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| Product | Description | |
|---|---|---|
| S,S-Diphenylsulfilimine Monohydrate | S,S-Diphenylsulfilimine Monohydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 68837-61-6. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. |  Worldwide |
| Sse9 I | One unit of the enzyme is the amount required to hydrolyze 1 μg of pBR322 DNA in 1 hour at 55°C in a total reaction volume of 50 μl. Applications: After 5-fold overdigestion with enzyme more than 95% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 500 U; 2500U. ↑AATT TTAA&darr. Activity: 5000u.a./ml. Appearance: 10 X SE-buffer B, BSA. Storage: -20°C. Form: Liquid. Source: An E.coli strain that carries the cloned Sse9 I gene from Sporosarcina species. Pack: 10 mM Tis-HCl (pH 7.5); 50 mM NaCl; 0.1 mM EDTA; 1 mM DTT; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1180RE. |  |
| S, S'-Ethylenebis (glutathione) | S, S'-Ethylenebis (glutathione) is a haloethane-glutathione conjugate formed via GSH transferases. S, S'-Ethylenebis (glutathione) formation is used to study the polymorphism in glutathione conjugation activity of human erythrocytes towards ethylene dibromide. Group: Biochemicals. Alternative Names: 2,2'-(1,2-Ethanediyl)bis[L-γ-glutamyl-L-cysteinylglycine. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| 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-(?)-SKF-38393 hydrochloride | solid. Group: Fluorescence/luminescence spectroscopy. |  |
| Ssp I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 10-fold overdigestion with enzyme 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 500 U; 2500U. AAT↑ATT TTA↓TAA. Activity: 10000u.a./ml. Appearance: 10 X SE-buffer K, BSA. Storage: -20°C. Form: Liquid. Source: An E.coli strain, that carries the cloned gene SspI from Sphaerotilus species. Pack: 10 mM Tris-HCl (pH 7.5); 200 mM NaCl; 0,1 mM EDTA; 1 mM DTT; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1181RE. | |
| 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. | |
| SSR 146977 hydrochloride | SSR 146977 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 264618-38-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| 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. | |
| SSR 69071 | SSR 69071. Group: Biochemicals. Grades: Purified. CAS No. 344930-95-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| s,s,s-Csdphen | s,s,s-Csdphen. Uses: Designed for use in research and industrial production. Additional or Alternative Names: S,S,S-CsDphen, 676270-65-8. Product Category: Heterocyclic Organic Compound. CAS No. 676270-65-8. Molecular formula: C23H28N2O3S. Mole weight: 412.545020 [g/mol]. Purity: 0.96. IUPACName: N-[(1S,2S)-2-amino-1,2-diphenylethyl]-7,7-dimethyl-3-oxobicyclo[2.2.1]heptane-4-sulfonamide. Canonical SMILES: CC1(C2CCC1(C(=O)C2)S(=O)(=O)NC(C3=CC=CC=C3)C(C4=CC=CC=C4)N)C. Density: 1.28g/cm³. Product ID: ACM676270658. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 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. | |
| SSTF | SSTF. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 10-Phenyl-2'-(triphenylsilyl)-10H-spiro[acridine-9,9'-fluorene]. Product Category: Organic Light Emitting Diode (OLED). CAS No. 1454372-37-2. Molecular formula: C49H35NSi. Mole weight: 665.89 g/mol. Product ID: ACM1454372372. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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-succinylglutathione hydrolase | This enzyme belongs to the family of hydrolases, specifically those acting on thioester bonds. The systematic name of this enzyme class is S-succinylglutathione hydrolase. Group: Enzymes. Enzyme Commission Number: EC 3.1.2.13. CAS No. 50812-22-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3548; S-succinylglutathione hydrolase; EC 3.1.2.13; 50812-22-1. Cat No: EXWM-3548. | |
