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 | |
|---|---|---|
| CID-1067700 | CID-1067700 (ML282) is a pan GTPase inhibitor, and competitively inhibits Ras-related in brain 7 (Rab7) with a Ki of 13 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ML282. CAS No. 314042-01-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13452. |  |
| CID 16020046 | CID 16020046 is a potent and selective GPR55 antagonist and inhibits GPR55 constitutive activity with an IC 50 of 0.15 μM. CID 16020046 inhibits GPR55-mediated Ca 2+ signaling and GPR55-mediated ERK1/2 phosphorylation. CID 16020046 reduces wound healing in endothelial cells and is involved in the regulation of platelet function [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 834903-43-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16697. | |
| CID 2745687 | CID 2745687 acts as a specific, reversible and competitive GPR35 antagonist with a Ki of 12.8 nM[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 264233-05-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107537. | |
| CID 697851 | CID 697851 is an AddAB and RecBCD inhibitor, with IC 50 s of 13 and 33 nM. CID 697851 can be used for antibacterial research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 312508-42-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-151221. | |
| Cidofovir | Cidofovir (GS 0504) is an acyclic monophosphate nucleotide analogue and CMV inhibitor with antiviral activity. Cidofovir inhibits cytomegalovirus (CMV) replication by selectively inhibiting viral DNA polymerase. Cidofovir induces apoptosis and can be used in studies of AIDS cytomegalovirus retinitis, herpes, and cancer [1] [3]. Cidofovir also has anti- orthopoxvirus and anti-variola activities [4]. Uses: Scientific research. Group: Natural products. Alternative Names: GS 0504; HPMPC; (S)-HPMPC. CAS No. 113852-37-2. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17438. | |
| Ciforadenant | Ciforadenant (CPI-444) is a potent, orally active and selective adenosine A2A receptor ( A2AR ) antagonist, which induces antitumor responses [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CPI-444; V81444. CAS No. 1202402-40-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101978. | |
| Ciglitazone | Ciglitazone is a potent and selective PPARγ agonist ( EC 50 =3 μM). Ciglitazone inhibits proliferation and differentiation of th17 cells. Ciglitazone is a hypoglycemic agent orally active in the obese-hyperglycemic animal models. Ciglitazone induces apoptosis accompanied by activation of p38 MAPK and nuclear translocation of apoptosis inducing factor (AIF) in opossum kidney (OK) renal epithelial cells [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ADD-3878; U-63287. CAS No. 74772-77-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-W011220. | |
| CIL56 | CIL56 is a potent and selective ferroptosis inducer. Ferroptosis is an iron-dependent form of regulated cell death (RCD). Uses: Scientific research. Group: Signaling pathways. CAS No. 300802-28-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112063. | |
| Cilastatin | Cilastatin (MK0791) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC 50 of 0.1 μM. Cilastatin inhibits the bacterial metallob-lactamase enzyme CphA with an IC 50 of 178 μM. Cilastatin is an antibacterial adjunct [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK0791. CAS No. 82009-34-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-A0166. | |
| Cilastatin sodium | Cilastatin sodium (MK0791 sodium) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC 50 of 0.1 μM. Cilastatin sodium inhibits the bacterial metallob-lactamase enzyme CphA with an IC 50 of 178 μM. Cilastatin sodium is an antibacterial adjunct [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK0791 sodium. CAS No. 81129-83-1. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-A0166A. | |
| Cilazapril monohydrate | Cilazapril Monohydrate is a angiotensin-converting enzyme (ACE) inhibitor used for the treatment of hypertension and congestive heart failure. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 31-2848 monohydrate. CAS No. 92077-78-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0043A. | |
| Cilengitide | Cilengitide (EMD 121974) is a potent integrins antagonist with IC50s of 0.61 nM (???3), 8.4 nM (???5) and 14.9 nM (?5?1), respectively. Cilengitide inhibits the binding of ???3 and ???5 to Vitronectin with IC50s of 4 nM and 79 nM, respectively. Cilengitide inhibits TGF-?/Smad signaling, mediates PD-L1 expression. Cilengitide also induces apoptosis, shows antiangiogenic effect in the research against glioblastoma and other cancers[1][2][3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EMD 121974. CAS No. 188968-51-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16141. | |
