A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Super yellow light-emitting PPV copolymer. CAS No. 26009-24-5. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications.
Supinoxin
Supinoxin (RX-5902) is an orally active inhibitor of phosphorylated-p68 RNA helicase (P-p68) and a potent first-in-class anti-cancer agent. Supinoxin interacts with Y593 phosphorylated-p68 and attenuates the nuclear shuttling of β-catenin. Supinoxin induces cell apoptosis and inhibits growth of TNBC cancer cell lines with IC50s ranging from 10 nM to 20 nM[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: RX-5902. CAS No. 888478-45-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-123611.
Suplatast Tosylate
Suplatast Tosylate is an antiallergic drug. Suplatast Tosylate inhibits antigen-induced histamine release from mast cells as well as IgE antibody formation. Suplatast Tosylate suppresses interleukin (IL)-4 release from T cells, however in human peripheral basophils, Suplatast Tosylate inhibited the antigen-induced release of IL-13 but not IL-4. Group: Biochemicals. Alternative Names: [3- [ [4- (3-ethoxy-2-hydroxypropoxy) phenyl] amino] -3-oxopropyl] dimethylsulfonium 4-Methyl Benzene sulfonate; (±) - [2- [4- (3-Ethoxy-2-hydroxypropoxy) phenylcarbamoyl] ethyl] dimethylsulfonium p-toluenesulfonate; IPD 1151T; Suplatast tosilate. Grades: Highly Purified. CAS No. 94055-76-2. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
Suplatast Tosylate
Suplatast tosylate is a Th2 cytokine inhibitor that attenuates IL-2, IL-5 and IL-13 production and has no effect on IFN-γ production. Acts as an immunoregulator that suppresses IgE production, eosinophil infiltration and histamine release. Shows antiasthmatic, anti-inflammatory and antifibrotic activity in vivo. Suplatast Tosilate (ST) is an innovative anti-allergic medication that has emerged in recent years. It is a synthetic compound known as the l-tosylate ester of suplatast, which is a novel anti-allergic substance. Suplatast Tosilate can hinder the production of pro-inflammatory cytokines, including interleukin-4 and interleukin-5. Moreover, it has also been found to suppress the activity of enzymes involved in generating inflammatory mediators such as cyclooxygenase-2 and phospholipase A2. Category: Active pharmaceutical ingredients. CAS No. 94055-76-2. Product ID: API94055762. Molecular formula: C23H33NO7S2. Mole weight: 499.641. Appearance: Powder.
Suplite RB Nanopowder
Suplite RB Nanopowder. Purity: >99%.
Suprofen
Suprofen. Group: Biochemicals. Alternative Names: a-Methyl-4- (2-thienylcarbonyl) benzeneacetic acid; p-(2-Thenoyl)hydratropic acid; Sutoprofen. Grades: Highly Purified. CAS No. 40828-46-4. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C14H12O3S. US Biological Life Sciences.
Suramin Hexasodium Salt (Germanin, NSC 34936, SK 24728)
Sodium salt of Suramin, a hepatitis C virus NS3 helicase inhibitor. Also used in the treatment of arthritis due to problematic collagen.A P2x and P2y purinergic receptor antagonist that displays antitumor, antiangiogenic and antiparasitic activities. Inhibits sirtuin 1, sirtuin 5 and topoisomerase II. Inhibits the cell surface binding of various growth factors including PDGF, EGF, FGFa and FGFb. Blocks association of G protein alpha and b/g-subunits. Potent competitive inhibitor of reverse transcriptase and protects T lymphocytes against in vitro human immunodeficiency virus infection.Potent ATPase inhibitor. Potent competitive inhibitor of reverse transcriptase.lfonic Acid Hexasodium Salt; 309F; 8,8'-[Ureylenebis[m-phenylene carbonylimino (4-methyl-m-phenylene) carbonylimino]]di (1, 3, 5-naphthalenetrisulfonic Acid) Hexasodium Salt; Antrypol; BAY 205; Bayer 205; CI 1003; Fourneau 309; Germanin; Germanin (pharmaceutical); Hexasodium Sym.-bis(m-aminobenzoyl)-m-amino-p-methylbenzoyl-1-naphthylamino-4,6,8-trisulfonate) Carbamide; Moranyl; NF 060; Naganin; Naganine; Naphuride; Naphuride sodium; Sodium Suramin; Suramin Hexasodium; Suramin Sodium; Suramine Sodium. Grades: Highly Purified. CAS No. 129-46-4. Pack Sizes: 50mg, 100mg, 250mg. Molecular Formula: C??H??N?Na?O??S?, Molecular Weight: 1429.17. US Biological Life Sciences.
