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| Product | Description | |
|---|---|---|
| Samarium (Sm) | Samarium (Sm). Alternative Names: High Purity Samarium (Sm); 99.9% Samarium (Sm); 99.99% Samarium (Sm); 99.999% Samarium (Sm). Purity: 3N-5N. |  |
| Samarium (Sm) Sputtering Targets | Samarium (Sm) Sputtering Targets. Alternative Names: Samarium (Sm) Sputtering Targets, Sm Sputtering Target, Sm Sputter Target, Sm Target, Samarium Sputtering Target, Samarium Sputter Target, Samarium Target. Purity: 99.99%. | |
| Samarium Strontium Cobalt Oxide | Samarium Strontium Cobalt Oxide (Samarium Strontium Cobaltite, SSC) is used as a cathode material in high performance solid oxide fuel cells and is generally immediately available in most volumes. Alternative Names: Samarium Strontium Cobaltite, SSC, strontium- doped samarium cobaltite, Cobalt samarium strontium oxide , SmSrCo4Ox; 491845-26-2. Molecular formula: SrO ·Sm2O3 ·2Co3O4. Mole weight: 933.93196999999998. Purity: 99%|99.9%|99.99%|99.999%. IUPAC Name: oxocobalt;oxo(oxocobaltiooxy)cobalt;oxo(oxosamariooxy)samarium;oxostrontium. SMILES: O=[Co].O=[Co].O=[Co]O[Co]=O.O=[Co]O[Co]=O.O=[Sr].O=[Sm]O[Sm]=O. InChI: O=[Co].O=[Co].O=[Co]O[Co]=O.O=[Co]O[Co]=O.O=[Sr].O=[Sm]O[Sm]=O. | |
| Samarium Strontium Cobalt Oxide Nanoparticle Dispersion | Samarium Strontium Cobalt Oxide Nanopowder is used as material component in hHigh performance solid oxide fuel cells and is generally immediately available in most volumes. Alternative Names: Samarium Strontium Cobaltite, SSC, strontium- doped samarium cobaltite, Cobalt samarium strontium oxide , SmSrCo4Ox; 491845-26-2, Samarium Strontium Cobalt Oxide nanopowder suspension, aqueous Samarium Strontium Cobalt Oxide nanoparticle solution, Samarium Strontium Cobalt Oxide nanofluid. Molecular formula: SrO; Sm2O3; 2Co3O4. Mole weight: 934g/mol. IUPAC Name: oxocobalt; oxo(oxocobaltiooxy)cobalt; oxo(oxosamariooxy)samarium; oxostrontium. SMILES: O=[Co].O=[Co].O=[Co]O[Co]=O.O=[Co]O[Co]=O.O=[Sr].O=[Sm]O[Sm]=O. InChI: InChI=1S/6Co.12O.2Sm.Sr. | |
| Samarium Strontium Cobalt Oxide Nanoparticles / Nanopowder | Samarium Strontium Cobalt Oxide Nanopowder is used as material component in hHigh performance solid oxide fuel cells and is generally immediately available in most volumes. Alternative Names: Samarium Strontium Cobaltite. Molecular formula: SrO; Sm2O3; 2Co3O4. Mole weight: 934g/mol. Purity: 99%, 99.9%, 99.99%, 99.999%. IUPAC Name: oxocobalt; oxo(oxocobaltiooxy)cobalt; oxo(oxosamariooxy)samarium; oxostrontium. SMILES: O=[Co].O=[Co].O=[Co]O[Co]=O.O=[Co]O[Co]=O.O=[Sr].O=[Sm]O[Sm]=O. InChI: InChI=1S/6Co.12O.2Sm.Sr. | |
| Samarium Sulfate | Samarium Sulfate. Grades: 99.99% Extremely High (>=99%). CAS No. 13465-58-2. Pack Sizes: Gram Quantities: 25 gm, 100 gm. Order Number: 3106. |  www.prochemonline.com |
| Samarium Sulfate | SAMARIUM SULFATE, OCTAHYDRATE, 99.9% pure, -6 mesh, Formula: Sm2(SO4)3.8H2O. CAS No. 13465-58-2. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Samarium Sulfide (Sm2S3) | Samarium Sulfide (Sm2S3). Alternative Names: Samarium Sulfide Powder, Sm2S3 Powder, Samarium Sulfide, Sm2S3, 12067-22-0. Purity: 99.9%, 99.99%. | |
| Samarosporin | It is a peptide antibiotic produced by the strain of Samarospora sp. No. F-7762. It has anti-bacterial, yeast, fungi and protozoa effects, but the effect is not strong. The serum can reduce its activity. CAS No. 60304-25-8. Molecular formula: C71H107N15O18. Mole weight: 1458.70. |  |
