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 | |
|---|---|---|
| (R)-3-Hydroxytetradecanoic acid | (R)-3-Hydroxytetradecanoic acid is an ester product. Uses: Scientific research. Group: Signaling pathways. CAS No. 28715-21-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W288375. |  |
| (R)-4-Amino-3-hydroxybutyric acid | (R)-4-Amino-3-hydroxybutyric acid ((R)-GABOB) is a 4-aminobutyric acids ( GABAB ) agonist. (R)-4-Amino-3-hydroxybutyric acid is promising for research of nervous disorders [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (-)-γ-Amino-β-hydroxybutyric acid; (R)-GABOB; (-)-β-Hydroxy-GABA. CAS No. 7013-7-2. Pack Sizes: 100 mg; 250 mg; 500 mg; 1 g; 5 g. Product ID: HY-W005749. | |
| (R)-4-Benzyl-2-oxazolidinone | (R)-4-Benzyl-2-oxazolidinone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 102029-44-7. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g. Product ID: HY-W007664. | |
| (R)-4-Isopropyloxazolidin-2-one | (R)-4-Isopropyloxazolidin-2-one is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 95530-58-8. Pack Sizes: 10 g; 25 g. Product ID: HY-W002320. | |
| (R)-5,7-Dimethoxyflavanone | (R)-5,7-Dimethoxyflavanone shows potent antimutagenic activity against MeIQ mutagenesis in Ames test using the S. typhimurium TA100 and TA98 strains [1]. And (R)-5,7-Dimethoxyflavanone significantly and dose-dependently inhibits the inflammatory mediato [1]. Uses: Scientific research. Group: Natural products. CAS No. 1277188-85-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N5054. | |
| R715 | R715 is a selective bradykinin B1 receptor antagonist. R715 significantly attenuates the hyperalgesic effect developed in Streptozotocin(HY-13753)-diabetic mice [1]. Uses: Scientific research. Group: Peptides. CAS No. 185052-09-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-103290. | |
| R-96544 | R-96544 is an orally active 5-HT 2A receptor antagonist. R-96544 can inhibit platelet aggregation in vitro [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 167144-80-1. Pack Sizes: 5 mg. Product ID: HY-103136. | |
| Rabacfosadine | Rabacfosadine (GS-9219), a novel proagent of the nucleotide analogue PMEG, is designed as a cytotoxic agent that preferentially targets lymphoid cells. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-9219; VDC-1101. CAS No. 859209-74-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13640. | |
| Rabeprazole | Rabeprazole (LY307640) is a second-generation proton pump inhibitor ( PPI ) that irreversibly inactivates gastric H + /K + -ATPase. Rabeprazole induces apoptosis. Rabeprazole acts as an uridine nucleoside ribohydrolase ( UNH ) inhibitor with an IC 50 of 0.3 μM. Rabeprazole can be used for the research of gastric ulcerations and gastroesophageal reflux [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY307640. CAS No. 117976-89-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-B0656. | |
| Rabeprazole-d4 | Rabeprazole-d 4 is a deuterium labeled Rabeprazole. Rabeprazole is a second-generation proton pump inhibitor (PPI) that irreversibly inactivates gastric H+/K+-ATPase. Rabeprazole induces apoptosis. Rabeprazole acts as an uridine nucleoside ribohydrolase (UNH) inhibitor with an IC50 of 0.3 μM. Rabeprazole can be used for the research of gastric ulcerations and gastroesophageal reflux[1][2][3]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: LY307640-d4. CAS No. 934295-48-4. Pack Sizes: 1 mg. Product ID: HY-B0656S. | |
| Rabeprazole sodium | Rabeprazole sodium (LY307640 sodium) is a second-generation proton pump inhibitor ( PPI ) that irreversibly inactivates gastric H + /K + -ATPase. Rabeprazole sodium induces apoptosis. Rabeprazole sodium acts as an uridine nucleoside ribohydrolase ( UNH ) inhibitor with an IC 50 of 0.3 μM. Rabeprazole sodium can be used for the research of gastric ulcerations and gastroesophageal reflux [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY307640 sodium. CAS No. 117976-90-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0656A. | |
| (Rac)-1,2-Distearoyl-sn-Glycero-3-Phosphatidylglycerol sodium | (Rac)-1,2-Distearoyl-sn-Glycero-3-Phosphatidylglycerol (sodium) is an anionic phospholipid, can be used for drug delivery and the synthesis of liposomes [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 124011-52-5. Pack Sizes: 50 mg; 100 mg. Product ID: HY-112307A. | |
