phenamil methanesulfonate | Phenamil methanesulfonate, an analog of Amiloride (HY-B0285), is a more potent and less reversible epithelial sodium channel (ENaC) blocker with an IC 50 of 400 nM [2]. Phenamil methanesulfonate is also a competive inhibitor of TRPP3 and inhibits TRPP3-mediated Ca 2+ transport with an IC 50 of 140 nM in a Ca 2+ uptake assay [1]. Phenamil methanesulfonate is an intriguing small molecule to promote bone repair by strongly activating BMP signaling pathway [4]. Phenamil methanesulfonate is used for the research of cystic fibrosis lung disease [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1161-94-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-108464A. | |
| Phenanthrene | Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 85-01-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1727. | |
| Phenanthrene (Standard) | Phenanthrene (Standard) is the analytical standard of Phenanthrene. This product is intended for research and analytical applications. Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 85-01-8. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B1727R. | |
| Phenanthriplatin | Phenanthriplatin is a monovalent platinum(II)-based complex with a large cytotoxicity against cancer cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1416900-51-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139813. | |
| Phenazine | Phenazine is an electron shuttles, which modulates the redox state of cells and the downstream gene expression related to biofilm formation and bacterial survival. Phenazines is a biocontrol agents, which affects the growth of plants and induces the systemic resistance in plants [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 92-82-0. Pack Sizes: 10 mM * 1 mL; 10 g; 25 g; 50 g; 100 g. Product ID: HY-W016477. | |
| Phenazine-1-carboxylic acid | Phenazine-1-carboxylic acid is an antifungal agent. Additionally, Phenazine-1-carboxylic acid exhibits anticancer activity by inducing apoptosis in cancer cells through the regulation of ROS generation. Phenazine-1-carboxylic acid can upregulate the expression of IL-8 and ICAM-1 while inhibiting the release of RANTES and MCP-1, demonstrating its potential immunomodulatory effects. Phenazine-1-carboxylic acid holds significant research value in the areas of anti-infection, anticancer, and immune response modulation [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 2538-68-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 1 g. Product ID: HY-33037. | |
| Phenazine methylsulfate | Phenazine methylsulfate is a free radical generator that can act as an electron transfer reactant in cell viability assays. It also has insecticidal properties. Furthermore, Phenazine methylsulfate induces oxidative DNA damage and cell apoptosis , showing antitumor activity [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 5-Methylphenazinium methylsulfate. CAS No. 299-11-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-W004520. | |
| Phenazopyridine | Phenazopyridine is a competitive SARM1 inhibitor, with IC 50 145 μM. Phenazopyridine is a TRPM8 antagonist. Phenazopyridine has a local anesthetic/analgesic effect. Phenazopyridine is used to relieve painful symptoms of conditions such as cystitis and urethritis. Phenazopyridine can promote neuronal differentiation and can also be used in the study of traumatic brain injury, peripheral neuropathy and neurodegenerative diseases [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 94-78-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-B0985A. | |
| Phenazopyridine hydrochloride | Phenazopyridine hydrochlorideis a competitive SARM1 inhibitor, with IC 50 145 μM. Phenazopyridine hydrochlorideis a TRPM8 antagonist. Phenazopyridine hydrochloride has a local anesthetic/analgesic effect. Phenazopyridine hydrochlorideis used to relieve painful symptoms of conditions such as cystitis and urethritis. Phenazopyridine hydrochloridecan promote neuronal differentiation and can also be used in the study of traumatic brain injury, peripheral neuropathy and neurodegenerative diseases [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 136-40-3. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0985. | |
| Phen-DC3 Trifluoromethanesulfonate | Phen-DC3 Trifluoromethanesulfonate is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases with IC50s of 65±6 and 50±10 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Phen-DC3 Triflate. CAS No. 929895-45-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15594A. | |
| Phenelzine sulfate | Phenelzine sulfate is a non-selective and irreversible monoamine oxidase inhibitor (MAOI), used as an antidepressant and anxiolytic. Uses: Scientific research. Group: Signaling pathways. CAS No. 156-51-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1018A. | |
| Pheneturide (Standard) | Pheneturide (Standard) is the analytical standard of Pheneturide. This product is intended for research and analytical applications. Pheneturide (Ethylphenacemide, M 551), a decarboxylation product of Phenobarbital, can be used to prevent psychomotor seizures[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ethylphenacemide (Standard); M 551 (Standard). CAS No. 90-49-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-111177R. | |
| Phenformin | Phenformin (1-phenethylbiguanide) is an orally active antidiabetic and anticancer agent. Phenformin has an incidence of associated lactic acidosis. Phenformin acts through acting AMPK activation and blocking mTOR pathway. Phenformin is also a substrate of P-glycoprotein (P-gp), and an OXPHOS inhibitor. Phenformin induces cancer cell apoptosis [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Phenethylbiguanide. CAS No. 114-86-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16397. | |
| Phenformin hydrochloride | Phenformin hydrochloride is an anti-diabetic agent from the biguanide class, can activate AMPK activity. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Phenethylbiguanide hydrochloride. CAS No. 834-28-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-16397A. | |
| Phenibut hydrochloride | Phenibut (β-Phenyl-GABA) hydrochloride is an orally active GABA-B agonist [1]. Phenibut hydrochloride acts as a GABA-mimetic, primarily at GABAB receptors. Phenibut hydrochloride has anxiolytic and nootropic (cognition enhancing) effects [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: β-Phenyl-GABA hydrochloride; 4-Amino-3-phenylbutanoic acid hydrochloride; 4-Amino-3-phenylbutyric acid hydrochloride. CAS No. 3060-41-1. Pack Sizes: 100 mg. Product ID: HY-W041333. | |
