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 | |
|---|---|---|
| AZ304 | AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits wild type BRAF, V600E mutant BRAF and wild type CRAF, with IC 50 s of 79 nM, 38 nM and 68 nM, respectively. AZ304 also has significant effect on other kinases, such as p38 ( IC 50 , 6 nM), CSF1R ( IC 50 , 35 nM). Anti-tumor activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 942507-42-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-117273. |  |
| AZ31 | AZ31 is a a potent, highly selective, and orally active ATM inhibitor with an IC 50 of <1.2 nM for ATM enzyme, and an IC 50 of 46 nM for ATM in cell. AZ31 shows excellent selectivity over ATR (>500-fold) and excellent PIKK-family selectivity and pan-kinase selectivity. AZ31 is a potent radiosensitizer in vitro, it can be used for the research of cancer [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2088113-98-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-112198. | |
| AZ505 ditrifluoroacetate | AZ505 ditrifluoroacetate is a potent and selective SMYD2 inhibitor with IC 50 of 0.12 μM. Uses: Scientific research. Group: Signaling pathways. CAS No. 1035227-44-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15226A. | |
| AZ 628 | AZ 628 is a pan-Raf kinase inhibitor with IC 50 s of 105, 34 and 29 nM for B-Raf , B-RafV600E , and c-Raf-1 , respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 878739-06-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-11004. | |
| AZ683 | AZ683 is a potent and selective 3-amido-4-anilinoquinoline CSF1R inhibitor. AZ683 has high affinity for CSF1R ( K i =8 nM; IC 50 =6 nM). AZ683 has good oral bioavailability. [ 11 C]AZ683 can be used as a positron emission tomography (PET) radiotracer for colony stimulating factor 1 receptor (CSF1R) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 953798-95-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-159108. | |
| Azacyclonol | Azacyclonol (γ-pipradol), a metabolite of Terfenadine, is a central depressant agent. Azacyclonol is a ganglion-blocking agent. Azacyclonol can be used to diminish psychoses-induced hallucinations [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: γ-pipradol. CAS No. 115-46-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0530. | |
| Azadirachtin | Azadirachtin is an oral active triterpenoid compound with anticancer, antimalarial, anti-inflammatory, and insecticidal activities. Azadirachtin induces cell apoptosis through the mitochondrial pathway (by inhibiting Bcl-2/Bax ratio or activating Apaf-1 and caspase-3 ) or through death receptors (by inhibiting TNFR activation). Additionally, Azadirachtin exerts its anti-inflammatory effects by inhibiting NF-?B signaling pathway activation, and it exhibits insecticidal activity by inducing apoptosis in insect cells [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Natural products. CAS No. 11141-17-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-126741. | |
| Azamethiphos | Azamethiphos is an organophosphate insecticide and a neurotoxic agent, causing acetylcholinesterase (AChE) inhibition [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 35575-96-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg. Product ID: HY-114899. | |
| Azaperone | Azaperone (R-1929) acts as a dopamine antagonist but also has some antihistaminic and anticholinergic properties. Azaperone is a pyridinylpiperazine and butyrophenone neuroleptic agent with antiemetic effects, which is used mainly as a tranquilizer in veterinary medicine. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R-1929. CAS No. 1649-18-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B1470. | |
| Azaribine | Azaribine (2',3',5'-Tri-O-acetyl-6-azauridine) is a potent orotidine monophosphate decarboxylase (OMPD) inhibitor. Azaribine is an antiviral inhibitor of several RNA viruses and inhibits viral genome replication and gene transcription. Azaribine shows broad-spectrum antiviral activity ( EC 50 =3.80?nM-1.73?μM against influenza A and B viruses; EC 50 =1.62 μM against ZIKV Paraiba). Azaribine, a triacetate salt of Azauridine, has the potential for psoriasis research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 2',3',5'-Tri-O-acetyl-6-azauridine. CAS No. 2169-64-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-B1537. | |
| Azaserine | Azazerine (CI-337) is a competitive inhibitor of glutamine amidotransferase. Azaserine is an antibiotic , it shows antibacterial activities. Azazerine shows anti-tumor activities and it may also act as a tumor inducer. Azazerine can be used for the research of cancer and infection [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CI-337; O-Diazoacetyl-L-serine; P-165. CAS No. 115-02-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0919. | |
| Azasetron hydrochloride | Azasetron (Y-25130) hydrochloride, a benzamide derivative, is a potent and selective 5-HT3 receptor antagonist. Azasetron is used in the study for Chemotherapy-induced nausea and vomiting (CINV) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Y-25130 hydrochloride. CAS No. 123040-16-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0068. | |
