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 | |
|---|---|---|
| Vanillin | Vanillin (p-Vanillin) is a single molecule extracted from vanilla beans and also a popular odor used widely in perfume, food and medicine. Uses: Scientific research. Group: Natural products. Alternative Names: p-Vanillin; m-Methoxy-p-hydroxybenzaldehyde; p-Hydroxy-m-methoxybenzaldehyde. CAS No. 121-33-5. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g. Product ID: HY-N0098. |  |
| Vanillin acetate | Vanillin acetate is easily synthesized from vanillin by treatment with acetic anhydride [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 881-68-5. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-W009948. | |
| Vanillin (Standard) | Vanillin (Standard) is the analytical standard of Vanillin. This product is intended for research and analytical applications. Vanillin (p-Vanillin) is a single molecule extracted from vanilla beans and also a popular odor used widely in perfume, food and medicine. Uses: Scientific research. Group: Natural products. Alternative Names: p-Vanillin (Standard); m-Methoxy-p-hydroxybenzaldehyde (Standard); p-Hydroxy-m-methoxybenzaldehyde (Standard). CAS No. 121-33-5. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0098R. | |
| Vanilloid receptor antagonist 1 | Vanilloid receptor antagonist 1 is a potent vanilloid receptor TRPV1 antagonist extracted from patent US8349852B2, compound B8 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 871814-52-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114017. | |
| Vanillyl alcohol | Vanillyl alcohol (p-(Hydroxymethyl)guaiacol), derived from vanillin, is a phenolic alcohol and is used as a flavoring agent in foods and beverages [1]. Uses: Scientific research. Group: Natural products. Alternative Names: p-(Hydroxymethyl)guaiacol. CAS No. 498-00-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-N2067. | |
| Vanillylamine | Vanillylamine is a derivative of vanillin is synthesized through a transaminase reaction in the phenylpropanoid pathway of capsaicinoid synthesis [1]. Uses: Scientific research. Group: Natural products. CAS No. 1196-92-5. Pack Sizes: 10 mM * 1 mL; 1 g. Product ID: HY-W097899. | |
| Vanillyl butyl ether | Vanillyl butyl ether is a major contributor to the characteristic flavor and fragrance of vanilla. Vanillyl butyl ether is one of the eco-friendly and nontoxic substances. Vanillyl butyl ether exhibits mutually inhibitory effects on mammalian TRPV1 and TRPM8 channels. Vanillyl butyl ether shows repellency activity against Tribolium castaneum , T. confusum and L. bostrychophila. Vanillyl butyl ether acts as a mild warming agent, providing a warming sensation and enhancing blood circulation [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 82654-98-6. Pack Sizes: 10 mM * 1 mL; 25 g; 50 g. Product ID: HY-W014394. | |
| Vanillylmandelic acid | Vanillylmandelic acid is the endproduct of epinephrine and norepinephrine metabolism. Vanillylmandelic acid can be used as an indication of the disorder in neurotransmitter metabolism as well. Vanillylmandelic acid has antioxidant activity towards DPPH radical with an IC 50 value of 33 μM [1]. Uses: Scientific research. Group: Natural products. CAS No. 55-10-7. Pack Sizes: 10 mM * 1 mL; 25 mg. Product ID: HY-113121. | |
| Vanillylmandelic acid (Standard) | Vanillylmandelic acid (Standard) is the analytical standard of Vanillylmandelic acid. This product is intended for research and analytical applications. Vanillylmandelic acid is the endproduct of epinephrine and norepinephrine metabolism. Vanillylmandelic acid can be used as an indication of the disorder in neurotransmitter metabolism as well. Vanillylmandelic acid has antioxidant activity towards DPPH radical with an IC 50 value of 33 μM [1]. Uses: Scientific research. Group: Natural products. CAS No. 55-10-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113121R. | |
| Vanoxerine dihydrochloride | Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) is a competitive, potent, and highly selective dopamine reuptake inhibitor ( K i =1 nM). Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) binds to the target site on the dopamine transporter (DAT) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GBR-12909 dihydrochloride; I893 dihydrochloride. CAS No. 67469-78-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-13217. | |
