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 | |
|---|---|---|
| Canertinib | Canertinib (CI-1033;PD-183805) is a potent and irreversible EGFR inhibitor; inhibits cellular EGFR and ErbB2 autophosphorylation with IC50s of 7.4 and 9 nM. Canertinib is active against vaccinia virus respiratory infection in mice[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CI-1033; PD-183805. CAS No. 267243-28-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10367. |  |
| Canertinib dihydrochloride | Canertinib dihydrochloride (CI-1033 dihydrochloride) is a potent and irreversible EGFR inhibitor; inhibits cellular EGFR and ErbB2 autophosphorylation with IC50s of 7.4 and 9 nM. Canertinib dihydrochloride is active against vaccinia virus respiratory infection in mice[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CI-1033 dihydrochloride; PD-183805 dihydrochloride. CAS No. 289499-45-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-10367A. | |
| Cangrelor tetrasodium | Cangrelor tetrasodium, an adenosine triphosphate analogue, is a reversible and selective platelet P2Y12 antagonist, with prompt and potent antiplatelet effects. Cangrelor tetrasodium directly blocks adenosine diphosphate (ADP)-induced activation and aggregation of platelets. Cangrelor tetrasodium is also a nonspecific GPR17 antagonist[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AR-C69931MX tetrasodium. CAS No. 163706-36-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-19638A. | |
| Cannabisin A | Cannabisin A is a natural product in seeds in sprouts[1]. Uses: Scientific research. Category: Natural products. CAS No. 130508-46-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N1959. | |
| Cannabisin B | Cannabisin B (Compound 7) is a compound isolated from the aerial part of Tetragonia tetragonioides (New Zealand spinach)[1]. Uses: Scientific research. Category: Natural products. CAS No. 144506-17-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N10419. | |
| Cannflavin A | Cannflavin A can be isolated from Cannabis sativa L. Cannflavin A has anti-cancer, neuroprotective and anti-inflammatory activity. Cannflavin A inhibits Aβ1-42 aggregation. Cannflavin A also inhibits kynurenine-3-monooxygenase (KMO) (IC50 = 29.4 μM). Cannflavin A activates apoptosis via caspase-3 cleavage. Cannflavin A exerts anti-inflammatory effects by inhibiting pro-inflammatory enzymes, including prostaglandin E2 and cytochrome c oxidases I and II in PC12 cell line[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 76735-57-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W748591. | |
| Canrenone | Canrenone (Aldadiene) is an aldosterone antagonist extensively used as a diuretic agent. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Aldadiene; SC9376. CAS No. 976-71-6. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-B1438. | |
| Cantharidic acid disodium | Cantharidic acid disodium is the hydrolysis product of the acid anhydride Cantharidin that induces apoptosis in various human cancer cells. Cantharidic acid disodium is a selective protein phosphatase 2 (PP2A) and PP1 inhibitor withIC50 values of 50 nM and 600 nM, respectively[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1465-77-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-137135A. | |
| Canthaxanthin | Canthaxanthin is a red-orange carotenoid with various biological activities, such as antioxidant, antitumor properties. Uses: Scientific research. Category: Signaling pathways. Alternative Names: E 161g; all-trans-Canthaxanthin. CAS No. 514-78-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B1960. | |
| Canthin-6-one | Canthin-6-one is an indole alkaloid, displays antibacterial and anti-inflammatory activities[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 479-43-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-N3536. | |
| Cantrixil | Cantrixil (TRX-E-002-1), an active enantiomer of TRX-E-002, is a second-generation super-benzopyran (SBP) compound. Cantrixil increases phosphorylated c-Jun levels resulting in caspase-mediated apoptosis in ovarian cancer cells. Cantrixil has potent pan anti-cancer activity against a broad range of cancer phenotypes[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: TRX-E-002-1. CAS No. 2135511-22-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-114250. | |