| Samatasvir | Samatasvir (IDX71) is a potent, orally active NS5A inhibitor of HCV replication. Samatasvir is effective and selective against infectious HCV and replicons, with EC50s falling within a tight range of 2 to 24 pM in genotype 1 through 5 replicons[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: IDX719; IDX18719. CAS No. 1312547-19-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16784. |  |
| SAMβA | SAMβA is conjugated to the cell permeable peptide TAT47-57. SAMβA, a rationally designed selective antagonist of Mfn1-βIIPKC association. SAMβA is a selective inhibitor of mitofusin 1-βIIPKC association improves heart failure outcome in rats[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2429946-75-6. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P3429. | |
| Sambutoxin | Sambutoxin is natural alkaloid isolated from the rotted potato tubers, it can cause toxic effects in rats, including body weight loss, feed refusal, hemorrhage in the stomach and intestines. Synonyms: 3-[(2S,5R,6R)-6-[(E,4R,6S)-4,6-dimethyloct-2-en-2-yl]-5-methyloxan-2-yl]-4-hydroxy-5-(4-hydroxyphenyl)-1-methylpyridin-2-one. Grade: >98%. CAS No. 160047-56-3. Molecular formula: C28H39NO4. Mole weight: 453.6. | |
| Samelisant | Samelisant (SUVN-G3031) is a potent and selective histamine H3 receptor (H3R) inverse agonist with good brain penetration and oral bioavailability. Samelisant has a similar binding affinity towards human (hH3R; Ki=8.7 nM) and rat (rH3R;Ki=9.8 nM) H3R indicating no inter-species differences. Samelisant can be used for the research of sleep-related disorders[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SUVN-G3031. CAS No. 1394808-20-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120124. | |
| SAM Formation reagent for biotin terminated monolayer on gold surface | SAM Formation reagent for biotin terminated monolayer on gold surface. | |
| SAM Formation reagent for carboxylic acid terminated monolayer on gold surface | SAM Formation reagent for carboxylic acid terminated monolayer on gold surface. | |
| Samidorphan | Samidorphan (ALKS-33) is an orally active opioid system modulator that has a high affinity for binding with μ?opioid, κ?opioid, and δ?opioid receptors. Samidorphan acts as an antagonist at μ?opioid receptors and acts as a partial agonist at k-opioid and δ?opioid receptors. Samidorphan primarily acts as an opioid receptor antagonist in vivo. Samidorphan can improve the behavior of depressed animals[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ALKS-33; RDC-0313. CAS No. 852626-89-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-123689. | |
| Samidorphan Impurity 1 | Samidorphan Impurity 1. Uses: For analytical and research use. Molecular formula: C21H26N2O5. Mole weight: 386.45. Catalog: APB12177. |  |
| Samidorphan Impurity 2 | Samidorphan Impurity 2. Uses: For analytical and research use. Molecular formula: C21H24N2O5. Mole weight: 384.43. Catalog: APB12178. | |
| Samidorphan Impurity 3 | Samidorphan Impurity 3. Uses: For analytical and research use. CAS No. 852626-89-2. Molecular formula: C21H26N2O4. Mole weight: 370.45. Catalog: APB852626892. | |
| S-(-)-Aminoglutethimide D-tartrate salt | S-(-)-Aminoglutethimide D-tartrate salt. Group: Biochemicals. Alternative Names: S-(-)-3-(4-Aminophenyl)-3-ethyl-2,6-piperidinedione L-tartrate salt; l-Aminoglutethimide L-tartrate. Grades: Highly Purified. CAS No. 57288-04-7. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C17H22N2O8. US Biological Life Sciences. |  Worldwide |
