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 | |
|---|---|---|
| Levofloxacin hydrochloride | Levofloxacin hydrochloride is an orally active antibiotic. Levofloxacin inhibits DNA gyrase and topoisomerase IV activity, inducing Apoptosis. Levofloxacin hydrochloride has antibacterial activity against both Gram-positive and Gram-negative bacteria. Levofloxacin hydrochloride exhibits anticancer activity against lung cancer. Levofloxacin hydrochloride has anti-acnegenic, anxiogenic, and analgesic effects. Levofloxacin hydrochloride shortens sleep duration in mice. Levofloxacin hydrochloride can be used in the research of infectious diseases (such as tuberculosis, chronic periodontitis, bacterial infections associated with stable COPD, and BK viremia) and lung cancer[1][2][3][4][5][6][7][8][9][10]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (-)-Ofloxacin hydrochloride. CAS No. 177325-13-2. Pack Sizes: 10 mM * 1 mL in Water; 1 g; 5 g; 10 g. Product ID: HY-B0330B. |  |
| Levofloxacin N-oxide | Levofloxacin N-oxide is a minor metabolite of Levofloxacin (HY-B0330). Levofloxacin N-oxide does not exhibit significantly genotoxic risks. Levofloxacin is an orally active antibiotic and is active against both Gram-positive and Gram-negative bacteria[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 117678-38-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133787. | |
| Levoglucosan-13C6 | Levoglucosan-13C6 is the 13C labeled Levoglucosan[1]. Levoglucosan (1,6-Anhydro-β-D-glucopyranose) is an anhydrosugar produced through glucan pyrolysis and is widely found in nature[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 1,6-Anhydro-β-D-glucopyranose-13C6; 1,6-Anhydro-β-D-glucose-13C6. CAS No. 1375293-81-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-W050145S2. | |
| Levoketoconazole | Levoketoconazole ((-)-Ketoconazole) is the 2S,4R enantiomer derived from racemic Ketoconazole (HY-B0105). Levoketoconazole is a potent and orally active cortisol synthesis inhibitor. Levoketoconazole inhibits key steps in cortisol and testosterone synthesis by inhibiting CYP11B1, CYP11A1, and CYP17A1. Levoketoconazole can be used for research on endogenous Cushings syndrome[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (-)-Ketoconazole; (-)-Ketoconazol; (-)-R 41400. CAS No. 142128-57-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0105B. | |
| Levoleucovorin | Levoleucovorin (Levofolinic acid; Levofolene) is the pharmacologically and orally active levoisomer of Folinic acid (HY-17556), a synthetic folate analogue. Levoleucovorin can inhibit LOXL2 with an IC50 of 68.81 μM. Levoleucovorin can inhibit cancer cells proliferation, migration and induce apoptosis. Levoleucovorin can be used as a rescue agent for high-dose Methotrexate (HY-14519). Levoleucovorin can reduce the frequency of embryonic malformations. Levoleucovorin can be used for the research of can and endocrinology, such as breast cancer and osteosarcoma[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Levofolinic acid; Levofolene. CAS No. 68538-85-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-127009. | |
| Levomedetomidine hydrochloride | Levomedetomidine hydrochloride is an isomer of Medetomidine (HY-17034), and a cardioprotective agent with sedative and analgesic effects[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 190000-46-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-135735A. | |
| Levomefolate calcium | Levomefolate calcium is a synthetic calcium salt of L-5-methyltetrahydrofolate and an orally active and brain-penetrant folate supplement. Levomefolate calcium incorporates into body folate pools to increase plasma and red blood cell folate levels over time. Levomefolate calcium does not significantly increase folate concentrations in breast milk. Levomefolate calcium can be used for the research of neural tube defects and megaloblastic anemia[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 151533-22-1. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17383. | |
| Levomefolic acid | Levomefolic acid (L-5-MTHF) is an orally active, brain-penetrant natural active form of folic acid and is one of the most widely used folic acid food supplements[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-5-MTHF. CAS No. 31690-09-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14781. | |