| S-Sulfo-DL-cysteine-[2,3,3-d3] | S-Sulfo-DL-cysteine-[2,3,3-d3] is a labelled S-Sulfocysteine. S-Sulfocysteine is a potent NMDA-receptor agonist. Synonyms: White to off-white powder. Grade: 98%. CAS No. 2687960-80-9. Molecular formula: C3H4D3NO5S2. Mole weight: 204.24. |  |
| S-Sulfo-L-cysteine sodium salt | S-Sulfo-L-cysteine sodium salt. Group: Biochemicals. Grades: Purified. CAS No. 7381-67-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| S-Sulfo-L-cysteine Sodium Salt | S-Sulfo-L-cysteine sodium salt is an EAA receptor agonist. It is also reported to be an agonist at mGlu1α and mGlu5a subtypes expressed in clonal RGT cell lines. Synonyms: L-Cysteine, Hydrogen Sulfate (Ester), Monosodium Salt (6CI,8CI); L-Cysteine, Hydrogen Sulfate (Ester), Monosodium Salt (9CI); NSC 344479; S-Sulfocysteine Monosodium Salt; S-Sulfocysteine Sodium Salt; Sodium Cysteine-S-sulfonate. Grade: 85%. CAS No. 7381-67-1. Molecular formula: C3H6NNaO5S2. Mole weight: 223.20. | |
| S-(-)-Sulpiride | Dopamine D2 and D3-receptor antagonist. Antipsychotic; antidepressant; antiemetic. Group: Biochemicals. Alternative Names: 5-(Aminosulfonyl)-N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-2-benzamide; (-)-N-[(1-Ethyl-2-pyrrolidinyl)methyl]-5-sulfamoyl-o-anisamide; (-)-Sulpiride; L-Sulpiride; Levobren; Levopraid; Levosulpiride; S-(-)-Sulpiride; S-Sulpiride; l-Sulpiride; Levopride; Sulpid. Grades: Highly Purified. CAS No. 23672-07-3. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| ST034307 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| ST 1059. 1-(2,5-Dimethoxyphenyl)-2-aminoethanol, de-Glymidodrine, Desglymidodrine (1-(2,5-Dimethoxyphenyl)-2-aminoethanol, de-Glymidodrine, Desglymidodrine) | A metabolite of Midodrine. It induces alpha-adrenergic receptor stimulation of both arterial and venous systems without direct central nervous systme of cardiac effects. Group: Biochemicals. Alternative Names: 1-(2,5-Dimethoxyphenyl)-2-aminoethanol, de-Glymidodrine, Desglymidodrine. Grades: Highly Purified. CAS No. 3600-87-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| ST 1059-d6. (Desglymidodrine-d6) | ST 1059-d6(Desglymidodrine-d6). Group: Biochemicals. Alternative Names: 1-(2,5-Dimethoxyphenyl)-2-aminoethanol-d6; α-(Aminomethyl)-2,5-dimethoxy-benzyl Alcohol-d6; α-(Aminomethyl)-2,5-dimethoxy-benzenemethanol-d6; de-Glymidodrine, Desglymidodrine-d6. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C10H9D6NO3, Molecular Weight: 203.27. US Biological Life Sciences. | Worldwide |
| ST 1059(desglymidodrine) | ST 1059(desglymidodrine). Group: Biochemicals. Alternative Names: 1-(2',5'-Dimethoxyphenyl)-2-aminoethanol; a-(Aminomethyl)-2,5-dimethoxy-benzyl alcohol; a-(Aminomethyl)-2,5-dimethoxy-benzenemethanol. Grades: Highly Purified. CAS No. 3600-87-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C10H15NO3. US Biological Life Sciences. | Worldwide |
| ST1326 | ST1326. Group: Others. Synonyms: Teglicar. Purity: >99%. Mole weight: 399.611. Stability: 1 Year. Storage: -20°C. Avanti Polar Lipids; lipid products; bioactive lipids; fluorescent lipids; singnal transduction; cell pathways; Teglicar; ST1326; (R)-3-(3-tetradecylureido)-4-(trimethylammonio)butanoate. Cat No: FLBZ-089. | |
| ST1926 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| 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. | |
| ST1936 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| ST 1936 oxalate | ST 1936 oxalate. Group: Biochemicals. Grades: Purified. CAS No. 1210-81-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| ST247 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| 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. | |
| ST638 | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| 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. | |