| Cantuzumab | Cantuzumab is a monoclonal antibody that can binds the CanAg antigen. Cantuzumab is typically linked to one of several cytotoxic agents, yielding antibody-drug conjugates (ADC), such as Cantuzumab mertansine (HY-P99492) and Cantuzumab ravtansine (HY-P99493)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1204740-23-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99967. | |
| Canvuparatide | Canvuparatide (MBX 2109) is a prodrug for parathyroid hormone (PTH) peptide that releases the bioactive PTH[1-32] peptide agonist that retains a fatty acylated lysine (Lys33) at the C-terminus, thereby extending the halflife of Canvuparatide. Canvuparatide can be used for the symptoms of hypoparathyroidism such as hypocalcemia and hyperphosphatemia[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MBX 2109. CAS No. 2925554-87-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P10909. | |
| Capecitabine | Capecitabine is an oral proagent that is converted to its active metabolite, 5-FU, by thymidine phosphorylase. Uses: Scientific research. Category: Signaling pathways. CAS No. 154361-50-9. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g; 5 g. Product ID: HY-B0016. | |
| Capivasertib | Capivasertib (AZD5363) is an orally active and potent pan-AKT kinase inhibitor with IC50 of 3, 7 and 7 nM for Akt1,Akt2 and Akt3, respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AZD5363. CAS No. 1143532-39-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-15431. | |
| Caplacizumab (His Tag) | Caplacizumab (His Tag) is a humanized anti-von Willebrand factor (vWF) nanobody. Caplacizumab (His Tag) inhibits the binding of vWF with platelet glycoprotein (GP) Ibα. Caplacizumab (His Tag) inhibits the vWF-mediated platelet adhesion and prevents further microthrombi formation. Caplacizumab (His Tag) can be used for the research of thrombotic thrombocytopenic purpura (TTP)[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ALX-0681; ALX-0081. CAS No. 915810-67-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P99227. | |
| Capmatinib | Capmatinib (INC280; INCB28060) is a potent, orally active, selective, and ATP competitive c-Met kinase inhibitor (IC50=0.13 nM). Capmatinib can inhibit phosphorylation of c-MET as well as c-MET pathway downstream effectors such as ERK1/2, AKT, FAK, GAB1, and STAT3/5. Capmatinib potently inhibits c-MET-dependent tumor cell proliferation and migration and effectively induces apoptosis. Antitumor activity. Capmatinib is largely metabolized by CYP3A4 and aldehyde oxidase[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: INC280; INCB28060. CAS No. 1029712-80-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-13404. | |
| Capmatinib dihydrochloride hydrate | Capmatinib (INC280; INCB28060) dihydrochloride hydrate is a potent, orally active, selective, and ATP competitive c-Met kinase inhibitor (IC50=0.13 nM). Capmatinib dihydrochloride hydrate can inhibit phosphorylation of c-MET as well as c-MET pathway downstream effectors such as ERK1/2, AKT, FAK, GAB1, and STAT3/5. Capmatinib dihydrochloride hydrate potently inhibits c-MET-dependent tumor cell proliferation and migration and effectively induces apoptosis. Antitumor activity. Capmatinib dihydrochloride hydrate is largely metabolized by CYP3A4 and aldehyde oxidase[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: INC280 dihydrochloride hydrate; INCB-28060 dihydrochloride hydrate. CAS No. 1865733-40-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-13404C. | |
| Capreomycin sulfate | Capreomycin sulfate is a macrocyclic peptide antibiotic that inhibits phenylalanine synthesis in mycobacterial ribosomal translation. Capreomycin sulfate has anti-amyloidogenic and pro-fibrinolytic activities, reducing amyloid-induced cytotoxicity by inhibiting the occurrence of amyloid fibrillation. Capreomycin sulfate can be used in the study of multidrug-resistant tuberculosis, type 2 diabetes, Alzheimer's disease and Parkinson's disease[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1405-37-4. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-17566. | |