| Levomenol | Levomenol ((-)-α-Bisabolol), a monocyclic sesquiterpene alcohol, exerts antioxidant, anti-inflammatory, and anti-apoptotic activities. Levomenol also has neuroprotective effects and prevents neuronal damage and memory deficits through reduction of proinflammatory markers induced by permanent focal cerebral ischemia in mice. Levomenol attenuates nociceptive behaviour and central sensitisation in a rodent model of trigeminal neuropathic pain. Orally active[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (-)-α-Bisabolol. CAS No. 23089-26-1. Pack Sizes: 1 mL; 10 mM * 1 mL in DMSO; 5 mL. Product ID: HY-N6967. | |
| Levomepromazine | Levomepromazine (Methotrimeprazine) is an orally active antipsychotic compound and Ca2+ release inducer. Levomepromazine inhibits SERCA pump and induces an increase in cytoplasmic Ca2+ levels. Levomepromazine has antagonistic effects on a variety of neurotransmitter receptors, including dopamine, cholinergic, serotonin, and histamine receptors. Levomepromazine can induce adaptive ER stress and autophagy. In addition, Levomepromazine has antiviral, anti-inflammatory, neuroprotective and analgesic, sedative and anti-injurious activities. Levomepromazine can be used in the study psychiatric disorders and relieving nausea and vomiting[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Methotrimeprazine. CAS No. 60-99-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1693. | |
| Levonadifloxacin | Levonadifloxacin ((S)-(-)-Nadifloxacin; WCK 771) is a broad-spectrum anti-staphylococcal agent. Levonadifloxacin shows antibacterial activity against Methicillin (HY-121544)-susceptible Staphylococcus aureus (MSSA) and Methicillin-resistant S. aureus (MRSA) strains, with a reduction of which phagocytized in THP-1 monocytes[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (S)-(-)-Nadifloxacin; WCK 771. CAS No. 154357-42-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14926. | |
| Levonordefrin | Levonordefrin ((-)-Cobefrin; (-)-α-Methylnoradrenaline; (-)-Nordefrin) is an α-adrenergic receptor agonist with blood pressure regulatory properties. Levonordefrin is a key metabolite responsible for the hypotensive effect of α-methyldopa. By stimulating central α-adrenergic receptors in the nucleus tractus solitarius region of the medulla oblongata, Levonordefrin induces centrally mediated hypotension and bradycardia. When administered intravenously, Levonordefrin increases mean arterial blood pressure in a dose-dependent manner. Levonordefrin is applicable for research on the pathophysiology of hypertension and drug metabolism[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (-)-Cobefrin; (-)-α-Methylnoradrenaline; (-)-Nordefrin. CAS No. 829-74-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-107915. | |
| Levonorgestrel | Levonorgestrel is an orally active inhibitor of progesterone (HY-N0437). Levonorgestrel has anticancer activity and can induce Apoptosis. Levonorgestrel can be used as a contraceptive and in combination with other medications. Levonorgestrel can be used in the study of osteoporosis and uterine leiomyoma[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: D-Norgestrel. CAS No. 797-63-7. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg. Product ID: HY-B0257. | |
| Levonorgestrel (Standard) | Levonorgestrel (Standard) is the analytical standard of Levonorgestrel. This product is intended for research and analytical applications. Uses: Scientific research. Category: Signaling pathways. Alternative Names: D-Norgestrel (Standard). CAS No. 797-63-7. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg; 500 mg. Product ID: HY-B0257R. | |
| Levosimendan | Levosimendan (Simsndan; OR-1259) is a calcium sensitiser used in the management of acutely decompensated congestive heart failure. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Simsndan; OR-1259. CAS No. 141505-33-1. Pack Sizes: 100 mg; 500 mg. Product ID: HY-14286. | |
| Levosulpiride | Levosulpiride (RV-12309) is the (S)-enantiomer of sulpiride, which is a D2 receptor a antagonist, an atypical antipsychotic agent of the benzamide class. Uses: Scientific research. Category: Signaling pathways. Alternative Names: RV-12309; S-(-)-Sulpiride. CAS No. 23672-07-3. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg. Product ID: HY-B1059. | |
