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 | |
|---|---|---|
| (±)-Naproxen-d3 | (±)-Naproxen-d 3 is the deuterium labeled (±)-Naproxen. (±)-Naproxen is a non-steroidal anti-inflammatory drug (NSAID)[1]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: (Rac)-Naproxen-d3. CAS No. 958293-79-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-15029S. |  |
| Naproxen sodium | Naproxen sodium is a COX-1 and COX-2 inhibitor with IC 50 s of 8.72 and 5.15 μM, respectively in cell assay. Uses: Scientific research. Group: Signaling pathways. CAS No. 26159-34-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-15030A. | |
| Naptumomab | Naptumomab is a fusion protein of a tumor-targeting superantigen (TTS). Naptumomab stimulates the immune system to recognize and kill tumor cells and can be used in the study of refractory solid tumors such as renal cell carcinoma [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1412892-09-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99035. | |
| N-Arachidonoylserotonin | N-Arachidonoylserotonin (Arachidonyl serotonin; AA-5-HT) is a potent fatty acid amide hydrolase (FAAH) inhibitor with an IC 50 value of 1~12 μM. N-Arachidonoylserotonin acts also as an antagonist of transient receptor potential vanilloid-type 1 (TRPV1) channels (IC 50 =70~100 nM). N-Arachidonoylserotonin is analgesic in rodents [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Arachidonyl serotonin; AA-5-HT. CAS No. 187947-37-1. Pack Sizes: 5 mg (108.07 mM * 0.1 mL in methyl acetate); 10 mg (108.07 mM * 0.2 mL in methyl acetate); 25 mg (108.07 mM * 0.5 mL in methyl acetate); 50 mg (108.07 mM * 1 mL in methyl acetate). Product ID: HY-103337. | |
| N-Arachidonyldopamine | N-Arachidonyldopamine is a potent and selective endogenous CB1 receptor agonist with a K i of 250 nM [1]. N-Arachidonyldopamine is also a potent and selective TRPV1 agonist an with EC 50 of ~ 50 nM [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 199875-69-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110018. | |
| N-Arachidonyl-GABA | N-Arachidonoyl-GABA is one member of a new class of lipoamino acids related to anandamide identified in bovine brain. N-Arachidonoyl-GABA displays analgesic activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 128201-89-8. Pack Sizes: 1 mg (64.17 mM * 40 μL in Ethanol); 5 mg (64.17 mM * 200 μL in Ethanol). Product ID: HY-103507. | |
| N-Arachidonylglycine | N-Arachidonylglycine (NA-Gly), a carboxylic analog of the endocannabinoid anandamide (AEA), is a GPR18 agonist ( EC 50 = 44.5 nM). Unlike AEA, N-Arachidonylglycine has no activity at either CB1 or CB2 receptors. N-Arachidonylglycine inhibits GLYT2 ( IC 50 = 5.1 μM). N-Arachidonylglycine also is an effective activator of endometrial cell migration [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: NA-Gly. CAS No. 179113-91-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103332. | |
| N-Arachidonylglycine-d8 | N-Arachidonylglycine-d8 is a deuterated labeled N-Arachidonylglycine [1]. N-Arachidonylglycine (NA-Gly), a carboxylic analog of the endocannabinoid anandamide (AEA), is a GPR18 agonist ( EC 50 = 44.5 nM). Unlike AEA, N-Arachidonylglycine has no activity at either CB1 or CB2 receptors. N-Arachidonylglycine inhibits GLYT2 ( IC 50 = 5.1 μM). N-Arachidonylglycine also is an effective activator of endometrial cell migration [2] [3]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: NA-Gly-d8. CAS No. 1159908-44-7. Pack Sizes: 1 mg (2.71 mM * 1 mL in Ethanol). Product ID: HY-103332S. | |
| Narasin | Narasin is a cationic ionophore antibiotic and coccidiostat agent. Narasin inhibits NF-κB signaling and induces tumor cells apoptosis. Narasin has antimicrobial, antiviral anticancer activity. Narasin inhibits tumor metastasis and growth of ERα - positive breast cancer cells by inactivation of the TGF-β/SMAD3 and IL - 6/STAT3 signaling pathways [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 55134-13-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-121410. | |
| Naratriptan hydrochloride | Naratriptan hydrochloride is a selective 5-HT1 receptor subtype agonist and is a triptan drug that is used for the treatment of migraine headaches. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GR-85548A hydrochloride. CAS No. 143388-64-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B0197A. | |