| Rac1-IN-3 | Rac1-IN-3 (Compound 2) is a Rac1 inhibitor with an IC 50 of 46.1 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 380470-06-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-156668. | |
| rac-BHFF | rac-BHFF is a potent and orally active allosteric enhancer of GABA B receptor [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 123557-91-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103519. | |
| (Rac)-BINAP | (Rac)-BINAP is the isomer of (R)-BINAP (HY-W017757), and can be used as an experimental control. (R)-BINAP is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. CAS No. 98327-87-8. Pack Sizes: 5 g; 10 g. Product ID: HY-Y0003. | |
| Racecadotril | Racecadotril (Acetorphan) is a neutral endopeptidase ( NEP ) inhibitor. Racecadotril and its active metabolite Thiorphan inhibits purified NEP activity from mouse brain with K i s of 4500 and 6.1 nM, , respectively. Antidiarrheal agent [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Acetorphan. CAS No. 81110-73-8. Pack Sizes: 10 mM * 1 mL; 200 mg; 1 g. Product ID: HY-17399. | |
| (Rac)-JBJ-04-125-02 | (Rac)-JBJ-04-125-02 is the racemate of JBJ-04-125-02. JBJ-04-125-02 is a potent, mutant-selective, allosteric and orally active EGFR inhibitor [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2140807-05-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-135805A. | |
| Raclopride | Raclopride is a dopamine D 2 / D 3 receptor antagonist with potential antipsychotic effects. Raclopride binds to D 2 and D 3 receptor s with K i s of 1.8 nM and 3.5 nM, respectively [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 84225-95-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-103414. | |
| (Rac)-Nebivolol | (Rac)-Nebivolol ((Rac)-R 065824) is a racemic isomer of Nebivolol. Nebivolol is a selective β1-adrenergic receptor antagonist with an IC 50 value of 0.8 nM. Nebivolol can prevent up-regulation of Nox2/NADPH oxidase and lipoperoxidation in the early stages of ethanol-induced cardiac toxicity. Vasodilatory activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (Rac)-R 065824. CAS No. 99200-09-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-B0203B. | |
| Racotumomab | Racotumomab (Anti-Human NGcGM3 Recombinant Antibody) is an anti-idiotype monoclonal antibody (MAb). Racotumomab reacts to Neu-glycolyl (NeuGc)-containing gangliosides, sulfatides, and other antigens expressed in tumors. Racotumomab is an active anticancer agent for lung cancer [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: 1E10. CAS No. 946832-34-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99254. | |
| (Rac)-Pyrotinib | (Rac)-Pyrotinib ((Rac)-SHR-1258) is the racemic form of Pyrotinib (HY-104065). Pyrotinib is a potent and selective dual EGFR/HER2 receptor inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (Rac)-SHR-1258. CAS No. 1246089-97-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-104065A. | |
| (Rac)-Rhododendrol | (Rac)-Rhododendrol ((Rac)-Betuligenol) is an aromatic compound with pro-oxidant activity. (Rac)-Rhododendrol may be useful in the suppression of liver diseases. (Rac)-Rhododendrol can be toxic to melanocytes, leading to cell death. The metabolite of (Rac)-Rhododendrol, RD-quinone, is cytotoxic and causes enzyme inactivation and endoplasmic reticulum stress by binding to thiol proteins. (Rac)-Rhododendrol-derived melanin exhibits potent pro-oxidant activity and may cause oxidative stress [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (Rac)-Betuligenol. CAS No. 69617-84-1. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-136913. | |
| RAD51-IN-3 | RAD51-IN-3 is a Rad51 inhibitor extracted from patent WO2019051465A1, compound Example 66A [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2301084-99-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136604. | |
| Radafaxine hydrochloride | Radafaxine hydrochloride (GW-353162A) is a DAT (dopamine transporter) and NET(norepinephrine transporter) transporters inhibitor, and nAChR family modulator. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (S,S)-Hydroxybupropion hydrochloride; GW-353162A; BW-306U. CAS No. 106083-71-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-17590. | |
| Rademikibart | Rademikibart (CBP-201) is a human monoclonal antibody targeting IL-4Rα with a KD of 20.7 pM when binding to human IL-4Rα epitopes. Rademikibart does not bind to IL-4Rα from other species. Rademikibart inhibits IL-4 and IL-13-mediated STAT6 signaling, TF-1 cell proliferation and TARC production in PBMCs. Rademikibart has the potential for moderate-to-severe Th2 inflammatory diseases research [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: CBP-201. CAS No. 2648260-80-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990090. | |