| Levulinic acid | Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate. Levulinic acid is also a 5-keto-pentanoic acid. Levulinic acid can be utilized by the cells as a cosubstrate for biopolymer synthesis. Levulinic acid can be used in antibacterial research[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 4-Oxovaleric acid; NSC 3716. CAS No. 123-76-2. Pack Sizes: 10 mM * 1 mL in DMSO; 25 g; 50 g; 100 g; 500 g; 1 k g. Product ID: HY-Y0839. | |
| Lewis a trisaccharide | Lewis a trisaccharide (Lewis a) is a trisaccharide that has been found to be present in the glycan structures of spermatozoa. Lewis a trisaccharide also is a major component of the glycan structures on the surface of HL-60 cells[1]. Uses: Scientific research. Category: Natural products. Alternative Names: Lewis a. CAS No. 56570-03-7. Pack Sizes: 1 mg. Product ID: HY-N10531. | |
| Lewis-b tetrasaccharide | Lewis-b tetrasaccharide is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 80081-06-7. Pack Sizes: 1 mg; 2 mg; 5 mg. Product ID: HY-W854445. | |
| Lewis X trisaccharide | Lewis X trisaccharide (Lewis X, Lex) is a potent TH2 regulator, antagonizes LPS-induced IL-12 immune expression. Lewis X trisaccharide is a human histo-blood group antigen, plays an key role in cell-cell adhesion, and servers as a tumor marker. Lewis X trisaccharide is highly expressed in the outer membrane of the parasite, can be used for the immunology research of schistosomiasis[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Lewis X. CAS No. 71208-06-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N10534. | |
| Lexatumumab | Lexatumumab (HGS-ETR 2) is a human agonistic TRAIL receptor 2 (TRAIL-R2, DR5, APO-2) IgG4κ type monoclonal antibody. Lexatumumab induces apoptosis in malignant mesothelioma. Lexatumumab can be used for malignant pleural mesothelioma (MPM) research[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: HGS-ETR 2; ETR2-ST01. CAS No. 845816-02-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99299. | |
| Lexibulin | Lexibulin (CYT-997) is a potent and orally active tubulin polymerisation inhibitor with IC50s of 10-100 nM in cancer cell lines; with potent cytotoxic and vascular disrupting activity in vitro and in vivo[1][2]. Lexibulin induces cell apoptosis and induces mitochondrial ROS generation in GC cells[3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CYT-997. CAS No. 917111-44-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10498. | |
| LF3 | LF3 is an antagonist of the β-Catenin/TCF4 interaction with antitumor activity; has an IC50 of 1.65 μM[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 664969-54-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101486. | |
| LFHP-1c | LFHP-1c is an PGAM5 inhibitor with neuroprotective activity in brain ischemic stroke. LFHP-1c protects blood-brain barrier integrity from ischemia-induced injury. LFHP-1c binds to endothelial PGAM5 to inhibit the activity of PGAM5 phosphatase and the interaction of PGAM5 with NRF2. LFHP-1c exhibits in vitro and in vivo protection[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2102347-47-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139598. | |
| L-fucokinase/GDP-fucose pyrophos-phorylase (FKP) | L-fucokinase/GDP-fucose pyrophos-phorylase (FKP) is an enzyme that catalyzes the chemical reaction. L-fucokinase/GDP-fucose pyrophos-phorylase (FKP) has substrate of L-fucose. L-fucokinase/GDP-fucose pyrophos-phorylase (FKP) induces L-fucose phosphorylation to form L-fucose-L-phosphate[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 37278-00-5. Pack Sizes: 5 U; 10 U; 25 U. Product ID: HY-E70026. | |
| LG100268 | LG100268 (LG268) is a potent, selective and orally active retinoid X receptor (RXR) agonist with EC50 values of 4 nM, 3 nM, and 4 nM for RXR-α, RXR-β, and RXR-γ, respectively[1]. LG100268 displays >1000-fold selectivity for RXR over RAR, the Ki values are 3.4 nM, 6.2 nM and 9.2 nM for RXR-α, RXR-β, and RXR-γ, respectively[2]. LG100268 activates RXR homodimers to induce transcriptional activation. LG100268 can be used for the study of lung carcinogenesisy[3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LG268. CAS No. 153559-76-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15340. | |
