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| Product | Description | |
|---|---|---|
| Survivin Inhibitor III, LLP-3 (Survivin-Ran Interaction Blocker, LLP3, 4-(3,5-bis(Benzyloxy)phenyl)-6-(5-chloro-2-hydroxyphenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile) | A cell-permeable, dihydropyridinone compound that selectively disrupts survivin-Ran interaction in cell-free binding assays (IC50 <0.3uM) and in U87 glioma cells (by 55% in 24h; 20uM) via direct binding at survivin protein-protein interaction interface, while exhibiting much reduced or little potency against survivin-Smac/DIABLO, survivin-survivin, or XIAP-Smac/DIABLO interaction. LLP-3 treatment abrogates neurosphere formation in GMB cultures (IC50 ≤35uM) by selectively depleting CD133+ GSC population via apoptosis induction. TMZ, in comparison, enriches GMB GSC population by preferentially eradicating non-GSC population. LLP-3 is also efficacious in treating human GMB xenograft in mice in vivo (25mg/kg/day via i.p.). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Survivin Inhibitor, YM155 (Survivin Inhibitor I, Interleukin Enhancer-Binding Factor 3 Inhibitor) | A cell-permeable imidazolium derivative that suppresses survivin expression, blocks survivin promoter activity, and induces apoptosis in a variety of tumor cell lines (IC50 = 540nM) in a dose-dependent manner. The main target of YM155 appears to be the interleukin enhancer-binding factor 3 (ILF3/NF110) with shorter C-terminal lengths associated with reduced binding. Exhibits potent anti-tumor effects without any severe systemic toxicity in murine models. Reported to induce tumor regression by suppressing intratumor survivin levels in PC3-xenograph tumor models (by 47% and 80% at 1 and 5mg/kg, respectively. Group: Biochemicals. Grades: Highly Purified. CAS No. 781661-94-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Survodutide | Survodutide (BI 456906) is a potent, selective glucagon receptor/GLP-1 receptor (GCGR/GLP-1R) dual agonist with EC 50 s 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. Group: Peptides. Alternative Names: BI 456906. CAS No. 2805997-46-8. Pack Sizes: 1 mg; 5 mg; 10 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. Grades: >95%. Molecular formula: C175H261N45O52S2. Mole weight: 3891.39. | |
| Suspended Graphene on TEM Grids | Suspended Graphene on TEM Grids. Group: Cvd graphene. |  |
| Suspended Monolayer Graphene on Cavities | Suspended Monolayer Graphene on Cavities. Group: Cvd graphene. | |
| 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. Uses: Graphene film on tem grid is useful for high resolution tem imaging of nanoscale materials because it preserves the same focal plane over the whole grid mesh. Group: Carbon nano materials. | |
| Suspended PVC Resin ALFA01 | This product is a thermoplastic PVC resin, insoluble in water, gasoline and alcohol. Uses: Mainly used in the production of pvc pipes, pvc fittings, pvc profiles, pvc sheets, pvc films, pvc pipes, pvc sheets, pvc cables and wires, pvc bottles and containers, pvc leather, pvc flooring, etc. Group: Pvc resins. Alternative Names: Suspended poly(vinyl chloride) resins. | |
| Suspended PVC Resin ALFA02 | This product is a thermoplastic PVC resin, insoluble in water, gasoline and alcohol. Uses: Mainly used in the production of pvc pipes, pvc fittings, pvc profiles, pvc sheets, pvc films, pvc pipes, pvc sheets, pvc cables and wires, pvc bottles and containers, pvc leather, pvc flooring, etc. Group: Pvc resins. Alternative Names: Suspended poly(vinyl chloride) resins. | |
| Suspended PVC Resin ALFA03 | This product is a thermoplastic PVC resin, insoluble in water, gasoline and alcohol. Uses: Mainly used in the production of pvc pipes, pvc fittings, pvc profiles, pvc sheets, pvc films, pvc pipes, pvc sheets, pvc cables and wires, pvc bottles and containers, pvc leather, pvc flooring, etc. Group: Pvc resins. Alternative Names: Suspended poly(vinyl chloride) resins. | |