| Radicicol | Radicicol is an inhibitor of Hsp90 with an IC 50 value < 1 μM, and leads to proteasomal degradation [1]. Radicicol exhibits inhibition on PDK with IC 50 s of 230 μM ( PDK1 ) and 400 μM ( PDK3 ). Radicicol is an antifungal and antimalarial antibiotic, impairs mitochondrial replication by targeting P. falciparum topoisomerase VIB [2]. Radicicol is also an inhibitor of fat mass and obesity-associated protein ( FTO ), with an IC 50 value of 16.04 μM [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Monorden. CAS No. 12772-57-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N6769. | |
| Radiprodil | Radiprodil (RGH-896) is an orally active and selective NMDA NR2B antagonist. A potential therapeutic agent in treatment of neuropathic pain and possibly other chronic pain conditions [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RGH-896. CAS No. 496054-87-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14777. | |
| Radotinib | Radotinib(IY-5511) is a novel and selective BCR-ABL1 tyrosine kinase inhibitor with IC50 of 34 nM for wild-type BCR-ABL1 kinase. Uses: Scientific research. Group: Signaling pathways. Alternative Names: IY-5511. CAS No. 926037-48-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15728. | |
| Raffinose | Raffinose (Melitose), a non-digestible short-chain oligosaccharide, is a trisaccharide composed of galactose, glucose, and fructose and can be found in many plants. Raffinose (Melitose) can be hydrolyzed to D-galactose and sucrose by the enzyme α-galactosidase (α-GAL) [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Melitose. CAS No. 512-69-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N7088. | |
| Rafigrelide | Rafigrelide is a platelet-lowering agent, and also has antithrombotic properties. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 3,3-Dimethylanagrelide. CAS No. 1029711-88-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-U00383. | |
| Raf inhibitor 2 | Raf inhibitor 2 is a potent raf kinase (IC 50 <1.0 μM) inhibitor, compound 32, extracted from patent EP1003721B1. Raf inhibitor 2 can be used for cancer research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 220904-99-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-109574. | |
| Rafoxanide | Rafoxanide is a poent, orally active halogenated salicylaniline agent with antiparasitic activity. Rafoxanide interferes with energy metabolism in trematodes by uncoupling oxidative phosphorylation. Rafoxanide is also found to be a potent inhibitor of the BRAF V600E mutant protein , which is important in colorectal cancer. Rafoxanide can be used for the control of infestation with Hemonchus species or Fasciola species in sheep and cattle as well as Oestrus ovis in sheep. Rafoxanide can also be used for cancer research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 22662-39-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-17598. | |
| RAGE antagonist peptide | RAGE antagonist peptide is an advanced glycation end products (RAGE) antagonist. RAGE antagonist peptide prevents RAGE from binding with several of its most important ligands, including HMGB-1, S100P, and S100A4. RAGE antagonist peptide (RAP) possesses anti-tumor and anti-inflammatory activities [1] [2]. Uses: Scientific research. Group: Peptides. CAS No. 1092460-91-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2268. | |
| Ralfinamide | Ralfinamide (FCE-26742A) is an orally available Na + blocker derived from α-aminoamide, with function of suppressing pain [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FCE-26742A. CAS No. 133865-88-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-101437. | |
| Ralinepag | Ralinepag is a potent, orally bioavailable and non-prostanoid prostacyclin (IP) receptor agonist, with EC 50 s of 8.5 nM, 530 nM and 850 nM for human and rat IP receptor and human DP1 receptor, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: APD811. CAS No. 1187856-49-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16751. | |