| Vantictumab | Vantictumab (OMP-18R5) is a fully human IgG2 monoclonal antibody. Vantictumab inhibits Wnt pathway signaling by binding to FZD1/2/5/7/8 receptors. Vantictumab can be studied against cancers through direct actions on tumor cells, including CSCs, and effects on the stroma, such as metastatic HER2-negative breast cancer and metastatic pancreatic adenocarcinoma [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: OMP-18R5. CAS No. 1345009-45-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9974. | |
| Vanucizumab | Vanucizumab is a first-in-class, bispecific IgG1-like monoclonal antibody that simultaneously blocks VEGF-A and angiopoietin-2 (Ang-2) from interacting with their receptors. Vanucizumab has antiangiogenic and anticancer effects [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-Human VEGFA Recombinant Antibody; RO5520985. CAS No. 1448221-05-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99330. | |
| Vanzacaftor | Vanzacaftor (VX-121) is an orally active noval corrector of Cystic fibrosis transmembrane conductance regulator ( CFTR ). Vanzacaftor improves processing and trafficking of CFTR protein as well as increases chloride transport in triple combined with Tezacaftor (HY-15448) and Deutivacaftor. Vanzacaftor-Tezacaftor-Deutivacaftor is safe and well tolerated, improving lung function, respiratory symptoms, and CFTR function with cystic fibrosis, which is promising for research in the field of cystic fibrosis diseases [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: VX-121. CAS No. 2374124-49-7. Pack Sizes: 1 mg. Product ID: HY-145603. | |
| Vapreotide | Vapreotide is a neurokinin-1 (NK1) receptor antagonist, with an IC 50 of 330 nM. Uses: Scientific research. Group: Peptides. Alternative Names: RC160; BMY 41606. CAS No. 103222-11-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P0061. | |
| Vapreotide acetate | Vapreotide acetate (RC-160 acetate; BMY-41606 acetate) is a neurokinin-1 (NK1) receptor antagonist, with an IC 50 of 330 nM. Uses: Scientific research. Group: Peptides. Alternative Names: RC-160 acetate; BMY-41606 acetate. CAS No. 849479-74-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P0061A. | |
| Vardenafil | Vardenafil is a selective and orally active inhibitor of phosphodiesterase-5 ( PDE5 ), with an IC 50 of 0.7 nM. Vardenafil shows inhibitory towards PDE1, PDE6 with IC 50 s of 180 nM, and 11 nM, while IC 50 s are >1000 nM for PDE3 and PDE4 [1]. Vardenafil competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels [2]. Vardenafil can be used for the research of erectile dysfunction, hepatitis, diabetes [1]-[6]. Uses: Scientific research. Group: Natural products. CAS No. 224785-90-4. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-B0442. | |
| Vardenafil hydrochloride | Vardenafil hydrochloride is a selective and orally active inhibitor of phosphodiesterase-5 ( PDE5 ), with an IC 50 of 0.7 nM. Vardenafil hydrochloride shows inhibitory towards PDE1, PDE6 with IC 50 s of 180 nM, and 11 nM, while IC 50 s are >1000 nM for PDE3 and PDE4 [1]. Vardenafil hydrochloride competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels [2]. Vardenafil hydrochloride can be used for the research of erectile dysfunction, hepatitis, diabetes [1]-[6]. Uses: Scientific research. Group: Natural products. CAS No. 224785-91-5. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-B0442A. | |
| Vardenafil hydrochloride trihydrate | Vardenafil hydrochloride trihydrate is a selective and orally active inhibitor of phosphodiesterase-5 ( PDE5 ), with an IC 50 of 0.7 nM. Vardenafil hydrochloride trihydrate shows inhibitory towards PDE1, PDE6 with IC 50 s of 180 nM, and 11 nM, while IC 50 s are >1000 nM for PDE3 and PDE4 [1]. Vardenafil hydrochloride trihydrate competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels [2]. Vardenafil hydrochloride trihydrate can be used for the research of erectile dysfunction, hepatitis, diabetes [1]-[6]. Uses: Scientific research. Group: Natural products. CAS No. 330808-88-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0442B. | |
| Varenicline | Varenicline (CP 526555) is an orally active partial agonist of α4β2 nicotinic acetylcholine receptor (α4β2 nAChR, IC 50 = 250 nM), which is the principal mediator of nicotine dependence. Varenicline is also a partial agonist of α6β2 nAChR and a full agonist of α6β2 nAChR. Varenicline blocks the direct agonist effects of nicotine on nAChR while stimulates nAChR in a more moderate way, being widely used as an aid of smoking cessation [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP 526555. CAS No. 249296-44-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10019. | |
