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 | |
|---|---|---|
| Guanoclor | Guanoclor is an antihypertensive compound. Guanoclor is an adrenergic neurone-blocking agent, which also interferes with noradrenaline synthesis by inhibition of the enzyme dopamine beta-hydroxylase [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Vatensol. CAS No. 5001-32-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100796. |  |
| Guanosine | Guanosine (DL-Guanosine) is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a β-N9-glycosidic bond. Guanosine possesses anti- HSV activity. Uses: Scientific research. Group: Natural products. Alternative Names: DL-Guanosine; Vernine. CAS No. 118-00-3. Pack Sizes: 10 mM * 1 mL; 1 g. Product ID: HY-N0097. | |
| Guanosine-13C10,15N5 | Guanosine- 13 C 10 , 15 N 5 is the 13 C and 15 N labeled Guanosine (HY-N0097). Guanosine (DL-Guanosine) is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a β-N9-glycosidic bond. Guanosine possesses anti-HSV activity [1]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: DL-Guanosine- 13 C10, 15 N5; Vernine- 13 C10, 15 N5. CAS No. 202406-81-3. Pack Sizes: 1 mg. Product ID: HY-N0097S6. | |
| Guanosine 5'-diphosphate disodium salt | Guanosine 5'-diphosphate (GDP) disodium salt, a purine nucleoside diphosphate, is interconverted to guanosine by the action of exonucleotidase and phosphorylation of nucleoside to guanine. Guanosine 5'-diphosphate disodium salt activates adenosine 5'-triphosphate-sensitive K + channel and is used to study the kinetics and characteristics of GTPases such as those associated with G-protein coupled receptors (GPCR). Guanosine 5'-diphosphate disodium salt is a potential iron mobilizer, which prevents the Hepcidin (HY-P70400)- ferroportin interaction and modulates the interleukin-6 (IL-6)/stat-3 pathway. Elevated levels of guanosine 5-diphosphate are associated with the pathogenesis of neurological diseases. Guanosine 5'-diphosphate disodium salt is promising for the research of inflammation, such as anemia of inflammation (AI) [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: GDP disodium salt. CAS No. 7415-69-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-113066A. | |
| Guanylate cyclase-IN-1 | Guanylate cyclase-IN-1 (Example 46) is a guanylate cyclase inhibitor that can be used for cardiovascular diseases research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1361569-23-4. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-W021162. | |
| Guanylyl imidodiphosphate lithium | Guanylyl imidodiphosphate (Gpp(NH)p) lithium, a non-hydrolyzable GTP analogue, increases adenylate cyclase activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Gpp(NH)p lithium. CAS No. 64564-03-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-137167. | |
| Gue1654 | Gue1654 is a modulator of OXE-R. Gue1654 inhibits Gβγ but not Gα signaling triggered upon activation of Gα(I)-βγ by the chemoattractant receptor OXE-R. Gue1654 does not interfere nonspecifically with signaling directly at or downstream of Gβγ [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 397290-30-1. Pack Sizes: 1 mg. Product ID: HY-110114. | |
| Guggulsterone | Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products ( IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin ), modulation of cell cycle proteins ( cyclin D1 and c-Myc ), activation of caspases and JNK , inhibition of Akt [1]. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC 50 s of 17 and 15 μM for Z- and E-Guggulsterone, respectively [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Z/E-Guggulsterone. CAS No. 95975-55-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107738. | |
| Gum arabic | Gum Arabic (Arabic gum) is a branched-chain, complex polysaccharide derive from A. Senegal. Gum Arabic is an anti-oxidant, and can protect against experimental hepatic-, renal- and cardiac toxicities. Gum Arabic also can be used in immunohistochemistry [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Arabic gum. CAS No. 9000-1-5. Pack Sizes: 10 g; 25 g. Product ID: HY-N6664. | |
| Guselkumab | Guselkumab is a recombinant human IgG1 monoclonal antibody against the IL-23p19 subunit. Guselkumab binds to human and cynomolgus monkey IL-23 with K d values of 3.3 and 1.9 pmol/L, respectively. Guselkumab inhibits production of cytokines lying downstream of the IL-23 signaling pathway and can be used for psoriatic arthritis research [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: CNTO 1959. CAS No. 1350289-85-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P9931. | |
| Guvacine hydrochloride | Guvacine hydrochloride is an alkaloid from the nut of Areca catechu , acts as an inhibitor of GABA transporter , and dispalys modest selectivity for cloned GABA transporters with IC 50 s of 14 μM (human GAT-1), 39 μM (rat GAT-1), 58 μM (rat GAT-2), 119 μM (human GAT-3), 378 μM (rat GAT-3), and 1870 μM (human BGT-3). Uses: Scientific research. Group: Natural products. CAS No. 6027-91-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-100809. | |
| Guvacoline hydrochloride | Guvacoline hydrochloride, a pyridine alkaloid found in Areca triandra , can act as a weak full agonist of atrial and ileal muscarinic receptors [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 6197-39-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N5016. | |