| Raloxifene | Raloxifene (Keoxifene) is a benzothiophene-derived selective estrogen receptor modulator (SERM). Raloxifene has estrogen-agonistic effects on bone and lipids and estrogen-antagonistic effects on the breast and uterus. Raloxifene is used for breast cancer and osteoporosis research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Keoxifene; LY156758 free base; LY139481. CAS No. 84449-90-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-13738. | |
| Raloxifene hydrochloride | Raloxifene hydrochloride (Keoxifene hydrochloride) is a second generation selective and orally active estrogen receptor modulator. Raloxifene hydrochloride produces estrogen-agonistic effects on bone and lipid metabolism and estrogen-antagonistic effects on uterine endometrium and breast tissue [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Keoxifene hydrochloride; LY156758; LY139481 hydrochloride. CAS No. 82640-04-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-13738A. | |
| Raloxifene (hydrochloride) (Standard) | Raloxifene (hydrochloride) (Standard) is the analytical standard of Raloxifene (hydrochloride). This product is intended for research and analytical applications. Raloxifene hydrochloride (Keoxifene hydrochloride) is a second generation selective and orally active estrogen receptor modulator. Raloxifene hydrochloride produces estrogen-agonistic effects on bone and lipid metabolism and estrogen-antagonistic effects on uterine endometrium and breast tissue [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Keoxifene (hydrochloride)(Standard); LY156758(Standard); LY139481 (hydrochloride) (Standard). CAS No. 82640-04-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13738AR. | |
| (R)-(-)-α-Methylhistamine dihydrochloride | (R)-(-)-α-Methylhistamine dihydrochloride is a potent, selective and brain-penetrant agonist of H3 histamine receptor, with a K d of 50.3 nM [1] [2]. (R)-(-)-α-Methylhistamine dihydrochloride can enhance memory retention, attenuates memory impairment in rats [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 75614-89-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-W014941. | |
| (R)-(-)-α-Phellandrene | (R)-(-)-α-Phellandrene ((-)-α-Phellandrene) is an the (R)-(-)-stereoisomer of α-phellandrene. α-phellandrene is an orally active cyclic monoterpene that attenuates inflammatory response, and induces DNA damage [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: (-)-α-Phellandrene. CAS No. 4221-98-1. Pack Sizes: 1 mL. Product ID: HY-N9487. | |
| Raltegravir | Raltegravir is a potent integrase (IN) inhibitor, used to treat HIV infection. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-0518. CAS No. 518048-05-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-10353. | |
| Raltegravir potassium | Raltegravir (MK 0518) potassium is a potent integrase (IN) inhibitor, used to treat HIV infection. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK 0518 potassium. CAS No. 871038-72-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10353A. | |
| Raltitrexed | Raltitrexed is an antimetabolite agent used in chemotherapy, acting by inhibiting thymidylate synthase. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ZD1694; D1694; ICI-D1694. CAS No. 112887-68-0. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10821. | |
| Raludotatug | Raludotatug is a humanized immunoglobulin G1-kappa, anti-CDH6 monoclonal antibody. Raludotatug is an antineoplastic [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2610074-56-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990028. | |
| Ramatroban | Ramatroban is a selective thromboxane A 2 ( TxA 2 , IC 50 =14 nM) antagonist, which also antagonizes CRTH2 ( IC 50 =113 nM) by inhibiting PGD 2 binding. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY u3405. CAS No. 116649-85-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0745. | |
| Ramelteon | Ramelteon is a potent, highly selective, and orally active agonist of MT1/MT2 with Ki values of 14 and 112 pM, respectively. Ramelteon has the potential for the research of insomnia. Ramelteon consistently reduces sleep onset after long-term treatment, with no next-morning residual effects or rebound insomnia or withdrawal symptoms upon discontinuation [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-375. CAS No. 196597-26-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-A0014. | |
| (R)-Aminocarnitine | (R)-Aminocarnitine (Emeriamine) is a fatty acid oxidation inhibitor. (R)-Aminocarnitine reduces hyperglycaemia and ketosis. (R)-Aminocarnitine can be used in the study of metabolic diseases [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Emeriamine. CAS No. 98063-21-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-126221A. | |