| Capromorelin Tartrate | Capromorelin Tartrate is an orally active, potent growth hormone secretagogue receptor (GHSR) agonist, with Ki of 7 nM for hGHS-R1a. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CP 424391-18. CAS No. 193273-69-7. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15243. | |
| Caprylic/Capric Triglyceride | Caprylic/Capric Triglyceride is a mixed triester of Octanoic acid (Caprylic acid) (HY-41417) and Capric acid oil possessing excellent oxidation stability. Caprylic/Capric Triglyceride is used as a food additive and used in cosmetics[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 65381-09-1. Pack Sizes: 100 mg. Product ID: HY-135087. | |
| CAPS | CAPS, cyclohexylaminopropane sulfonic acid, is a surfactant. CAPS can be used as biological buffer (0.05 M, pH 11) for dialysis[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: N-Cyclohexyl-3-aminopropanesulfonic acid. CAS No. 1135-40-6. Pack Sizes: 10 mM * 1 mL in DMSO; 25 g; 50 g; 100 g. Product ID: HY-D0869. | |
| Capsaicin | Capsaicin ((E)-Capsaicin), an active component of chili peppers, is a TRPV1 agonist. Capsaicin induces a nociceptive response by binding to its receptors. Capsaicin has analgesic effects on neurological disorders. Capsaicin has antioxidant, anti-inflammatory, anti-cancer effects[1][2]. Uses: Scientific research. Category: Induced disease models products. Alternative Names: (E)-Capsaicin. CAS No. 404-86-4. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-10448. | |
| Capsaicin (Purity 65%) | Capsaicin (Purity 65%) is a mixture of Capsaicin and Dihydrocapsaicin (Ratio >2:1). Capsaicin (Purity 65%) is an orally active capsaicin receptor (TRPV1) agonist[1][2]. Uses: Scientific research. Category: Induced disease models products. CAS No. 404-86-4. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg. Product ID: HY-10448A. | |
| Capsaicin (Standard) | Capsaicin (Standard) is the analytical standard of Capsaicin. This product is intended for research and analytical applications. Capsaicin ((E)-Capsaicin), an active component of chili peppers, is a TRPV1 agonist. Capsaicin induces a nociceptive response by binding to its receptors. Capsaicin has analgesic effects on neurological disorders. Capsaicin has antioxidant, anti-inflammatory, anti-cancer effects[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (E)-Capsaicin (Standard). CAS No. 404-86-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10448R. | |
| Capsazepine | Capsazepine is a synthetic analogue of the sensory neurone excitotoxin, and an antagonist of TRPV1 receptor with an IC50 of 562 nM. Uses: Scientific research. Category: Signaling pathways. CAS No. 138977-28-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15640. | |
| Captopril | Captopril (SQ 14225), antihypertensive agent, is a thiol-containing competitive, orally active angiotensin-converting enzyme (ACE) inhibitor (IC50=0.025 μM) and has been widely used for research of hypertension and congestive heart failure. Captopril is also a New Delhi metallo-β-lactamase-1 (NDM-1) inhibitor with an IC50 of 7.9 μM[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SQ 14225. CAS No. 62571-86-2. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B0368. | |
| Capzimin | Capzimin is a potent and moderately specific proteasome isopeptidase Rpn11 inhibitor. Uses: Scientific research. Category: Signaling pathways. CAS No. 2084868-04-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110404. | |
| Caraphenol A | Caraphenol A is a resveratrol trimer and is able to transiently reduce interferon-induced transmembrane (IFITM) protein expression. Caraphenol A safely enhances lentiviral vector gene delivery to hematopoietic stem and progenitor cells[1]. Caraphenol A also inhibits human cystathionine β-synthase (hCBS) and human cystathionine γ- lyase (hCSE) with IC50s of 5.9 μM and 12.1 μM, respectively[2]. Uses: Scientific research. Category: Natural products. CAS No. 354553-35-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N3540. | |
| Carazolol | Carazolol is a β1/β2 adrenoceptor antagonist of high potency used in the research of hypertension. Carazolol is also a potent, selective β3-adrenoceptor agonist[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (±)-Carazolol; DL-Carazolol; Suacron. CAS No. 57775-29-8. Pack Sizes: 10 mM * 1 mL in DMSO; 10 mg; 25 mg; 50 mg. Product ID: HY-107327. | |