| Varenicline dihydrochloride | Varenicline (CP 526555-18) is an orally active partial agonist of α4β2 nicotinic acetylcholine receptor (α4β2 nAChR, IC 50 = 250 nM), which is the principal mediator of nicotine dependence. Varenicline is also a partial agonist of α6β2 nAChR and a full agonist of α6β2 nAChR. Varenicline blocks the direct agonist effects of nicotine on nAChR while stimulates nAChR in a more moderate way, being widely used as an aid of smoking cessation [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP 526555 dihydrochloride. CAS No. 866823-63-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10019A. | |
| Varenicline Hydrochloride | Varenicline (CP 526555) is an orally active partial agonist of α4β2 nicotinic acetylcholine receptor (α4β2 nAChR, IC 50 = 250 nM), which is the principal mediator of nicotine dependence. Varenicline is also a partial agonist of α6β2 nAChR and a full agonist of α6β2 nAChR. Varenicline blocks the direct agonist effects of nicotine on nAChR while stimulates nAChR in a more moderate way, being widely used as an aid of smoking cessation [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP 526555 hydrochloride. CAS No. 230615-23-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10020. | |
| Varenicline Tartrate | Varenicline (CP 526555) is an orally active partial agonist of α4β2 nicotinic acetylcholine receptor (α4β2 nAChR, IC 50 = 250 nM), which is the principal mediator of nicotine dependence. Varenicline is also a partial agonist of α6β2 nAChR and a full agonist of α6β2 nAChR. Varenicline blocks the direct agonist effects of nicotine on nAChR while stimulates nAChR in a more moderate way, being widely used as an aid of smoking cessation [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP 526555-18. CAS No. 375815-87-5. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10021. | |
| Varespladib | Varespladib (LY315920) is a potent and selective group IIA, secretory phospholipase A 2 (sPLA 2 ) inhibitor with an IC 50 of 9 nM. Varespladib exhibits the significant inhibitory effect on sPLA2 activity in serum from various species including rat, rabbit, guinea pig and human with IC 50 s of 8.1 nM, 5.0 nM, 3.2 nM and 6.2 nM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY315920. CAS No. 172732-68-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13402. | |
| Varespladib sodium | Varespladib sodium (LY315920 sodium) is a potent and selective group IIA, secretory phospholipase A 2 (sPLA 2 ) inhibitor with an IC 50 of 9 nM. Varespladib sodium exhibits the significant inhibitory effect on sPLA2 activity in serum from various species including rat, rabbit, guinea pig and human with IC 50 s of 8.1 nM, 5.0 nM, 3.2 nM and 6.2 nM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY315920 sodium. CAS No. 172733-42-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13402A. | |
| Varlilumab | Varlilumab (CDX-1127) is a first-in-class human IgG1 anti- CD27 monoclonal antibody. Varlilumab has an anti-tumor activity [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: CDX-1127. CAS No. 1393344-72-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99057. | |
| Varlilumab (anti-CD27) | Varlilumab (anti-CD27) is a first-in-class human IgG1 anti- CD27 monoclonal antibody. Varlilumab has an anti-tumor activity [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1393344-72-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99057A. | |
| Varlitinib | Varlitinib (ASLAN001) is a potent, reversible, small molecule pan- EGFR inhibitor with IC 50 s of 7, 2, 4 nM for HER1, HER2 and HER4, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ASLAN001; ARRY-334543. CAS No. 845272-21-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10530. | |
| Vasculotide | Vasculotide, an angiopoietin-1 mimetic, is a Tie-2 activator and induces Tie-2 phosphorylation. Vasculotide has anti-inflammatiory effect and anti-permeability. Vasculotide ameliorates endotoxin-induced endothelial barrier dysfunction. Vasculotide promotes angiogenesis in a mouse model of diabetic ulcer. Vasculotide protects mice from vascular leakage and reduces mortality in murine abdominal sepsis. Vasculotide decreases microvascular leakage and improves microcirculatory perfusion in a rat model of hemorrhagic shock [1] [2] [3]. Uses: Scientific research. Group: Peptides. CAS No. 1359657-45-6. Pack Sizes: 1 mg. Product ID: HY-P10580. | |
| Vasicine | Vasicine (peganine) is a quinazoline alkaloid isolated from Justicia adhatoda. Vasicine (peganine) possesses anti- tuberculosis activity [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Peganine. CAS No. 6159-55-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N1103. | |