| Azathioprine | Azathioprine (BW 57-322) is an orally active immunosuppressive agent. Azathioprine can be converted in vivo to the active metabolite 6-mercaptopurine (6-MP). Azathioprine has myelosuppressive effects and induces apoptosis [1] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BW 57-322. CAS No. 446-86-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0256. | |
| AZD0156 | AZD0156 is a potent, selective and orally active ATM inhibitor with an IC 50 of 0.58 nM. AZD0156 inhibits the ATM -mediated signaling, prevents DNA damage checkpoint activation, disrupts DNA damage repair, and induces tumor cell apoptosis [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1821428-35-6. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-100016. | |
| AZD0780 | PCSK9-IN-12 is a heteroaryl compound. PCSK9-IN-12 has bind affinity for PCSK9 with a K d value of ?200 nM. PCSK9-IN-12 can be used for the research of cholesterol metabolism [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PCSK9-IN-12. CAS No. 2455427-91-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148673. | |
| AZD1208 | AZD1208 is an orally bioavailable, highly selective PIM kinases inhibitor [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1204144-28-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-15604. | |
| AZD1390 | AZD1390 is a potent, highly selective, orally bioavailable, brain-penetrant ATM inhibitor with an IC 50 of 0.78 nM in cell [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2089288-03-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109566. | |
| AZD1656 | AZD1656 is a potent, selective and orally active glucokinase activator with an EC 50 of 60 nM. AZD1656 has the potential for type 2 diabetes research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 919783-22-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15675. | |
| AZD1981 | AZD1981 is a potent and selective CRTh2 antagonist; displaces radio-labelled PGD2 from human recombinant DP2 with high potency (pIC50 = 8. Uses: Scientific research. Group: Signaling pathways. CAS No. 802904-66-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15950. | |
| AZD 2066 | AZD-2066 is a selective, orally active and blood-brain barrier-permeating mGluR5 antagonist. AZD 2066 activates the BDNF/trkB signaling pathway. AZD 2066 can be used in the research of neuropathic pain, major depressive disorder and gastroesophageal reflux disease [1] [2] [3] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 934282-55-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-110255. | |
| AZD3229 | AZD3229 is a potent pan- KIT mutant inhibitor for the treatment of gastrointestinal stromal tumors. AZD3229 inhibits c-KIT with an IC 50 value of 223.3 nM [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2248003-60-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112802. | |
| AZD3229 Tosylate | AZD3229 Tosylate is a potent pan-KIT mutant inhibitor for the treatment of gastrointestinal stromal tumors. Uses: Scientific research. Group: Signaling pathways. CAS No. 2248003-71-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112802A. | |
| AZD3839 free base | AZD3839 free base is a potent and selective orally active, brain-permeable BACE1 inhibitor ( K i=26 nM). AZD3839 free base shows 14 and >1000-fold selectivity against BACE2 and cathepsin D, respectively. AZD3839 free base exhibits dose- and time-dependent lowering of plasma, brain, and cerebrospinal fluid Aβ levels in mouse, guinea pig, and non-human primate. AZD3839 free base can be used for the research of Alzheimer's disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1227163-84-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-13438. | |
| AZD3965 | AZD3965 is a selective MCT1 inhibitor with a K i of 1.6 nM, showing 6-fold selectivity over MCT2. Uses: Scientific research. Group: Signaling pathways. CAS No. 1448671-31-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12750. | |
| AZD4320 | AZD4320 is a novel BH3-mimicking dual BCL2/BCLxL inhibitor with IC 50 s of 26 nM, 17 nM, and 170 nM for KPUM-MS3, KPUM-UH1, and STR-428 cells, respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 1357576-48-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-112416. | |
| AZD4573 | AZD4573 is a potent and highly selective CDK9 inhibitor ( IC 50 of <4 nM) that enables transient target engagement for the treatment of hematologic malignancies [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2057509-72-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-112088. | |
| AZD4694 Precursor | AZD4694 Precursor (AZ13040214) is the precursor of [ 18 F] AZD4694 for the synthesis of [ 18 F] AZD4694, an amyloid-β imaging ligand with high affinity for amyloid-β plaques [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZ13040214; NAV4614. CAS No. 1211333-20-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139516. | |