| LG100754 | LG100754 (UVI 2112) is a RXR dimers modulater. LG100754 acts as a RXR:RXR homodimer antagonist, but functions as a agonist towards RXR:PPARα and RXR:PPARγ heterodimers. LG100754 is an insulin sensitizer that functions through RXR[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: UVI 2112. CAS No. 180713-37-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108523. | |
| L-γ-Glutamyl-L-glutamic acid | L-γ-Glutamyl-L-glutamic acid (γ-Glu-Glu) is the isomer of D-γ-Glutamyl-D-glutamic acid (HY-118090A), and can be used as an experimental control. D-γ-Glutamyl-D-glutamic acid is a poly(γ-glutamic acid) of clusters of D- and D-glutamic acid repeating units in a linear chain[1]. Uses: Scientific research. Category: Peptides. Alternative Names: γ-Glu-Glu; H-γ-Glu-Glu-OH. CAS No. 1116-22-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-118090. | |
| L-gamma-Glutamyl-L-threonine | L-gamma-Glutamyl-L-threonine (gamma-Glutamylthreonine; H-γ-Glu-Thr-OH; γ-Glu-Thr) is a dipeptide obtained through the formal condensation of the L-glutamic acid side chain carboxyl group and the L-threonine amino group. L-gamma-Glutamyl-L-threonine is present in high concentrations in human urine and exhibits antibacterial activity against Gram-negative bacterial. L-gamma-Glutamyl-L-threonine is also a flavor compound. Gamma-Glutamylthreonine is a metabolite catalyzed by γ-glutamyl transpeptidase and is associated with immune regulation. Gamma-Glutamylthreonine can be used in research on inflammation and bacterial infections[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: gamma-Glutamylthreonine; H-γ-Glu-Thr-OH; γ-Glu-Thr. CAS No. 5652-48-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N13356. | |
| LGD-6972 | LGD-6972 is a selective and orally active glucagon receptor antagonist. LGD-6972 has the potential for type 2 diabetes research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1207989-09-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12525. | |
| LGK974 | LGK974 (WNT974) is an orally bioavailable and specific Porcupine (PORCN) inhibitor with an IC50 of 0.1 nM[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: WNT974. CAS No. 1243244-14-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17545. | |
| L-Glutamic acid | L-Glutamic acid is an excitatory amino acid neurotransmitter that acts as an agonist for all subtypes of glutamate receptors (metabolic rhodophylline, NMDA, and AMPA). L-Glutamic acid has an agonist effect on the release of DA from dopaminergic nerve endings. L-Glutamic acid can be used in the study of neurological diseases. L-Glutamic acid acts at ionotropic and metabotropic glutamate receptors[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 56-86-0. Pack Sizes: 10 mM * 1 mL in Water; 1 g; 5 g. Product ID: HY-14608. | |
| L-Glutamic acid-1-13C | L-Glutamic acid-1-13C is the 13C-labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. Uses: Scientific research. Category: Signaling pathways. CAS No. 81201-99-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14608S1. | |
| L-Glutamic acid-13C5 | L-Glutamic acid-13C5 is the 13C-labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. Uses: Scientific research. Category: Signaling pathways. CAS No. 55443-55-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-14608S5. | |
| L-Glutamic acid-13C5,15N | L-Glutamic acid-13C5,15N is the 13C- and 15N-labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. Uses: Scientific research. Category: Signaling pathways. CAS No. 202468-31-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-14608S3. | |
| L-Glutamic acid-15N | L-Glutamic acid-15N is the 15N-labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 21160-87-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-14608S2. | |
| L-Glutamic acid-5-13C | L-Glutamic acid-5-13C is the 13C-labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. Uses: Scientific research. Category: Signaling pathways. CAS No. 81202-00-8. Pack Sizes: 5 mg. Product ID: HY-14608S6. | |
| L-Glutamic acid ammonium | L-Glutamic acid ammonium is an excitatory amino acid neurotransmitter that acts as an agonist for all subtypes of glutamate receptors (metabolic rhodophylline, NMDA, and AMPA). L-Glutamic acid ammonium has an agonist effect on the release of DA from dopaminergic nerve endings. L-Glutamic acid can be used in the study of neurological diseases. L-Glutamic acid ammonium acts at ionotropic and?metabotropic glutamate receptors[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 7558-63-6. Pack Sizes: 10 mM * 1 mL in Water; 1 g; 5 g; 10 g; 25 g. Product ID: HY-W419700. | |