| Cilengitide TFA | Cilengitide is a potent and selective integrin inhibitor for ?v?3 and ?v?5 receptor, with IC50 values of 4 nM and 79 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EMD 121974 TFA. CAS No. 199807-35-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16143. | |
| Cilgavimab | Cilgavimab (AZD-1061; COV2-2130) is a human SARS-CoV-2 -neutralizing monoclonal antibody, can compose monoclonal-antibody combination AZD7442 with Tixagevimab (HY-P99556). Cilgavimab shows protective action on mouse models of SARS-CoV-2 infection [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: AZD-1061; COV2-2130. CAS No. 2420563-99-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99604. | |
| Ciliobrevin A | Ciliobrevin A (HPI-4) is a hedgehog (Hh) signaling pathway inhibitor with median inhibitory concentration (IC50) less than 10 ?M[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HPI-4. CAS No. 302803-72-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100790. | |
| Ciliobrevin D | Ciliobrevin D is a cell-permeable, reversible and specific inhibitor of AAA+ ATPase motor cytoplasmic dynein. Ciliobrevin D inhibits Hedgehog (Hh) signaling and primary cilia formation. Ciliobrevin D inhibits dynein-dependent microtubule gliding and ATPase activity in vitro[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1370554-01-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-122632. | |
| Cilnidipine | Cilnidipine is a long-acting, second-generation dihydropyridine Ca 2+ -channel blocker on L and N-type Ca 2+ channel [1] [2] [3] [4]. Antihypertensive effects [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FRC-8653. CAS No. 132203-70-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17404. | |
| Cilofexor | Cilofexor (GS-9674) is a potent, selective and orally active nonsteroidal FXR agonist with an EC 50 of 43 nM. Cilofexor has anti-inflammatory and antifibrotic effects. Cilofexor has the potential for primary sclerosing cholangitis (PSC) and nonalcoholic steatohepatitis (NASH) research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-9674. CAS No. 1418274-28-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109083. | |
| Cilomilast | Cilomilast (SB-207499) is a potent, selective and orally active inhibitor of Phosphodiesterase 4 (PDE4) , with IC 50 s of ~100 and 120 nM for LPDE4 and HPDE4, respectively. Cilomilast shows selectivity for PDE4 over PDE1, PDE2, PDE3 and PDE5 ( IC 50=74, 65, >100, and 83 μM, respectively). Cilomilast has anti-inflammatory and immunomodulatory effects and can be used for thr research of asthma and chronic obstructive pulmonary disease (COPD) [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SB-207499. CAS No. 153259-65-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10790. | |
| Cilostamide | Cilostamide is a selective and potent PDE3 inhibitor, with IC50s of 27 nM and 50 nM for PDE3A and PDE3B, respectively, and has antithrombotic and anti-intimal hyperplastic activity. Uses: Scientific research. Group: Signaling pathways. Alternative Names: OPC3689. CAS No. 68550-75-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101312. | |
| Cilostazol | Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A , the isoform of PDE 3 in the cardiovascular system, with an IC 50 of 0.2 μM [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: OPC 13013. CAS No. 73963-72-1. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-17464. | |
| CIM0216 | CIM0216, a synthetic TRPM3 ligand, acts as a potent and selective agonist of TRPM3. CIM0216 exhibits selectivity for TRPM3 over TRPM1, TRPM2 and TRPM4-8. CIM0216 acts in a TRPM3-dependent manner to induce pain and evoke neuropeptide release from sensory nerve terminals in vitro. CIM0216 is a powerful tool for studies of the physiological functions of TRPM3, and can be used for neurogenic inflammation research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1031496-06-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110220. | |
| Cimetidine | Cimetidine (SKF-92334) is an orally active and inverse histamine H2 receptor antagonist with a K i of 0.6 μM. Cimetidine is a gastric acid reducer, and can be used for duodenal and gastric ulcers research. Cimetidine has anti-cancer and anti-inflammatory activity [1] [2] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SKF-92334. CAS No. 51481-61-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 1 g; 5 g; 10 g. Product ID: HY-14289. | |
| Cimetropium Bromide | Cimetropium Bromide (DA-3177) is a mAChR antagonist for long-term treatment of irritable bowel syndrome. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DA-3177. CAS No. 51598-60-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-U00106. | |