| AZD5153 | AZD5153 (Compound 13) is a trivalent triazolpyrazine bromide domain (BRD), bromodomain and extraterminal (BET) inhibitor. AZD5153 has down-regulated c-Myc gene and tumor growth inhibition activity. AZD5153 can be used in the study of BET small molecule inhibitors [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1869912-39-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-100653. | |
| AZD5153 6-Hydroxy-2-naphthoic acid | AZD5153 6-Hydroxy-2-naphthoic acid is the 6-Hydroxy-2-naphthoic acid of AZD5153. AZD5153 is a potent, selective, and orally available BET/BRD4 bromodomain inhibitor; disrupts BRD4 with an IC 50 of 1.7 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 1869912-40-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100653A. | |
| AZD5423 | AZD5423 is an inhaled, potent, selective, and non-steroidal glucocorticoid receptor (GR) modulator (SGRM) [1]. AZD5423 effectively reduces allergen-induced responses in subjects with mild allergic asthma [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1034148-04-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108243. | |
| AZD7325 | AZD7325 is a potent and orally active partial selective PAM of GABAAα2 and Aα3 receptor ( K i =0.3 and 1.3 nM, respectively), and has less antagonistic efficacy at the Aα1 and Aα5 receptor subtypes [1] [4]. AZD7325 is a moderate CYP1A2 and a potent CYP3A4 inducer in vitro [2]. AZD7325 has the potential for the investigation of anxiety and dravet syndrome [3]. PAM: positive allosteric modulator. Uses: Scientific research. Group: Signaling pathways. CAS No. 942437-37-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-111052. | |
| AZD-8055 | AZD-8055 is a potent, selective, and orally bioavailable ATP-competitive mTOR kinase inhibitor with an IC 50 of 0.8 nM. AZD-8055 inhibits both mTORC1 and mTORC2 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1009298-09-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10422. | |
| AZD8186 | AZD8186 is a PI3K inhibitor, which potently inhibits PI3Kβ (IC 50 =4 nM) and PI3Kδ (IC50 50 =12 nM) with selectivity over PI3Kα (IC 50 =35 nM) and PI3Kγ (IC 50 =675 nM). Uses: Scientific research. Group: Signaling pathways. CAS No. 1627494-13-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12330. | |
| AZD-8529 | AZD-8529 is a potent, highly selective and orally bioavailable positive allosteric modulator of mGluR2 , with an EC 50 of 285 nM, and shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes. Uses: Scientific research. Group: Signaling pathways. CAS No. 1092453-15-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107457. | |
| AZD-8529 mesylate | AZD-8529 mesylate is a potent, highly selective and orally bioavailable positive allosteric modulator of mGluR2 , with an EC 50 of 285 nM, and shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1314217-69-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107457A. | |
| AZD9496 | AZD9496 is an effective, selective estrogen receptor ( ERα ) antagonist with an IC 50 of 0.28 nM. AZD9496 is an orally active, selective estrogen receptor degrader (SERD). Uses: Scientific research. Group: Signaling pathways. CAS No. 1639042-08-2. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12870. | |
| AZD9496 maleate | AZD9496 maleate is a potent and selective estrogen receptor ( ERα ) antagonist with IC 50 of 0.28 nM. AZD9496 maleate is an orally bioavailable selective oestrogen receptor degrader (SERD). Uses: Scientific research. Group: Signaling pathways. CAS No. 1639042-28-6. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-12870A. | |
| AzddMeC | AzddMeC (CS-92) is an antiviral nucleoside analogue and a potent potent, selective and orally active HIV-1 reverse transcriptase and HIV-1 replication inhibitor. In HIV-1 -infected human PBM cells and HIV-1 -infected human macrophages, the EC 50 values of AzddMeC are 9 nM and 6 nM, respectively [1] [2]. AzddMeC is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CS-92. CAS No. 87190-79-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105268. | |
| Azelaic acid | Azelaic acid is a nine-carbon dicarboxylic acid. Azelaic acid has antimicrobial activity against Propionibacterium acnes and Staphylococcus epidermidis through inhibition of microbial cellular prorein synthesis. Azelaic acid has hypopigmentation action resulting from its ability to scavenge free radicals [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Nonanedioic acid. CAS No. 123-99-9. Pack Sizes: 10 mM * 1 mL; 25 g. Product ID: HY-B0704. | |
| Azelastine hydrochloride | Azelastine hydrochloridem, an antihistamine, is a potent and selective histamine 1 (H 1 ) antagonist. Azelastine hydrochloride can be used for the research of allergic rhinitis, asthma, diabetic hyperlipidemic and SARS-CoV-2 [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 79307-93-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg. Product ID: HY-B0462. | |
| Azelnidipine | Azelnidipine (CS 905) is a dihydropyridine calcium channel blocker that is effective orally. Azelnidipine inhibits the intracellular calcium ion flow and lower blood pressure by selectively blocking L-type calcium channel on the membrane of vascular smooth muscle. Azelnidipine inhibits esophageal squamous cell carcinoma proliferation by targeting MEK1/2. Azelnidipine also has anti-inflammatory, antioxidant and neuroprotective effects [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CS 905. CAS No. 123524-52-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0023. | |