| Carbamazepine | Carbamazepine is an orally active pressure-sensitive sodium ion channel blocker with an IC50 of 131 μM. Carbamazepine blocks voltage gated Na+, Ca2+, and K+ channels, and is also a HDAC inhibitor (IC50: 2 μM). Carbamazepine is an anticonvulsant and can be used for research of epilepsy and neuropathic pain[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CBZ; NSC 169864. CAS No. 298-46-4. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg. Product ID: HY-B0246. | |
| Carbamazepine 10,11-epoxide | Carbamazepine 10,11-epoxide is a metabolite of Carbamazepine (HY-B0246). Carbamazepine 10,11-epoxide can be used to monitor for Carbamazepine[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 36507-30-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W013378. | |
| Carbamazepine 10,11-epoxide (Standard) | Carbamazepine 10,11-epoxide (Standard) is the analytical standard of Carbamazepine 10,11-epoxide (HY-W013378). Carbamazepine 10,11-epoxide is a metabolite of Carbamazepine (HY-B0246). Carbamazepine 10,11-epoxide can be used to monitor for Carbamazepine[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 36507-30-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W013378R. | |
| Carbamyl-PAF | Carbamyl-PAF is an analog and agonist of platelet-activating factor (PAF). Carbamyl-PAF is not significantly metabolized by Raji lymphoblasts at 37°C, making it a useful tool for inflammation research. [1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: C-PAF. CAS No. 91575-58-5. Pack Sizes: 1 mg (18.56 mM * 100 μL in Ethanol); 5 mg (18.56 mM * 500 μL in Ethanol). Product ID: HY-137257. | |
| Carbazeran | Carbazeran, a potent phosphodiesterase inhibitor, is aldehyde oxidase substrate. Carbazeran can be used for the research of metabolic disease[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 70724-25-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0051. | |
| Carbendazim | Carbendazim is a potent and orally active broad-spectrum benzimidazole fungicide and can be acts as a pesticide for fungal diseases research, such as Seproria, Fusarium and Sclerotina[1][3]. Carbendazim is a benzimidazole (HY-Y1825) derivative with antitumor activity and used for cancer research, especially advanced solid tumors and lymphoma[3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 10605-21-7. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-13582. | |
| Carbenicillin disodium | Carbenicillin disodium (Sodium carbenicillin) is a broad-spectrum semi-synthetic penicillin antibiotic for gram-negative bacteria. Carbenicillin disodium can interfere the cell wall synthesis while displaying low toxicity to plant tissue[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Sodium carbenicillin. CAS No. 4800-94-6. Pack Sizes: 250 mg; 1 g; 5 g; 10 g; 25 g. Product ID: HY-B0525A. | |
| Carbenoxolone | Carbenoxolone is a blood-brain barrier-permeable Pannexin1 inhibitor, gap junction (Gap junction) blocker, and β-amyloid 42 inhibitor. Carbenoxolone modulates voltage-gated currents of wild-type and mutant Panx1, and inhibits stimulus-activated Panx1 channel function. Carbenoxolone interacts with stable residues of β-amyloid 42 peptides, fibrils and oligomers, thereby inhibiting their aggregation. Carbenoxolone alleviates liver fibrosis. Carbenoxolone exerts neuroprotective and nootropic effects. Carbenoxolone can be used in studies related to Alzheimer's disease and liver fibrosis[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 5697-56-3. Pack Sizes: 10 mM * 1 mL in DMSO; 10 mg; 25 mg; 50 mg. Product ID: HY-B1588. | |
| Carbenoxolone disodium | Carbenoxolone disodium is the active metabolite of Glycyrrhizic acid (HY-N0184) and the inhibitor of human 11β-HSD and bacterial 3α, 20β-HSD[1]. Carbenoxolone disodium is an uncoupling agent for gap junctions and a potent inhibitor of Vaccinia virus replication[2]. Carbenoxolone disodium is used for the study of peptic, esophageal and oral ulceration and inflammation. Carbenoxolone disodium inhibits Vaccinia virus replication. Uses: Scientific research. Category: Signaling pathways. CAS No. 7421-40-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1367. | |
