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| Product | Description | |
|---|---|---|
| S-Hydroxychloroquine-[d4] | A labelled analogue of Hydroxychloroquine. Hydroxychloroquine is a medication used for the treatment of certain malaria. Synonyms: (S)-2-[[4-[(7-Chloro-4-quinolinyl)amino]pentyl]ethylamino-d4]ethanol. Grade: >98%. Molecular formula: C18H22D4ClN3O. Mole weight: 339.89. |  |
| S-(hydroxymethyl)glutathione dehydrogenase | The substrate, S-(hydroxymethyl)glutathione, forms spontaneously from glutathione and formaldehyde; its rate of formation is increased in some bacteria by the presence of EC 4.4.1.22, S-(hydroxymethyl)glutathione synthase. This enzyme forms part of the pathway that detoxifies formaldehyde, since the product is hydrolysed by EC 3.1.2.12, S-formylglutathione hydrolase. The human enzyme belongs to the family of zinc-dependent alcohol dehydrogenases. Also specifically reduces S-nitrosylglutathione. Group: Enzymes. Synonyms: NAD-linked formaldehyde dehydrogenase (incorrect); formaldehyde dehydrogenase (incorrect); formic dehydrogenase (incorrect); class III . Enzyme Commission Number: EC 1.1.1.284. 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-0192; S-(hydroxymethyl)glutathione dehydrogenase; EC 1.1.1.284; NAD-linked formaldehyde dehydrogenase (incorrect); formaldehyde dehydrogenase (incorrect); formic dehydrogenase (incorrect); class III alcohol dehydrogenase; ADH3; χ-ADH; FDH (incorrect); formaldehyde dehydrogenase (glutathione) (incorrect); GS-FDH (incorrect); glutathione-dependent formaldehyde dehydrogenase (incorrect); NAD-dependent formaldehyde dehydrogenase; GD-FALDH; NAD- and glutathione-dependent formaldehyde dehydrogenase. Cat No: EXWM-0192. |  |
| S-(hydroxymethyl)glutathione synthase | The enzyme from Paracoccus denitrificans accelerates the spontaneous reaction in which the adduct of formaldehyde and glutathione is formed, i.e. the substrate for EC 1.1.1.284, S-(hydroxymethyl)glutathione dehydrogenase, in the formaldehyde-detoxification pathway. Group: Enzymes. Synonyms: glutathione-dependent formaldehyde-activating enzyme; Gfa; S-(hydroxymethyl)glutathione formaldehyde-lyase. Enzyme Commission Number: EC 4.4.1.22. CAS No. 425642-27-9. 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-5324; S-(hydroxymethyl)glutathione synthase; EC 4.4.1.22; 425642-27-9; glutathione-dependent formaldehyde-activating enzyme; Gfa; S-(hydroxymethyl)glutathione formaldehyde-lyase. Cat No: EXWM-5324. | |
| S-(hydroxymethyl)mycothiol dehydrogenase | S-hydroxymethylmycothiol is believed to form spontaneously from formaldehyde and mycothiol. This enzyme oxidizes the product of this spontaneous reaction to S-formylmycothiol, in a reaction that is analogous to EC 1.1.1.284, S-(hydroxymethyl)glutathione dehydrogenase. Group: Enzymes. Synonyms: NAD/factor-dependent formaldehyde dehydrogenase; mycothiol-dependent formaldehyde dehydrogenase. Enzyme Commission Number: EC 1.1.1.306. CAS No. 192140-85-5. 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-0217; S-(hydroxymethyl)mycothiol dehydrogenase; EC 1.1.1.306; 192140-85-5; NAD/factor-dependent formaldehyde dehydrogenase; mycothiol-dependent formaldehyde dehydrogenase. Cat No: EXWM-0217. | |
