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 | |
|---|---|---|
| SS-208 | SS-208 is a selective HDAC6 inhibitor, with an IC 50 of 12 nM. SS-208 possesses anti-tumor activity in melanoma [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AVS100. CAS No. 2245942-72-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-126330. |  |
| (S)-Salsolinol | (S)-Salsolinol ((-)-Salsolinol) is a dopamine-derived endogenous metabolite [1]. Uses: Scientific research. Group: Natural products. Alternative Names: (-)-Salsolinol. CAS No. 27740-96-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-113316B. | |
| (S,S)-CPI-1612 | (S,S)-CPI-1612 is the isomer of CPI-1612 (HY-136285), and can be used as an experimental control. CPI-1612 is a highly potent, orally active EP300/CBP histone acetyltransferase (HAT) inhibitor with an IC 50 of 8.1 nM for EP300 HAT. CPI-1612 has an anticancer activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2374971-82-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-145386. | |
| SSI-4 | SSI-4 is an inhibitor of Stearoyl CoA desaturase 1 (SCD1) , which can be modified with 11 C, used as a ligand to in vivo small animal PET/CT imaging of SCD1 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1875084-68-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-155033. | |
| SSK1 | SSK1, a senescence-specific killing compound, is a ?-galactosidase-targeted proagent attenuates inflammation. SSK1 is activated by lysosomal ?-galactosidase and selectively killed senescent cells through the activation of p38 MAPK and induction of apoptosis[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2629250-69-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-138936. | |
| (S)-SNAP5114 | (S)-SNAP5114 is a selective GABA transport inhibitor, with IC 50 values of 5 μM and 21 μM for hGAT-3 and rGAT-2, respectively. (S)-SNAP5114 is an anticonvulsant agent [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 157604-55-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103504. | |
| ß-pBrPh-Glc | β-pBrPh-Glc is a small-molecule ice recrystallization inhibitor. β-pBrPh-Glc can control the rate and extent of intracellular ice recrystallization in the nuclei over a broad range of subzero temperatures. β-pBrPh-Glc is an important tool to improve the recovery and function of cryopreserved cells and tissues [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 30572-42-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-124020. | |
| SSR128129E | SSR128129E is an orally available and allosteric FGFR inhibitor with an IC 50 of 1.9 μM for FGFR1. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SSR. CAS No. 848318-25-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15599. | |
| SSR180711 hydrochloride | SSR180711 hydrochloride is an orally active, selective and reversible α7 acetylcholine nicotinic receptor (n-AChRs) partial agonist. SSR180711 hydrochloride can act on rat α7 n-AChR ( K i =22 nM; IC 50 =30 nM) and human α7 n-AChR ( K i =14 nM; IC 50 =18 nM). SSR180711 hydrochloride increases glutamatergic neurotransmission, ACh release and long-term potentiation (LTP) in the hippocampus [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 446031-79-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19411. | |
| SSR504734 | SSR504734 is an orally active, selective and reversible inhibitor of human, rat, and mouse GlyT1 ( IC 50 =18, 15, and 38?nM, respectively). SSR504734 shows anti-schizophrenia, anti-anxiety and anti-depression activities [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 615571-23-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10715. | |
| SSTC3 | SSTC3 is a casein kinase 1? (CK1?) activator (Kd = 32 nM) that inhibits WNT signaling (EC50 = 30 nM). SSTC3 exhibits minimal gastrointestinal toxicity compared to other classes of WNT inhibitors[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1242422-09-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-120675. | |
| SSTR5 antagonist 2 hydrochloride | SSTR5 antagonist 2 hydrochloride is a highly potent, oral active and selective somatostatin (receptor) subtype 5 (SSTR5) antagonist and has potential for the research of type 2 diabetes mellitus (T2DM) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2988224-31-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114191B. | |
| (S,S)-TsDPEN | (S,S)-N-p-Toluenesulfonyl-1,2-diphenylethylenediamine 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. 167316-27-0. Pack Sizes: 5 g; 10 g. Product ID: HY-Y1108. | |
| (S)-STX-478 | (S)-STX-478 is the S-enantiomer of STX-478. STX-478 is a selective inhibitor of PI3Kα mutants, preventing metabolic dysfunction and demonstrating antitumor activity in xenograft mouse models with PI3Kα mutant tumors [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2883540-91-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156681A. | |