| Azemiglitazone | Azemiglitazone (MSDC-0602) is an orally active thiazolidinedione (TZD) -like molecule, which binds to PPARγ with low binding and activating affinity. Azemiglitazone inhibits mitochondrial pyruvate carrier ( MPC ), which inhibits Alzheimers disease and diminishes nonalcoholic steatohepatitis (NASH) caused liver injury [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MSDC-0602. CAS No. 1133819-87-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-108022. | |
| Azemiglitazone potassium | Azemiglitazone potassium (MSDC-0602K), a PPARγ -sparing thiazolidinedione (Ps-TZD), binds to PPARγ with the IC 50 of 18.25 μM [1]. Azemiglitazone potassium modulates the mitochondrial pyruvate carrier (MPC). Azemiglitazone potassium can be used for the research of fatty liver including dysfunctional lipid metabolism, inflammation, and insulin resistance [2]. Azemiglitazone potassium, an insulin sensitizer, improves insulinemia and fatty liver disease in mice, alone and in combination with Liraglutide [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MSDC-0602K. CAS No. 1314533-27-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-108022A. | |
| Azenosertib | Azenosertib (ZN-c3) is a selective, orally active inhibitor for Wee1 inhibitor ( IC 50 =3.9 nM). Azenosertib exhibits antitumor activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ZN-c3. CAS No. 2376146-48-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132295. | |
| Azepan-2-one | Azepan-2-one is a kind of biological materials or organic compounds that are widely used in life science research [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 105-60-2. Pack Sizes: 25 g; 50 g. Product ID: HY-W010542. | |
| Azetidine-2-carboxylic acid | Azetidine-2-carboxylic acid is a non proteinogenic amino acid homologue of proline. Found in common beets. Azetidine-2-carboxylic acid can be misincorporated into proteins in place of proline in many species, including humans. Toxic and teratogenic agent [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 2517-4-6. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g; 10 g. Product ID: HY-75308. | |
| Azetidine-3-carboxylic acid | Azetidine-3-carboxylic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Azetidine-3-carboxylic acid 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. 36476-78-5. Pack Sizes: 10 g; 25 g. Product ID: HY-Y0530. | |
| Azetidine hydrochloride | Azetidine 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. Alternative Names: Trimethyleneimine hydrochloride. CAS No. 36520-39-5. Pack Sizes: 5 g; 10 g. Product ID: HY-W010628. | |
| Azetukalner | KCNQ2/3 activator-1 is an activator of Kv7.2/Kv7.3 ( KCNQ2/3 ) potassium channel. KCNQ2/3 activator-1 has the potential in relieving pain (the main problem from medical treatment) (extracted from patent WO2021113757A1, compound A) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: XEN1101. CAS No. 1009344-33-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-139791. | |
| Azidoacetic Acid | Azidoacetic Acid (2-Azidoacetic acid) (compound 92-1) is a click chemistry reagent containing an azide group. Azidoacetic Acid can be used as a small molecule tool for the synthesis of PROTAC [1]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 2-Azidoacetic acid. CAS No. 18523-48-3. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-151719. | |
| Azido-PEG4-NHS-ester | Azido-PEG4-NHS-ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Azido-PEG4-NHS-ester is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. Uses: Scientific research. Group: Signaling pathways. CAS No. 1807534-82-2. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-140765. | |
| Azilsartan | Azilsartan (TAK-536) is an orally active, potent, selective and specific angiotensin II type 1 receptor (AT1) antagonist. Azilsartan induces ROS formation and apoptosis in HepG2 cells. Azilsartan shows neuroprotective and anticancer activity. Azilsartan can be used for hypertension and stroke research [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-536. CAS No. 147403-03-0. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-14914. | |
| Azilsartan medoxomil | Azilsartan medoxomil (TAK 491) is an orally administered angiotensin II receptor type 1 antagonist with IC 50 of 0.62 nM, which used in the treatment of adults with essential hypertension [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-491. CAS No. 863031-21-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-14736. | |
| Azimilide | Azimilide(NE-10064) is a class III antiarrhythmic compound, inhibits I(Ks) and I(Kr) in guinea-pig cardiac myocytes and I(Ks) (minK) channels expressed in Xenopus oocytes. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NE-10064. CAS No. 149908-53-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-18600. | |