| S-Hydroxy Topiramate | A metabolite of Topiramate. Group: Biochemicals. Alternative Names: 4,5-O-[(1S)-2-Hydroxy-1-methylethylidene]-2,3-O-(1-methylethylidene)- β-D-fructopyranose 1-Sulfamate; 9-Hydroxy Topiramate. Grades: Highly Purified. CAS No. 198215-62-2. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| S-Hypoglycine A, 85% | S-Hypoglycine A, 85%. Group: Biochemicals. Grades: Highly Purified. CAS No. 156-56-9. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Shz 1 | Shz 1. Group: Biochemicals. Grades: Purified. CAS No. 326886-05-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Shz-1 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Shz-1 | Shz-1, a small cardiogenic molecule, induces various cardiac-specific genes including sarcomeric tropomyosin in P19CL6 cells. Shz-1 induces Nkx2.5 expression in mouse. Shz-1 activates the axolotl TPM4 promoter-driven ectopic expression in C2C12 cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 326886-05-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108440. |  |
| Shz-1 (2-hydrazide benzenesulfonic acid) | Enhancer of myocardial regenerative repair by stem cells. Potent inducer of Nkx2.5 and a subset of other cardiac markers, including myocardin, and sarcomeric-tropomyosin (SalphaTM) in a variety of different stem/progenitor cells. Group: Biochemicals. Alternative Names: 2-hydrazide benzenesulfonic acid. Grades: Highly Purified. CAS No. 326886-05-9. Pack Sizes: 1mg, 5mg. Molecular Formula: C13H11BrN2O3S. US Biological Life Sciences. | Worldwide |
| SI-109 | SI-109 is a potent STAT3 SH2 domain inhibitor (Ki=9 nM) with antitumor activity. SI-109 effectively inhibits the transcriptional activity of STAT3 (IC50=3 ?M). SI-109 and an analog of CRBN ligand lenalidomide have been used to design PROTAC STAT3 degrader SD-36[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2429877-30-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-129603. | |
| SI-113 | SI-113 is a SGK1 inhibitor, with an IC50 of 600 nM. SI113 induces autophagy[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1392816-46-4. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-117357. | |
| SI-2 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| SI-2 hydrochloride | SI-2 (EPH 116 hydrochloride) is a highly promising SRC-3 inhibitor (PPI). SI-2 (EPH 116 hydrochloride) has a much improved toxicity and pharmacokinetic profile, with acceptable oral availability [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EPH 116 hydrochloride. CAS No. 1992052-49-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-101447A. | |
| SIAB | SIAB. Pack Sizes: Milligram Quantities: 100 mg. Order Number: CL204. |  www.prochemonline.com |
| SIA Crosslinker | SIA Crosslinker is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Synonyms: 2,5-Dioxopyrrolidin-1-yl 2-iodoacetate; N-Succinimidyl Iodoacetate; Iodoacetic acid N-hydroxysuccinimide ester. Grade: > 99.3 %. CAS No. 39028-27-8. Molecular formula: C6H6INO4. Mole weight: 283.02. | |
| SIAIS100 TFA | SIAIS100 TFA is a potent BCR-ABL PROTAC degrader with an DC50 value of 2.7 nM. SIAIS100 TFA can be used to research chronic myeloid leukemia (CML)[1]. Uses: Scientific research. Group: Signaling pathways. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-152036A. | |
| sialate O-acetylesterase | Acts on free and glycosidically bound N-acetyl- or N-glycoloyl-neuraminic acid; acts mainly on the 4-O- and 9-O-acetyl groups. Also acts on some other O-acetyl esters, both cyclic and acyclic compounds, which are not sialic acids. Group: Enzymes. Synonyms: N-acetylneuraminate acetyltransferase; sialate 9(4)-O-acetylesterase; sialidase. Enzyme Commission Number: EC 3.1.1.53. CAS No. 89400-31-7. 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-3481; sialate O-acetylesterase; EC 3.1.1.53; 89400-31-7; N-acetylneuraminate acetyltransferase; sialate 9(4)-O-acetylesterase; sialidase. Cat No: EXWM-3481. | |