| GW0742 | GW0742 is a potent PPARβ and PPARδ agonist, with an IC 50 of 1 nM for human PPARδ in binding assay, and EC 50 s of 1 nM, 1.1 μM and 2 μM for human PPARδ , PPARα, and PPARγ, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GW610742. CAS No. 317318-84-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13928. | |
| GW274150 | GW274150 is a potent, selective, orally active and NADPH-dependent inhibitor of human inducible nitric oxide synthase (iNOS) ( IC 50 =2.19 μM; K d =40 nM) and rat iNOS ( ED 50 =1.15 μM). GW274150 also displays less potency for both humans or rats endothelial NOS ( eNOS ) and neuronal NOS ( nNOS ). GW274150 exerts a protective role in an acute model of lung injury inflammation [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 210354-22-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12119. | |
| GW274150 phosphate | GW274150 phosphate is a potent, selective, orally active and NADPH-dependent inhibitor of human inducible nitric oxide synthase (iNOS) ( IC 50 =2.19 μM; K d =40 nM) and rat iNOS ( ED 50 =1.15 μM). GW274150 phosphate displays less potency for both humans or rats endothelial NOS ( eNOS ) and neuronal NOS ( nNOS ). GW274150 phosphate exerts a protective role in an acute model of lung injury inflammation [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 438542-15-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12119A. | |
| GW3965 hydrochloride | GW3965 hydrochloride is a potent and selective liver X receptor (LXR) agonist with EC 50 s of 190 nM and 30 nM for hLXRα and hLXRβ, respectively [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 405911-17-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10627A. | |
| GW-405833 | GW-405833 (L768242) is a potent, selective cannabinoid receptor 2 (CB 2 ) agonist with an EC 50 of 50.7 nM. GW-405833 also behaves as a noncompetitive CB 1 antagonist. GW-405833 suppresses inflammatory and neuropathic pain [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: L768242. CAS No. 180002-83-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-110036. | |
| GW405833 hydrochloride | GW-405833 (L768242) hydrochloride is a potent, selective cannabinoid receptor 2 (CB 2 ) agonist with an EC 50 of 50.7 nM. GW-405833 hydrochloride also behaves as a noncompetitive CB 1 antagonist. GW-405833 hydrochloride suppresses inflammatory and neuropathic pain [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: L768242 hydrochloride. CAS No. 1202865-22-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110036A. | |
| GW4869 | GW4869 is a noncompetitive neutral sphingomyelinase (N-SMase) inhibitor with an IC 50 of 1 μM. GW4869 is an inhibitor of exosome biogenesis/release [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 6823-69-4. Pack Sizes: 2 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-19363. | |
| GW 501516 | GW 501516 (GW 1516) is a PPARδ agonist with an EC 50 of 1.1 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GW 1516; GSK-516. CAS No. 317318-70-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10838. | |
| GW791343 dihydrochloride | GW791343 dihydrochloride is a potent human P2X7 receptor negative allosteric modulator (exhibits species-specific activity), produces a non-competitive antagonist effect on human P2X7 receptor, with a pIC 50 of 6.9-7.2. GW791343 dihydrochloride can enhance ATP rhythm. GW791343 dihydrochloride can be used in study of neurological disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1019779-04-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-15469. | |
| GYKI 52466 dihydrochloride | GYKI 52466 dihydrochloride is an orally active, highly selective and noncompetitive AMPA/kainate receptor antagonist with the IC 50 values of 7.5 and 11μM, respectively. GYKI 52466 dihydrochloride has good blood brain barrier permeability and anticonvulsant effect. GYKI 52466 dihydrochloride can be used in Parkinson's disease research [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2319722-40-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103234A. | |
| GYKI 53655 hydrochloride | GYKI 53655 (LY300168) hydrochloride is an α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid ( AMPA ) antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY300168 hydrochloride. CAS No. 143692-48-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-103228. | |
| Gymnemic acid I | Gymnemic acid I is a bioactive triterpene saponin found in Gymnema sylvestre. Gymnemic acid I decreases the apoptosis under the high glucose stress [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 122168-40-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N2541. | |
| Gynostemma Extract | Gynostemma Extract (Ginsenoside C-Mx1) is a natural product. Uses: Scientific research. Group: Natural products. Alternative Names: Ginsenoside C-Mx1; Gypenoside IX. CAS No. 80321-63-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0167. | |
| H2DCFDA | H2DCFDA (DCFH-DA) is a cell-permeable probe used to detect intracellular reactive oxygen species (ROS) (Ex/Em=488/525 nm) [1]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: DCFH-DA; 2',7'-Dichlorodihydrofluorescein diacetate. CAS No. 4091-99-0. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-D0940. | |