| (R)-(+)-Aminoglutethimide | (R)-(+)-Aminoglutethimide is a potent and orally active aromatase inhibitor. (R)-(+)-Aminoglutethimide has the potential for the research of breast cancer [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: d-Aminoglutethimide. CAS No. 55511-44-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W392925. | |
| Ramipril | Ramipril (HOE-498) is an angiotensin-converting enzyme (ACE) inhibitor with IC 50 of 5 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HOE-498. CAS No. 87333-19-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B0279. | |
| (R)-Amlodipine-d4 | (R)-Amlodipine-d 4 is the deuterium labeled (R)-Amlodipine[1]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1346616-97-4. Pack Sizes: 500 μg; 1 mg. Product ID: HY-B0317DS. | |
| Ramoplanin | Ramoplanin is a broad-spectrum lipoglycodepsipeptide antibiotic derived from the Actinoplanes spp with with activity against gram-positive bacteria [1] [2]. Uses: Scientific research. Group: Peptides. CAS No. 76168-82-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129034. | |
| Ramosetron Hydrochloride | Ramosetron (YM060 free base) Hydrochloride is an orally active 5-HT 3 antagonist that improves dysphoria, interference with activity and food avoidance. Ramosetron Hydrochloride is promising for research of irritable bowel syndrome with diarrhea [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: YM060. CAS No. 132907-72-3. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0595. | |
| Ramucirumab (anti-VEGFR) | Ramucirumab (anti-VEGFR) is a human VEGFR-2 antagonist for the treatment of solid tumors. Ramucirumab (anti-VEGFR) is a recombinant human immunoglobulin G1 monoclonal antibody that binds to the extracellular binding domain of VEGFR-2 and prevents the binding of VEGFR ligands: VEGF-A, VEGF-C, and VEGF-D. Ramucirumab (anti-VEGFR) is also an angiogenesis inhibitor [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 947687-13-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P9920A. | |
| Ranibizumab (anti-VEGF) | Ranibizumab (RG-6321) (anti-VEGF) is a humanized anti-VEGF monoclonal antibody fragment and can recognize all VEGF-A isoforms (VEGF110, VEGF121, and VEGF165) [1]. Ranibizumab (anti-VEGF) slows vision loss in vivo and is used for wet age-related macular degeneration (AMD) research [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: RG-6321 (anti-VEGF). CAS No. 347396-82-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9951A. | |
| Ranitidine | Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC 50 of 3.3 μM that inhibits gastric secretion. Ranitidine is a weak inhibitor of CYP2C19 and CYP2C9 [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 66357-35-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-B0693. | |
| Ranitidine-d6 hydrochloride | Ranitidine-d 6 (hydrochloride) is the deuterium labeled Ranitidine hydrochloride. Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM that inhibits gastric secretion. Ranitidine hydrochloride is a weak inhibitor of CYP2C19 and CYP2C9[1][2]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1185238-09-8. Pack Sizes: 1 mg. Product ID: HY-B0281AS. | |
| Ranitidine hydrochloride | Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist with an IC 50 of 3.3 μM that inhibits gastric secretion. Ranitidine hydrochloride is a weak inhibitor of CYP2C19 and CYP2C9 [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 66357-59-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0281A. | |
| Ranolazine | Ranolazine (CVT 303) is an anti-angina drug that achieves its effects by inhibiting the late phase of inward sodium current ( I Na and I Kr with IC 50 values of 6 μM and 12 μM, respectively) without affecting heart rate or blood pressure (BP) [1] [2]. Ranolazine is also a partial fatty acid oxidation (FAO) inhibitor [3]. Antianginal agent. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CVT 303; RS 43285-003. CAS No. 95635-55-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-B0280. | |