| Sialic Acid Aldolase from Escherichia coli K12, Recombinant | In enzymology, a N-acetylneuraminate lyase (EC 4.1.3.3) is an enzyme that catalyzes the chemical reaction:N-acetylneuraminate<-> N-acetyl-D-mannosamine + pyruvate. Hence, this enzyme has one substrate, N-acetylneuraminate, and two products, N-acetyl-D-mannosamine and pyruvate. This enzyme belongs to the family of lyases, specifically the oxo-acid-lyases, which cleave carbon-carbon bonds. This enzyme participates in aminosugars metabolism. Sialic acid aldolases, or n-acetylneuraminate lyases, catalyze the reversible aldol cleavage of n-acetylneuraminic acid to form pyruvate and n-acetyl-d-mannosamine. in nature, n-acetylneuraminate lyase mainly occurs in pathogen...neuraminate pyruvate-lyase; N-acetylneuraminate pyruvate-lyase. Enzyme Commission Number: EC 4.1.3.3. CAS No. 9027-60-5. NALase. Activity: > 3.0 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing Tris-HCl and NaCl. Source: E. coli BL21. Species: Escherichia coli K12. EC 4.1.3.3; Sialic Acid Aldolase; N-Acetylneuraminate lyase; N-Acetylneuraminate pyruvate-lyase (N-acetyl-D-mannosamine-forming); N-acetylneuraminic acid aldolase; acetylneuraminate lyase; sialic aldolase; sialate lyase; N-acetylneuraminic aldolase; neuraminic aldolase; N-acetylneuraminate aldolase; neuraminic acid aldolase; N-acetylneuraminic acid aldolase; neuraminate aldolase; N | |
| Sialidase 33A from Bacteroides fragilis, Recombinant | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. At least four mammalian sialidase homologs have been described in the human genome (see NEU1, NEU2, NEU3, NEU4). Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Purity: >90% as judged by SDS-PAGE. Neuraminidase. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides fragilis. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Cat No: NATE-1511. | |
| Sialidase 33A from Clostridium perfringens, Recombinant | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. At least four mammalian sialidase homologs have been described in the human genome (see NEU1, NEU2, NEU3, NEU4). Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminida. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Purity: >90% as judged by SDS-PAGE. Neuraminidase. Mole weight: 53.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium perfringens. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Cat No: NATE-1512. | |
| Sialidase 33A from Streptococcus pneumoniae, Recombinant | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. At least four mammalian sialidase homologs have been described in the human genome (see NEU1, NEU2, NEU3, NEU4). Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuramini. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Purity: >90% as judged by SDS-PAGE. Neuraminidase. Mole weight: 16.3 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Streptococcus pneumoniae. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Cat No: NATE-1513. | |
| SIalpha1 | SIalpha1 is an antibacterial peptide isolated from Sorghum bicolor (Seeds). It has activity against fungi. | |
| SIalpha2 | SIalpha2 is an antibacterial peptide isolated from Sorghum bicolor (Seeds). It has activity against fungi. | |
| Sialyl lewis a,sodium salt | Sialyl lewis a,sodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Sialyl Lewis a, Sialyl Lea tri, Sialyl-Lewis a, SLea, 3-Sialyl Lewis A, 3-SLea, CID643993, a-NeuNAc-(2>3)-b-D-Gal-(1>3)-(a-L-Fuc-[1>4])-D-GlcNAc, 92448-22-1, D-Glucose, O-(N-acetyl-a-neuraminosyl)-(2>3)-O-b-D-galactopyranosyl-(1>3)-O-[6-deoxy-a-L-galactopyranosyl-(1>4)]-2-(acetylamino)-2-deoxy- (9CI), D-glucose, O-5-(acetylamino)-3,5-dideoxy-D-glycero-alpha-D-galacto-2-nonulopyranonosyl-(2->3)-O-beta-D-galactopyranosyl-(1->3)-O-[6-deoxy-alpha-L-galactopyranosyl-(1->4)]-2-(acetylamino)-2-deoxy-. Product Category: Heterocyclic Organic Compound. CAS No. 92448-22-1. Molecular formula: C31H52N2O23. Mole weight: 820.74. Purity: 0.96. IUPACName: (2S,4S,5R,6R)-5-acetamido-2-[(2R,3R,4S,5S,6R)-2-[(2R,3R,4R,5R)-2-acetamido-5,6-dihydroxy-1-oxo-4-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyhexan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropy. Canonical SMILES: CC1C(C(C(C(O1)OC(C(CO)O)C(C(C=O)NC(=O)C)OC2C(C(C(C(O2)CO)O)OC3(CC(C(C(O3)C(C(CO)O)O)NC(=O)C)O)C(=O)O)O)O)O)O. Density: 1.66g/cm³. Product ID: ACM92448221. Alfa Chemistry ISO 9001:2015 Certified. Categories: 3'-Sialyl-Lewis-a tetrasaccharide. |  |