| (S)-Subasumstat | (S)-Subasumstat is the isomer of Subasumstat (HY-111789). 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: (S)-TAK-981. CAS No. 1858282-76-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111789A. | |
| ST-193 | ST-193 is a potent broad-spectrum arenavirus inhibitor; inhibits Guanarito, Junin, Lassa and Machupo virus with IC50 values of 0.44, 0.62, 1.4 and 3.1 nM, respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 489416-12-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101441. | |
| ST1936 | ST1936 is a selective, nanomolar affinity 5-HT 6 receptor agonist with K i values of 13 nM, 168 nM and 245 nM for human 5-HT 6 , 5-HT 7 and 5-HT 2B receptors, respectively. ST1936 also shows moderate affinity (K i of 300 nM) for human and rat α2 adrenergic receptor [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1210-81-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103110. | |
| ST271 | ST271 is a potent inhibitor of protein tyrosine kinase ( PTK ), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC 50 s of 6.7 and 9 μM, respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 106392-48-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-103097. | |
| ST 2825 | ST 2825 is a specific MyD88 dimerization inhibitor. ST2825 interferes with recruitment of IRAK1 and IRAK4 by MyD88, causing inhibition of IL-1?-mediated activation of NF-?B transcriptional activity[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 894787-30-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-50937. | |
| ST-401 | ST-401, a microtubule-targeting agent (MTA), is a brain-penetrant microtubule (MT) assembly inhibitor. ST-401 disrupts microtubule (MT) function through gentle and reverisible reduction in MT assembly that triggers mitotic delay and cell death in interphase. ST-401 shows a potent antitumor activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2419942-78-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-163737. | |
| ST91 | ST91 is a α 2 -adrenoceptor (α 2 AR) agonist. ST91 activates both α 2A AR and non-α 2A AR subtypes to produce spinal antinociception [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 4749-61-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-103203. | |
| Stachydrine | Stachydrine is a major constituent of Chinese herb leonurus heterophyllus sweet used to promote blood circulation and dispel blood stasis. Stachydrine can inhibit the NF-κB signal pathway. Uses: Scientific research. Group: Natural products. CAS No. 471-87-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0298. | |
| Stachydrine hydrochloride | Stachydrine hydrochloride is the major active constituent of Leonurus artemisia , which is a potential therapy for cardiovascular diseases [2]. Stachydrine can inhibit the NF-κB signal pathway. Anti-hypertrophic activities [1]. Uses: Scientific research. Group: Natural products. CAS No. 4136-37-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N0738. | |
| Stachyose | Stachyose, a kind of oligosaccharides, act as a hypoglycemic agent [1]. Uses: Scientific research. Group: Natural products. CAS No. 470-55-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N7910. | |
| Stachyose hydrate | Stachyose hydrate is an orally active prebiotic that enhances the growth and activity of beneficial bacteria. Stachyose hydrate has hypoglycemic effects and can improve inflammation by regulating gut microbiota. In addition, Stachyose hydrate can induce plant cell apoptosis ( Apoptosis ). Stachyose hydrate can be used in research on inflammation, gastrointestinal diseases, and agriculture [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 54261-98-2. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0299. | |
| Stafia-1 | Stafia-1 is a potent STAT5a inhibitor ( K i =10.9 μM, IC 50 =22.2 μM). Stafia-1 displays high selectivity over STAT5b and other STAT family members [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2582757-90-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136546. | |
| Stafib-1 | Stafib-1 is the first selective inhibitor of the STAT5b SH2 domain, with a Ki of 44 nM and an IC50 of 154 nM[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1688703-26-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112647. | |
| Stafib-2 | Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b , with an IC 50 of 82 nM and 1.7 μM for STAT5b and STAT5a , respectively. Stafib-2 exhibits poor cell permeability [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2097938-74-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112648. | |
| Stains-All | Stains-All, a cationic carbocyanine dye, is a convenient probe to study the structural features of the individual calcium-binding sites of calmodulin (CaM) and related calcium-binding proteins (CaBP) [1] [2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 7423-31-6. Pack Sizes: 10 mM * 1 mL; 200 mg. Product ID: HY-D0987. | |