| Carbetocin | Carbetocin, an oxytocin (OT) analogue, is an oxytocin receptor agonist with a Ki of 7.1 nM. Carbetocin has high affinity to chimeric N-terminus (E1) of the oxytocin receptor (Ki=1.17 μM). Carbetocin has the potential for postpartum hemorrhage research. Carbetocin can crosse the blood-brain barrier and produces antidepressant-like activity via activation of oxytocin receptors in the CNS[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 37025-55-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17573. | |
| Carbetocin acetate | Carbetocin acetate, an oxytocin (OT) analogue, is an oxytocin receptor agonist with a Ki of 7.1 nM. Carbetocin acetate has high affinity to chimeric N-terminus (E1) of the oxytocin receptor (Ki=1.17 μM). Carbetocin acetate has the potential for postpartum hemorrhage research. Carbetocin acetate can crosse the blood-brain barrier and produces antidepressant-like activity via activation of oxytocin receptors in the CNS[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1631754-28-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17573A. | |
| Carbidopa | Carbidopa ((S)-(-)-Carbidopa), a peripheral decarboxylase inhibitor, can be used for the research of Parkinson's disease. Carbidopa is a selective aryl hydrocarbon receptor (AhR) modulator. Carbidopa inhibits pancreatic cancer cell and tumor growth[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (S)-(-)-Carbidopa. CAS No. 28860-95-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0311. | |
| Carbidopa-d3 monohydrate | Carbidopa-d3 (monohydrate) is the deuterium labeled Carbidopa monohydrate. Carbidopa ((S)-(-)-Carbidopa) monohydrate, a peripheral decarboxylase inhibitor, can be used for the research of Parkinson's disease. Carbidopa monohydrate is a selective aryl hydrocarbon receptor (AhR) modulator. Carbidopa monohydrate inhibits pancreatic cancer cell and tumor growth[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (S)-(-)-Carbidopa-d3 monohydrate. CAS No. 1276197-58-0. Pack Sizes: 1 mg. Product ID: HY-B0311AS. | |
| Carbidopa monohydrate | Carbidopa ((S)-(-)-Carbidopa) monohydrate, a peripheral decarboxylase inhibitor, can be used for the research of Parkinson's disease. Carbidopa monohydrate is a selective aryl hydrocarbon receptor (AhR) modulator. Carbidopa monohydrate inhibits pancreatic cancer cell and tumor growth[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (S)-(-)-Carbidopa monohydrate. CAS No. 38821-49-7. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-B0311A. | |
| Carbocisteine | Carbocisteine is an orally active mucolytic agent. Carbocisteine attenuates the phosphorylation of NF-κB p65 and ERK1/2. Carbocisteine modulates Nrf2/HO-1 and NFκB interplay. Carbocisteine inhibits Apoptosis. Carbocisteine is used in chronic obstructive pulmonary disease (COPD) research[1][2][3][4][5][6][7][8][9][10][11][12][13]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Carbocysteine. CAS No. 638-23-3. Pack Sizes: 500 mg; 1 g. Product ID: HY-D0205A. | |
| Carbomer 934 | Carbomer 934 (CBM 934) is an acrylic acid polymer, which can be used as a thickening agent. Carbomer 934 which forms a high viscosity gel, provides a stable gel matrix, and exhibits good heat, light and microbial contamination resistance. Carbomer 934 facilitates the drug release and local application, which can be used in the pharmaceutical industry[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CBM 934. CAS No. 9007-20-9. Pack Sizes: 25 g; 50 g; 100 g; 500 g. Product ID: HY-W250721B. | |
| Carbon-13C | Carbon-13C is the 13C labeled Carbon (HY-Y1213). Carbon possesses unique physicochemical properties such as electrical and structural characteristics, making it a core material in the field of fuel cells. Carbon also serves as a pharmaceutical excipient and can be used in the synthesis of other compounds[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 14762-74-4. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-Y1213S. | |
| Carbonic anhydrase, Bovine erythrocytes | Carbonic anhydrase, Bovine erythrocytes (EC 4.2.1.1) is ubiquitous zinc-containing metalloenzyme present in prokaryotes and eukaryotes. Carbonic anhydrase can catalyze reversible conversion of carbon dioxide to bicarbonate and protons. Carbonic anhydrase can be used for the research of cancer, glaucoma, obesity and epilepsy[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EC 4.2.1.1. CAS No. 9001-03-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1775. | |