| (±)?-?Vasicine | (±)-Vasicine is the racemate of Vasicine. Vasicine (Peganine) significantly inhibits H + -K + -ATPase activity in vitro with an IC 50 of 73.47 μg/mL. Anti-ulcer activity. Vasicine shows significant anti-secretory, antioxidant and cytoprotective effect [1]. Uses: Scientific research. Group: Natural products. Alternative Names: (±)?-Peganine. CAS No. 6159-56-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N7031. | |
| Vasicine hydrochloride | Vasicine hydrochloride (peganine hydrochloride) is a quinazoline alkaloid isolated from Justicia adhatoda. Vasicine (peganine) possesses anti- tuberculosis activity [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Peganine hydrochloride. CAS No. 7174-27-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N1103A. | |
| Vasicinone | Vasicinone is a quinazoline alkaloid isolated from the Adhatoda vasica. Vasicinone is a potential agent for Parkinson's disease and possibly other oxidative stress-related neurodegenerative disorders [1]. Uses: Scientific research. Group: Natural products. Alternative Names: (-)-Vasicinone. CAS No. 486-64-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N1100. | |
| Vasopressin | Vasopressin is a cyclic nonapeptide that is synthesized centrally in the hypothalamus. Vasopressin participates in the hypothalamic-pituitary-adrenal axis, and regulates pituitary corticotropin secretion by potentiating the stimulatory effects of corticotropin releasing factor. Vasopressin also can act as a neurotransmitter, exerting its action by binding to specific G protein-coupled receptors [1] [2] [3]. Uses: Scientific research. Group: Peptides. CAS No. 11000-17-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B1811. | |
| Vatalanib | Vatalanib (PTK787; ZK-222584; CGP-79787) is an inhibitor of VEGFR2/KDR with IC 50 of 37 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PTK787; ZK-222584; CGP-79787. CAS No. 212141-54-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10203. | |
| Vatalanib dihydrochloride | Vatalanib dihydrochloride (PTK787 dihydrochloride) is an inhibitor of VEGFR2/KDR with IC 50 of 37 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PTK787 dihydrochloride; ZK-222584 dihydrochloride; CGP-797870 dihydrochloride. CAS No. 212141-51-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12018. | |
| Vatelizumab | Vatelizumab (GBR500) is a monoclonal antibody targeting the α2 subunit (CD49b) of very late antigen-2 (VLA-2). Vatelizumab can be used for the research of multiple sclerosis [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: GBR500. CAS No. 1238217-55-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99524. | |
| Vatinoxan hydrochloride | Vatinoxan hydrochloride (MK-467 hydrochloride;L-659066 hydrochloride) is a peripheral α2 adrenergic receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-467 hydrochloride; L-659066 hydrochloride. CAS No. 130466-38-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-19057A. | |
| Vazegepant | Vazegepant (Zavegepant) is an orally active calcitonin gene-related peptide CGRP receptor antagonist with potential for acute research in migraine, can be administered intranasally. CGRP is an important trigger in migraine pathophysiology [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Zavegepant; BHV-3500. CAS No. 1337918-83-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-134992. | |
| VBIT-12 | VBIT-12 is a potent VDAC1 inhibitor. VBIT-12 directly interacts with VDAC1 and prevents VDAC1 oligomerization, and thus inhibits apoptotic action of VDAC1 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2089227-65-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-135885. | |
| VCH-916 | VCH-916 is a novel nonnucleoside HCV NS5B polymerase inhibitor. Uses: Scientific research. Group: Signaling pathways. CAS No. 1200133-34-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13465. | |
| Vecabrutinib | Vecabrutinib (SNS-062) is a potent, noncovalent BTK and ITK inhibitor, with K d values of 0.3 nM and 2.2 nM, respectively. Vecabrutinib shows an IC 50 of 24 nM for ITK [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SNS-062. CAS No. 1510829-06-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109078. | |
| Vecuronium bromide | Vecuronium (ORG NC 45) bromide is a non-depolarizing neuromuscular blocking agent that also acts as a nicotinic acetylcholine receptor ( nAChR ) inhibitor, a muscle relaxant, and can be used for pre-surgical anesthesia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ORG NC 45. CAS No. 50700-72-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0118A. | |