| Stapokibart | Stapokibart (CM310) is a humanised monoclonal antibody targeting IL-4Rα and efficiently blocks the interaction of cytokines IL-4 and IL-13 with their co-receptor subunit IL-4R&alpha. Stapokibart has the capacity to interact with IL-4Rα in humans, cynomolgus monkeys, and rats [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: CM310. CAS No. 2734715-10-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990093. | |
| Starch (from potato) | Starch from potato is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Edible corn starch (from potato). CAS No. 9005-25-8. Pack Sizes: 100 g. Product ID: HY-B2225A. | |
| Starch soluble | Starch soluble is a kind of biological materials or organic compounds that are widely used in life science research [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 9005-84-9. Pack Sizes: 5 g. Product ID: HY-W094695. | |
| STAT3-IN-13 | STAT3-IN-13 (compound 6f) is a potent STAT3 inhibitor. STAT3-IN-13 has anti-proliferative effects and binds to the STAT3 SH2 domain with a KD of 0.46 ?M. STAT3-IN-13 inhibits the phosphorylation of STAT3 Y705 and downstream target gene expression. STAT3-IN-13 induces apoptosis in vitro and suppresses the growth and metastasis of tumor in vivo. STAT3-IN-13 can be used for cancer research[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2248552-86-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-150603. | |
| STAT3-IN-14 | STAT3-IN-14 (Compound 1) is a STAT3 inhibitor and has STAT3 phosphorylation inhibitory activity. STAT3-IN-14 (Compound 1) can directly bind to the hinge region of STAT3 [1]. Uses: Scientific research. Group: Natural products. CAS No. 123297-90-5. Pack Sizes: 1 mg. Product ID: HY-N10472. | |
| STAT3-IN-17 | STAT3-IN-17 is a moderate STAT3 inhibitor ( IC 50 =0.7 μM; HEK-Blue IL-6), with antiproliferative activity in HeLa cells. STAT3-IN-17 has good pharmacokinetic characteristics. STAT3-IN-17 also inhibits pyruvate-ferredoxin oxidoreductase ( PFOR ), and inhibits Helicobacter pylori [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1245814-52-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148706. | |
| STAT3-IN-25 | STAT3-IN-25 (compound 2p) is a potent STAT3 inhibitor with a p-trifluoroethoxy benzyl substituent. STAT3-IN-25 shows STAT3 luciferase inhibition activity using HEK293T cells with an IC 50 of 22.3 nM and ATP production inhibition activity using BxPC-3 cells with an IC 50 of 32.5 nM. STAT3-IN-25 shows potent antiproliferation activities on BxPC-3 and Capan-2 cells. STAT3-IN-25 has the potential for pancreatic cancer research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2591440-75-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-160496. | |
| STAT5-IN-1 | STAT5-IN-1 is a STAT5 inhibitor with an IC50 of 47 ?M for STAT5? isoform. Uses: Scientific research. Group: Signaling pathways. CAS No. 285986-31-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101853. | |
| STAT6-IN-1 | STAT6-IN-1 (Compound 19a) is a STAT6 inhibitor with a high affinity for the SH2 domain of STAT6 (IC50=0.028 μM). STAT6-IN-1 can be used in studies of allergic lung disease, allergic rhinitis, chronic obstructive pulmonary disease or cancer[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1637532-68-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148096. | |
| STAT6-IN-2 | STAT6-IN-2 (Compound R-84) is a STAT6 inhibitor that can inhibit the tyrosine phosphorylation of STAT6. STAT6-IN-2 can also inhibit the secretion of eotaxin-3. STAT6-IN-2 can be used in the research of immune diseases and allergic inflammatory diseases such as asthma[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1355594-85-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153991. | |
| STAT6-IN-3 | STAT6-IN-3 is a phosphopeptide mimic targeting the SH2 domain of STAT6 and has a high affinity for STAT6 (IC50: 0.04 ?M). STAT6-IN-3 can be used in the research of inflammation such as asthma[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 371919-80-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-153992. | |
| STAT6-IN-4 | STAT6-IN-4 (Ex. 78) is a STAT6 inhibitor, with an IC50 of 0.34 ?M. STAT6-IN-4 can be used in the research of diseases such as inflammatory and allergic diseases[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3033742-14-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-158398. | |
| STAT6-IN-5 | STAT6-IN-5 (compound 84) is a STAT6 inhibitor (IC50=0.24 ?M), which can be used for the research of inflammatory diseases and allergic diseases (e.g. atopic dermatitis)[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3033742-22-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-158399. | |
| Statine | Statine is an unusual amino acid that occurs twice in the sequence of pepstatin, a protease inhibitor that is active against pepsin and other acid proteases. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (3S,4S)-Statine; (S,S)-Statine. CAS No. 49642-07-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-101877. | |