| Carbonic anhydrase (isoenzyme) | Carbonic anhydrase isoenzyme is the isoenzyme of Carbonic anhydrase (HY-P1775). Carbonic anhydrase isoenzyme is ubiquitous zinc-containing metalloenzyme present in prokaryotes and eukaryotes. Carbonic anhydrase isoenzyme catalyzes reversible conversion of carbon dioxide to bicarbonate and protons, and can be used for the research of cancer, glaucoma, obesity and epilepsy[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9001-03-0. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P1775A. | |
| Carboplatin | Carboplatin (NSC 241240) is a DNA synthesis inhibitor which binds to DNA, inhibits replication and transcription and induces cell death. Carboplatin (NSC 241240) is a derivative of CDDP and a potent anti-cancer agent. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NSC 241240. CAS No. 41575-94-4. Pack Sizes: 50 mg; 100 mg; 200 mg; 500 mg; 1 g; 2 g; 5 g; 10 g. Product ID: HY-17393. | |
| Carboplatin (Standard) | Carboplatin (Standard) is the analytical standard of Carboplatin. This product is intended for research and analytical applications. Carboplatin (NSC 241240) is a DNA synthesis inhibitor which binds to DNA, inhibits replication and transcription and induces cell death. Carboplatin (NSC 241240) is a derivative of CDDP and a potent anti-cancer agent. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NSC 241240 (Standard). CAS No. 41575-94-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17393R. | |
| Carboxyamidotriazole | Carboxyamidotriazole (L-651582) is an orally active cytostatic inhibitor of nonvoltage-operated calcium channels and calcium channel-mediated signaling pathways. Carboxyamidotriazole inhibits NF-κB, MAPK activation and NO production. Carboxyamidotriazole has anti-angiogenic and anti-inflammatory activities. Carboxyamidotriazole has anticancer activity against liver cancer, lung cancer and leukemia[1][2][3][4][5][6][7][8][9][10][11][12][13]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-651582; CAI. CAS No. 99519-84-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16126. | |
| Carboxyatractyloside dipotassium | Carboxyatractyloside dipotassium is a diterpenoid. Carboxyatractyloside dipotassium can be isolated from plants of the genus Xanthium. Carboxyatractyloside dipotassium is an ADP/ATP carrier inhibitor, inhibiting mitochondrial ADP/ATP transport. Carboxyatractyloside dipotassium promotes ROS production, induces Ca2+ release, and leads to mitochondrial dysfunction. Carboxyatractyloside dipotassium induces lethargy, weakness, and epileptic seizures in rats[1][2][3][4][5][6]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Gummiferin dipotassium. CAS No. 33286-30-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-N2522. | |
| Carboxyatractyloside tripotassium | Carboxyatractyloside tripotassium is a diterpenoid. Carboxyatractyloside tripotassium can be isolated from plants of the genus Xanthium. Carboxyatractyloside tripotassium is an ADP/ATP carrier inhibitor, inhibiting mitochondrial ADP/ATP transport. Carboxyatractyloside tripotassium promotes ROS production, induces Ca2+ release, and leads to mitochondrial dysfunction. Carboxyatractyloside tripotassium induces lethargy, weakness, and epileptic seizures in rats[1][2][3][4][5][6]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Gummiferin tripotassium. CAS No. 77228-71-8. Pack Sizes: 10 mM * 1 mL in Water; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N1502. | |
| Carboxybetaine methacrylate | Carboxybetaine methacrylate is an amphoteric ionic compound with excellent properties such as good hydrophilicity, antistatic property, and biocompatibility. Carboxybetaine methacrylate can be used to prepare tissue engineering scaffolds, drug carriers, and so on[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 24249-95-4. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 250 mg; 1 g; 5 g; 10 g. Product ID: HY-W110584. | |
| Carboxyl diazirine alkyne | Carboxyl diazirine alkyne is a protein cross-linking compound. Carboxyl diazirine alkyne plays a crucial role in the research on the inhibition and labeling of FTO protein by fluorescein derivatives[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1450754-37-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-W074785. | |