| Ranolazine dihydrochloride | Ranolazine dihydrochloride (CVT 303 dihydrochloride) is an anti-angina agent that achieves its effects by inhibiting the late phase of inward sodium current ( I Na and I Kr with IC 50 values of 6 μM and 12 μM, respectively) without affecting heart rate or blood pressure (BP) [1] [2]. Ranolazine dihydrochloride is also a partial fatty acid oxidation inhibitor [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CVT 303 dihydrochloride; RS 43285. CAS No. 95635-56-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg; 1 g; 5 g. Product ID: HY-17401. | |
| Rapacuronium bromide | Rapacuronium bromide (Org 9487), a non-depolarizing neuromuscular blocker, is an allosteric modulator of muscarinic acetylcholine receptor (mAChR) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Org 9487. CAS No. 156137-99-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16423. | |
| Rapamycin | Rapamycin (Sirolimus; AY 22989) is a potent and specific mTOR inhibitor with an IC 50 of 0.1 nM in HEK293 cells. Rapamycin binds to FKBP12 and specifically acts as an allosteric inhibitor of mTORC1 [1]. Rapamycin is an autophagy activator, an immunosuppressant [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Sirolimus; AY-22989. CAS No. 53123-88-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g; 2 g; 5 g. Product ID: HY-10219. | |
| Rapamycin-d3 | Rapamycin-d 3 is the deuterium labeled Rapamycin. Rapamycin is a potent and specific mTOR inhibitor with an IC 50 of 0.1 nM in HEK293 cells. Rapamycin binds to FKBP12 and specifically acts as an allosteric inhibitor of mTORC1. Rapamycin is an autophagy activator, an immunosuppressant [1] [2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Sirolimus-d3; AY-22989-d3. CAS No. 392711-19-2. Pack Sizes: 500 μg; 1 mg. Product ID: HY-10219S. | |
| Rapastinel Trifluoroacetate | Rapastinel Trifluoroacetate (GLYX-13 Trifluoroacetate) is an NMDA receptor modulator with glycine-site partial agonist properties. Rapastinel Trifluoroacetate has the potential for major depressive disorder treatment. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GLYX-13 Trifluoroacetate. CAS No. 1435786-04-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-16728B. | |
| Rasagiline | Rasagiline (R-AGN1135) is a highly potent selective irreversible mitochondrial monoamine oxidase ( MAO ) inhibitor with IC 50 s of 4.43 nM and 412 nM for rat brain MAO B and A activity, respectively [1]. Rasagiline is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (R)-AGN1135; TVP1012. CAS No. 136236-51-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 250 mg. Product ID: HY-14605A. | |
| Rasagiline mesylate | Rasagiline (R-AGN1135) mesylate is a highly potent selective irreversible mitochondrial monoamine oxidase ( MAO ) inhibitor with IC 50 s of 4.43 nM and 412 nM for rat brain MAO B and A activity, respectively [1]. Rasagiline (mesylate) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (R)-AGN1135 mesylate; TVP1012 mesylate. CAS No. 161735-79-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14605. | |
| Rasburicase | Rasburicase is a recombinant urate oxidase and a hyperuricemia inhibitor. Rasburicase converts uric acid into allantoin, making it easier to be cleared by the kidneys and improving the elevated level of uric acid in the blood [1]. Uses: Scientific research. Group: Natural products. CAS No. 134774-45-1. Pack Sizes: 1 mg. Product ID: HY-108844. | |
| Raspberry ketone | Raspberry ketone is a major aromatic compound of red raspberry, widely used as a fragrance in cosmetics and as a flavoring agent in foodstuff; also shows PPAR-α agonistic activity. Uses: Scientific research. Group: Natural products. Alternative Names: Frambione; 4-(4-Hydroxyphenyl)-2-butanone. CAS No. 5471-51-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N1426. | |
| Rat CGRP-(8-37) | Rat CGRP-(8-37) (VTHRLAGLLSRSGGVVKDNFVPTNVGSEAF) is a highly selective CGRP receptor antagonist. Uses: Scientific research. Group: Peptides. CAS No. 129121-73-9. Pack Sizes: 500 μg; 1 mg; 5 mg. Product ID: HY-P0209. | |
| (R)-(+)-Atenolol | (R)-(+)-Atenolol is the less active enantiomer of the (R,S)-atenolol. (R,S)-atenolol is a β-adrenergic receptor antagonist [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 56715-13-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-B2111. | |
| Rauwolscine | Rauwolscine is a selective α2-adrenoceptor antagonist that inhibits tumor growth and induces apoptosis [1]. Uses: Scientific research. Group: Natural products. Alternative Names: α-Yohimbine; Corynanthidine; Isoyohimbine. CAS No. 131-03-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-12710. | |
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