| L-Glutamic acid-d3 | L-Glutamic acid-d3 is the deuterium labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. Uses: Scientific research. Category: Signaling pathways. CAS No. 203805-84-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-14608S8. | |
| L-Glutamic acid-d5 | L-Glutamic acid-d5 is the deuterium labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. Uses: Scientific research. Category: Signaling pathways. CAS No. 2784-50-1. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-14608S7. | |
| L-Glutamic acid monosodium salt | L-Glutamic acid monosodium salt is an excitatory amino acid neurotransmitter that acts as an agonist for all subtypes of glutamate receptors (metabolic rhodophylline, NMDA, and AMPA). L-Glutamic acid monosodium salt has an agonist effect on the release of DA from dopaminergic nerve endings. L-Glutamic acid monosodium salt can be used in the study of neurological diseases. L-Glutamic acid monosodium salt acts at ionotropic and metabotropic glutamate receptors[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 142-47-2. Pack Sizes: 10 mM * 1 mL in Water; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-14608A. | |
| L-Glutamine | L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Glutamic acid 5-amide. CAS No. 56-85-9. Pack Sizes: 25 g; 50 g; 100 g; 500 g; 1000 g. Product ID: HY-N0390. | |
| L-Glutamine-1-13C | L-Glutamine-1-13C is the 13C-labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na+-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Glutamic acid 5-amide-1-13C. CAS No. 159663-16-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-N0390S5. | |
| L-Glutamine-13C5 | L-Glutamine-13C5 is the 13C-labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na+-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Glutamic acid 5-amide-13C5. CAS No. 184161-19-1. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0390S1. | |
| L-Glutamine-13C5,15N2 | L-Glutamine-13C5,15N2 is the 13C- and 15N-labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na+-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Glutamic acid 5-amide-13C5,15N2. CAS No. 285978-14-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N0390S6. | |
| L-Glutamine-15N | L-Glutamine-15N is the 15N-labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na+-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Glutamic acid 5-amide-15N. CAS No. 80143-57-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0390S. | |
| L-Glutamine-15N-1 | L-Glutamine-15N-1 is the 15N-labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na+-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Glutamic acid 5-amide-15N-1. CAS No. 59681-32-2. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0390S9. | |
| L-Glutamine-15N2 | L-Glutamine-15N2 is the 15N-labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na+-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Glutamic acid 5-amide-15N2. CAS No. 204451-48-9. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg. Product ID: HY-N0390S8. | |
| L-Glutathione reduced | L-Glutathione reduced (GSH; γ-L-Glutamyl-L-cysteinyl-glycine) is an endogenous antioxidant and is capable of scavenging oxygen-derived free radicals. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GSH; γ-L-Glutamyl-L-cysteinyl-glycine. CAS No. 70-18-8. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-D0187. | |
| L-Glutathione reduced-13C2,15N | L-Glutathione reduced-13C2,15N is the 13C- and 15N-labeled L-Glutathione reduced. L-Glutathione reduced (GSH) is an endogenous antioxidant and is capable of scavenging oxygen-derived free radicals. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GSH-13C2,15N; γ-L-Glutamyl-L-cysteinyl-glycine-13C2,15N. CAS No. 815610-65-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-D0187S. | |
| L-Glutathione reduced (Standard) | L-Glutathione reduced (Standard) is the analytical standard of L-Glutathione reduced. This product is intended for research and analytical applications. L-Glutathione reduced (GSH; γ-L-Glutamyl-L-cysteinyl-glycine) is an endogenous antioxidant and is capable of scavenging oxygen-derived free radicals. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GSH (Standard); γ-L-Glutamyl-L-cysteinyl-glycine (Standard). CAS No. 70-18-8. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg; 500 mg. Product ID: HY-D0187R. | |