Worldwide
Suramin sodium salt
Suramin sodium salt(Suramin hexasodium salt) is a reversible and competitive protein-tyrosine phosphatases (PTPases) inhibitor[1]. Suramin sodium salt is a potent inhibitor of sirtuins: SirT1 (IC50=297 nM), SirT2 (IC50=1.15 μM), and SirT5 (IC50=22 μM)[2]. Suramin sodium salt is a competitive inhibitor of reverse transcriptase (DNA topoisomerase II: IC50=5 μM)[3][4]. Suramin sodium salt is a potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor[5]. Suramin sodium salt efficiently inhibits IP5K and is an antiparasitic, anti-neoplastic and anti-angiogenic agent[6][7][8]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Suramin hexasodium salt. CAS No. 129-46-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0879A.
Suramin sodium salt (Standard)
Suramin (sodium salt) (Standard) is the analytical standard of Suramin (sodium salt). This product is intended for research and analytical applications. Suramin sodium salt (Suramin hexasodium salt) is a reversible and competitive protein-tyrosine phosphatases (PTPases) inhibitor[1]. Suramin sodium salt is a potent inhibitor of sirtuins: SirT1 (IC50=297 nM), SirT2 (IC50=1.15 μM), and SirT5 (IC50=22 μM)[2]. Suramin sodium salt is a competitive inhibitor of reverse transcriptase (DNA topoisomerase II: IC50=5 μM)[3][4]. Suramin sodium salt is a potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor[5]. Suramin sodium salt efficiently inhibits IP5K and is an antiparasitic, anti-neoplastic and anti-angiogenic agent[6][7][8]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Suramin hexasodium salt (Standard). CAS No. 129-46-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B0879AR.
Surface IgG (sA20-Ig) of A20 (106-114)
Surface IgG (sA20-Ig) of A20 (106-114) is a peptide corresponding to residues 106-114 of Surface IgG (sA20-Ig) of A20. Inoculation of the Id-peptide in A20-engrafted mice caused apoptosis of tumor cells and resulted in tumor growth inhibition and extended survival of diseased animals. Synonyms: Surface IgG (sA20-Ig) of A20 B-lymphoma cell line (106-114).
Surfactin is a lipopeptide antibiotic and biosurfactant. Group: Biochemicals. Grades: Highly Purified. CAS No. 24730-31-2. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C53H93N7O13. US Biological Life Sciences.
Worldwide
Surfactin
Surfactin is a lipopeptide antibiotic and biosurfactant from Bacillus subtilis. Synonyms: surfactin C. CAS No. 24730-31-2. Molecular formula: C53H93N7O13. Mole weight: 1036.34.
Surfactin
Surfactin is a potent cyclic lipopeptide biosurfactants consists of four isomers (Surfactin A, B, C and D), which mediates flux of mono-and divalent cations, such as calcium, across lipid bilayer membranes. Surfactin can act as an antimicrobial adjuvant with anti-bacterial, anti-fungal, antimycoplasma and hemolytic effects[1][2]. Surfactin also has antiviral activity against a variety of enveloped viruses[3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 252023-70-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129555.
Surfen dihydrochloride
Surfen dihydrochloride is a potent heparan sulfate antagonist. Surfen inhibits FGF2 binding and signal transduction. Surfen binds to glycosaminoglycans and reduces tau hyperphosphorylation. Surfen dihydrochloride inhibits the activity of recombinant uronyl 2-O-sulfotransferase with an IC50 of approximately 2 μM. Surfen dihydrochloride inhibits HSV-1 viral infection. Surfen dihydrochloride inhibits neural differentiation, delays remyelination, and alleviates EAE[1][2][3][4][5][6]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Aminoquinuride dihydrochloride. CAS No. 5424-37-3. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-122704A.
Surfynol 104 E (technical grade)
Surfynol 104 E (technical grade). CAS No. 8043-35-4. Purity: Tech. Product ID: ACM8043354-1. Alfa Chemistry - ISO 9001:32057 Certified.