| Phenidone | Phenidone, an orally active dual inhibitor of cyclooxygenase (COX) and lipoxygenase (LOX) , ameliorates rat paralysis in experimental autoimmune encephalomyelitis. Phenidone is a potent hypotensive agent in the spontaneously hypertensive rat [1] [2]. Phenidone is used as a photographic developer [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 92-43-3. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-W010144. | |
| Phenindione | Phenindione is an anticoagulant and can act as a vitamin K antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Rectadione. CAS No. 83-12-5. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-B0325. | |
| Pheniprazine hydrochloride | Pheniprazine hydrochloride is a potent and long acting inhibitor of monoamine oxidase. Pheniprazine has the potential for the research of depression [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: β-Phenylisopropylhydrazine hydrochloride. CAS No. 66-05-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W224327A. | |
| Pheniramine maleate | Pheniramine (Prophenpyridamine; Tripoton) maleate is a first-generation histamine H1 receptor antagonist, acts on the central nervous system (CNS) with sedative and hypnotic effect. Pheniramine maleate displays antitumor effect and induces leukemia cells apoptosis. Pheniramine maleate is also a safe and effective local agent that can suppress or relieve pain, with antipruritic effects [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Prophenpyridamine maleate; Tripoton maleate; Pheniramine maleate. CAS No. 132-20-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-B0971. | |
| Phenmedipham | Phenmedipham is a carbamate herbicide [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 13684-63-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B2032. | |
| Phenolphthalein | Phenolphthalein is an acid-base indicator that is colorless in an acidic environment and pink in an alkaline environment. Phenolphthalein is genotoxic and potentially carcinogenic to mice. In addition, phenolphthalein is also a blood indicator [1] [2] [3]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 77-09-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-D0211. | |
| Phenol Red | Phenol red (Phenolsulfonephthalein) is a pH indicator dye, relying on a distinct color change from pink to yellow in case of a positive reaction [1] [2]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Phenolsulfonephthalein. CAS No. 143-74-8. Pack Sizes: 5 g; 25 g. Product ID: HY-D0169. | |
| Phenothiazine | Phenothiazine is an antibiotic which has insecticidal, fungicidal, antibacterial and anthelmintic activities. Phenothiazine also can be used for the research of neurological diseases [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Thiodiphenylamine. CAS No. 92-84-2. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-Y0055. | |
| Phenothrin | Phenothrin is a synthetic pyrethroid that kills adult fleas and ticks. Uses: Scientific research. Group: Signaling pathways. CAS No. 26002-80-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-B1072. | |
| Phenoxazine | Phenoxazine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 135-67-1. Pack Sizes: 5 g; 10 g. Product ID: HY-34463. | |
| Phenoxyacetic acid | Phenoxyacetic acid is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 122-59-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-Y0267. | |
| Phenoxyacetone | Phenoxyacetone is a acetylcholinesterase ( AChE ) inhibitor [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Phenoxy-2-propanone. CAS No. 621-87-4. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-116792. | |
| Phenoxybenzamine hydrochloride | Phenoxybenzamine hydrochloride is a nonselective, irreversible, orally active α-adrenoceptor antagonist that is commonly used for the research of hypertension, specifically caused by pheochromocytoma. Phenoxybenzamine hydrochloride also shows antitumor activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 63-92-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B0431A. | |
| Phenoxyethanol | Phenoxyethanol has a broad spectrum of antimicrobial agent. Phenoxyethanol is an uncouple agent in oxidative phosphorylation from respiration and competitively inhibits malate dehydrogenase. Phenoxyethanol is used as a preservative in cosmetic, vaccine, and textile, et al [1]. Uses: Scientific research. Group: Natural products. CAS No. 122-99-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1729. | |
| Phenprocoumon | Phenprocoumon is a coumarin derivative that acts as a long acting oral anticoagulant and an antagonist of vitamin K. Uses: Scientific research. Group: Signaling pathways. CAS No. 435-97-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-A0145. | |
| Phenserine | Phenserine ((-)-Eseroline phenylcarbamate) is a derivative of Physostigmine and is a potent, noncompetitive, long-acting and selective AChE inhibitor. Phenserine reduces β-amyloid precursor protein (APP) and β-amyloid peptide (Aβ) formation. Phenserine improves cognitive performance and attenuates the progression of Alzheimer's disease [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (-)-Eseroline phenylcarbamate; (-)-Phenserine. CAS No. 101246-66-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-103374. | |
| Phenthoate | Phenthoate is an organophosphorus pesticide having low toxicity in animals. Phenthoate is also a AChE inhibitor [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2597-3-7. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-118165. | |
| Phentolamine | Phentolamine is a potent, selective and orally active α1 adrenergic and α2 adrenergic receptor antagonist. Phentolamine can be used for the research of erectile dysfunction [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 50-60-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-12717. | |
| Phentolamine hydrochloride | Phentolamine hydrochloride is an orally active adrenergic α receptor -blocking agent [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 73-05-2. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-12717A. | |
| Phentolamine mesylate | Phentolamine mesylate (Phentolamine methanesulfonate) is a reversible, non-selective, and orally active blocker of α1 and α2 adrenergic receptor that expands blood vessels to reduce peripheral vascular resistance. Phentolamine mesylate can be used for the research of pheochromocytoma-related hypertension, heart failure and erectile dysfunction [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Phentolamine methanesulfonate. CAS No. 65-28-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0362A. | |
| Phenyl 2-bromoacetate | Phenyl 2-bromoacetate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 620-72-4. Pack Sizes: 25 g. Product ID: HY-41413. | |
| Phenyl acetate | Phenyl acetate is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 122-79-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-128733. | |
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