| ST 91 | ST 91. Group: Biochemicals. Grades: Purified. CAS No. 4749-61-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| STA-21 | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| STA-4783 | STA-4783 Inhibitor. Uses: Scientific use. Product Category: T6170. CAS No. 488832-69-5. |  |
| Stabilized Gold Nanoparticles | Stabilized Gold Nanoparticles. Uses: Conjugate development, immunostaining, lateral flow assays, biological sensor development (e.g. lspr-based assays), electron microscopy, dark field microscopy, surface enhanced raman spectroscopy (sers). Group: other s. |  |
| Stabilizer 9000 (technical grade) | Stabilizer 9000 (technical grade). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,4-Diisocyanato-1,3,5-tris(1-methyl)-benzene homopolymer. Product Category: Promotional Products. CAS No. 29963-44-8. Purity: Tech. Product ID: ACM29963448-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Stachartin A | Stachartin A is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrysin; 3-Buten-2-one, 4-[(1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6',7',8',8'a-octahydro-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethylspiro[benzofuran-2(3H), 1'(2'H)-naphthalen]-7-yl]-, (3E)-. Grade: 98.0%. CAS No. 1978388-54-3. Molecular formula: C26H36O5. Mole weight: 428.56. | |
| Stachartin B | Stachartin B is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrylactone B; Spiro[benzo[2,1-b:3,4-c']difuran-2(8H),1'(2'H)-naphthalen]-8-one, 3,3',4',4'a,5',6,6',7',8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-. Grade: 97.5%. CAS No. 1978388-55-4. Molecular formula: C23H30O5. Mole weight: 386.48. | |
| Stachartin C | Stachartin C is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrylactone C. Grade: 98.0%. CAS No. 1978388-56-5. Molecular formula: C29H41NO6. Mole weight: 499.64. | |
| Stachartin D | Stachartin D is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrylactone D. Grade: 97.0%. CAS No. 1978388-57-6. Molecular formula: C30H43NO6. Mole weight: 513.67. | |
| Stachartin E | Stachartin E is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrylactone E. Grade: 98.0%. CAS No. 1978388-58-7. Molecular formula: C33H41NO6. Mole weight: 547.68. | |
| Stachybocin A | It is a receptor antagonist produced by the strain of Stachybotrys sp. M6222. It inhibits the binding of I-ET-1 to rat ETA receptors with IC50 of 2.3 X 10-5 (mol/L). It also inhibits the binding of I-ET-1 to human ETA receptors and human ETB receptors with IC50 (mol/L) of 1.3 X 10-5 and 7.9 X 10-6, respectively. Synonyms: Spirodihydrobenzofuranlactam ?; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-[(1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl]-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, (aS,1'R,2'R,4'aS,6'R,8'aS)-; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-(3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, [1'R-[1'a[S*(1'R*,2'R*,4'aS*,6'R*,8'S*)],2'a,4'aa,6'a,8'ab]]-; AM 6222A. CAS No. 158827-60-2. Molecular formula: C52H70N2O10. Mole weight: 883.12. | |
| Stachybocin B | It is a receptor antagonist produced by the strain of Stachybotrys sp. M6222. It inhibits the binding of I-ET-1 to rat ETA receptors with IC50 of 2.8 X 10-5 (mol/L). It also inhibits the binding of I-ET-1 to human ETA receptors and human ETB receptors with IC50 (mol/L) of 1.2 X 10-5 and 9.5 X 10-6, respectively. Synonyms: Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-[(1'R,2'R,4'aS,6'S,7'R,8'aS)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6',7'-trihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl]-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, (aS,1'R,2'R,4'aS,6'R,8'aS)-; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-(3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6',7'-trihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, [1'R-[1'a[S*(1'R*,2'R*,4'aS*,6'R*,8'S*)],2'a,4'aa,6'a,7'a,8'ab]]-; AM 6222B. CAS No. 158827-61-3. Molecular formula: C52H70N2O11. Mole weight: 899.12. | |