| Azimilide dihydrochloride | Azimilide (NE-10064) dihydrochloride is a class III antiarrhythmic compound, inhibits I(Ks) and I(Kr) in guinea-pig cardiac myocytes and I(Ks) (minK) channels expressed in Xenopus oocytes. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NE-10064 dihydrochloride. CAS No. 149888-94-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-18600A. | |
| Azimsulfuron | Azimsulfuron (DPX-A8947) is a sulfonylurea herbicide useful in controlling weeds in paddy fields [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DPX-A8947. CAS No. 120162-55-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121079. | |
| Azintuxizumab | Azintuxizumab is an anti- SLAMF7 human IgG4κ monoclonal antibody. Azintuxizumab can be used in the synthesis of antibody-drug conjugate (ADC), Azintuxizumab vedotin [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1826819-57-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99453. | |
| Azithromycin | Azithromycin is a macrolide antibiotic useful for the treatment of a number of bacterial infections. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP 62993. CAS No. 83905-01-5. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-17506. | |
| Azithromycin hydrate | Azithromycin hydrate is a macrolide antibiotic useful for the treatment of a number of bacterial infections. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP-62993 dihydrate. CAS No. 117772-70-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-17506A. | |
| Azobenzene | Azobenzene can be used as an optical trigger for the design and synthesis of a large variety of photoresponsive systems. Uses: Scientific research. Group: Signaling pathways. CAS No. 103-33-3. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g; 10 g. Product ID: HY-B2127. | |
| Azomethine-H monosodium | Azomethine-H monosodium is a colour-forming reagent. Azomethine-H monosodium is also a reagent for boron determinations [1] [2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 5941-7-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-D0797. | |
| Azomycin | Azomycin (2-Nitroimidazole) is an antibiotic which can be active against aerobic Gram-positive and Gram-negative bacteria. Uses: Scientific research. Group: Natural products. Alternative Names: 2-Nitroimidazole. CAS No. 527-73-1. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-N0195. | |
| Azosemide | Azosemide, a sulfonamide loop diuretic, is a potent NKCC1 inhibitor with IC 50 s of 0.246?μM and 0.197?μM for hNKCC1A and NKCC1B, respectively [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 27589-33-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107321. | |
| Azoxymethane | Azoxymethane is a colon carcinogen which leads to the formation of DNA adducts. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AOM. CAS No. 25843-45-2. Pack Sizes: 5 mg (135 mM * 500 μL in Water); 10 mg (135 mM * 1 mL in Water); 25 mg (135 mM * 2.5 mL in Water); 50 mg (135 mM * 5 mL in Water); 100 mg (135 mM * 10 mL in Water). Product ID: HY-111375. | |
| Azoxystrobin | Azoxystrobin is an orally active, broad-spectrum β-methoxyacrylate fungicide. Azoxystrobin inhibits mitochondrial respiration by binding to the Qo site of the cytochrome bc1 complex and inhibiting electron transfer. Azoxystrobin induces the production of reactive oxygen species (ROS) and induces cell apoptosis [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 131860-33-8. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-B0849. | |
| Aztreonam | Aztreonam (SQ-26,776) is a synthetic monocyclic beta-lactam antibiotic, which has a very high affinity for penicillin-binding protein 3 (PBP-3). Uses: Scientific research. Group: Signaling pathways. Alternative Names: SQ-26,776. CAS No. 78110-38-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-B0129. | |
| Azulene | Azulene (Cyclopentacycloheptene) is as an isomer of naphthalene with high anti-HIV activity. Azulene, isolated from the distillation of chamomile oil, is a scaffold in medicinal chemistry [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Cyclopentacycloheptene. CAS No. 275-51-4. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-B0055. | |
| Azure A chloride | Azure A (chloride) is a phenothiazine dye. Azure A (chlorine) is formed by oxidation of methylene blue and has strong metachromatic. Azure A (chlorine) can be used for the study of stains and redox media for electrochemical biosensing [1] [2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 531-53-3. Pack Sizes: 1 g; 5 g. Product ID: HY-D0947. | |
| B220 | B220 is an antiviral agent which can inhibit the growth of HSV-1 , HSV-2 and human cytomegalovirus ( CMV ). Uses: Scientific research. Group: Signaling pathways. CAS No. 112228-65-6. Pack Sizes: 10 mM * 1 mL; 1 mg. Product ID: HY-100272. | |
| Bacampicillin hydrochloride | Bacampicillin hydrochloride is a penicillin antibiotic, is a prodrug of ampicillin with improved oral bioavailability. Uses: Scientific research. Group: Signaling pathways. CAS No. 37661-08-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B1149A. | |
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