| Samotolisib | Samotolisib (LY3023414) potently and selectively inhibits class I PI3K isoforms, DNA-PK, and mTORC1/2 with IC50s of 6.07 nM, 77.6 nM, 38 nM, 23.8 nM, 4.24 nM and 165 nM for PI3Kα, PI3Kβ, PI3Kδ, PI3Kγ, DNA-PK and mTOR, respectively. Samotolisib potently inhibits mTORC1/2 at low nanomolar concentrations[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LY3023414. CAS No. 1386874-06-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12513. | |
| Sampaquita Givco 138 | Sampaquita Givco 138. CAS No. MIXTURE. VIGON Item # 508472. Categories: Speciality Ingrdients Suppliers. |  America & Internationally |
| SAMPH1 | SAMPH1 is an antibacterial peptide isolated from Salmo salar. It has activity against gram-positive bacteria and gram-negative bacteria. Synonyms: Ala-Glu-Val-Ala-Pro-Ala-Pro-Ala-Ala-Ala-Ala-Pro-Ala-Lys-Ala-Pro-Lys-Lys-Lys-Ala-Ala-Ala-Lys-Pro-Lys-Lys-Ala-Gly-Pro-Ser. Grade: >97%. Molecular formula: C126H217N37O34. Mole weight: 2794.34. | |
| Samrotamab | Samrotamab (PR-1498487) is a humanized IgG1-κ chimeric antibody targeting LRRC15. Samrotamab markedly reduces bladder cancer cells viability and inhibits clonogenic growth, migratory and invasive capabilities. Samrotamab significantly increases LRRC15 mRNA level while suppressing SCG5 mRNA expression. Samrotamab can be used for synthesis of ADC ABBV-085[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PR-1498487. CAS No. 2052591-32-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99899. | |
| SAMS | SAMS peptide, a synthetic peptide substrate for AMPK based on the sequence around Ser79 on acetyl-CoA carboxylase, is more selective for the kinase than acetyl CoA carboxylase itself, and provides a convenient and sensitive assay for AMPK. Synonyms: (Ser76, Arg86.87)-ACC-α (73-87) (dephosphorylated) (E.coli, rat); (Ser76, Arg86.87)-Acetyl-CoA Carboxylase 1 (73-87) (dephosphorylated) (E.coli, rat); (Ser77, Arg87.88)-ACC-α (74-88) (dephosphorylated) (bovine, ovine); (Ser77, Arg87.88)-Acetyl-CoA Carboxyla; H-His-Met-Arg-Ser-Ala-Met-Ser-Gly-Leu-His-Leu-Val-Lys-Arg-Arg-OH; L-histidyl-L-methionyl-L-arginyl-L-seryl-L-alanyl-L-methionyl-L-seryl-glycyl-L-leucyl-L-histidyl-L-leucyl-L-valyl-L-lysyl-L-arginyl-L-arginine. Grade: >95%. CAS No. 125911-68-4. Molecular formula: C74H131N29O18S2. Mole weight: 1779.15. | |
| SAMS Peptide trifluoroacetate salt | SAMS Peptide trifluoroacetate salt. Uses: For analytical and research use. CAS No. 125911-68-4 (free base). Mole weight: 1779.15 (free base basis). Catalog: ALP125911684. | |
| Samuraciclib | Samuraciclib Inhibitor. Uses: Scientific use. Product Category: T10898. CAS No. 1805789-54-1. |  |
| Samuraciclib | Samuraciclib (CT7001) is a potent, selective, ATP-competitive and orally active CDK7 inhibitor, with an IC50 of 41 nM. Samuraciclib displays 45-, 15-, 230- and 30-fold selectivity over CDK1, CDK2 (IC50 of 578 nM), CDK5 and CDK9, respectively. Samuraciclib inhibits the growth of breast cancer cell lines with GI50 values between 0.2-0.3 μM. Samuraciclib has anti-tumor effects[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CT7001; ICEC0942. CAS No. 1805833-75-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-103712. | |