| H2N-PEG2-CH2COOtBu | H2N-PEG2-CH2COOtBu is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1122484-77-8. Pack Sizes: 100 mg; 250 mg; 1 g. Product ID: HY-135927. | |
| H3B-6527 | H3B-6527 is an orally active, highly selective and covalent FGFR4 inhibitor with an IC 50 of <1.2 nM. H3B-6527 has at least 250-fold selectivity over FGFR1-3 with IC 50 s of 320 nM, 1290 nM and 1060 nM respectively. H3B-6527 has potent anti-cancer activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1702259-66-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-100491. | |
| H3B-6545 | H3B-6545 is an oral, selective estrogen receptor covalent antagonist ( SERCA ) for the research of metastatic ER-positive, HER2-negative breast cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2052130-80-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-112596. | |
| H3B-6545 hydrochloride | H3B-6545 hydrochloride is an oral, selective estrogen receptor covalent antagonist ( SERCA ) for the research of metastatic ER-positive, HER2-negative breast cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2052132-51-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-112596A. | |
| H3B-8800 | H3B-8800 is a potent and orally active SF3B splicing modulator. H3B-8800 direct interaction with the SF3b complex and shows anti-cancer activity. H3B-8800 has the potential for the research of acute myeloid leukemia (AML) with SF3B1 mutant [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1825302-42-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111517. | |
| H4 Receptor antagonist 1 | H4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist, with an IC 50 of 19 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 848217-00-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-114025. | |
| H-8 dihydrochloride | H-8 (dihydrochloride) is a cell-permeable, reversible and ATP-competitive PKA inhibitor [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 113276-94-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-112465. | |
| H-9 Dihydrochloride | H-9 Dihydrochloride is a PKA (protein kinase) inhibitor. H-9 Dihydrochloride (10 μM) significantly reduces the excitatory response to 5-HT. H-9 Dihydrochloride also has a direct effect on pharyngeal activity. H-9 Dihydrochloride inhibits signal-transduction and cell growth in EGF (epidermal growth factor)-dependent epithelial cell lines [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 116700-36-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-100923. | |
| HA-100 | HA-100 is a potent protein kinase inhibitor, with IC 50 s of 4 μM, 8 μM, 12 μM and 240 μM for cGMP-dependent protein kinase (PKG) , cAMP-dependent protein kinase (PKA) , protein kinase C (PKC) and MLC-kinase , respectively. HA-100 also used as a ROCK inhibitor [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 84468-24-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100984. | |
| HA-1004 | HA-1004 is a selective inhibitor of PKA, which can inhibit lipolysis and induce vascular relaxation. HA-1004 is also a dual inhibitor of cyclic GMP-dependent protein kinase and cyclic AMP-dependent protein, and is involved in smooth muscle, second messenger, cyclic AMP and cyclic GMP regulation mechanisms. HA-1004 is an antagonist for calcium , that can be used as a vasodilator to inhibit the contraction of rabbit aortic strips, or to antagonize ERK and tyrosine hydroxylase (TH) phosphorylation in morphine abstinence rat models [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 91742-10-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-123468. | |
| HA130 | HA130 is a selective autotaxin (ATX) inhibitor with an IC 50 of 28 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 1229652-21-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-19329. | |
| HA155 | HA-155 is a potent and selective autotaxin (ATX) inhibitor with an IC 50 of 5.7 nM [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1312201-00-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-116100A. | |
| HADA hydrochloride | HADA hydrochloride (HCC-Amino-D-alanine hydrochloride) is a blue (λ em ~450 nm) fluorescent D-amino acid (FDAA). FDAAs are efficiently incorporated into the peptidoglycans (PGs) of diverse bacterial species at the sites of PG biosynthesis, allowing specific and covalent probing of bacterial growth with minimal perturbation [1]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: HCC-Amino-D-alanine hydrochloride. CAS No. 2253733-10-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-131045. | |
| HAE | HAE is a 3-amino acid peptide which consists of histidine, alanine and glutamate. Uses: Scientific research. Group: Peptides. CAS No. 64111-99-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1232. | |
| HAEGTFT | HAEGTFT is the first N-terminal 1-7 residues of GLP-1 peptide. Uses: Scientific research. Group: Peptides. CAS No. 926018-95-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1228. | |
| HAEGTFTSDVSSYLE | HAEGTFTSDVSSYLE is a polypeptide from patent CN 102920658 B. GLP-I analog contains the sequence. Uses: Scientific research. Group: Peptides. CAS No. 926018-57-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1445. | |