| Cimicoxib | Cimicoxib (CX) is an orally active potent and selective COX-2 (cyclo-oxygenase-2) inhibitor. Cimicoxib exhibits promising anti-inflammatory and analgesic activity. The PK parameters of Cimicoxib in dogs given precise (2 mg/kg) and approximate doses (1.95-2.5 mg/kg) are similar [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: UR-8880. CAS No. 265114-23-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-100516. | |
| Cimlanod | Cimlanod (BMS-986231) is a second-generation Nitroxyl (HNO) donor for heart failure. Cimlanod (BMS-986231) delivers HNO via pH-dependent chemical breakdown when exposed to the neutral pH environment of the bloodstream. Cimlanod (BMS-986231) possesses positive lusitropic and inotropic as well as vasodilatory effects [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMS-986231; CXL-1427. CAS No. 1620330-72-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-118643. | |
| Cinacalcet | Cinacalcet (AMG 073) is an orally active, allosteric agonist of Ca receptor (CaR) , used for cardiovascular disease research. Uses: Scientific research. Group: Natural products. Alternative Names: AMG 073. CAS No. 226256-56-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-70037. | |
| Cinacalcet hydrochloride | Cinacalcet hydrochloride (AMG-073 hydrochloride) is an orally active, allosteric agonist of Ca receptor (CaR) , used for cardiovascular disease treatment. Uses: Scientific research. Group: Natural products. Alternative Names: AMG-073 hydrochloride. CAS No. 364782-34-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-70037A. | |
| Cinaciguat | Cinaciguat is an activator of guanylate cyclase (sGC) , and used for acute decompensated heart failure. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 58-2667. CAS No. 329773-35-5. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14181. | |
| Cinaciguat hydrochloride | Cinaciguat hydrochloride is a potent soluble guanylate cyclase ( GC ) activator with EC 50 of 15 nM in platelets. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 58-2667 hydrochloride. CAS No. 646995-35-9. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14181A. | |
| Cinanserin hydrochloride | Cinanserin hydrochloride (SQ 10643) is a potent, selective and highly affinity 5-HT 2 receptor antagonist with a K i of 41 nM. Cinanserin hydrochloride has a much higher binding affinity for the 5-HT 2 than for the 5-HT 1 receptor ( K i of 3500 nM). Cinanserin is also an inhibitor of 3C-like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SQ 10643. CAS No. 54-84-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-100943. | |
| Cinchonidine | Cinchonidine (α-Quinidine) is a cinchona alkaloid found in Cinchona officinalis and Gongronema latifolium. A building block used in asymmetric synthesis in organic chemistry. Weak inhibitor of serotonin transporter (SERT) with K i s of 330, 4.2, 36, 196, 15 μM for dSERT, hSERT, hSERT I172M, hSERT S438T, hSERT Y95F, respectively. Antimalarial activities [1]. Uses: Scientific research. Group: Natural products. Alternative Names: α-Quinidine. CAS No. 485-71-2. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-N0173. | |
| Cinchonine | Cinchonine is a natural compound present in Cinchona bark with antimalarial, antitumor, anti-inflammatory, anti platelet-aggregation and anti-obesity properties. Cinchonine inhibits cells proliferation and autophagy and induces apoptosis through activation of Caspase-3. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells [1]. Uses: Scientific research. Group: Natural products. Alternative Names: (8R,9S)-Cinchonine; LA40221. CAS No. 118-10-5. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-Y0152. | |
| Cinepazide Maleate | Cinepazide Maleate (MD-67350) is a piperazine derivative and acts as a weak calcium channel blocker. Cinepazide Maleate is a potent vasodilator and can be used for the research of cerebrovascular diseases, including ischemic stroke, brain infarct et. al [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MD-67350. CAS No. 26328-04-1. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-66010. | |
| Cinitapride | Cinitapride is a nonselective 5-HT1 and 5-HT4 receptors agonist and a 5-HT2 and D2 antagonist. Cinitapride can be used in functional dyspepsia (FD) and gastroesophageal reflux disease (GERD) research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 66564-14-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B2089. | |
