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 | |
|---|---|---|
| STF-31 | STF-31 is a selective inhibitor of glucose transporter 1 (GLUT1), with an IC50 of 1 ?M. STF-31 is also a NAMPT inhibitor. STF-31 inhibits glucose uptake in renal cell carcinoma (RCC) 4 cells[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 724741-75-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18728. |  |
| STF-62247 | STF-62247 is an autophagy inducer that selectively cytotoxic to VHL-deficient renal cell carcinoma ( IC 50 of 0.625 μM and 16 μM in RCC4 and RCC4/VHL cells, respectively) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 315702-99-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-100746. | |
| STh | STh, an Escherichia coli heat-stable toxin, is a 19 amino acid polypeptide encompassing three disulfide bridges. STh is an antigen of interest in the search for a broad coverage enterotoxigenic Escherichia coli (ETEC) vaccine [1]. Uses: Scientific research. Group: Peptides. CAS No. 118447-40-8. Pack Sizes: 1 mg. Product ID: HY-P2695. | |
| (S)-Thalidomide | (S)-Thalidomide ((S)-(-)-Thalidomide) is the S-enantiomer of Thalidomide. (S)-Thalidomide has immunomodulatory, anti-inflammatory, antiangiogenic and pro-apoptotic effects [1] [2] [3]. (S)-Thalidomide induces teratogenic effects by binding to cereblon (CRBN) [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (S)-(-)-Thalidomide. CAS No. 841-67-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14658A. | |
| (S)-Thioctic acid | (S)-Thioctic acid ((S)-lipoic acid; (S)-5-(1,2-Dithiolan-3-yl)pentanoic acid) is a biochemical reagent that can be used as a biological material or organic compound for life science related research [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: (S)-lipoic acid; (S)-5-(1,2-Dithiolan-3-yl)pentanoic acid. CAS No. 1077-27-6. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-W014590. | |
| Stigmasta-4,22-dien-3-one | Stigmasta-4,22-dien-3-one is an antitubercular agent. Stigmasta-4,22-dien-3-one shows cytotoxicity against human HT1080 tumoral cell line with an IC 50 of 0.3 mM [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 20817-72-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N9596. | |
| Stigmastanol | Stigmastanol is the 6-amino derivative isolated from Hypericum riparium. Hypericum riparium A. Chev. is a Cameroonian medicinal plant belonging to the family Guttiferae [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 83-45-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113494. | |
| Stigmasterol | Stigmasterol is a plant sterol which has been focused on the cholesterol-lowering activity and is valued as an anti-stiffness factor in the therapy of rheumatic diseases. Uses: Scientific research. Group: Natural products. CAS No. 83-48-7. Pack Sizes: 100 mg. Product ID: HY-N0131. | |
| Stilbamidine dihydrochloride | Stilbamidine dihydrochloride is a diamidine compound derived from Stilbene and used chiefly in the form of its crystalline isethionate salt in treating various fungal infections. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ba 2652 dihydrochloride; Stilbamidin dihydrochloride. CAS No. 6935-63-3. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-U00007A. | |
| (S)-Timolol maleate | (S)-Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic β-adrenoceptor blocker. (S)-Timolol Maleate is widely used as standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. (S)-Timolol Maleate can be used for hypertension, angina pectoris and myocardial infarction [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (S)-L-714,465 maleate; MK 950. CAS No. 26921-17-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg. Product ID: HY-17380. | |
| STING agonist-1 | STING agonist-1 (G10) is human-specific STING agonist that elicits antiviral activity against emerging Alphaviruses. G10 potently blocks replication of Alphavirus species Venezuelan Equine Encephalitis Virus (VEEV) with IC 90 of 24.57 μM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: G10. CAS No. 702662-50-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-19711. | |
| STING agonist-20 | STING agonist-20 (compound 95) is a potent STING agonist used in the synthesis of XMT-2056. STING agonist-20 can be used as a vaccine adjuvant in the study of cancer and other inflammatory, immune diseases[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2591300-72-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-148068. | |