| Halazone | Halazone is an atypical antimicrobial sulfonamide derivative and a carbonic anhydrase II inhibitor with a K d value of 1.45 μM. Halazone protects sodium channels from inactivation. Halazone is widely used for disinfection of drinking water [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 80-13-7. Pack Sizes: 50 mg; 100 mg; 250 mg. Product ID: HY-B1386. | |
| Halcinonide | Halcinonide (SQ-18566) is a high potency corticosteroid used topically in the treatment of certain skin conditions. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SQ-18566. CAS No. 3093-35-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-B0877. | |
| Halicin | Halicin (SU3327) is a potent, selective and substrate-competitive JNK inhibitor with an IC 50 of 0.7 μM. Halicin also inhibits protein-protein interactions between JNK and JNK Interacting Protein (JIP) with an IC 50 of 239 nM. Halicin shows less active against p38α and Akt kinase [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SU3327. CAS No. 40045-50-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-107597. | |
| Halobetasol | Halobetasol (Ulobetasol) is a corticosteroid. Halobetasol can be used for research of severe localized psoriasis [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ulobetasol. CAS No. 98651-66-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-113783. | |
| Halobetasol (propionate) | Halobetasol propionate is a synthetic corticosteroid for topical dermatological use; exhibits anti-inflammatory, antipruritic, and vasoconstrictive properties. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMY-30056; CGP-14458; Ulobetasol propionate. CAS No. 66852-54-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0878. | |
| Halobetasol (propionate) (Standard) | Halobetasol (propionate) (Standard) is the analytical standard of Halobetasol (propionate). This product is intended for research and analytical applications. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMY-30056(Standard); CGP-14458(Standard); Ulobetasol propionate (Standard). CAS No. 66852-54-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0878R. | |
| Halocarban | Halocarban is a chemical with antibacterial properties sometimes used in deodorant and soap [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cloflucarban. CAS No. 369-77-7. Pack Sizes: 25 mg; 50 mg. Product ID: HY-116587. | |
| Halofantrine hydrochloride | Halofantrine hydrochloride (SKF-102886) is a blocker of delayed rectifier potassium current via the inhibition of human-ether-a-go-go-related gene (HERG) channel and a potent antimalarial compound [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SKF-102886; WR-171669 hydrochloride. CAS No. 36167-63-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-A0148A. | |
| Halofuginone | Halofuginone (RU-19110), a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a K i of 18.3 nM [1] [2]. Halofuginone is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity [3] [4]. Halofuginone is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca 2+ channels. Halofuginone has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects [5]. Uses: Scientific research. Group: Natural products. Alternative Names: RU-19110. CAS No. 55837-20-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1584. | |
| Halofuginone hydrobromide | Halofuginone (RU-19110) hydrobromid, a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a K i of 18.3 nM [1] [2]. Halofuginone hydrobromid is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity [3] [4]. Halofuginone hydrobromid is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca 2+ channels. Halofuginone hydrobromid has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects [5]. Uses: Scientific research. Group: Natural products. Alternative Names: RU-19110 hydrobromide. CAS No. 64924-67-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-N1584A. | |
| Halofuginone lactate | Halofuginone lactate, a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a K i of 18.3 nM [1] [2]. Halofuginone lactate is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity [3] [4]. Halofuginone lactate is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca 2+ channels. Halofuginone lactate has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RU-19110 lactate. CAS No. 82186-71-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1584C. | |
| Halofuginone (Standard) | Halofuginone (Standard) is the analytical standard of Halofuginone. This product is intended for research and analytical applications. Halofuginone (RU-19110), a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a Ki of 18.3 nM [1] [2]. Halofuginone is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity [3] [4]. Halofuginone is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca2+ channels. Halofuginone has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects [5]. Uses: Scientific research. Group: Natural products. CAS No. 55837-20-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1584R. | |
| Haloperidol | Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic. Uses: Scientific research. Group: Signaling pathways. CAS No. 52-86-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-14538. | |
| Haloperidol decanoate | Haloperidol decanoate shows antipsychotic activity. Haloperidol decanoate can be used in schizophrenia and schizoaffective disorder research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 74050-97-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107969. | |