| Naratuximab | Naratuximab (Anti-TSPAN26/CD37 Reference Antibody (naratuximab)) is a humanized monoclonal antibody that binds CD37 (TSPAN26). Naratuximab can be used to synthesize an ADC compound, Naratuximab emtansine [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-TSPAN26/CD37 Reference Antibody (naratuximab). CAS No. 1622327-39-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99374. | |
| Narazaciclib | Narazaciclib (ON123300), a strong and brain-penetrant [1] multi-kinase inhibitor, inhibits CDK4 ( IC 50 =3.9 nM), Ark5 ( IC 50 =5 nM), PDGFRβ ( IC 50 =26 nM), FGFR1 ( IC 50 =26 nM), RET ( IC 50 =9.2 nM), and FYN ( IC 50 =11 nM). Single agent Narazaciclib causes a dose-dependent suppression of phosphorylation of Akt as well as activation of Erk in brain tumors [2]. Narazaciclib inhibits CDK6 with an IC 50 of 9.82 nM [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ON123300. CAS No. 1357470-29-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12624. | |
| Narciclasine | Narciclasine is a plant growth modulator. Narciclasine modulates the Rho/Rho kinase/LIM kinase/cofilin signaling pathway, greatly increasing GTPase RhoA activity as well as inducing actin stress fiber formation in a RhoA-dependent manner. Uses: Scientific research. Group: Natural products. Alternative Names: Lycoricidinol. CAS No. 29477-83-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-16563. | |
| Nardosinone | Nardosinone, isolated from Nardostachys chinensis , is the first enhancer of the neuritogenic action of dbcAMP and staurosporine. Nardosinone may become a useful pharmacological tool for studying the mechanism of action of not only nerve growth factor (NGF) but also both the neuritogenic substances [1]. Uses: Scientific research. Group: Natural products. CAS No. 23720-80-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg; 50 mg; 100 mg. Product ID: HY-N0380. | |
| Naringenin | Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti- dengue virus (DENV) activity. Uses: Scientific research. Group: Natural products. CAS No. 480-41-1. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0100. | |
| (±)-Naringenin | (±)-Naringenin is an orally available anti-inflammatory agent that can regulate both acute and chronic inflammation responses, while also showing antioxidant, neuroprotective, liver-protective, and anti-cancer effects. (±)-Naringenin promotes vasodilation in endothelial cells by activating BK Ca channels in muscle cells. It also exerts protective effects against experimental colitis by inhibiting Toll-like receptor 4 / NF-κB signaling, making it useful in studies related to sepsis, fulminant hepatitis, fibrosis, and cancer research [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 67604-48-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W011641. | |
| Naringenin chalcone | Naringenin chalcone is an orally active intermediate in flavonol biosynthesis. Naringenin chalcone induces Apoptosis. Naringenin chalcone inhibits the production of MCP-1 and NO. Naringenin chalcone exhibits anticancer activity against glioblastoma. Naringenin chalcone has anti-inflammatory and anti-allergic properties [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Natural products. CAS No. 73692-50-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N3007. | |
| Naringin | Naringin is a major flavanone glycoside obtained from tomatoes, grapefruits, and many other citrus fruits. Naringin exhibits biological properties such as antioxidant, anti-inflammatory, and antiapoptotic activities. Naringin also inhibits proliferation and invasion and induces apoptosis in human osteosarcoma cells by inhibiting zinc finger E-box binding homeobox 1 ( Zeb1 ) [1] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: Naringoside. CAS No. 10236-47-2. Pack Sizes: 10 mM * 1 mL; 200 mg; 10 g. Product ID: HY-N0153. | |
| Naringinase | Naringinase, a hydrolytic enzymatic complex, possesses the activity of both ?-L-rhamnosidase and ?-D-glucosidase. Naringinase has wide occurrence in nature. Naringinase can be used in the biotransformation of steroids, antibiotics, and mainly on glycosides hydrolysis[1][2]. Uses: Scientific research. Group: Natural products. CAS No. 9068-31-9. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-129217. | |