| Sialyl-Lewis X | Sialyl-Lewis X (sLeX) is a sialylated fucosylated tetrasaccharide, an endogenous antigen. Sialyl-Lewis X is a high-affinity ligand for selectins (E-, P-, and L-selectin) [1]. Sialyl-Lewis X binds to ELAM-1 and CD62 and has the ability to inhibits CD62-mediated neutrophil recruitment to sites of inflammation [2]. Uses: Scientific research. Group: Natural products. Alternative Names: sLeX. CAS No. 98603-84-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-W020790. | |
| Sialyltransferase Inhibitor, 3Fax-Peracetyl Neu5Ac | The Sialyltransferase Inhibitor, 3Fax-Peracetyl Neu5Ac controls the biological activity of Sialyltransferase. Group: Fluorescence/luminescence spectroscopy. | |
| Siamenoside I | Siamenoside I is one of the mogrosides that has several kinds of bioactivities. Uses: Scientific research. Group: Natural products. CAS No. 126105-12-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0612. | |
| Siamenoside I | Siamenoside I. Group: Biochemicals. Grades: Plant Grade. CAS No. 126105-12-2. Pack Sizes: 10mg. Molecular Formula: C54H92O24, Molecular Weight: 1125.29. US Biological Life Sciences. | Worldwide |
| Siamycin I | Siamycin I is a tricyclic peptide antibiotic originally isolated from Streptomyces sp. AA6532. It exhibits antiviral and antibacterial effects against HIV and HSV, as well as B. subtilis, M. luteus and S. aureus. Synonyms: Siamycin I; 164802-68-0; BMY 29304; CLGVGSCNDFAGCGYAIVCFW; FR901724; FR 901724; MS 271; DTXSID70167811; DA-51269. Grade: ≥85%. CAS No. 164802-68-0. Molecular formula: C97H131N23O26S4. Mole weight: 2163.48. | |
| Siamycin II | Siamycin II is an antibacterial peptide isolated from Streptomyces strains AA3891. It has activity against viruses. Synonyms: Cys-Leu-Gly-Ile-Gly-Ser-Cys-Asn-Asp-Phe-Ala-Gly-Cys-Gly-Tyr-Ala-Ile-Val-Cys-Phe-Trp. CAS No. 164802-69-1. Molecular formula: C98H133N23O26S4. Mole weight: 2177.50. | |
| Siastatin B | A-72363 B is a Heparanase inhibitor produced by Streptomyces nobilis SANK 60192. Synonyms: A-72363 B; 3-Piperidinecarboxylic acid, 6-(acetylamino)-4,5-dihydroxy-, (3S-(3-alpha,4-alpha,5-alpha,6-beta))-; Siastatin B microbial; (2s,3r,4s,5s)-2-(Acetylamino)-5-Carboxy-3,4-Dihydroxypiperidinium. Grade: 95%. CAS No. 54795-58-3. Molecular formula: C8H14N2O5. Mole weight: 218.21. | |
| Siastatin B | Siastatin B. Group: Biochemicals. Alternative Names: (3S,4S,5R,6R)-6-(Acetylamino-4,5-dihydroxy-3-piperidinecarboxylic acid. Grades: Highly Purified. CAS No. 54795-58-3. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C8H14N2O5. US Biological Life Sciences. | Worldwide |
| Siastatin B | lyophilized powder, from microbial. Group: Fluorescence/luminescence spectroscopy. | |
| SIB 1508Y maleate | SIB 1508Y maleate. Group: Biochemicals. Grades: Purified. CAS No. 192231-16-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SIB-1553A | SIB-1553A is an orally bioavailable nicotinic acetylcholine receptors (nAChRs) agonist, with selectivity for β4 subunit-containing nAChRs. SIB-1553A is also a selective neuronal nAChR ligand. SIB-1553A is a cognitive enhancer, and has therapeutic potential for the symptomatic treatment of Alzheimers disease and other cognitive disorders [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 191611-89-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-107676. | |