| STING agonist-26 | STING agonist-26 (CF508) is a non-nucleotide small-molecule STING agonist. STING agonist-23 activates STING, increases phosphorylation of STING , TBK1 and IRF3. STING agonist-23 promotes the levels of IFN-β , IL-6 , CXCL-10 , TNF-α , ISG-15 , and CCL-5 in tumor cells. STING agonist-23 exhibits activity against SARS-CoV series strains [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2868261-48-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-152959. | |
| STING agonist-3 | STING agonist-3, extracted from patent WO2017175147A1 (example 10), is a selective and non-nucleotide small-molecule STING agonist with a pEC50 and pIC50 of 7.5 and 9.5, respectively. STING agonist-3 has durable anti-tumor effect and tremendous potential to improve treatment of cancer[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2138299-29-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103665. | |
| STING antagonist 1 | STING antagonist 1 is an antagonist of STING with an IC50 of 3.8 nM. STING antagonist 1 can be used in the research of autoimmune diseases, inflammatory diseases, and others[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3036981-21-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-162664. | |
| STING-IN-2 | STING-IN-2 (C-170) is a potent and covalent STING inhibitor. STING-IN-2 efficiently inhibits both mouse STING (mmSTING) and human STING (hsSTING). STING-IN-2 can be used for autoinflammatory disease research[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 346691-38-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-138682. | |
| STING ligand-3 | STING ligand-3 is a Ligand for Target Protein for PROTAC activity control. STING ligand-3 can be used to synthesize Anti-inflammatory agent 70 (HY-157570) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2762552-73-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-47709. | |
| Stiripentol | Stiripentol (STP) is an anticonvulsant agent, which can inhibit N-demethylation of CLB to NCLB mediatated by CYP3A4 (noncompetitively) and CYP2C19 (competitively) with K i of 1.59±0.07 and 0.516±0.065 μM and IC 50 of 1.58 and 3.29 μM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BCX2600. CAS No. 49763-96-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103392. | |
| STL001 | STL001 is potent and selective FOXM1 inhibitor. STL001 induces the translocation of nuclear FOXM1 to the cytoplasm and promotes its autophagic degradation. STL001 sensitizes human cancers to a broad-spectrum of cancer therapies [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3047493-70-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-158420. | |
| STL1267 | STL1267 is a potent and cross-the-blood-brain barrier REV-ERB agonist with a Ki value of 0.16 μM for REV-ERB?. STL1267 shows no cytotoxicity. STL1267 inhibits the gene expression of BMAL1[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1429024-58-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148711. | |
| STL127705 | STL127705 (Compound L) is a potent Ku 70/80 heterodimer protein inhibitor with an IC50 of 3.5 ?M. STL127705 interferes the binding of Ku70/80 to DNA and by inhibits the activation of the DNA-PKCS kinase. STL127705 shows antiproliferative and anticancer activity. STL127705 induces apoptosis[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1326852-06-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-122727. | |
| STM2457 | STM2457 is a first-in-class, highly potent, selective and orally active METTL3 inhibitor with an IC50 of 16.9 nM. STM2457 can be used for the research of acute myeloid leukaemia (AML)[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2499663-01-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-134836. | |
| STM3006 | STM3006 is a highly potent, selective, and orally active inhibitor of METTL3 (IC50: 5 nM). STM3006 can reduce the m6A level, promote the formation of dsRNA, trigger a cell-intrinsic interferon response, and enhance the killing effect of T cells on tumors. STM3006 has anti-tumor activity, and its combination with anti-PD-1 immunotherapy yields better results[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2499664-52-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156773. | |