Surlorian
Surlorian is a ryanodine receptor (RyR) stabilizer[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ARM210. CAS No. 1467605-57-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-159502.
Surovatamig
Surovatamig (AZD0486; TNB-486) is a fully human anti-CD19/CD3 IgG4 bispecific antibody. Surovatamig triggers T cell activation, releases cytotoxic granules, and induces T cell-dependent cellular cytotoxicity and tumor cell lysis. Surovatamig can reduces release of pro-inflammatory cytokines including IL-2, IFNγ, TNF. Surovatamig can be used for the research of cancer, such as B cell non-Hodgkin lymphoma[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AZD0486; TNB-486. CAS No. 2892667-02-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P991028.
Survivin (18-27)
A peptide fragment of Survivin. Survivin, also called BIRC5 , is a member of the apoptosis inhibitor protein family containing a baculovirus domain. Survivin is overexpressed in most human cancers but rarely expressed in normal differentiated adult tissues. Synonyms: Survivin (18-27)(modK); Sur18K10; Baculoviral IAP repeat-containing protein 5 (18-27).
Survivin-3A (96-104)
Survivin-3A (96-104) is a 9-aa peptide. Survivin is the smallest member of the Inhibitor of apoptosis (IAP) family of proteins, involved in inhibition of apoptosis and regulation of cell cycle.
Survivin (80-88)
A peptide fragment of Survivin. Survivin, also called BIRC5 , is a member of the apoptosis inhibitor protein family containing a baculovirus domain. Survivin is overexpressed in most human cancers but rarely expressed in normal differentiated adult tissues. Synonyms: Baculoviral IAP repeat-containing protein 5 (80-88).
Survivin (96-104)
A peptide fragment of Survivin. Survivin, also called BIRC5 , is a member of the apoptosis inhibitor protein family containing a baculovirus domain. Survivin is overexpressed in most human cancers but rarely expressed in normal differentiated adult tissues. Synonyms: NSC-742276 (96-104). Molecular formula: C51H86N10O12S. Mole weight: 1063.3499999999999.
Survodutide
Survodutide is a dual peptide agonist of the glucagon-like peptide 1 receptor (GLP-1R) and glucagon receptor (GCGR). Synonyms: BI-456906. CAS No. 2805997-46-8. Molecular formula: C192H289N47O61. Mole weight: 4231.62.
Survodutide
Survodutide (BI 456906) is a potent, selective glucagon receptor/GLP-1 receptor (GCGR/GLP-1R) dual agonist with EC50s of 0.52 nM and 0.33 nM in CHO-K1 cells, respectively. Survodutide, a 29-amino-acid peptide, is a potent acylated peptide containing a C18 fatty acid. Survodutide has robust anti-obesity efficacy achieved by increasing energy expenditure and decreasing food intake[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BI 456906. CAS No. 2805997-46-8. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P4146.
Sushi peptide 1
Sushi peptide 1 is a protein-derived peptide, which has activity against gram-positive bacteria. Synonyms: Gly-Phe-Lys-Leu-Lys-Gly-Met-Ala-Arg-Ile-Ser-Cys-Leu-Pro-Asn-Gly-Gln-Trp-Ser-Asn-Phe-Pro-Pro-Lys-Cys-Ile-Arg-Glu-Cys-Ala-Met-Val-Ser-Ser. Molecular formula: C164H263N47O44S5. Mole weight: 3757.48.
Sushi peptide 3
Sushi peptide 3 is a protein-derived peptide. It has activity against gram-negative bacteria. Synonyms: His-Ala-Glu-His-Lys-Val-Lys-Ile-Gly-Val-Glu-Gln-Lys-Tyr-Gly-Gln-Phe-Pro-Gln-Gly-Thr-Glu-Val-Thr-Tyr-Thr-Cys-Ser-Gly-Asn-Tyr-Phe-Leu-Met. Grade: >95%. Molecular formula: C175H261N45O52S2. Mole weight: 3891.39.
Suspended Graphene on TEM Grids
Suspended Graphene on TEM Grids.
Suspended Monolayer Graphene on Cavities
Suspended Monolayer Graphene on Cavities.
Suspended Monolayer Graphene on TEM Grids (Quantifoil Gold) - Pack 4 units
Suspended Monolayer Graphene on TEM Grids (Quantifoil Gold) - Pack 4 units.