| Stachybocin C | It is a receptor antagonist produced by the strain of Stachybotrys sp. M6222. It inhibits the binding of I-ET-1 to rat ETA receptors with IC50 of 2.9 X 10-5 (mol/L). It also inhibits the binding of I-ET-1 to human ETA receptors and human ETB receptors with IC50 (mol/L) of 1.5 X 10-5 and 9.4 X 10-6, respectively. Synonyms: Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-[(1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl]-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6',7'-trihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, (aS,1'R,2'R,4'aS,6'S,7'R,8'aS)-; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-(3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6',7'-trihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, [1'R-[1'a[S*(1'R*,2'R*,4'aS*,6'R*,8'aS*)],2'a,4'aa,6'a,7'a,8'ab]]-; AM 6222C. CAS No. 158827-62-4. Molecular formula: C52H70N2O11. Mole weight: 899.12. | |
| Stachybotramide | Stachybotramide is produced by the mycelia and culture broth of Stachybotrys sp. Stachybotramide can stimulate the plasma cholesteryl ester transfer protein (CETP)-mediated transfer of cholesteryl esters (CE) from high density lipoprotein (HDL) to very low density lipoprotein (VLDL) and low density lipoprotein (LDL). Synonyms: Spirodihydrobenzofuranlactam II; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one, 3',4',4'a,5',6',7,7',8,8',8'a-decahydro-4,6'-dihydroxy-7-(2-hydroxyethyl)-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-; (1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6',7,7',8,8',8'a-Decahydro-4,6'-dihydroxy-7-(2-hydroxyethyl)-2',5',5',8'a-tetramethylspiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one; Stachybotrin; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one, 3',4',4'a,5',6',7,7',8,8',8'a-decahydro-4,6'-dihydroxy-7-(2-hydroxyethyl)-2',5',5',8'a-tetramethyl-, [1'R-(1'α,2'α,4'aα,6'α,8'aβ)]-. Grade: 97.5%. CAS No. 149598-71-0. Molecular formula: C25H35NO5. Mole weight: 429.55. | |
| Stachybotrin A | It is produced by the strain of Stachyborrys sp. It has antimicrobial and antifungal activity. CAS No. 144373-26-2. Molecular formula: C23H31NO5. Mole weight: 401.49. | |
| Stachybotrin B | It is produced by the strain of Stachyborrys sp. It has antimicrobial and antifungal activity. Synonyms: (+)-Stachybotrin B. CAS No. 144385-02-4. Molecular formula: C23H31NO4. Mole weight: 385.50. | |
| Stachybotrin C | It is a neuritogenic agent produced by the strain of Stachyborrys parvispora F4708. It promotes the enlargement of the neural sinus of P12 cells, and the effect of Stachybotrin C is obvious, but the effect of Parvisporin is weak. Synonyms: Pyrano[2,3-e]isoindol-7(2H)-one, 2-[(3E)-4,8-dimethyl-3,7-nonadien-1-yl]-3,4,8,9-tetrahydro-3,5-dihydroxy-8-[2-(4-hydroxyphenyl)ethyl]-2-methyl-, (2R,3R)-rel-; Pyrano[2,3-e]isoindol-7(2H)-one, 2-(4,8-dimethyl-3,7-nonadienyl)-3,4,8,9-tetrahydro-3,5-dihydroxy-8-[2-(4-hydroxyphenyl)ethyl]-2-methyl-, [2a(E),3a]-; Antibiotic NG 245. CAS No. 150351-23-8. Molecular formula: C31H39NO5. Mole weight: 505.64. | |
| Stachybotrolide | Stachybotrolide is produced by Stachybotrys alternans. Synonyms: Stachybotrylactone; (2R,2'R,4a'S,6'R,8a'S)-4,6'-dihydroxy-2',5',5',8a'-tetramethyl-3',4',4a',5',6',7',8',8a'-octahydro-2'H,3H-spiro[benzo[2,1-b:3,4-c']difuran-2,1'-naphthalen]-6(8H)-one; Spiro[benzo[2,1-b:3,4-c']difuran-2(3H),1'(2'H)-naphthalen]-6(8H)-one, 3',4',4'a,5',6',7',8',8'a-octahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, [1'R-(1'α,2'α,4'aα,6'α,8'aβ)]-; Spiro[benzo[2,1-b:3,4-c']difuran-2(3H),1'(2'H)-naphthalen]-6(8H)-one, 3',4',4'a,5',6',7',8',8'a-octahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-. Grade: 97.5%. CAS No. 149691-31-6. Molecular formula: C23H30O5. Mole weight: 386.48. | |