| (S)-TNG260 | (S)-TNG260 is an isomer of TNG260 (HY-153358). TNG260 is a CoREST selective deacetylase (CoreDAC) inhibitor. TNG260 inhibits HDAC1 with 10-fold selectivity over HDAC3. TNG260 causes HDAC1 inhibition and reverses anti-PD1 resistance driven by STK11 deletion. TNG260 reduces intratumoral infiltration of neutrophils. TNG260 exhibits immune-mediated cell killing. Uses: Scientific research. Group: Signaling pathways. CAS No. 2935964-93-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153358A. | |
| STO-609 | STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KK? and CaM-KK?, respectively. STO-609 inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 ~0.02 g/ml. Uses: Scientific research. Group: Signaling pathways. CAS No. 52029-86-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19805. | |
| Streptavidin | Streptavidin is a ~60 kDa homotetramer. Streptavidin binds four molecules of biotin with the highest affinity. The binding affinity of biotin to streptavidin is one of the highest reported for a non-covalent interaction to date, with a K D ~ 0.01 pM [1]. Streptavidin has an immunosuppressive role [2]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 9013-20-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3152. | |
| Streptolysin O | Streptolysin O, a group A streptococcal toxin, is a well-characterized oxygen-labile prototype of a cholesterol-binding bacterial exotoxin. Streptolysin O causes both lysis of cells and cardiotoxicity. Streptolysin O is widely used for the controlled permeabilization of cell membranes. Streptolysin O exists in two forms, a reduced active state and an oxidized reversibly inactive state [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 98072-47-0. Pack Sizes: 25 KU. Product ID: HY-135416. | |
| Streptomycin | Streptomycin (Agrept) is an effective antibiotic against M. tuberculosis , is used for the research of tuberculosis (TB). Streptomycin also is a bacteriocidal agent that can be used for the research of a number of bacterial infections. Streptomycin can bind strongly to nucleic acids, interferes and blocks protein synthesis while permitting continued RNA and DNA synthesis. Streptomycin, as a common antibiotic used in culture media, also is a blocker of stretch-activated and mechanosensitive ion channels in neurons and cardiac myocytes [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Agrept; Agrimycin; Streptomycin A. CAS No. 57-92-1. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1906. | |
| Streptomycin sulfate | Streptomycin sulfate is an aminoglycoside antibiotic, that inhibits protein synthesis. Uses: Scientific research. Group: Natural products. CAS No. 3810-74-0. Pack Sizes: 10 mM * 1 mL; 500 mg; 10 g; 50 g. Product ID: HY-B0472. | |
| Streptonigrin | Streptonigrin (Bruneomycin), a natural product produced by Streptomyces flocculus , possesses both anti-tumor and anti-bacterial activity. Streptonigrin acts as a pan-PAD inhibitor with IC 50 s of 48.3±34.2 μM, 26.1±0.3 μM, 0.43±0.03 μM, and 2.5±0.4 μM for PAD1 , PAD2 , PAD3 , and PAD4 , respectively [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Bruneomycin. CAS No. 3930-19-6. Pack Sizes: 500 μg; 1 mg. Product ID: HY-124586. | |
| Streptozotocin | Streptozotocin (Streptozocin; STZ) is an antibiotic widely used in experimental animal models of induced diabetes. Streptozotocin enters B cells via the glucose transporter (GLUT2) and causes the alkylation of DNA ( DNA-methylating ). Streptozotocin can induce the apoptosis of β cells [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Streptozocin; NSC-85998; U 9889. CAS No. 18883-66-4. Pack Sizes: 100 mg; 500 mg. Product ID: HY-13753. | |
| Strictinin | Strictinin is a phenolic compound isolated from Pu'er teas. Strictinin has potential antiviral, antibacterial and laxative activities. Strictinin occurs by accelerating intestinal transit rather than enhancing gastric emptying, increasing food intake, or inducing diarrhea in rats. Uses: Scientific research. Group: Natural products. CAS No. 517-46-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-135319. | |