| Cinnabarinic acid | Cinnabarinic acid is a specific orthosteric agonist of mGlu 4 by interacting with residues of the glutamate binding pocket of mGlu4, has no activity at other mGlu receptors. Cinnabarinic acid is an endogenous metabolite of the kynurenine pathway of tryptophan. Cinnabarinic acid induces cell apoptosis [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 606-59-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W011417. | |
| Cinnamic acid | Cinnamic acid has potential use in cancer intervention, with IC 50 s of 1-4.5 mM in glioblastoma, melanoma, prostate and lung carcinoma cells. Uses: Scientific research. Group: Natural products. Alternative Names: 3-Phenylacrylic acid; β-Phenylacrylic acid. CAS No. 621-82-9. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N0610A. | |
| Cinnamyl-3,4-dihydroxy-α-cyanocinnamate | Cinnamyl-3,4-dihydroxy-α-cyanocinnamate (CDC) is a potent 12/15-Lipoxygenases (LO) inhibitor. Cinnamyl-3,4-dihydroxy-α-cyanocinnamate has the potential for the research of type 1 diabetes mellitus [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CDC. CAS No. 132465-11-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-138688. | |
| Cinnamyl acetate | Cinnamyl acetate has a wide application in the flavor and fragrance industry [1]. Cinnamyl acetate is a new broad spectrum antibacterial agent [2]. Uses: Scientific research. Group: Natural products. CAS No. 103-54-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-N7125. | |
| Cinnamyl Alcohol | Cinnamyl Alcohol is an active component from chestnut flower, inhibits increased PPARγ expression, with anti-obesity activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 104-54-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-Y0078. | |
| Cinnamyl Alcohol (Standard) | Cinnamyl Alcohol (Standard) is the analytical standard of Cinnamyl Alcohol. This product is intended for research and analytical applications. Cinnamyl Alcohol is an active component from chestnut flower, inhibits increased PPARγ expression, with anti-obesity activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 104-54-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-Y0078R. | |
| Cinnamyl cinnamate | Cinnamyl cinnamate (Styracin) is a natural product. Cinnamyl cinnamate can be produced from Liquidambar orientalis Mill [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Styracin. CAS No. 122-69-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N3588. | |
| Cinnamylideneacetic acid | Cinnamylideneacetic acid is a photoresponsive compound which is capable of a photoinduced [2+2] cycloaddition [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Cinnamalacetic acid. CAS No. 1552-94-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N7129. | |
| Cinnarizine | Cinnarizine is an antihistamine and a calcium channel blocker, promote cerebral blood flow, used to treat cerebral apoplexy, post-trauma cerebral symptoms, and cerebral arteriosclerosis. Uses: Scientific research. Group: Signaling pathways. CAS No. 298-57-7. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B1090. | |
| Cinnarizine-d8 | Cinnarizine-d 8 is a deuterium labeled Cinnarizine. Cinnarizine is an antihistamine and a calcium channel blocker. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1185242-27-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-B1090S. | |
| Cinobufagin | Cinobufagin is an anticancer agent that can be secreted by the Asiatic toad Bufo gargarizans. Cinobufagin induces the cell cycle arrests in the G1 phase or G2/M phase, leading to apoptosis in cancer cells. Cinobufagin inhibits tumor growth in melanoma and glioblastoma multiforme xenograft mouse models [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Cinobufagine. CAS No. 470-37-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0421. | |
| Cinobufaginol | Cinobufaginol is a natural bufadienolide isolated from toad venom which has been widely used for centuries in China to treat different diseases, especially for cancer. Cinobufaginol potently inhibits the activity against human nasopharyngeal carcinoma cell lines with IC 50 s of 803 μΜ and 1.270 μΜ for CNE-1 and CNE-2Z, respectively [1]. Uses: Scientific research. Group: Natural products. CAS No. 6691-83-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N7020. | |
| Cinoxacin | Cinoxacin (Compound 64716), a synthetic antimicrobial related to the quinolone class of orally active antibacterial agent. Cinoxacin has antibacterial activity against many gram-negative aerobic bacteria and inhibits bacterial DNA synthesis. Cinoxacin can be used for the research of urinary tract infections and bacterial prostatitis [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Compound 64716. CAS No. 28657-80-9. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-B1085. | |