| Suspended PVC Resin ALFA04 | This product is a thermoplastic PVC resin, insoluble in water, gasoline and alcohol. Uses: Mainly used in the production of pvc pipes, pvc fittings, pvc profiles, pvc sheets, pvc films, pvc pipes, pvc sheets, pvc cables and wires, pvc bottles and containers, pvc leather, pvc flooring, etc. Group: Pvc resins. 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. Group: Signaling pathways. Alternative Names: PNU-100480; U-100480; PF-02341272. CAS No. 168828-58-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10392. | |
| Sutezolid | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Sutezolid | Sutezolid, also called as PNU-100480, is an oxazolidinone antibacterial compound to reach Phase-II clinical research for Tuberculosis. Synonyms: N-[[(5S)-3-(3-fluoro-4-thiomorpholin-4-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamidePF-02341272; PF02341272; PF 02341272; PNU-100480; PNU 100480; PNU100480; U-100480; U 100480; U100480; Sutezolid.168828-58-8. Grades: 95%. CAS No. 168828-58-8. Molecular formula: C16H20FN3O3S. Mole weight: 353.41. | |
| Sutherlandia Frutescens Herb Powder (Aerial Parts) | Sutherlandia Frutescens Herb Powder (Aerial Parts). |  CA, FL & NJ |
| Sutimlimab | Sutimlimab is a humanized monoclonal antibody that targets the C1s protein in the classical complement pathway. Sutimlimab has been approved by US FDA for the treatment of adults with cold agglutinin disease (CAD). Synonyms: Enjaymo. CAS No. 2049079-64-1. | |
| Sutimlimab | Sutimlimab, a first-in-class complement protein component 1, s subcomponent ( C1s ) inhibitor, can be used for the research of cold agglutinin disease. C1s is a serine protease which cleaves C4 and C2 to form the C3 convertase [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2049079-64-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99050. | |
| SUV39H1 full length Active human | recombinant, expressed in baculovirus infected insect cells. Group: Fluorescence/luminescence spectroscopy. | |
| SUV39H1 human | recombinant, expressed in E. coli, ?50% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| SUV39H2 human | recombinant, expressed in E. coli, ?70% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| SUV4-20H1 human | recombinant, expressed in E. coli, ?20% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| SUV4-20h2 human | recombinant, expressed in E. coli, ?80% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| 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. Group: Signaling pathways. Alternative Names: MK-8998; CX-8998; JZP385. CAS No. 953778-58-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-101096. | |
| SUVN-1507035 | SUVN-1507035 is an agent potentially used for the treatment of anxiety and schizophrenia. Study showed that it has high affinity for mumltiple neural targets, such as 5-HT1A,5-HT2A receptor,D2S,D2L receptor and adrenoreceptor alpha1B. Uses: The potential treatment of anxiety and schizophrenia. Synonyms: SUVN 1507035; SUVN1507035. | |
| SUVN-502 | SUVN-502 is a 5-HT6 receptor antagonist originated by Suven Life Sciences. It has >1200-fold selectivity over 5-HT2A receptor with a superior profile that differentiates from competitor 5-HT6 antagonists. Phase II clinical trials for the treatment of Alzheimer's disease and Schizophrenia are on-going. Uses: Alzheimer's disease; schizophrenia. Synonyms: SUVN-502; SUVN 502; SUVN502; 1-((2-bromophenyl)sulfonyl)-5-methoxy-3-((4-methylpiperazin-1-yl)methyl)-1H-indole. Grades: 98%. CAS No. 701205-60-9. Molecular formula: C21H24BrN3O3S. Mole weight: 478.41. | |
| SUVN-911 | SUVN-911 is a potent, selective, brain penetrated and orally bioavailable neuronal nicotinic acetylcholine α4β2 receptor antagonist, with a K i of 1.5 nM. SUVN-911 has antidepressant activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2414674-71-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-136146. | |
| SUVN-D4010 | SUVN-D4010 is a selective Serotonin 4 receptor partial agonist originated by Suven Life Sciences. Phase I clinical trials for the treatment of Alzheimer's disease and Schizophrenia are on-going. Uses: Alzheimer's disease; schizophrenia. Synonyms: SUVN-D4010; SUVN-D 4010; SUVN D4010; SUVN-1004028; SUVN-D-1208045; SUVN-D1003019; SUVN-D1104010; SUVN-D1108121;2-(1-isopropyl-1H-indazol-3-yl)-5-(1-(3-methoxypropyl)piperidin-4-yl)-1,3,4-oxadiazole. Grades: 98%. CAS No. 1428862-32-1. Molecular formula: C21H29N5O2. Mole weight: 383.49. | |