| S-Trityl-L-cysteine | S-Trityl-L-cysteine (NSC 83265) is a selective and allosteric kinesin Eg5 inhibitor with an IC50 of 1 ?M for the inhibition of basal ATPase activity and 140 nM for the microtubule-activated ATPase activity. S-Trityl-L-cysteine has antitumor activities[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NSC 83265; S-Tritylcysteine; 3-Tritylthio-L-alanine. CAS No. 2799-7-7. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-W011102. | |
| (S)-Trolox | (S)-Trolox is an analogue of vitamin E, in which the phytyl chain is replaced with a carboxyl group. (S)-Trolox is frequently used as a model compound for studies of structural features, as well as a standard for evaluation of antioxidant activity. (S)-Trolox has potent and specific neuroprotective and antioxidant effects[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 53174-06-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-101445B. | |
| Strontium chloride,anhydrous grade,99.99% metals basis | Strontium chloride,anhydrous grade,99.99% metals basis is a biochemical reagent. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 10476-85-4. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-22009A. | |
| Strontium Ranelate | Strontium Ranelate (S12911) is an antiosteoporotic agent that acts by reducing bone resorption and promoting bone formation, thereby inducing a positive bone balance. Strontium Ranelate can also activate the calcium-sensing receptor (CaSR) in non skeletal cells, resulting in the activation of inositol 1, 4, 5-triphosphate production and mitogen-activated protein kinase signaling [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Distrontium renelate; S12911. CAS No. 135459-87-9. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-17397. | |
| Strophanthidin | Strophanthidin is a naturally available cardiac glycoside [1]. Strophanthidin 0.1 and 1 nmol/L increases and 1~100 μmol/L inhibits the Na+/K+-ATPase activities, but Strophanthidin 10 and 100 nmol/L does not affect Na+/K+-ATPase activities in cardiac sarcolemmal [2]. Strophanthidin increases both diastolic and systolic intracellular Ca 2+ concentration [3]. Uses: Scientific research. Group: Natural products. CAS No. 66-28-4. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-114252. | |
| STX-0119 | STX-0119 is a selective, orally active STAT3 dimerization inhibitor. STX-0119 inhibits STAT3 transcription with an IC50 of 74 ?M[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 851095-32-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103692. | |
| STX-478 | STX-478 (compound 80) is an oral CNS-penetrant allosteric mutant-selective PI3Kα inhibitor. STX-478 shows robust and durable tumor regression and can be used in cancer research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2883540-92-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156681. | |
| STX-721 | STX-721 is a mutant-selective inhibitor of EGFR and HER2 Exon 20 insertion (ex20ins) mutants [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2765525-82-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-157229. | |
| (±)-Stylopine | (±)-Stylopine (Tetrahydrocoptisine) is an alkaloid compound originally isolated from Corydalis tubers that exhibits anti-inflammatory and anti-parasitic activities [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Tetrahydrocoptisine. CAS No. 4312-32-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N0924. | |
| (±)-Stylopine hydrochloride | (±)-Stylopine (Tetrahydrocoptisine) hydrochloride is an alkaloid compound originally isolated from Corydalis tubers that exhibits anti-inflammatory and anti-parasitic activities [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Tetrahydrocoptisine hydrochloride. CAS No. 96087-21-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N0924A. | |
| SU0268 | SU0268 is a potent and specific inhibitor of 8-Oxoguanine DNA glycosylase 1 (OGG1). SU0268 regulates inflammatory responses during Pseudomonas aeruginosa infection[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2210228-45-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139056. | |
| SU056 | SU056 is a YB-1 inhibitor. SU056 induces cell-cycle arrest, apoptosis, and inhibits cell migration in ovarian cancer cells. SU056 interacts with YB-1 and inhibits and its associated downstream proteins and pathways. SU056 can enhance the cytotoxic effects of Paclitaxel (HY-B0015)[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2376580-08-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-150231. | |