| Stattic | Stattic is a potent STAT3 inhibitor and inhibits STAT3 phosphorylation (at Y705 and S727) [1]. Stattic inhibits the binding of a high affinity phosphopeptide for the SH2 domain of STAT3 [2]. Stattic ameliorates the renal dysfunction in Alport syndrome (AS) mice [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 19983-44-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13818. | |
| Staurosporine | Staurosporine is a potent, ATP-competitive and non-selective inhibitor of protein kinases with IC50s of 6 nM, 15 nM, 2 nM, and 3 nM for PKC, PKA, c-Fgr, and Phosphorylase kinase respectively. Staurosporine also inhibits TAOK2 with an IC50 of 3 ?M. Staurosporine is an apoptosis inducer[1][2][3][4][5]. Uses: Scientific research. Group: Natural products. Alternative Names: Antibiotic AM-2282; STS; AM-2282. CAS No. 62996-74-1. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15141. | |
| Stavudine | Stavudine (d4T) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Stavudine has activity against HIV-1 and HIV-2. Stavudine also inhibits the replication of mitochondrial DNA (mtDNA). Stavudine reduces NLRP3 inflammasome activation and modulates Amyloid-β autophagy. Stavudine induces apoptosis [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: d4T. CAS No. 3056-17-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0116. | |
| Stavudine (Standard) | Stavudine (Standard) is the analytical standard of Stavudine. This product is intended for research and analytical applications. Stavudine (d4T) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Stavudine has activity against HIV-1 and HIV-2. Stavudine also inhibits the replication of mitochondrial DNA (mtDNA). Stavudine reduces NLRP3 inflammasome activation and modulates Amyloid-β autophagy. Stavudine induces apoptosis [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3056-17-5. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0116R. | |
| STC-15 | STC-15 is an orally active RNA methyltransferase METTL3 inhibitor with the activity of activating anti-tumor immunity and reshaping the tumor microenvironment. STC-15 inhibits tumor growth by activating anti-cancer immune responses associated with increased interferon signaling and synergizes with T-cell checkpoint blockade. STC-15 can be used in the study of proliferative diseases such as cancer and autoimmune diseases[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2648257-56-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156677. | |
| Stearamide | Stearamide is a primary fatty acid amide. Stearamide displays cytotoxic and ichthytoxic activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 124-26-5. Pack Sizes: 250 mg; 500 mg; 1 g; 5 g; 10 g; 25 g. Product ID: HY-W130610. | |
| Stearic acid | Stearic acid is a long-chain dietary saturated fatty acid that can significantly reduce visceral fat by inducing apoptosis of preadipocytes. Stearic acid can be used in the study of cardiovascular and metabolic diseases [1]. Uses: Scientific research. Group: Natural products. CAS No. 57-11-4. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B2219. | |
| Stearic acid-13C18 | Stearic acid- 13 C 18 is the 13 C-labeled Stearic acid. Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 287100-83-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-B2219S2. | |
| Stearic Acid-d35 | Stearic Acid-d 35 is the deuterium labeled Stearic acid. Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 17660-51-4. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-B2219S4. | |
| Stearic acid (Standard) | Stearic acid (Standard) is the analytical standard of Stearic acid. This product is intended for research and analytical applications. Stearic acid is a long-chain dietary saturated fatty acid that can significantly reduce visceral fat by inducing apoptosis of preadipocytes. Stearic acid can be used in the study of cardiovascular and metabolic diseases [1]. Uses: Scientific research. Group: Natural products. CAS No. 57-11-4. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B2219R. | |
| Stearidonic acid | Stearidonic acid (6Z,9Z,12Z,15Z-Octadecatetraenoic acid) is an intermediate fatty acid in the biosynthetic pathway from α-linolenic acid to VLC ω-3 PUFA. The conversion efficiency of stearidonic acid is higher than that of alpha-linolenic acid. Increasing the intake of stearidonic acid can increase the content of eicosapentaenoic acid (EPA) in red blood cells. Stearidonic acid can also be isolated from methanolic extracts of the brown alga Brachyphyllum gracilis [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: 6Z,9Z,12Z,15Z-Octadecatetraenoic acid. CAS No. 20290-75-9. Pack Sizes: 1 mg (36.18 mM * 100 μL in Ethanol); 5 mg (36.18 mM * 500 μL in Ethanol); 10 mg (36.18 mM * 1 mL in Ethanol). Product ID: HY-113120. | |
| Stearoylethanolamide | Stearoylethanolamide is an endocannabinoid-like compound with pro-apoptotic activity. Uses: Scientific research. Group: Natural products. CAS No. 111-57-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113015. | |