| SUVN-G3031 hydrochloride | SUVN-G3031 is a Histamine H3 receptor antagonist originated by Suven Life Sciences. Blockade of Histamine H3 receptor can augment the pre-synaptic release of both histamine and other neurotransmitters including acetylcholine from cholinergic neurons. In Aug 2016, Suven Life Sciences initiated a phase I pharmacokinetics trial for treatment of Cognition disorders in Healthy volunteers in USA. Uses: Cognition disorders. Synonyms: N-[4-(1-cyclobutyl piperidin-4-yloxy)-phenyl]-2-(morpholin-4-yl) acet amide dihydrochloride;1394808-82-2 (free base). Grades: 98%. CAS No. 1394808-20-8. Molecular formula: C21H33Cl2N3O3. Mole weight: 446,41. | |
| SUVN-I-6107 | SUVN-I-6107 is a positive allosteric modulators of muscarinic acetylcholine M1 receptor with high selectivity and activity, which is promisingly used for the treatment of Alzheimer's disease. It has the excellent stability, and exhibits satisfactory safety in mouse study. Uses: The potential treatment of alzheimer's disease. Synonyms: SUVN I 6107. | |
| 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. Group: Inhibitory antibodies. 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. | Worldwide |
| Suxibuzone | Suxibuzone is a compound used for the study of joint and muscle pain, and it is a prodrug of the non-steroidal anti-inflammatory drug Phenylbutazone. Uses: Scientific research. Group: Signaling pathways. CAS No. 27470-51-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-B1079. | |
| Suzetrigine | Suzetrigine (VX-548) is an orally active and highly selective Na V 1.8 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. Group: Signaling pathways. Alternative Names: VX-548. CAS No. 2649467-58-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148800. | |
| 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. Grades: ≥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. Grades: ≥95%. Molecular formula: C58H104N20O18S. Mole weight: 1401.65. | |
| 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 |
| S-Verapamil HCl | S-Verapamil HCl is an inhibitor of the p-glycoprotein efflux pump in multidrug resistant tumor cells. Synonyms: (S)-(-)-Verapamil Hydrochloride; (α S) -α -[3-[[2- (3, 4-Dimethoxyphenyl) ethyl]methylamino]propyl]-3, 4-dimethoxy-α - (1-methylethyl) -benzeneacetonitrile Hydrochloride; (S)-Verapamil Hydrochloride; (-)-Verapamil Hydrochloride (α S) -α -[3-[[2- (3, 4-Dimethoxyphenyl) ethyl]methylamino]propyl]-3, 4-dimethoxy-α - (1-methylethyl) -benzeneacetonitrile Hydrochloride; (S)-Verapamil Hydrochloride; (-)-Verapamil Hydrochloride. CAS No. 36622-28-3. Molecular formula: C27H38N2O4. HCl. Mole weight: 491.07. | |
| S(?)-Verapamil hydrochloride hydrate | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| S(+)-?-Vigabatrin | solid. Group: Fluorescence/luminescence spectroscopy. | |
| SW033291 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| SW033291 | SW033291 is a potent and selective 15-hydroxyprostaglandin dehydrogenase (15-PGDH) enzyme inhibitor. SW033291 has been shown to promote hematopoietic recovery following murine transplant. Synonyms: SW-033291; SW 033291; 2-(butane-1-sulfinyl)-4-phenyl-6-(thiophen-2-yl)thieno[2,3-b]pyridin-3-amine. Grades: >98%. CAS No. 459147-39-8. Molecular formula: C21H20N2OS3. Mole weight: 412.58. | |
| SW044248 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| SW044248 | SW044248 is a potent and selective Topoisomerase I inhibitor. SW044248 killed approximately 15% of a panel of 74 NSCLC cell lines and was nontoxic to immortalized human bronchial cell lines. Synonyms: SW044248; SW-044248; SW 044248. Grades: 98%. CAS No. 522650-83-5. Molecular formula: C22H23N5O2S. Mole weight: 421.52. | |
| SW-100 | SW-100, a selective histone deacetylase 6 (HDAC6) inhibitor with an IC 50 of 2.3 nM, shows at least 1000-fold selectivity for HDAC6 relative to all other HDAC isozymes. SW-100 displays a significantly improved ability to cross the blood-brain-barrier [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2126744-35-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-115475. | |