| Narirutin | Narirutin, one of the active constituents isolated from citrus fruits, has antioxidant and anti-inflammatory activities. Narirutin is a shikimate kinase inhibitor with anti-tubercular potency [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 14259-46-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N0804. | |
| Narmafotinib | Narmafotinib (AMP-945) is an orally active inhibitor of the enzyme focal adhesion kinase (FAK, KD=0.21 nM). Narmafotinib inhibits autophosphorylation of 397Y-FAK in MDA-MB-231 cells with an IC50=7 nM and exhibits low general cellular toxicity (IC50=2.7 ?M, MDA-MB-231 cells). Narmafotinib can be used for anti-cancer study[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMP-945. CAS No. 1393653-34-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145652. | |
| Narnatumab | Narnatumab (IMC-RON8) is a neutralizing human monoclonal antibody that blocks RON binding to its ligand, macrophage-stimulating protein (MSP) , with a K d of 32 pM. Narnatumab can be used for the research of cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: IMC-RON8; LY3012219; Anti-MSPR/RON/CD136 Reference Antibody (narnatumab). CAS No. 1188275-92-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99375. | |
| Naronapride | Naronapride (ATI-7505) is a potent prokinetic 5-HT 4 receptor agonist. Naronapride can be used for gastrointestinal diseases research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ATI-7505. CAS No. 860174-12-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-121826. | |
| Narsoplimab | Narsoplimab (OMS 721) is a high-affinity fully human immunoglobulin gamma 4 (IgG4) monoclonal antibody that binds MASP-2 and blocks lectin pathway activation. Narsoplimab can be used in research of hematopoietic stem-cell transplantation and SARS-CoV-2 [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: OMS 721; Anti-MASP2 Reference Antibody (narsoplimab). CAS No. 2108782-45-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99376. | |
| Naspm | Naspm (1-Naphthyl acetyl spermine), a synthetic analogue of Joro spider toxin, is a calcium permeable AMPA ( CP-AMPA ) receptors antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 1-Naphthylacetyl spermine. CAS No. 122306-11-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12506. | |
| Naspm trihydrochloride | Naspm trihydrochloride (1-Naphthylacetyl spermine trihydrochloride), a synthetic analogue of Joro spider toxin, is a calcium permeable AMPA (CP-AMPA) receptors antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 1-Naphthylacetyl spermine trihydrochloride. CAS No. 1049731-36-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12506A. | |
| Nasunin | Nasunin, an antioxidant anthocyanin, possesses antiangiogenic activity [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Delphinidin-3-(p-coumaroylrutinoside)-5-glucoside. CAS No. 28463-30-1. Pack Sizes: 500 μg; 1 mg; 5 mg. Product ID: HY-N9396. | |
| NAT | NAT is an initial hit of NAMPT activator. NAMPT is the rate-limiting enzyme in the NAD salvage pathway, which makes it an attractive target for the research of many diseases associated with NAD exhaustion such as neurodegenerative diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 831243-31-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-144776. | |
| Natalizumab | Natalizumab is a recombinant, humanized IgG4 monoclonal antibody, binds to α4β1- integrin and blocks its interaction with vascular cell adhesion molecule-1 (VCAM-1). Natalizumab can be used for the treatment of relapsing remitting multiple sclerosis and Crohn's disease. Natalizumab is also the first targeted therapy which blocks an essential mechanism for lymphocyte entry to the CNS and thus prevents acute demyelinating relapses [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 189261-10-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-108831. | |
| Natalizumab (Solution) | Natalizumab (Solution) is a recombinant, humanized IgG4 monoclonal antibody, binds to α4β1- integrin and blocks its interaction with vascular cell adhesion molecule-1 (VCAM-1). Natalizumab can be used for the treatment of relapsing remitting multiple sclerosis and Crohn's disease. Natalizumab is also the first targeted therapy which blocks an essential mechanism for lymphocyte entry to the CNS and thus prevents acute demyelinating relapses [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 189261-10-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108831A. | |