| Carboxyl methylstarch sodium | Sodium carboxyl methylstarch is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Category: Signaling pathways. CAS No. 9063-38-1. Pack Sizes: 25 g; 50 g; 100 g. Product ID: HY-W133963. | |
| Carboxymethyl-β-cyclodextrin sodium salt | Carboxymethyl-β-cyclodextrin sodium salt is a negatively charged β-cyclodextrin derivative, as well as a metal ion chelator and solubilizing reagent. Carboxymethyl-β-cyclodextrin sodium salt forms stable aqueous complexes with Ba2+, Ca2+, Cd2+, Ni2+, Pb2+, Sr2+, and Zn2+ ions. Carboxymethyl-β-cyclodextrin sodium salt derived hydrogel carriers support oral insulin delivery via paracellular permeation across Caco-2 monolayers and produce sustained hypoglycemic effects in diabetic mice. Carboxymethyl-β-cyclodextrin sodium salt can be conjugated onto folate-modified BSA nanoparticles to boost folate receptor-mediated endocytosis, elevate intracellular anticancer drug uptake and trigger cell apoptosis. Carboxymethyl-β-cyclodextrin sodium salt can be utilized for chiral separation in capillary electrophoresis, development of nanoscale drug carriers and nucleic acid transfection research[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2828447-14-7. Pack Sizes: 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-W1113135. | |
| Carboxymethyl chitosan | Carboxymethyl chitosan is a derivative of chitosan. Carboxymethyl chitosan inhibits Apoptosis and ROS. Carboxymethyl chitosan increases the expression of Bcl-2 and reduces the expression of Bax, cytochrome c and caspase-3. Carboxymethyl chitosan inhibits the migration of various cells. Carboxymethyl chitosan exerts antitumor effects on Lewis tumors and hepatocarcinoma[1][2][3][4][5][6][7][8]. Uses: Scientific research. Category: Signaling pathways. CAS No. 83512-85-0. Pack Sizes: 1 g; 5 g. Product ID: HY-W250111. | |
| Carboxypeptidase B (MS grade) | Carboxypeptidase B (MS grade) is a peptide exonuclease that can specifically degrade peptide chains. Carboxypeptidase B (MS grade) is progressively degraded from the C-terminal to release free amino acids. Carboxypeptidase B (MS grade) hydrolyzes only peptide bonds with basic amino acids (such as arginine and lysine) as C-terminal residues[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EC 3.4.2.2 (MS grade). CAS No. 9025-24-5. Pack Sizes: 100 U. Product ID: HY-E70201. | |
| Carboxypeptidase B, Porcine pancreas | Carboxypeptidase B, Porcine pancreas (EC 3.4.2.2) is a peptide exonuclease that can specifically degrade peptide chains. Carboxypeptidase B is progressively degraded from the C-terminal to release free amino acids. Carboxypeptidase B hydrolyzes only peptide bonds with basic amino acids (such as arginine and lysine) as C-terminal residues[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EC 3.4.2.2. CAS No. 9025-24-5. Pack Sizes: 100 U; 500 U; 1 KU. Product ID: HY-P2746. | |
| Carboxy-PTIO potassium | Carboxy-PTIO potassium is a potent nitric oxide (NO) scavenger that can make a quick reaction with NO to produce NO2. Carboxy-PTIO potassium can prevent hypotension and endotoxic shock through the direct scavenging action against NO in lipopolysaccharide-stimulated rat model[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 148819-94-7. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18734A. | |
| Carboxy pyridostatin trifluoroacetate salt | Carboxy pyridostatin trifluoroacetate salt is a G-quadruplex ligand. Carboxy pyridostatin trifluoroacetate salt has a highly molecular specificity to RNA on DNA G4s and reduces ATF-5 protein. Carboxy pyridostatin trifluoroacetate salt reduces cell proliferation and hinders stress granule (SG) formation[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2444713-88-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112680A. | |
| Carboxy-SNARF 1 (5/6-mixture) | Carboxy-SNARF 1 (5/6-mixture) (SNARF 1) is a fluorescent probe that is sensitive to pH (Ex: 488 nm). Carboxy-SNARF 1 (5/6-mixture) can be used for measurement pH. Carboxy-SNARF 1 (5/6-mixture) exhibits a significant emission shift from yellow-orange (Em: 580 nm) to deep red fluorescence (Em: 640 nm) under acidic and basic conditions (pH=7-8), respectively[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SNARF 1. CAS No. 126208-12-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-D1094. | |