| SW155246 | SW155246 is an inhibitor of DNA methyltransferase 1 (DNMT1) with IC50 value of 1.2 μM, displaying 30-fold selectivity for inhibition of human DNMT1 versus human or murine DNMT3A or -3B. It was shown to inhibit global methylation in HeLa cells, and reactivate expression of the tumor suppressor gene RASSF1A in A549 cells. Synonyms: 4-chloro-N-(4-hydroxynaphthalen-1-yl)-3-nitrobenzenesulfonamide. Grades: ≥98%. CAS No. 420092-79-1. Molecular formula: C16H11ClN2O5S. Mole weight: 378.8. | |
| SW155246 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| 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 Granulated Seaweed | Seaweed Granules. Uses: Agriculture, horticulture, amenity & animal feed. Alternative Names: Soil improver & animal feed supplements. Grades: High. Pack Sizes: 500KG. Molecular formula: Fertilizer. Sold wholesale for blending & formulating. Categories: Seaweed granules, algae, Soil Conditioners. |  |
| 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 trifluoroacetate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| SW203668 trifluoroacetate salt | SW203668 is an irreversible inhibitor of stearoyl-CoA desaturase (IC50 = 54 nM). It is selectively cytotoxic to H2122, H460, HCC44, and HCC95 cell lines. Synonyms: SW203668 TFA; 4-(aminophenylmethyl)-N-(6-methoxy-2-benzothiazolyl)-benzamide trifluoroacetate salt. Grades: ≥98%. CAS No. 2117405-48-6. Molecular formula: C22H19N3O2S·CF3COOH. Mole weight: 503.49. | |
| SW2 Refined seaweed granules | Refined Seaweed Granules. Uses: Agriculture, horticulture, amenity. Alternative Names: Soil improver. Pack Sizes: 500KG. Molecular formula: Fertilizer with greater water holding capacity. Categories: Seaweed granules, algae, Soil Conditioners. | |
| SW2+ Refined seaweed granules with beneficial soil microbes | Refined Seaweed Granule with beneficial soil microbes. Uses: Agriculture, horticulture, amenity. Alternative Names: Soil improver. Pack Sizes: 500KG. Molecular formula: Fertilizer with greater water holding capacity. Categories: Seaweed granules, algae, Soil Conditioners. | |
| SW480 Cell Lysate, LiCl-treated | Western Blot positive control cell lysate for C2069-48D. Cell lysate from SW480 cells. Serum starved cells were treated for 15min with LiCl. Group: Biologicals. Grades: Lysate. Pack Sizes: 200ul. US Biological Life Sciences. | Worldwide |
| Swainsonine | Swainsonine. Group: Biochemicals. Grades: Purified. CAS No. 72741-87-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Swainsonine | synthetic. Group: Fluorescence/luminescence spectroscopy. | |
| Swainsonine | Swainsonine. CAS No. 72741-87-8. Product ID: 8-04858. Molecular formula: C8H15NO3. Mole weight: 173.2. Properties: antibiotic. |  |
| Swainsonine | Swainsonine (Tridolgosir) is an natural indolizidine alkaloid, a potent and reversible α-mannosidase inhibitor. Swainsonine induces apoptosis and cell cycle arrest at G2/M phase. Swainsonine shows anti-tumor activity [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Tridolgosir. CAS No. 72741-87-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N6722. | |
| Swainsonine (8a,b-Octahydroindolizidine-1a,2a,8b-triol) | Swainsonine is a plant alkaloid derived from Swainsona canes. Group: Biochemicals. Alternative Names: 8a,b-Octahydroindolizidine-1a,2a,8b-triol. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Swalpamycin | Swalpamycin is a 16-membered ring macrolide antibiotic produced by Str.sp.Y-84, 30967. Activity against gram-positive bacteria. Synonyms: Oxacyclohexadeca-3,11,13-triene-2,10-dione, 15-(((6-deoxy-2,3-di-O-methyl-beta-D-allopyranosyl)oxy)methyl)-6-(((4S,5R,6R,7S,9R)-6-hydroxy-4,9-dimethyl-2-oxo-1,3,8-trioxaspiro(4.5)dec-7-yl)oxy)-5,7,9,16-tetramethyl-, (3E,5S,6S,7S,9R,11E,13E,15R,16R)-. Grades: >98%. CAS No. 112008-27-2. Molecular formula: C37H56O14. Mole weight: 724.83. | |
| SWCNT | SWCNT. Group: Single wall cnt. CAS No. 308068-56-6. >98% (SWNT). | |
| SWCNT (Amino Functional Group) | SWCNT (Amino Functional Group). Group: Single wall cnt. >80% (SWCNT). | |
| SWCNT COOH | SWCNT COOH. Group: Single wall cnt. >95% (SWNT). | |
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