| SIB 1553A hydrochloride | SIB 1553A hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 191611-89-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SIB 1757 | ?99% (HPLC), crystalline. Group: Fluorescence/luminescence spectroscopy. | |
| SIB 1757 | SIB 1757. Group: Biochemicals. Grades: Purified. CAS No. 31993-01-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SIB-1757 | SIB-1757 is a highly selective and noncompetitive antagonist of mGlu5 receptor with an IC 50 of 0.4 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 31993-01-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-102095. | |
| SIB 1893 | >99%, solid. Group: Fluorescence/luminescence spectroscopy. | |
| SIB 1893 | SIB 1893. Group: Biochemicals. Grades: Purified. CAS No. 6266-99-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SIBA | SIBA (5'-Isobutylthioadenosine) is a transmethylation inhibitor ( SAH (HY-19528) analogue), with potent anti-proliferative activity. SIBA reversibly inhibits the production of HSV-1 by blocking methylation, specifically by blocking the 5' end-capping of viral mRNA. SIBA also inhibits the growth of tumour cells in vitro and metastatic spread in vivo. SIBA can be used in cancer, HSV-1 infection and anti-malaria studies [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 5'-Isobutylthioadenosine; 5'-Deoxy-5'-isobutylthioadenosine. CAS No. 35899-54-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-18684. | |
| Sibanomicin | It is produced by the strain of Micronconospora sp. SF2364. It has weak effect against gram-positive bacteria. Mice inoculated with leukemic P388 cells were given 2.1 and 1.0 mg/kg, which extended the survival time by 96% and 69% compared with the control group. Synonyms: 7-[[3-C-Methyl-4-(methylamino)-4,6-dideoxy-α-L-mannopyranosyl]oxy]-1,2,3,11a-tetrahydro-2-[(E)-propylidene]-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one; 5H-Pyrrolo[2,1-c][1,4]benzodiazepin-5-one, 7-[[4,6-dideoxy-3-C-methyl-4-(methylamino)-a-L-mannopyranosyl]oxy]-1,2,3,11a-tetrahydro-2-propylidene-, (2E)-; Antibiotic SF 2364. CAS No. 117782-84-0. Molecular formula: C23H31N3O5. Mole weight: 429.51. | |
| Sibenadet | Sibenadet. Group: Biochemicals. Alternative Names: 4-Hydroxy-7- [2- [ [2- [ [3- (2-phenylethoxy) propyl] sulfonyl] ethyl] amino] ethyl] -2 (3H) -benzothiazolone; AR-C 68397; AR-C 68397XX. Grades: Highly Purified. CAS No. 154189-40-9. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C22H28N2O5S2. US Biological Life Sciences. | Worldwide |
| Sibeprenlimab | Sibeprenlimab (VIS649) is a humanized IgG2 monoclonal antibody which inhibits a proliferation-inducing ligand ( APRIL ). Sibeprenlimab suppresses pathogenic immunoglobulins ( IgA and IgM ), while preserving antibody responses to mRNA-based vaccines against SARS-COV-2. Sibeprenlimab reduces urinary protein-to-creatinine ratio (UPCR) and glomerular filtration rate (GFR). Sibeprenlimab is promising for the research of IgA nephropathy (IgAN) [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: VIS649. CAS No. 2382896-07-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99901. | |
| Siberian Cocklebur Fruit Extract | Siberian Cocklebur Fruit Extract. Applications: Used for health care products, dietary supplements, herb medecine to anti-allergy and anti-bacterial. Group: Others. Synonyms: Siberian Cocklebur Fruit Extract; Xanthium sibiricum Patr. Purity: 10:1 by TLC. Appearance: Brown yellow fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Fruit. Species: Xanthium sibiricum Patr. Siberian Cocklebur Fruit Extract; Xanthium sibiricum Patr; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-149. | |