| Cardanol monoene | Cardanol monoene (Cardanol C15:1) is a phenolic compound which can be found in cashew nut shell liquid. Cardanol monoene can inhibit cancer cells proliferation, migration, cause S phase arrest, induce apoptosis, ROS production and mitochondrial depolarization. Cardanol monoene downregulates MMP-2, MMP-9, cyclinA1 expression, regulates CDK2, p53, Bax, cytochrome c, cleaved caspase-3, cleaved PARP, Apaf-1 expression and Bax/Bcl-2 ratio. Cardanol monoene shows weak DPPH radical scavenging activity and AChE inhibition activity. Cardanol monoene is lethal to Artemia salina nauplii. Cardanol monoene. Cardanol monoene can be used for the research of cancer, infection and inflamation[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Cardanol C15:1. CAS No. 501-26-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-119979. | |
| Cardiolipin (Heart, Bovine) sodium | Cardiolipin (Heart, Bovine) sodium is a mitochondria-exclusive phospholipid that can be extracted from Bovine hear. Cardiolipin (Heart, Bovine) sodium can maintain mitochondrial function, regulate cellular metabolism and signaling and induce apoptosis and autophagy. Cardiolipin (Heart, Bovine) sodium can be coated on microtitre plates for ELISA assay. Cardiolipin (Heart, Bovine) sodium can be used for the researches of inflammation, immunology, cardiovascular and neurological disease[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 383907-10-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-134238. | |
| Cardiomyocyte proliferation promoting agent-1 | Cardiomyocyte proliferation promoting agent-1 ((E/Z)-GA-002), which is an E/Z mixture, is a cardiomyocyte proliferation promoter. GA-002 (single E configuration) is a kinase inhibitor for LATS1 and LATS2, with its IC50 values being 3.93 nM and 3.87 nM respectively. GA-002 can induce the expression of genes regulated by the Hippo pathway, inhibit the phosphorylation of YAP/TAZ, and induce the nuclear translocation of YAP[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (E/Z)-GA-002. CAS No. 2351906-71-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-164254. | |
| Cardiotoxin Analog (CTX) IV (6-12) | Cardiotoxin Analog (CTX) IV (6-12) is a membrane active peptide that specifically targets negatively charged phospholipid membranes (such as phosphatidylserine and phosphatidylinositol). Cardiotoxin Analog (CTX) IV (6-12) was discovered in the venom of the Taiwan cobra. Cardiotoxin Analog (CTX) IV (6-12) is a chemically synthesized snake venom cardiotoxin that binds to cell membranes and embeds into lipid bilayers through hydrophobic interactions and electrostatic attraction, thereby destroying the stability of membrane structure. Cardiotoxin Analog (CTX) IV (6-12) can induce membrane lipid disorder and cell lysis, exhibiting hemolysis and cytotoxicity[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 115722-23-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1902. | |
| Cardiotoxin Analog (CTX) IV (6-12) TFA | Cardiotoxin Analog (CTX) IV (6-12) TFA is a membrane active peptide that specifically targets negatively charged phospholipid membranes (such as phosphatidylserine and phosphatidylinositol). Cardiotoxin Analog (CTX) IV (6-12) TFA was discovered in the venom of the Taiwan cobra. Cardiotoxin Analog (CTX) IV (6-12) TFA is a chemically synthesized snake venom cardiotoxin that binds to cell membranes and embeds into lipid bilayers through hydrophobic interactions and electrostatic attraction, thereby destroying the stability of membrane structure. Cardiotoxin Analog (CTX) IV (6-12) TFA can induce membrane lipid disorder and cell lysis, exhibiting hemolysis and cytotoxicity[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2918768-05-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1902A. | |
| Carfilzomib | Carfilzomib (PR-171) is an irreversible proteasome inhibitor with an IC50 of 5 nM in ANBL-6 and RPMI 8226 cells. Uses: Scientific research. Category: Induced disease models products. Alternative Names: PR-171. CAS No. 868540-17-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-10455. | |
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