| Natamycin | Natamycin (Pimaricin) is a macrolide antibiotic agent produced by several Streptomyces strains. Natamycin inhibits the growth of fungi via inhibition of amino acid and glucose transport across the plasma membrane. Natamycin is a food preservative, an antifungal agent in agriculture, and is widely used for fungal keratitis research [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Pimaricin. CAS No. 7681-93-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-B0133. | |
| Nateglinide | Nateglinide, a D-phenylalanine derivative, is an orally active and short-acting insulinotropic agent and a DPP IV inhibitor. Nateglinide inhibits ATP-sensitive K + channels in pancreatic β-cells. Nateglinide is used for the treatment of type 2 (non-insulin-dependent) diabetes mellitus [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: A4166; Senaglinide. CAS No. 105816-04-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0422. | |
| Nattokinase, Natto fermentation | Nattokinase, Natto fermentation is a potent fibrinolytic enzyme. Nattokinase can break down blood clots by directly hydrolyzing fibrin and plasmin substrate. Nattokinase can be used for the research of cardiovascular diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 133876-92-3. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-P2373. | |
| Nav1.7 inhibitor | Nav1.7 inhibitor (compound II), a sulfonamide, is a potent Nav1.7 inhibitor. Nav1.7 inhibitor has the potential for a wide range of disorders, particularly pain [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1355631-24-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13985. | |
| NAV 26 | NAV 26 (compound 26) is a selective voltage-gated sodium channel Nav1.7 blocker with an IC 50 of 0.37 μM. NAV 26 can be used for pain research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1198160-14-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-118048. | |
| Navacaprant | Navacaprant (BTRX-335140) is a selective and orally active κ opioid receptor (KOR) antagonist, has antagonist activity for κOR, μOR and δOR with IC 50 values of 0.8 nM, 110 nM, and 6500 nM, respectively. Navacaprant endows with favorable in vitro ADMET and in vivo pharmacokinetic profiles and medication-like duration of action in rats. Navacaprant distributes well into the CNS and can be used for the research of neuropathy [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BTRX-335140; CYM-53093. CAS No. 2244614-14-8. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-124754. | |
| Navarixin | Navarixin (SCH 527123) is a potent, allosteric and orally active antagonist of both CXCR1 and CXCR2, with Kd values of 41 nM for cynomolgus CXCR1 and 0.20 nM, 0.20 nM, 0.08 nM for mouse, rat and cynomolgus monkey CXCR2, respectivelly[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SCH 527123; MK-7123. CAS No. 473727-83-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10198. | |
| Navitoclax | Navitoclax (ABT-263) is a potent and orally active Bcl-2 family protein inhibitor that binds to multiple anti-apoptotic Bcl-2 family proteins, such as Bcl-x L , Bcl-2 and Bcl-w, with a K i of less than 1 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-263. CAS No. 923564-51-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-10087. | |
| Navlimetostat | Navlimetostat is a potent, orally active, selective PRMT5-MTA complex inhibitor, with IC50 of 3.6 and 20.5 nM for PRMT5-MTA and PRMT5. Navlimetostat binds to the PRMT5-MTA complex, with KD value of 0.14 pM. Navlimetostat shows antineoplastic activity in vitro and in vivo, and can be used for cancer study[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MRTX-1719. CAS No. 2630904-45-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139611. | |
| Navocaftor | Navocaftor (GLPG 3067), as a cystic fibrosis transmembrane regulator ( CFTR ), is a protein modulator (US 20200377491 Al, example 1) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GLPG 3067; ABBV-3067. CAS No. 2159103-66-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109152. | |
| Navoximod | Navoximod (GDC-0919; NLG-?919) is a potent IDO (indoleamine-(2,3)-dioxygenase) pathway inhibitor with Ki/EC50 of 7 nM/75 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GDC-0919; NLG-?919. CAS No. 1402837-78-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18770B. | |