| Vedaprofen | Vedaprofen (Quadrisol) is a COX-1 selective nonsteroidal anti-inflammatory agent (NSAID) for serum TxB2 and exudate PGE2 inhibition [1]. Vedaprofen is a Escherichia coli ( E. coli ) sliding clamp (SC) inhibitor with the IC 50 of 222 μM [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Quadrisol; CERM 10202; PM 150. CAS No. 71109-09-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-118827. | |
| Vedolizumab | Vedolizumab is a humanized IgG1 monoclonal antibody that targets the α4β7 integrin for the treatment of ulcerative colitis and Crohn's disease. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-Human lymphocyte α4β7 integrin, Humanized Antibody. CAS No. 943609-66-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9911. | |
| Vedolizumab (anti-α4β7-integrin) | Vedolizumab (anti-α4β7-integrin) is a humanized IgG1 monoclonal antibody that targets the α4β7 integrin for the treatment of ulcerative colitis and Crohn's disease [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 943609-66-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9911A. | |
| VEGFR2-IN-2 | VEGFR2-IN-2 (compound 6e) is a potent and selective VEGFR2 inhibitor with an IC 50 of 19.32 nM. VEGFR2-IN-2 can be used for researching. Uses: Scientific research. Group: Signaling pathways. CAS No. 737818-56-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147133. | |
| VEGFR-2-IN-29 | VEGFR-2-IN-29 (Compound 5) is a VEGFR-2 inhibitor with an IC 50 of 16.5 nM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 62802-77-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148040. | |
| VEGFR-2-IN-39 | VEGFR-2-IN-39 (PROTAC-5) is a PROTAC targeting VEGFR-2 ( IC 50 : 208.6 nM). VEGFR-2-IN-39 has low toxicity.VEGFR-2-IN-39 inhibits the proliferation of EA.hy926, one of HUVECs, in a concentration-dependent manner, with an IC 50 of 38.65 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2353417-86-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-160259. | |
| VEGFR-2-IN-5 hydrochloride | VEGFR-2-IN-5 hydrochloride is a VEGFR2 inhibitor extracted from patent WO2013055780A1, Page 69 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2700435-52-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18625A. | |
| VEGFR-IN-1 | VEGFR-IN-1 (compound 3) is a potent angiogenesis inhibitor with IC 50 s of 0.02, 0.18, 0.24 7.3, and 7 μM for KDR , Flt-1 , c-Kit, EGF-R, and c-Src, respectively [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 269390-69-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-101219. | |
| Velagliflozin | Velagliflozin is an orally available sodium-glucose cotransporter 2 ( SGLT2 ) inhibitor, with anti-diabetic activity. Uses: Scientific research. Group: Signaling pathways. CAS No. 946525-65-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-109018. | |
| Velagliflozin proline | Velagliflozin proline is an oral sodium-glucose cotransporter 2 ( SGLT2 ) inhibitor with antidiabetic activity. Velagliflozin proline reduces renal glucose reabsorption and stimulates glycosuria, which lowers blood sugar and insulin concentrations [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1539295-26-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-109018A. | |
| Veldoreotide TFA | Veldoreotide (DG3173) TFA a somatostatin analogue, binds to and activate the somatostatin receptors (SSTR) 2, 4, and 5. Veldoreotide TFA inhibits growth hormone (GH) secretion in adenomas compared with Octreotide (HY-P0036). Veldoreotide has the potential to be used as pain modulating agent [1]. Uses: Scientific research. Group: Peptides. Alternative Names: DG3173 TFA; PTR-3173 TFA. CAS No. 2126831-23-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P0024A. | |
| Veligrotug | Veligrotug is an IgG1-kappa, anti- IGF1R (insulin-like growth factor 1 receptor, CD221) chimeric monoclonal antibody [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2728655-31-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990084. | |
| Veliparib | Veliparib (ABT-888) is a potent PARP inhibitor, inhibiting PARP1 and PARP2 with K i s of 5.2 and 2.9 nM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-888. CAS No. 912444-00-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10129. | |
| Veliparib dihydrochloride | Veliparib (dihydrochloride) is a potent inhibitor of PARP1 and PARP2 with K i s of 5.2 nM and 2.9 nM in cell-free assays, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-888 dihydrochloride. CAS No. 912445-05-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10130. | |
| Velnacrine maleate | Velnacrine maleate (HP 029) is an orally active cholinesterase inhibitor that can be used for the research of Alzheimer's disease [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HP 029; Hydroxytacrine maleate. CAS No. 118909-22-1. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W011246. | |