| Siberian Ginseng (Eleutherococcus Senticosus) Powder | Siberian Ginseng (Eleutherococcus Senticosus) Powder. |  CA, FL & NJ |
| Siberian ginseng extract | Siberian ginseng extract. Applications: Functional food, health care products and pharmaceuticals. Group: Others. Purity: 0.8%, 1.0%, 1.2%. Appearance: Brown-yellow powder. Source: Siberian ginseng is a shrub native to the Far East that grows 3 - 10 feet high. Its leaves are attached to a main stem by long branches. Both the branches and the stem are covered with thorns. Flowers, yellow or violet, grow in umbrella-shaped clusters, and turn into round, black berries in late summer. The root itself is woody and is brownish, wrinkled, and twisted. Siberian ginseng (Eleutherococcus senticosus), also known as eleuthero, has been used for centuries in Eastern countries, including China and Russia. Despite its name, it is only a distant relative of American (Panax quinquefolius) and Asian ginseng (Panax ginseng), and it has different active chemical components. The active ingredients in Siberian ginseng, called eleutherosides, are thought to stimulate the immune system. Siberian ginseng extract. Cat No: EXTC-202. | |
| Siberian Ginseng Liquid Extract (Eleutherococcus Senticosus) | Siberian Ginseng Liquid Extract (Eleutherococcus Senticosus). Categories: sulbutiamine; bisibutiamine. | CA, FL & NJ |
| Siberian Ginseng Root Ext 0.8 % Eleutherosides HPLC (Eleutherococcus senticosus) | Siberian Ginseng Root Ext 0.8 % Eleutherosides HPLC (Eleutherococcus senticosus). | CA, FL & NJ |
| sibiricaxanthone B | sibiricaxanthone B. Group: Biochemicals. Grades: Plant Grade. CAS No. 241125-81-5. Pack Sizes: 20mg. Molecular Formula: C24H26O14, Molecular Weight: 538.46. US Biological Life Sciences. | Worldwide |
| Sibiricose A5 | Sibiricose A5. Group: Biochemicals. Alternative Names: 3?-Feruloylsucrose; Arillanin B. Grades: Plant Grade. CAS No. 107912-97-0. Pack Sizes: 20mg. Molecular Formula: C22H30O14, Molecular Weight: 518.465. US Biological Life Sciences. | Worldwide |
| Sibiricose A6 | Sibiricose A6. Group: Biochemicals. Grades: Plant Grade. CAS No. 241125-75-7. Pack Sizes: 20mg. Molecular Formula: C23H32O15, Molecular Weight: 548.49. US Biological Life Sciences. | Worldwide |
| Sibiromycin | Sibiromycin is a naturally produced glycosylated pyrrolobenzodiazepines (PBDs). Sibiromycin is also a potent antitumor antibiotic that binds covalently to DNA in the minor groove at the NH2 of guanine [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 12684-33-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N9460. | |
| Sibiromycin | Sibiromycin is a natural compound with antitumor activity. Sibiromycin is also a potent antitumor antibiotic that binds covalently to DNA in the minor groove at the NH2 of guanine. Uses: Designed for use in research and industrial production. Product Category: Others. Appearance: Solid powder. CAS No. 12684-33-2. Molecular formula: C24H33N3O7. Mole weight: 475.54. Purity: >98%. IUPACName: 5H-Pyrrolo[2,1-c][1,4]benzodiazepin-5-one,7-[[4,6-dideoxy-3-C-methyl-4-(methylamino)-a-L-mannopyranosyl]oxy]-1,10,11,11a-tetrahydro-9,11-dihydroxy-8-methyl-2-(1E)-1-propen-1-yl-,(11R,11aS)-. Canonical SMILES: O=C1N2[C@](CC(/C=C/C)=C2)([H])[C@@H](O)NC3=C(O)C(C)=C(O[C@H]4[C@@H]([C@]([C@@H](NC)[C@H](C)O4)(C)O)O)C=C13. Product ID: ACM12684332. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sibiromycin | It is an aminoglycoside antibiotic produced by the strain of Streptosporangium sibiricum. It has anti-bacterial effect and has an inhibitory effect on reticuloendothelial sarcoma RAB-1 and oncogenic AK/LY cells. Two times of the maximum tolerated dose of intravenous administration can inhibit OZH-5 tumor and lymphosarcoma Lic-1. It has very high DNA binding affinity and cytotoxicity against cancer cell lines. Synonyms: Sybiromycin; 5H-Pyrrolo(2,1-c)(1,4)benzodiazepin-5-one, 7-((4,6-dideoxy-3-C-methyl-4-(methylamino)-alpha-L-mannopyranosyl)oxy)-1,10,11,11a-treahydro-9,11-dihydroxy-8-methyl-2-(1E)-1-propenyl-, (11R,11aS)-. CAS No. 12684-33-2. Molecular formula: C24H33N3O7. Mole weight: 475.54. | |