| L-Glycero-D-mannoheptose | L-Glycero-D-mannoheptose is a biochemical assay reagent. Uses: Scientific research. Category: Signaling pathways. CAS No. 4305-74-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W415916. | |
| L-Guluronic acid sodium salt | L-Guluronic acid sodium salt is an uronic acid that can produce D-glucosaccharic acid on oxidation[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 32510-76-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N7700C. | |
| LHF-535 | LHF-535 is an antiviral agent extracted from patent WO2013123215A2, Compound 38, has EC50s of <1 μM, <1 μM, <1 μM, and 1-10 μM for Lassa, Machupo, Junin, and VSVg virus, respectively[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1450929-77-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-112762. | |
| L-Histidine | L-Histidine is an essential amino acid for infants. L-Histidine is an inhibitor of mitochondrial glutamine transport. Uses: Scientific research. Category: Signaling pathways. CAS No. 71-00-1. Pack Sizes: 10 mM * 1 mL in Water; 500 mg; 1 g. Product ID: HY-N0832. | |
| L-Histidine-13C6,15N3 hydrochloride hydrate | L-Histidine-13C6,15N3 hydrochloride hydrate is the 13C- and 15N-labeled L-Histidine hydrochloride hydrate (HY-W014423). L-Histidine hydrochloride hydrate is an endogenous metabolite. L-Histidine hydrochloride hydrate scavenges hydroxyl radicals and singlet oxygen, regulate the absorption of zinc, copper and iron, exhibits anti-inflammatory and antioxidant activities. L-Histidine hydrochloride hydrate is blood brain barrier penetrable[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: H-His-OH-13C6,15N3 hydrochloride hydrate. CAS No. 202468-43-7. Pack Sizes: 1 mg. Product ID: HY-W014423S3. | |
| L-Histidine-13C6 hydrochloride hydrate | L-Histidine-13C6 (hydrochloride hydrate) is the 13C-labeled L-Histidine hydrochloride hydrate (HY-W014423). L-Histidine hydrochloride hydrate is an endogenous metabolite. L-Histidine hydrochloride hydrate scavenges hydroxyl radicals and singlet oxygen, regulate the absorption of zinc, copper and iron, exhibits anti-inflammatory and antioxidant activities. L-Histidine hydrochloride hydrate is blood brain barrier penetrable[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: H-His-OH-13C6 hydrochloride hydrate. CAS No. 201740-88-7. Pack Sizes: 5 mg. Product ID: HY-W014423S2. | |
| L-Histidine-13C hydrochloride hydrate | L-Histidine-13C hydrochloride hydrate is the 13C-labeled L-Histidine hydrochloride hydrate (HY-W014423). L-Histidine hydrochloride hydrate is an endogenous metabolite. L-Histidine hydrochloride hydrate scavenges hydroxyl radicals and singlet oxygen, regulate the absorption of zinc, copper and iron, exhibits anti-inflammatory and antioxidant activities. L-Histidine hydrochloride hydrate is blood brain barrier penetrable[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: H-His-OH-13C hydrochloride hydrate. CAS No. 2483735-43-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-W014423S. | |
| L-Histidine-d5 hydrochloride hydrate | L-Histidine-d5 hydrochloride hydrate is the deuterium labeled L-Histidine hydrochloride hydrate (HY-W014423). L-Histidine hydrochloride hydrate is an endogenous metabolite. L-Histidine hydrochloride hydrate scavenges hydroxyl radicals and singlet oxygen, regulate the absorption of zinc, copper and iron, exhibits anti-inflammatory and antioxidant activities. L-Histidine hydrochloride hydrate is blood brain barrier penetrable[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: H-His-OH-d5 hydrochloride hydrate. CAS No. 2483831-75-8. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W014423S4. | |
| L-Histidinol dihydrochloride | L-Histidinol dihydrochloride is an orally active histidyl-tRNA synthetase inhibitor. L-Histidinol dihydrochloride interferes with the initiation stage of protein synthesis, thus affecting cell proliferation and metabolism. L-Histidinol dihydrochloride has the effect of modulating the sensitivity of tumor cells to chemotherapeutic agents. L-Histidinol dihydrochloride reduces the toxicity of certain chemotherapeutic agents to normal tissues and enhance the sensitivity of tumor cells to chemotherapeutic agents[1][2][3][4][5][6][7][8][9][10]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1596-64-1. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 200 mg. Product ID: HY-W014233. | |