| Stearoyl-L-carnitine chloride | Stearoyl-L-carnitine chloride is an endogenous long-chain acylcarnitine. Stearoyl-L-carnitine chloride is a less potent inhibitor of GlyT2. Stearoyl-L-carnitine chloride inhibits glycine responses by 16.8% at concentrations up 3 μM [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 32350-57-5. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-130466. | |
| Stearyl glycyrrhetinate | Stearyl glycyrrhetinate, a major component in licorice extract, has a MIC against S. aureus strains of more than 256 mg/L. Stearyl glycyrrhetinate has antibacterial effects [1]. Uses: Scientific research. Group: Natural products. CAS No. 13832-70-7. Pack Sizes: 500 mg. Product ID: HY-N2417. | |
| Stem bromelain | Stem bromelain (EC 3.4.22.32) is a cysteine proteinase, isolated from pineapple ( Ananas comosus ) stem. Stem bromelain is a major bromelain, which exhibits various fibrinolytic, antiedematous, antithrombotic, and anti-inflammatory activities. Stem bromelain has in vivo antitumoral and antileukemic activity, as well as antimetastatic action [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 37189-34-7. Pack Sizes: 5 g; 25 g; 100 g. Product ID: HY-P2970. | |
| Stemregenin 1 | Stemregenin 1 is a potent aryl hydrocarbon receptor ( AhR ) antagonist with IC 50 of 127 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SR1. CAS No. 1227633-49-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15001. | |
| Stenoparib | Stenoparib (E7449) is a potent PARP1 and PARP2 inhibitor and also inhibits TNKS1 and TNKS2 , with IC 50 s of 2.0, 1.0, ?50 and ?50 nM for PARP1, PARP2, TNKS1 and TNKS2, respectively, using 32 P-NAD + as substrate. Uses: Scientific research. Group: Signaling pathways. Alternative Names: E7449; 2X-121. CAS No. 1140964-99-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12418. | |
| Sterculic acid | Sterculic acid is a stearoyl-CoA desaturase-1 ( SCD1 ) inhibitor. Sterculic acid specifically inhibits the delta-9 desaturase ( Δ9D ) activity with an IC 50 value of 0.9 μM [1]. Uses: Scientific research. Group: Natural products. CAS No. 738-87-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-127143. | |
| Sterigmatocystine | Sterigmatocystine is a precursor of aflatoxins and a mycotoxin produced by common mold strains from Aspergillus versicolor [1] [2]. Sterigmatocystine, a inhibitor of G1 Phase and DNA synthesis, is used to inhibit p21 activity. Sterigmatocystine has teratogenic, and carcinogenic effects in animals [3]. Uses: Scientific research. Group: Natural products. CAS No. 10048-13-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N6725. | |
| Sterile 10 mM Histidine, pH 5.5 buffer | Sterile 10 mM Histidine, pH 5.5 buffer is a sterile solution using 10 mM histidine as the solute with its pH adjusted to 5.5, possessing both buffering capacity and biocompatibility. Sterile 10 mM Histidine, pH 5.5 buffer is widely applied in laboratory research, pharmaceutical production, cosmetics and other fields[1]. Uses: Scientific research. Group: Biochemical assay reagents. Pack Sizes: 10 mL; 30 mL. Product ID: HY-Y1968A. | |
| (S)-(-)-tert-Butylsulfinamide | (S)-(-)-tert-Butylsulfinamide is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: S-(-)-T-Butylsulfinimide. CAS No. 343338-28-3. Pack Sizes: 10 mM * 1 mL; 25 g; 100 g. Product ID: HY-40229. | |
| (S)-Tetrahydrofuran-3-ol | (S)-tetrahydrofuran-3-ol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: (+)-3-Hydroxytetrahydrofuran. CAS No. 86087-23-2. Pack Sizes: 25 g. Product ID: HY-76476. | |
| (S)-Tetrahydrofurfurylamine | (S)-Tetrahydrofurfurylamine 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. 7175-81-7. Pack Sizes: 250 mg; 1 g; 5 g. Product ID: HY-W010600. | |
| Steviol | Steviol is a major metabolite of the sweetening compound stevioside. Steviol slows renal cyst growth by reducing AQP2 expression and promoting AQP2 degradation [1]. Uses: Scientific research. Group: Natural products. CAS No. 471-80-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N2057. | |
| Stevioside | Stevioside is an orally active sweetener that can be isolated from Stevia rebaudiana , with antihypertensive, antihyperglycemic, antioxidant, anti-inflammatory and anti-tumor activities [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 57817-89-7. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0669. | |
| STF-083010 | STF-083010 is a specific IRE1? inhibitor. STF-083010 inhibits Ire1 endonuclease activity, without affecting its kinase activity, after endoplasmic reticulum stress. Uses: Scientific research. Group: Signaling pathways. CAS No. 307543-71-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-15845. | |
| STF-118804 | STF-118804 is a highly specific NAMPT inhibitor. STF-118804 activates AMPK and inhibits mTOR pathways. STF-118804 has antitumor activity against pancreatic cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 894187-61-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12808. | |
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