| Sibrafiban | Sibrafiban (RO 48-3657) is the orally active, nonpeptide, double-proagent of Ro 44-3888 and a selective glycoprotein IIb/IIIa receptor antagonist. Sibrafiban inhibits platelet aggregation [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RO 48-3657. CAS No. 172927-65-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10309. | |
| Sibrotuzumab | Sibrotuzumab (BIBH 1) is a humanized IgG1 monoclonal antibody targets fibroblast activation protein ( FAP ). Sibrotuzumab can be used for the research of colorectal cancer and non-small cell lung cancer (NSCLC) [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BIBH 1; Anti-Human FAP Recombinant Antibody. CAS No. 216669-97-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99269. | |
| Sibutramine-d6 | Deuterated Sibutramine, a serotonin and noradrenaline reuptake inhibitor (SNR). Decreases calorie intake and increases energy expenditure. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Sibutramine Hydrochloride | Sibutramine Hydrochloride is a 5-HT and noradrenaline reuptake inhibitor. Group: Biochemicals. Alternative Names: BTS 54-524; 1- (4-chlorophenyl) -N, N-di methyl - α - (2- methyl propyl ) -cyclobutane methanamine, monohydrochloride. Grades: Highly Purified. CAS No. 84485-00-7. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C17H26NCl HCl, Molecular Weight: 316.31. US Biological Life Sciences. | Worldwide |
| Sibutramine, Hydrochloride Monohydrate (BTS-54524, Reductil, Meridia) | A serotonin and noradrenaline reuptake inhibitor (SNR). Decreases calorie intake and increases energy expenditure. Group: Biochemicals. Alternative Names: BTS-54524, Reductil, Meridia. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Sibutramine Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sibutramine Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sibutramine Related Compound C | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Siccanin | It is a terpene antibiotic roduced by the strain of Helminthosporium siccans BH-34. It has activity against gram-negative bacteria, mycobacteria and fungi. Synonyms: Siccaninum; Sicanina; Siccanine; 13H-Benzo(a)furo(2,3,4-mn)xanthen-11-ol, 1,2,3,4,4a,5,6,6a,11b,13b-decahydro-4,4,6a,9-tetramethyl-, (4aS-(4aalpha,6aalpha,11balpha,13aR*,13balpha))-; 1H,11bH,13H-Benzo[a]furo[2,3,4-mn]xanthen-11-ol,2,3,4,4a,5,6,6a,13b-octahydro-4,4,6a,9-tetramethyl-, (4aS,6aS,11bR,13aS,13bS)-; (-)-Siccanin; NSC 135048. Grade: >98% by HPLC. CAS No. 22733-60-4. Molecular formula: C22H30O3. Mole weight: 342.47. | |
| Sicilic Acid, magnesium sodium salt (technical grade) | Sicilic Acid, magnesium sodium salt (technical grade). Uses: Designed for use in research and industrial production. Product Category: Promotional Products. CAS No. 101659-01-2. Purity: Tech. Product ID: ACM101659012-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| SiC Nanowire | SiC Nanowire. Group: Nanowires. |  |
| SiC Nanowire | SiC Nanowire. Group: Nanoparticles. | |
| SiC Nanowires | SiC Nanowires. Uses: Designed for use in research and industrial production. Product Category: One-Dimensional Nanomaterials. CAS No. 1568-80-5. Purity: ~98%. Product ID: ACM1568805-4. Alfa Chemistry ISO 9001:2015 Certified. | |
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