| Haloperidol (Standard) | Haloperidol (Standard) is the analytical standard of Haloperidol. This product is intended for research and analytical applications. Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic. Uses: Scientific research. Group: Signaling pathways. CAS No. 52-86-8. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14538R. | |
| Haloprogin | Haloprogin is a potent antifungal agent. Haloprogin has activity against dermatophytes, Candida spp and a limited number of Gram-positive bacteria [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 777-11-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16246. | |
| Halosulfuron-methyl | Halosulfuron-methyl is a pyrazole sulfonylurea herbicide [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Inpool; MON 12000; Manage. CAS No. 100784-20-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-B1850. | |
| Haloxon | Haloxon is an anti-parasitic agent. Haloxon can be used for the research of infections of Parascaris equorum, Oxyuris equi and Strongylus vulgaris. Haloxon also can be used in control of ascarids and hookworms in domesticated animals in combination with Bidimazium [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 321-55-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-17532. | |
| Haloxyfop-methyl | Haloxyfop-methyl is a high-efficacy herbicide. Haloxyfop-methyl selectively controls several annual and perennial grasses in soybeans and other dicotyledenous crops [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 69806-40-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W286307. | |
| Hamamelitannin | Hamamelitannin, a polyphenol extracted from the bark of Hamamelis virginiana , is a quorum-sensing (QS) inhibitor. Hamamelitannin increases antibiotic susceptibility of staphylococcus aureus biofilms by affecting peptidoglycan biosynthesis and eDNA release [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 469-32-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N4117. | |
| HAP-1 | HAP-1 is a synovial-targeted transduction peptide. HAP-1 facilitates specific internalization of protein complexes into human and rabbit synovial cells. HAP-1 fused to an antimicrobial peptide, (KLAK) 2 , to generate a proapoptotic peptide DP2 [1]. Uses: Scientific research. Group: Peptides. CAS No. 329004-38-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P4096. | |
| HA Peptide | HA Peptide (HA tag) is a nine amino acids peptide derived from the human influenza hemagglutinin (HA). HA Peptide is extensively used to isolate, purify, detect, and track the protein of interest in cell biology and biochemistry. Uses: Scientific research. Group: Peptides. CAS No. 92000-76-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P0239. | |
| HAPSBC | HAPSBC is an S-benzyl iron chelator that mobilizes intracellular 59 Fe distribution [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1376545-81-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156776. | |
| Hapten C | Hapten C is a derivative of histamine. Hapten C is utilized for synthesis of immunogens and coating antigens, that can quantitative determine the histamine via ELISA [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 90579-19-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108026. | |
| H-Arg-NH2 hydrochloride | H-Arg-NH2 (hydrochloride) is a nucleophilic reagent that can be used in experiments related to enzyme activity center detection [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 14975-30-5. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W011985. | |
| Harmalol hydrochloride | Harmalol hydrochloride, a beta carboline alkaloid, presents in several medicinal plants such as Peganum harmala. Harmalol hydrochloride, main metabolite of Harmaline, significantly inhibits the dioxin-mediated induction of CYP1A1 at the transcriptional and posttranslational levels. Harmalol hydrochloride possesses antioxidant and hydroxyl radical-scavenging properties [1]. Uses: Scientific research. Group: Natural products. CAS No. 6028-7-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N2625A. | |
| Harmane | Harmane is a benzodiazepine receptor inhibitor ( IC 50 =7 μM), with IC 50 values for mACh , Opioid Receptor , MAO-A/B , and α2-adrenergic receptor of 24 μM, 2.8 μM, 0.5 μM, 5 μM, and 18 μM, respectively. Harmane inhibits the I1 imidazoline receptor ( IC 50 = 30 nM) to reduce blood pressure and has antidepressant, anti-anxiety, anticonvulsant, and analgesic effects. Harmane inhibits dopamine biosynthesis by decreasing tyrosine hydroxylase (TH) activity and enhancing L-DOPA-induced cytotoxicity in PC12 cells. Additionally, Harmane can increase the mutagenic effect induced by 2-acetylaminofluorene (AAF) [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Natural products. CAS No. 486-84-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-101392. | |
| Harmine | Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase ( DYRK ) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT 2A serotonin receptor , with an K i of 397 nM [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Telepathine. CAS No. 442-51-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-N0737A. | |
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