| SU11274 | SU11274 is a selective Met inhibitor with IC 50 of 10 nM, but has no effects on PGDFRβ, EGFR or Tie2. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PKI-SU11274. CAS No. 658084-23-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12014. | |
| SU11652 | SU11652 is a potent receptor tyrosine kinase (RTK) inhibitor. SU11652 also inhibits several members of the split kinase family of RTKs, including VEGFR, FGFR, PDGFR, and Kit. SU11652 can be uesd for spontaneous cancers expressing Kit mutations research[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 326914-10-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112452. | |
| SU1261 | SU1261 is an IKK inhibitor with Ki values of 10 nM and 680 nM for IKK? and IKK?, respectively. SU1261 can inhibit non-canonical NF-?B signaling in U2OS osteosarcoma cells[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3061890-98-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-169053. | |
| SU14813 | SU14813 is a multi-targeted receptor tyrosine kinases inhibitor with IC 50 s of 50, 2, 4, 15 nM for VEGFR2 , VEGFR1 , PDGFRβ and KIT. Uses: Scientific research. Group: Signaling pathways. CAS No. 627908-92-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10501. | |
| SU14813 maleate | SU14813 maleate is a multi-targeted receptor tyrosine kinases inhibitor with IC 50 s of 50, 2, 4, 15 nM for VEGFR2 , VEGFR1 , PDGFRβ and KIT. Uses: Scientific research. Group: Signaling pathways. CAS No. 849643-15-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-10501A. | |
| SU1498 | SU1498 (AG 1498) is a selective inhibitor of the VEGFR2 ; inhibits Flk-1 with an IC 50 of value of 700 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AG 1498; Tyrphostin SU 1498. CAS No. 168835-82-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19326. | |
| SU 5402 | SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC 50 of 20 nM, 30 nM, and 510 nM for VEGFR2 , FGFR1 , and PDGFRβ , respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 215543-92-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10407. | |
| SU6656 | SU6656 is a Src family kinases inhibitor with IC 50 s of 280, 20, 130, 170 nM for Src, Yes, Lyn, and Fyn, respectively. SU6656 inhibits FAK phosphorylation at Y576/577, Y925, Y861 sites. SU6656 also inhibits p-AKT. Uses: Scientific research. Group: Signaling pathways. CAS No. 330161-87-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0789. | |
| SU9516 | SU9516 is a potent CDK2 inhibitor, with an IC 50 of 22 nM, and also shows inhibitory effects on CDK1 and CDK4, with IC 50 s of 40, 200 nM, respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 377090-84-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-18629. | |
| Subasumstat | Subasumstat (TAK-981) is a first in class and selective inhibitor of the SUMOylation enzymatic cascade, with potential immune-activating and antineoplastic activities[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-981. CAS No. 1858276-04-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-111789. | |
| Suberic acid | Suberic acid (Octanedioic acid) is an orally active crystalline dibasic acid. Suberic acid activates the Akt signaling pathway and regulates the expression of molecules related to the TGF-β and MAPK signaling pathways. Suberic acid inhibits skin dryness [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Octanedioic acid. CAS No. 505-48-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 1 g; 5 g. Product ID: HY-W015300. | |
| Suberylglycine | Suberylglycine is an acyl glycine, which is a normally minor metabolite of fatty acid. Uses: Scientific research. Group: Natural products. CAS No. 60317-54-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-113367. | |
| Submandibular mucin | Submandibular mucin is a high molecular weight glycoprotein that is used as a substrate for the viral enzyme neuraminidase [1]. Uses: Scientific research. Group: Peptides. CAS No. 84195-52-8. Pack Sizes: 50 mg; 100 mg; 500 mg. Product ID: HY-P3008. | |
| Substance P | Substance P (Neurokinin P) is a neuropeptide, acting as a neurotransmitter and as a neuromodulator in the CNS. The endogenous receptor for substance P is neurokinin 1 receptor ( NK1-receptor , NK1R ). Uses: Scientific research. Group: Peptides. Alternative Names: Neurokinin P. CAS No. 33507-63-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P0201. | |