| Cinpanemab | Cinpanemab (BIIB054) is a human-derived monoclonal antibody that binds to α-synuclein. Cinpanemab can be used for the research of Parkinson's disease [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BIIB054; Anti-Alpha-synuclein Reference Antibody (cinpanemab). CAS No. 2094516-02-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99356. | |
| Cinrebafusp alfa | Cinrebafusp alfa (PRS 343) is a high affinity CD137/HER2 bispecfic anticalin-based drug. Cinrebafusp alfa binds to recombinant human HER2 ( K d =0.3 nM) and human monomeric CD137 (4-1BB; K d =5 nM). Cinrebafusp alfa facilitates T-cell costimulation by tumor-localized, HER2-dependent 4-1BB clustering and activation, further enhancing T-cell receptor-mediated activity and leading to tumor destruction. Cinrebafusp alfa has the potential for HER2+ solid tumors research [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: PRS 343. CAS No. 2218515-90-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99605. | |
| Cintirorgon | Cintirorgon (LYC-55716) is a first-in-class, selective and orally bioavailable ROR? agonist. Cintirorgon (LYC-55716) modulates gene expression of ROR? expressing T lymphocyte immune cells, resulting in enhanced effector function, as well as decreased immunosuppression, resulting in decreased tumor growth, and improved survival[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LYC-55716. CAS No. 2055536-64-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-104037. | |
| Cipargamin | Cipargamin (NITD609) is an potent antimalarial compound, with an IC 50 of appr 1 nM against P. falciparum. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NITD609; KAE609. CAS No. 1193314-23-6. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14430. | |
| Cipralisant | Cipralisant (GT-2331) is an orally active, low-toxicity, potent, selective, high affinity histamine H3 receptor full antagonist in vivo, and an agonist in vitro, with a pK i of 9.9 for histamine H3 receptor and a K i of 0.47 nM for rat histamine H3 receptor. Cipralisant has the potential for attention-deficit hyperactivity disorder research [1] [2] [3] [4]. Cipralisant is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GT-2331. CAS No. 213027-19-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-106993. | |
| Cipralisant maleate | Cipralisant (GT-2331) (maleate) is an orally active, low-toxicity, potent, selective, high affinity histamine H3 receptor full antagonist in vivo, and an agonist in vitro, with a pK i of 9.9 for histamine H3 receptor and a K i of 0.47 nM for rat histamine H3 receptor. Cipralisant (maleate) has the potential for attention-deficit hyperactivity disorder research [1] [2] [3] [4]. Cipralisant (maleate) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GT-2331 maleate. CAS No. 223420-20-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106993A. | |
| Ciprofibrate | Ciprofibrate (Win35833) is a potent peroxisome proliferator and increases the phosphorylation level of the PPARalpha [1]. Ciprofibrate acts as an orally active hypolipidaemic agent and can be used for the research of primary hyperlipidaemias [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Win35833. CAS No. 52214-84-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0664. | |
| Ciprofloxacin | Ciprofloxacin (Bay-09867) is a potent, orally active topoisomerase IV inhibitor. Ciprofloxacin induces mitochondrial DNA and nuclear DNA damage and lead to mitochondrial dysfunction, ROS production. Ciprofloxacin has anti-proliferative activity and induces apoptosis. Ciprofloxacin is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bay-09867. CAS No. 85721-33-1. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-B0356. | |
| Ciprofloxacin hydrochloride monohydrate | Ciprofloxacin (Bay-09867) hydrochloride monohydrate is a potent, orally active topoisomerase IV inhibitor. Ciprofloxacin hydrochloride monohydrate induces mitochondrial DNA and nuclear DNA damage and lead to mitochondrial dysfunction, ROS production. Ciprofloxacin hydrochloride monohydrate has anti-proliferative activity and induces apoptosis. Ciprofloxacin hydrochloride monohydrate is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bay-09867 hydrochloride monohydrate. CAS No. 86393-32-0. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-B0356B. | |
| Ciprofloxacin monohydrochloride | Ciprofloxacin (Bay-09867) monohydrochloride is a potent, orally active topoisomerase IV inhibitor. Ciprofloxacin monohydrochloride induces mitochondrial DNA and nuclear DNA damage and lead to mitochondrial dysfunction, ROS production. Ciprofloxacin monohydrochloride has anti-proliferative activity and induces apoptosis. Ciprofloxacin monohydrochloride is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity[1][2][3][4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bay-09867 monohydrochloride. CAS No. 93107-08-5. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-B0356A. | |