| Stachybotrylactam | An unusual spirodihydrobenzofuranlactam mycotoxin isolated from Stachybotrys sp. It shows immunosuppressant and weak HIV protease activity and shows diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition. Synonyms: Stachybotrylactam; 163391-76-2; 3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-furo[2,3-e]isoindole]-6'-one; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one, 3',4',4'a,5',6',7,7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-; CID 45934402; Compound NP-020819; DTXSID70672955; CHEBI:201797; AKOS040737949; J-010041; (3R,4aS,7R,8R,8aS)-3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-uro[2,3-e]isoindole]-6'-one; 4,6'-DIHYDROXY-2',5',5',8'A-TETRAMETHYL-3',4',4'A,6',7,7',8,8'-OCTAHYDRO-2'H,3H-SPIRO[FURO[2,3-E]ISOINDOLE-2,1'-NAPHTHALEN]-6-ONE. Grade: >95% by HPLC. CAS No. 163391-76-2. Molecular formula: C23H31NO4. Mole weight: 385.50. | |
| Stachybotrylactam (2-deoxy Antibiotic F1839A) | Isolated from a Stachybotrys sp., this unusual spirodi hydrobenzofuranlactam mycotoxin shows immuno-suppressant and weak HIV protease activity. Members of this structural class show diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition. Group: Biochemicals. Alternative Names: 2-deoxy Antibiotic F1839A. Grades: Highly Purified. CAS No. 163391-76-2. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| 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 | Stachydrine. Group: Biochemicals. Grades: Plant Grade. CAS No. 471-87-4. Pack Sizes: 20mg. Molecular Formula: C7H13NO2, Molecular Weight: 143.18. US Biological Life Sciences. | Worldwide |
| Stachydrine hydrochloride | Stachydrine hydrochloride is extracted from the flower of Chrysanthemum parthenium. It promoted the protein expression of IL-12 and IL-6, as well as the mRNA expression of T-bet and RORγt, while inhibiting the mRNA expression of GATA-3 and Foxp3. Synonyms: Pyrrolidinium, 2-carboxy-1,1-dimethyl-, chloride (1:1), (2S)-; Pyrrolidinium, 2-carboxy-1,1-dimethyl-, chloride, (2S)-; Pyrrolidinium, 2-carboxy-1,1-dimethyl-, chloride, (S)-; Stachydrine, chloride; Cadabine hydrochloride; (S)-2-Carboxy-1,1-dimethylpyrrolidinium chloride; (S)-2-Carboxy-1,1-dimethylpyrrolidin-1-ium chloride. Grade: >98%. CAS No. 4136-37-2. Molecular formula: C7H14ClNO2. Mole weight: 179.64. | |
| 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. | |
| Stachydrine Hydrochloride | Stachydrine hydrochloride is extracted from the flower of Chrysanthemum parthenium. It promoted the protein expression of IL-12 and IL-6, as well as the mRNA expression of T-bet and RORγt, while inhibiting the mRNA expression of GATA-3 and Foxp3. Group: Biochemicals. Alternative Names: Turicine HCl; (S)-2-Carboxy-1,1-dimethylpyrrolidinium chloride; 2-Carboxy-1,1-dimethylpyrrolidinium chloride. Grades: Highly Purified. CAS No. 4136-37-2. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| 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. | |
| S Tag Peptide | S Tag Peptide, a 15 amino acid peptide derived from RNase A, is an oligopeptide used for improving protein solubility. Synonyms: Lys-Glu-Thr-Ala-Ala-Ala-Lys-Phe-Glu-Arg-Gln-His-Met-Asp-Ser; L-lysyl-L-alpha-glutamyl-(3xi)-L-threonyl-L-alanyl-L-alanyl-L-alanyl-L-lysyl-L-phenylalanyl-L-alpha-glutamyl-L-arginyl-L-glutaminyl-L-histidyl-L-methionyl-L-alpha-aspartyl-L-serine; S Tag. Grade: ≥95%. Molecular formula: C73H117N23O25S. Mole weight: 1748.91. | |
| Stainless Steel disc, 102mm (4.0in) dia x 12.7mm (0.5in) thick, Type 304 | Stainless Steel disc, 102mm (4.0in) dia x 12.7mm (0.5in) thick, Type 304. Group: Alloys. | |
| Stainless Steel disc, 152mm (6.0in) dia x 12.7mm (0.5in) thick, Type 304 | Stainless Steel disc, 152mm (6.0in) dia x 12.7mm (0.5in) thick, Type 304. Group: Alloys. | |
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