| Navtemadlin | Navtemadlin (AMG 232) is a potent, selective and orally available inhibitor of p53-MDM2 interaction, with an IC 50 of 0.6 nM. Navtemadlin binds to MDM2 with a K d of 0.045 nM [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMG 232; KRT-232. CAS No. 1352066-68-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12296. | |
| Naxitamab | Naxitamab (Hu3F8) is a humanized monoclonal antibody targeting the disialoganglioside GD2. Naxitamab can be used in research of neuroblastoma, osteosarcoma and other GD2-positive cancers [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Naxitamab-gqgk; Humanized 3F8; Hu3F8. CAS No. 1879925-92-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99206. | |
| NAZ2329 | NAZ2329, the first cell-permeable inhibitor of R5 subfamily of receptor-type protein tyrosine phosphatases (RPTPs), allosterically and preferentially inhibits PTPRZ (IC50=7.5 μM for hPTPRZ1) and PTPRG (IC50=4.8 μM for hPTPRG) over other PTPs. NAZ2329 binds to the active D1 domain and more potently inhibits PTPRZ-D1 fragment (IC50 of 1.1 μM) than the whole intracellular (D1?+?D2) fragment (IC50 of 7.5 μM). NAZ2329 can effectively inhibit tumor growth of the glioblastoma cells and suppress stem cell-like properties[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2809469-05-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103693. | |
| Nazartinib | Nazartinib (EGF816) is a covalent mutant-selective EGFR inhibitor, with Ki and Kinact of 31 nM and 0.222 min?1 on EGFR(L858R/790M) mutant, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EGF816. CAS No. 1508250-71-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-12872. | |
| NB-598 | NB-598 is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway. NB-598 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. CAS No. 131060-14-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16343. | |
| NBDHEX | NBDHEX is a potent glutathione S-transferase P1-1 (GSTP1-1) inhibitor. NBDHEX induces apoptosis of tumor cells. NBDHEX acts as an anticancer agent by inhibiting GSTs catalytic activity, avoiding inconvenience of the inhibitor extrusion from the cell by specific pumps and disrupting the interaction between the GSTP1-1 and key signaling effectors. NBDHEX can also act as late-phase autophagy inhibitor[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 787634-60-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-135318. | |
| NBD-PE | NBD-PE is an effective lipid fluorescent probe (Excitation/Emission: 465/535 nm; Color: Green). NBD-PE offers a wide array of applications in membrane and cell biology [1] [2] [3]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 178119-00-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-D1683. | |
| NBD Sphingosine | NBD Sphingosine (NBD-Sph), a fluorochrome, is a fluorescence-labeled sphingosine. NBD Sphingosine can be uesd for fluorescence assay for sphingosine kinases [1] [2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 1449370-25-5. Pack Sizes: 50 μg (523.45 μM * 200 μL in Ethanol). Product ID: HY-130433. | |
| NBD-X, SE | NBD-X, SE, the acceptor fluorophore, can be used to create environment sensitive bioconjugates [1]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 145195-58-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-134566. | |
| N-Benzoyl-(2R,3S)-3-phenylisoserine | N-Benzoyl-(2R,3S)-3-phenylisoserine is a Taxol C-13 Side Chain and crucial for the strong antitumor activity of Taxol [1]. Uses: Scientific research. Group: Natural products. CAS No. 132201-33-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N2380. | |
| N-Benzoylcytidine | N-Benzoylcytidine is a substrate for uracil-cytidine kinase 1 (UCK1) and UCK2. N-Benzoylcytidine can be used to synthesize 2-OH protective groups for solid-phase RNA synthesis, as well as synthetic oligonucleotides for UV induction and targeted gene silencing in zebrafish embryos [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 13089-48-0. Pack Sizes: 10 mM * 1 mL; 5 g; 25 g. Product ID: HY-78574. | |
| N-Benzoyl-DL-arginine-4-nitroanilide hydrochloride | N-Benzoyl-DL-arginine-4-nitroanilide hydrochloride 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. 911-77-3. Pack Sizes: 100 mg; 250 mg; 500 mg. Product ID: HY-W008953. | |