| Substance P(1-7) TFA | Substance P(1-7) TFA is a fragment of the neuropeptide, substance P (SP). Substance P(1-7) TFA gives depressor and bradycardic effects when applied to the nucleus tractus solitarius [1]. Uses: Scientific research. Group: Peptides. CAS No. 2828433-22-1. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P1485A. | |
| Substance P TFA | Substance P TFA (Neurokinin P TFA) is a neuropeptide, acting as a neurotransmitter and as a neuromodulator in the CNS. The endogenous receptor for substance P is neurokinin 1 receptor ( NK1-receptor , NK1R ) [1]. Uses: Scientific research. Group: Peptides. Alternative Names: Neurokinin P TFA. CAS No. 148470-19-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P0201A. | |
| Subtilisin | Subtilisin, or rubinase, is a bacterial serine protease. Subtilisin can be used as a detergent additive with thermal stability, pH tolerance, and calcium dependent stability [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EC 3.4.21.14. CAS No. 9014-1-1. Pack Sizes: 50 mg; 100 mg. Product ID: HY-P2729. | |
| Subtilisin, bacillus licheniformis | Subtilisin (Compound proteinase) (EC 3.4.21.62) is a proteolytic enzyme, isolated from Bacillus licheniformis. Subtilisin (Compound proteinase) has catalytic activity in anhydrous dimethyl formamide. Subtilisin (Compound proteinase) can be used as a catalyst for easy coupling between sugars and amino acids [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bacillopeptidaseb. CAS No. 9014-1-1. Pack Sizes: 25 g; 100 g; 1 g; 5 g. Product ID: HY-E70076. | |
| Suc-AAPF-AMC | Suc-AAPF-AMC is an ?-chymotrypsin fluorogenic substrate for the quantitative determination of chymotrypsin activity[1]. Uses: Scientific research. Group: Peptides. Alternative Names: Suc-Ala-Ala-Pro-Phe-AMC. CAS No. 88467-45-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-137811. | |
| Suc-AAPK-pNA | Suc-AAPK-pNA is a chromogenic substrate for the determination of serine/threonine kinase activity and enzyme kinetic parameters [1]. Uses: Scientific research. Group: Peptides. CAS No. 108929-39-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P4484. | |
| Succimer | Succimer is a widely used chelating agent for the treatment of Pb poisoning. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Dimercaptosuccinic acid; DMSA. CAS No. 304-55-2. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1768. | |
| Succinaldehydic acid | Succinaldehydic acid is a catabolite of GABA. Uses: Scientific research. Group: Natural products. CAS No. 692-29-5. Pack Sizes: 1 mg; 2.5 mg. Product ID: HY-104071. | |
| Succinic acid | Succinic acid is an anti-anxiety agent with oral activity. Disodium succinate is the salt form of Succinic acid. Succinic acid is an intermediate product of the tricarboxylic acid cycle. Succinic acid is an important platform chemical. Succinic acid can be used as surfactant, additive, ion chelating agent, flavoring agent and other applications in chemical, pharmaceutical and food fields [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: Wormwood acid. CAS No. 110-15-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N0420. | |
| Succinic anhydride | Succinic anhydride is a cyclic anhydride and a nonclaevable ADC linker extracted from patent WO2009064913A1. Succinic anhydride can react with compound 4 of the patent to link the proagent to an amine or hydroxy 1 group of a targeting polypeptide [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 108-30-5. Pack Sizes: 25 g; 50 g. Product ID: HY-79369. | |
| Succinimide | Succinimide is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Succinimide is utilized in the development of antiepileptic agent [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: pyrrolidine-2,5-dione. CAS No. 123-56-8. Pack Sizes: 5 g; 10 g. Product ID: HY-41877. | |
| Succinobucol | Succinobucol is a phenolic antioxidant with anti-inflammatory and antiplatelet effects. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AGI-1067; Probucol monosuccinate. CAS No. 216167-82-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14937. | |
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