| Velneperit | Velneperit (S-2367) is a novel neuropeptide Y (NPY) Y5 receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S2367. CAS No. 342577-38-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14423. | |
| Velpatasvir | Velpatasvir (VEL, GS-5816) is a novel pan-genotypic hepatitis C virus (HCV) nonstructural protein 5A (NS5A) inhibitor with activity against genotype 1 (GT1) to GT6 HCV replicons. Velpatasvir is also a SARS-CoV 3CL pro inhibitor with an IC 50 of 2.16 μM [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-5816. CAS No. 1377049-84-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12530. | |
| Veltuzumab | Veltuzumab (IMMU-106) is a humanized anti-CD20 monoclonal antibody. Veltuzumab has low EC 50 value of 0.08-0.09 μg/mL in the Daudi cell line. Veltuzumab can be used for the research of cancer including non-Hodgkin lymphoma (NHL) [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: IMMU-106; hA20. CAS No. 728917-18-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99224. | |
| Velufenacin | Velufenacin is a muscarinic receptor antagonist [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DA-8010. CAS No. 1648737-78-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109196. | |
| Velusetrag | Velusetrag (TD-5108) is an orally active, potent and selective agonist of serotonin 5-HT 4 receptor (5-HT4R) , with a pK i of 7.7. Velusetrag exhibits no affinity (K i >10 μM) for 5-HT 2A and 5-HT 2B receptors. Velusetrag can be used for the research of gastrointestinal diseases and Parkinson's disease [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TD-5108. CAS No. 866933-46-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10457. | |
| Velusetrag hydrochloride | Velusetrag (TD-5108) hydrochloride is an orally active, potent and selective agonist of serotonin 5-HT 4 receptor (5-HT 4 R) , with a pK i of 7.7. Velusetrag hydrochloride exhibits no affinity (K i >10 μM) for 5-HT 2A and 5-HT 2B receptors. Velusetrag hydrochloride can be used for the research of gastrointestinal diseases and Parkinson's disease [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TD-5108 hydrochloride. CAS No. 866933-51-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10457A. | |
| Vemircopan | Vemircopan (ALXN2050) is an orally active complement factor D inhibitor. Vemircopan is promising for research of paroxysmal nocturnal hemoglobinuria [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ALXN2050; ACH 0145228; ACH-5228. CAS No. 2086178-00-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139588. | |
| Vemurafenib | Vemurafenib (PLX4032) is a first-in-class, selective, potent inhibitor of B-RAF kinase, with IC 50 s of 31 and 48 nM for RAF V600E and c-RAF-1, respectively [1] [4]. Vemurafenib induces cell autophagy [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PLX4032; RG7204; RO5185426. CAS No. 918504-65-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-12057. | |
| Venetoclax | Venetoclax (ABT-199; GDC-0199) is a highly potent, selective and orally bioavailable Bcl-2 inhibitor with a K i of less than 0.01 nM. Venetoclax induces autophagy [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-199; GDC-0199; RG7601. CAS No. 1257044-40-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-15531. | |
| Venlafaxine | Venlafaxine (Wy 45030) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Wy 45030. CAS No. 93413-69-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0196. | |
| Venlafaxine-d6 | Venlafaxine-d 6 is the deuterium labeled Venlafaxine. Venlafaxine (Wy 45030) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant[1]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1020720-02-8. Pack Sizes: 5 mg. Product ID: HY-B0196S. | |
| Venlafaxine-d6 hydrochloride | Venlafaxine-d 6 (hydrochloride) is the deuterium labeled Venlafaxine hydrochloride. Venlafaxine hydrochloride (Wy 45030 hydrochloride) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant[1]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Wy 45030-d6 hydrochloride. CAS No. 1062606-12-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-B0196AS1. | |
| Venlafaxine hydrochloride | Venlafaxine hydrochloride (Wy 45030 hydrochloride) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Wy 45030 hydrochloride. CAS No. 99300-78-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B0196A. | |
Would you like to list your products on USA Chemical Suppliers?
Our database is helping our users find suppliers everyday.