| N-Benzoyl-Gly-His-Leu hydrate | N-Benzoyl-Gly-His-Leu hydrate is a leucine derivative, a polypeptide. N-Benzoyl-Gly-His-Leu hydrate exerts function with angiotensin converting enzyme (ACE) substrate. Uses: Scientific research. Group: Peptides. CAS No. 207386-83-2. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-137875. | |
| N-Benzoyl-L-arginine ethyl ester hydrochloride | N-Benzoyl-L-arginine ethyl ester hydrochloride is an arginine derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 2645-8-1. Pack Sizes: 1 g; 5 g. Product ID: HY-W008694. | |
| N-Benzoyl-L-leucine | N-Benzoyl-L-leucine is a leucine derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 1466-83-7. Pack Sizes: 100 mg. Product ID: HY-W142035. | |
| N-Benzylhydroxylamine hydrochloride | N-Benzylhydroxylamine hydrochloride 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. 29601-98-7. Pack Sizes: 25 g. Product ID: HY-W002216. | |
| N-Benzyllinoleamide | N-Benzyllinoleamide can be isolated from Lepidium meyenii Walp., has pharmaceutical property against exercise-induced fatigue [1]. Uses: Scientific research. Group: Natural products. CAS No. 18286-71-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N2361. | |
| N-Benzyloctadecanamide | N-Benzyloctadecanamide (N-Benzylstearamide) is a macamide, a distinct class of secondary metabolites in Lepidium meyenii Walp. (Maca) [1]. Uses: Scientific research. Group: Natural products. Alternative Names: N-Benzylstearamide. CAS No. 5327-45-7. Pack Sizes: 5 mg; 10 mg; 20 mg. Product ID: HY-N4188. | |
| N-(Benzyloxycarbonyloxy)succinimide | N-(Benzyloxycarbonyloxy)succinimide 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. 13139-17-8. Pack Sizes: 100 g. Product ID: HY-75200. | |
| NBI-31772 | NBI-31772 is a non-selective IGFBP inhibitor ( K i =47 nM). NBI-31772 has neuroprotective effects and reduces infarct volume during cerebral ischemia. NBI-31772 can also restore or enhance proteoglycan synthesis in osteoarticular chondrocytes. In addition, NBI-31772 also increases the effect of IGF3 on zebrafish oocyte maturation [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 374620-70-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110135. | |
| NBI-74330 | NBI-74330 is a potent antagonist for CXCR3, and exhibits potent inhibition of (125I)CXCL10 and (125I)CXCL11 specific binding with Ki of 1.5 and 3.2 nM, respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 855527-92-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15320. | |
| N-Boc-4-bromopiperidine | N-Boc-4-Bromopiperidine 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. 180695-79-8. Pack Sizes: 10 g; 25 g. Product ID: HY-W001478. | |
| N-Boc-4-hydroxypiperidine | N-Boc-4-hydroxypiperidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. CAS No. 109384-19-2. Pack Sizes: 5 g. Product ID: HY-75026. | |
| N-Boc-4-piperidinemethanol | N-Boc-4-piperidinemethanol (compound 4) is an acetylcholinesterase (AChE) inhibitor. N-Boc-4-piperidinemethanol can used ti study Alzheimers Disease [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 123855-51-6. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-21629. | |
| N-Boc-cis-4-Hydroxy-D-proline | N-Boc-cis-4-Hydroxy-D-proline is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N-Boc-cis-4-Hydroxy-D-proline is also a alkyl chain-based PROTAC linker that can be used in the Synthesis of ADCs or PROTACs. Uses: Scientific research. Group: Signaling pathways. CAS No. 135042-12-5. Pack Sizes: 25 g; 100 g. Product ID: HY-W002887. | |
| N-Boc-cis-4-hydroxy-L-proline | N-Boc-cis-4-hydroxy-L-proline is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N-Boc-cis-4-hydroxy-L-proline is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[2. Uses: Scientific research. Group: Signaling pathways. CAS No. 87691-27-8. Pack Sizes: 10 g; 25 g. Product ID: HY-W002886. | |
| N-Boc-diethanolamine | N-Boc-diethanolamine is an Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs. N-Boc-diethanolamine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 103898-11-9. Pack Sizes: 25 g; 50 g; 100 g. Product ID: HY-W044078. | |
| N-Boc-D-proline | Boc-D-proline 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. 37784-17-1. Pack Sizes: 5 g. Product ID: HY-40115. | |
| N-Boc-D-prolinol | N-Boc-D-prolinol 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. 83435-58-9. Pack Sizes: 25 g. Product ID: HY-78924. | |
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