| L-Homocysteine | L-Homocysteine, an amino acid, is a homocysteine that has L configuration. Homocysteine is an essential intermediate in normal mammalian metabolism of methionine. L-Homocysteine induces upregulation of Cathepsin V that mediates vascular endothelial inflammation in hyperhomocysteinaemia[1][2]. Uses: Scientific research. Category: Induced disease models products. CAS No. 6027-13-0. Pack Sizes: 10 mM * 1 mL in Water; 25 mg; 50 mg; 100 mg. Product ID: HY-W010347. | |
| L-Homocysteine (Standard) | L-Homocysteine (Standard) is the analytical standard of L-Homocysteine. This product is intended for research and analytical applications. L-Homocysteine, an amino acid, is a homocysteine that has L configuration. Homocysteine is an essential intermediate in normal mammalian metabolism of methionine. L-Homocysteine induces upregulation of Cathepsin V that mediates vascular endothelial inflammation in hyperhomocysteinaemia[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 6027-13-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W010347R. | |
| L-Homocystine | L-Homocystine is the oxidized member of the L-homocysteine. Homocysteine is a pro-thrombotic factor, vasodilation impairing agent, pro-inflammatory factor and endoplasmatic reticulum-stress inducer used to study cardiovascular disease mechanisms. Uses: Scientific research. Category: Signaling pathways. CAS No. 626-72-2. Pack Sizes: 100 mg; 500 mg; 1 g. Product ID: HY-W011690. | |
| L-Homopropargylglycine | L-Homopropargylglycine is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. L-homopropargylglycine is an amino acid analog of methionine containing an alkyne moiety that can undergo a classic click chemical reaction with azide containing Alexa Fluor[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 98891-36-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 1 g. Product ID: HY-140345. | |
| L-Homopropargylglycine hydrochloride | L-Homopropargylglycine hydrochloride is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. L-homopropargylglycine hydrochloride is an amino acid analog of methionine containing an alkyne moiety that can undergo a classic click chemical reaction with azide containing Alexa Fluor[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 942518-19-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-140345A. | |
| L-Homoserine | L-Homoserine is a nonessential chiral amino acid and the precursor of L-Threonine (HY-N0658) and L-Methionine (HY-N0326). L-Homoserine wide applications in the fields of pharmaceutical, agricultural, cosmetic and fragrance industries[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 672-15-1. Pack Sizes: 50 mg; 100 mg; 1 g; 5 g; 10 g; 25 g; 50 g; 100 g. Product ID: HY-W002292. | |
| L-Homoserine lactone hydrochloride | L-Homoserine lactone hydrochloride is the core structural unit of the bacterial quorum-sensing signal molecule N-acyl-L-homoserine lactone (AHLs). As an important intermediate, L-Homoserine lactone hydrochloride acylated derivatives have potent immunosuppressive activity[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2185-3-7. Pack Sizes: 10 mM * 1 mL in DMSO; 25 g. Product ID: HY-W015800. | |
| LHRH free acid | LHRH (free acid), the luteinizing hormone-releasing hormone, is a neuropeptide hypothalamic. LHRH regulates reproduction. LHRH can be used for the research of cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 35263-73-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P4675. | |
| LHVS | LHVS is a potent, non-selective, irreversible, cell-permeable cysteine protease and cathepsin inhibitor. LHVS decreases actin ring formation. LHVS inhibits T. gondii invasion with an IC50 of 10 μM[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 170111-28-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-128971. | |
| L-Hydroxyproline | L-Hydroxyproline, one of the hydroxyproline (Hyp) isomers, is a useful chiral building block in the production of many pharmaceuticals. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid. CAS No. 51-35-4. Pack Sizes: 10 mM * 1 mL in Water; 500 mg; 5 g; 10 g; 25 g; 50 g; 100 g; 500 g. Product ID: HY-40135. | |
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