| Ciproxifan | Ciproxifan (FUB 359) is a potent, selective, orally bioavailable and competitive antagonist of histamine H 3 -receptor , with an IC 50 of 9.2 nM. Ciproxifan displays low apparent affinity at other receptor subtypes. Ciproxifan can be used for the research of aging disorders and Alzheimer's disease [1] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FUB-359. CAS No. 184025-18-1. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-14567. | |
| Ciproxifan maleate | Ciproxifan maleate (FUB 359 maleate) is a potent, selective, orally bioavailable and competitive antagonist of histamine H 3 -receptor , with an IC 50 of 9.2 nM. Ciproxifan maleate displays low apparent affinity at other receptor subtypes. Ciproxifan maleate can be used for the research of aging disorders and Alzheimer's disease [1] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FUB 359 maleate. CAS No. 184025-19-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-15289. | |
| CIQ | CIQ is a subunit-selective potentiator of NMDA receptors containing the NR2C or NR2D subunit. Uses: Scientific research. Group: Signaling pathways. CAS No. 486427-17-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-18699. | |
| Ciraparantag | Ciraparantag is a thrombin and factor Xa inhibitor. Ciraparantag is a broad-spectrum reversal agent for anticoagulants, including low-molecular-weight heparin, unfractionated heparin, and certain direct oral anticoagulants. It is reported to antagonize the effects of all coagulants except VKAs and agratroban [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PER977. CAS No. 1438492-26-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18660. | |
| Ciraparantag acetate | Ciraparantag (PER977) acetate is a thrombin and factor Xa inhibitor. Ciraparantag acetate is a broad-spectrum reversal agent for anticoagulants, including low molecular weight heparins, unfractionated heparins, and some direct oral anticoagulants, but not VKAs [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PER977 acetate. CAS No. 1644388-83-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18660B. | |
| Cirazoline hydrochloride | Cirazoline hydrochloride (LD 3098 hydrochloride) is a potent competitive full α1A-adrenergic receptor (α1A-AR) agonist ( K i =120 nM) and only a partial agonist at α1B-AR ( K i = 960 nM) and α1D-AR ( K i =660 nM) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LD 3098 hydrochloride. CAS No. 40600-13-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-101300. | |
| Cirsilineol | Cirsilineol, a natural flavone compound, selectively inhibits IFN-γ/STAT1/T-bet signaling in intestinal CD4 + T cells. Cirsilineol has potent immunosuppressive and anti-tumor properties. Cirsilineol significantly ameliorates trinitro-benzene sulfonic acid (TNBS)-induced T-cell-mediated experimental colitis in mice [1]. Uses: Scientific research. Group: Natural products. CAS No. 41365-32-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-119347. | |
| Cirsiliol | Cirsiliol is a potent and selective 5-lipoxygenase inhibitor and a competitive low affinity benzodiazepine receptor ligand. Uses: Scientific research. Group: Natural products. CAS No. 34334-69-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110399. | |
| Cirsimarin | Cirsimarin is a potent antilipogenic flavonoid isolated from Microtea debilis. Cirsimarin exerts potent antilipogenic effect and decreases adipose tissue deposition in mice. The lipolytic activity of Cirsimarin resulting from both its antagonist activity on adenosin A1 receptor and its inhibitory effect on phosphodiesterase [1]. Uses: Scientific research. Group: Natural products. CAS No. 13020-19-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N7272. | |
| Cirsimaritin | Cirsimaritin binds weakly to the benzodiazepine site on GABA A receptors, with antidepressant, anxiolytic and antinociceptive activities. Uses: Scientific research. Group: Natural products. CAS No. 6601-62-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N6648. | |
| Cirsiumaldehyde | Cirsiumaldehyde can be isolated from the roots of Anemone altaica [1]. Uses: Scientific research. Group: Natural products. CAS No. 7389-38-0. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-W357642. | |
| Cirtociclib | Cirtociclib (BLU-222) is an orally active and highly selective CDK2 inhibitor. Cirtociclib disrupts Rb signaling and causes G1 arrest and apoptosis in CCNE1-amplified endometrial cancer cells [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BLU-222. CAS No. 2888704-84-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-160701. | |
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