Suspended monolayer graphene on TEM grid substrate (Quantifoil gold)
Transfer Method: Clean transfer method Size: 2 mm (TEM grid diameter) Appearance (Color): Transparent Coverage: >95% Number of graphene layers: single layer Thickness (theoretical): 0.345 nm FET Electron Mobility on Al2O3: 2; 000 cm2 /Vs FET Electron Mobility on SiO2/Si (expected): 4; 000 cm2 /Vs Sheet Resistance: 170 Ohms/sq. Grain size: up to 10 micrometer.
Suspended PVC Resin ALFA01
This product is a thermoplastic PVC resin, insoluble in water, gasoline and alcohol. Alternative Names: Suspended poly(vinyl chloride) resins.
Suspended PVC Resin ALFA02
This product is a thermoplastic PVC resin, insoluble in water, gasoline and alcohol. Alternative Names: Suspended poly(vinyl chloride) resins.
Suspended PVC Resin ALFA03
This product is a thermoplastic PVC resin, insoluble in water, gasoline and alcohol. Alternative Names: Suspended poly(vinyl chloride) resins.
Suspended PVC Resin ALFA04
This product is a thermoplastic PVC resin, insoluble in water, gasoline and alcohol. Alternative Names: Suspended poly(vinyl chloride) resins.
Sutezolid
Sutezolid (PNU-100480), an orally active oxazolidinone antimicrobial agent, acts by inhibiting bacterial protein synthesis. Sutezolid has potent activity against mycobacteria, and is used for the research of drug-resistant tuberculosis[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PNU-100480; U-100480; PF-02341272. CAS No. 168828-58-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10392.
Sutherlandia Frutescens Herb Powder (Aerial Parts)
Sutherlandia Frutescens Herb Powder (Aerial Parts).
CA, FL & NJ
Sutimlimab
Sutimlimab is a humanized monoclonal IgG4 antibody. Sutimlimab inhibits complement protein component 1, s subcomponent (C1s). Sutimlimab blocks C3 and C4 activation. Sutimlimab can be used for the research of cold agglutinin disease and complement-mediated hemolytic uremic syndrome[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BIVV009; IPN-009; TNT009. CAS No. 2049079-64-1. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P99050.
Suvecaltamide
Suvecaltamide (MK-8998) is a selective T-type calcium channel inhibitor with oral efficacy. Suvecaltamide exhibits no cytotoxicity in myeloma cell lines and does not affect the antitumor efficacy of Bortezomib (BTZ). Suvecaltamide reverses BTZ-induced peripheral neuropathy (CIPN) in mouse and rat models, and helps inhibit myeloma growth[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MK-8998; CX-8998; JZP385. CAS No. 953778-58-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-101096.
Suvigletistat
Suvigletistat is a Transglutaminase 2 (TG2) inhibitor with an IC50 <0.5 μM. Suvigletistat can be used for the research of inflammatory disorders[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2410912-75-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-177133.
SUVN-911
SUVN-911 is a potent, selective, brain penetrated and orally bioavailable neuronal nicotinic acetylcholine α4β2 receptor antagonist, with a Ki of 1.5 nM. SUVN-911 has antidepressant activity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2414674-71-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136146.
Suvorexant
Suvorexant is a first-in-class dual orexin receptor antagonist approved for the treatment of insomnia characterized by difficulties with sleep onset and/or sleep maintenance. It is available in oral tablet form and represents a novel mechanism distinct from traditional sedative-hypnotics such as benzodiazepines and Z-drugs. The drug selectively targets the orexin neuropeptide signaling system that promotes wakefulness. Applications: It is indicated for the treatment of insomnia in adults, specifically for patients who have difficulty falling asleep or staying asleep. unlike traditional hypnotics, suvorexant is not associated with tolerance or withdrawal at therapeutic doses, though next-morning somnolence and impaired driving ability are important safety considerations. it is classified as a controlled substance (schedule iv) due to potential for abuse, and the recommended dose is 10 to 20 mg taken within 30 minutes of bedtime. Category: Other apis. Synonyms: MK-4305; BELSOMRA; [(7R)-4-(5-Chloro-1,3-benzoxazol-2-yl)-7-methyl-1,4-diazepan-1-yl][5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone. CAS No. 1030377-33-3. Product ID: API0231546. Molecular formula: C23H23ClN6O2. Mole weight: 450.9. EINECS: 685-109-7. InChIKey: JYTNQNCOQXFQPK-MRXNPFEDSA-N. Appearance: Off-white powder.
Suvorexant impurity 1
Suvorexant impurity 1 is an impurity of Suvorexant. Uses: Scientific research. Category: Signaling pathways. CAS No. 2941-79-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-78572.
Suvratoxumab
Suvratoxumab (MEDI4893) is a long-acting, high-affinity human anti-α-toxin monoclonal antibody (IgG1κ type). Suvratoxumab potently neutralizes α-toxin, a key S. aureus virulence factor. Suvratoxumab improves survival and reduces lung injury in an immunocompromised mice model of pneumonia. Suvratoxumab also enhances the antibacterial activity of Vancomycin (HY-B0671) or Linezolid (HY-10394)[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MEDI4893. CAS No. 1629620-18-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99583.
Suxamethonium
Suxamethonium. Group: Biochemicals. Alternative Names: Succinylcholine chloride dihydrate. Grades: Highly Purified. CAS No. 6101-15-1. Pack Sizes: 50g, 100g, 250g. Molecular Formula: C14H30Cl2N2O4·2H2O. US Biological Life Sciences.
Suzetrigine (VX-548) is an orally active and highly selective NaV1.8 inhibitor that acts as an analgesic. Suzetrigine is also a blocker of sodium channel protein type 10 subunit alpha. Suzetrigine is promising for research of acute pain after abdominoplasty and bunionectomy[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: VX-548. CAS No. 2649467-58-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-148800.
Suzetrigine phenol
Suzetrigine phenol is the phenolate form of the sodium channel modulator Suzetrigine (HY-148800)[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2649467-91-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-160903.
SV40 large T antigen NLS
SV40 large T antigen NLS is from Large T antigen residue 47 to 55, enables protein import into cell nucleus. Uses: Scientific research. Category: Peptides. CAS No. 163815-24-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P0310.
SV40 large T antigen NLS
SV40 large T antigen NLS, a hexamer protein generated from Large T antigen residue 47 to 55, enables protein import into cell nucleus. Synonyms: Cys-Gly-Gly-Gly-Pro-Lys-Lys-Lys-Arg-Lys-Val-Glu-Asp. Grade: ≥95%. Molecular formula: C58H104N20O18S. Mole weight: 1401.63.
SV-40 Large T-antigen Nuclear Localization Signal (NLS)
It is a commonly used nuclear localization signal (NLS) peptide, which is derived from Large T antigen residue 47 to 55. It enables protein import into cell nucleus. Synonyms: H-Cys-Gly-Gly-Gly-Pro-Lys-Lys-Lys-Arg-Lys-Val-Glu-Asp-OH; SV40 Large T-antigen Nuclear Localization Signal (NLS) derived peptide. Grade: ≥95%. Molecular formula: C58H104N20O18S. Mole weight: 1401.65.
SV40 T-Ag-derived NLS peptide
SV40 T-Ag-derived NLS peptide, derived from the Large T antigen residues 47 to 56, is the nuclear localization signal DNA tagged to this peptide, which is effectively translocated into the nucleus. Synonyms: H-Pro-Lys-Lys-Lys-Arg-Lys-Val-Glu-Asp-Pro-Tyr-Cys-OH; SV40 T-Ag-derived Nuclear Localization Signal (NLS) Peptide; NLS Fragment 1; T-NLS peptide; L-Cysteine, L-prolyl-L-lysyl-L-lysyl-L-lysyl-L-arginyl-L-lysyl-L-valyl-L-α-glutamyl-L-α-aspartyl-L-prolyl-L-tyrosyl-. Grade: ≥95%. CAS No. 105425-98-7. Molecular formula: C66H111N19O18S. Mole weight: 1490.77.
SV40 T-Ag-derived NLS peptide acetate
SV40 T-Ag-derived NLS peptide, derived from the Large T antigen residues 47 to 56, is the nuclear localization signal DNA tagged to this peptide, which is effectively translocated into the nucleus. Molecular formula: C68H115N19O20S. Mole weight: 1550.82.
SVEC
SVEC. CAS No: 918822-70-5
Sarchem Laboratories New Jersey NJ
S-Venlafaxine
S-Venlafaxine. Group: Biochemicals. Alternative Names: 1-[ (1S) -2- (Dimethylamino) -1- (4-methoxyphenyl) ethyl]cyclohexanol; (-)-Venlafaxine. Grades: Highly Purified. CAS No. 93413-44-6. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C17H27NO2. US Biological Life Sciences.
Worldwide
S-Venlafaxine-di-p-toluoyl-L-tartrate Salt
A metabolite of Venlafaxine, a selective serotonin noradrenaline reuptake inhibitor. Used as an antidepressant. Group: Biochemicals. Grades: Highly Purified. CAS No. 272788-02-0. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
SW016789
SW016789 is a hypersecretion-inducer targeting VDAC1. SW016789 can induce insulin hypersecretion and Ca2+ influx in β-cells directly. SW016789 induces a transient endoplasmic reticulum stress response (ER stress), but does not cause beta cell death. SW016789 has reversible and non-apoptotic characteristics. SW016789 can be used for the study of Diabetes mellitus type 2 (T2DM) β-cell dysfunction[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 292613-04-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-176745.
SW033291
SW033291 is a potent and high-affinity inhibitor of 15-PGDH with a Ki of 0.1 nM. SW033291 increases prostaglandin PGE2 levels in bone marrow and other tissues. SW033291 also promotes tissue regeneration[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 459147-39-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16968.
SW083688
SW083688 is a selective TAOK2 inhibitor with an IC50 of 1.3 μM. SW083688 increases the abundance of p62 protein, inhibits autophagosome maturation, and blocks Autophagic flux. SW083688 is applicable for the research of non-small cell lung cancer and pancreatic cancer[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 422281-45-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-122232.
SW106065
SW106065 is an apoptosis inducer in malignant peripheral nerve sheath tumors (MPNST). SW106065 inhibits ATP consumption of sMPNST and other models of MPNST with an EC50 of 1 μM. SW106065 can be used for MPNST research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 62289-81-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-124778.
SW-163A
SW-163A is an immunosuppressant isolated from the culture broth of Streptomyces sp. SNA15896. It showed immunosuppressive and antimicrobial activities in vitro. Synonyms: SW-163 A. Molecular formula: C34H42N2O12. Mole weight: 670.7.
SW-163B
SW-163B is an immunosuppressant isolated from the culture broth of Streptomyces sp. SNA15896. It showed immunosuppressive and antimicrobial activities in vitro. Synonyms: SW-163 B. Molecular formula: C33H40N2O12. Mole weight: 656.7.
SW-163C
SW-163C is an antitumor depsipeptide produced by Streptomyces sp. SNA15896. The LD50 of SW-163C is > 100 mg/kg. Synonyms: SW-163 C. Molecular formula: C52H60N10O14S2. Mole weight: 1113.2.
SW-163E
SW-163E is an antitumor depsipeptide produced by Streptomyces sp. SNA15896. The LD50 of SW-163E is 0.6 mg/kg. Synonyms: SW-163 E. Molecular formula: C54H64N10O14S2. Mole weight: 1141.3.
SW1+ Pure granular seaweed meal with beneficial soil microbes
Seaweed Granules with beneficial soil microbes. Uses: Agriculture, horticulture, amenity. Alternative Names: Soil improver. Pack Sizes: 500KG. Molecular formula: Fertilizer. Sold wholesale for blending & formulating. Categories: Seaweed granules, algae, Soil Conditioners.
SW203668 TFA
SW203668 TFA is an irreversible stearoyl CoA desaturase (SCD) inhibitor with an IC50 of 54 nM. SW203668 TFA covalently binds and inhibits SCD, depletes unsaturated fatty acids, and triggers cell death in sensitive cells. SW203668 TFA requires demethylation by CYP4F11 to form its active SCD-inhibiting form; differential CYP4F11 expression drives selective cytotoxicity. SW203668 TFA exerts cytotoxicity toward CYP4F11-expressing non-small cell lung cancer (NSCLC) cells and spares CYP4F11-lacking NSCLC cells. SW203668 TFA inhibits tumor growth in immunodeficient mice bearing CYP4F11-expressing NSCLC xenografts and spares mouse skin sebocytes. SW203668 TFA can be used for the research of non-small cell lung cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2117405-48-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg. Product ID: HY-124084A.