| Samuraciclib hydrochloride | Samuraciclib hydrochloride (CT7001 hydrochloride) is a potent, selective, ATP-competitive and orally active CDK7 inhibitor, with an IC50 of 41 nM. Samuraciclib hydrochloride displays 45-, 15-, 230- and 30-fold selectivity over CDK1, CDK2 (IC50 of 578 nM), CDK5 and CDK9, respectively. Samuraciclib hydrochloride inhibits the growth of breast cancer cell lines with GI50 values between 0.2-0.3 μM. Samuraciclib hydrochloride has anti-tumor effects[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CT7001 hydrochloride; ICEC0942 hydrochloride. CAS No. 1805789-54-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103712A. | |
| S-(+)-a-Naphthyl glycidyl ether | S-(+)-a-Naphthyl glycidyl ether. Group: Biochemicals. Alternative Names: (2S) -2-[ (1-Naphthalenyloxy) methyl]oxirane. Grades: Highly Purified. CAS No. 61249-00-1. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C13H12O2. US Biological Life Sciences. | Worldwide |
| Sancycline | Sancycline is a tetracycline bacteriostatic antibiotic which also binds to the Tet repressor protein (TetR). Sancycline acts by reversibly binding to the 30S ribosomal subunit and inhibiting protein translation by blocking entry of aminoacyl-tRNA into the ribosome A site. Synonyms: Minocycline EP Impurity B; 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide; Norcycline; Bonomycin. Grade: >95%. CAS No. 808-26-4. Molecular formula: C21H22N2O7. Mole weight: 414.41. | |
| Sancycline-d6 Hydrochloride. | A semi-synthetic labeled antibiotic related to Tetracycline. Group: Biochemicals. Alternative Names: (4S,4aS,5aR,12aS)-4-(Dimethyl-d6-amino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1-11-dioxo-2-naphthacenecarboxamide Hydrochloride; Bonomycin-d6; Norcycline-d6; 6-Demethyl-6-deoxytetracycline-d6 Hydrochloride; GS 2147-d6. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Sancycline hydrochloride | The hydrochloride salt of a rare semi-synthetic tetracycline. It is prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of declomycin. It inhibits protein translation by reversibly binding to the 30S ribosomal subunit and blocking the entry of aminoacyl tRNA into the ribosomal A site. It is a semi-synthetic antibiotic with activity against tetracycline-resistant E. coli, S. aureus and E. faecalis. Synonyms: 6-Demethyl-6-deoxytetracycline hydrochloride; NSC 51812; (4S,4aS,5aR,12aS)-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1-11-dioxo-2-naphthacenecarboxamide Hydrochloride; Bonomycin; Norcycline; GS 2147; Minocycline EP Impurity B. Grade: >98% by HPLC. CAS No. 6625-20-3. Molecular formula: C21H23ClN2O7. Mole weight: 450.87. | |
| Sancycline hydrochloride | Sancycline hydrochloride. Group: Biochemicals. Alternative Names: (4S,4aS,5aR,12aS)-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1-11-dioxo-2-naphthacenecarboxamide hydrochloride; Bonomycin; Norcycline. Grades: Highly Purified. CAS No. 6625-20-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C21H23ClN2O7. US Biological Life Sciences. | Worldwide |
| Sancycline Impurity 1 | Sancycline Impurity 1. Uses: For analytical and research use. CAS No. 32598-29-1. Molecular formula: C24H29N3O7. Mole weight: 471.51. Catalog: APB32598291. | |
| Sancycline Impurity 2 | Sancycline Impurity 2. Uses: For analytical and research use. CAS No. 5679-1-6. Molecular formula: C21H23N3O13S. Mole weight: 557.48. Catalog: APB5679016. | |
| Sancycline Impurity 3 | Sancycline Impurity 3. Uses: For analytical and research use. CAS No. 2791-13-1. Molecular formula: C21H23N3O13S. Mole weight: 557.48. Catalog: APB2791131. | |
| Sancycline Impurity 4 | Sancycline Impurity 4. Uses: For analytical and research use. CAS No. 906364-48-5. Molecular formula: C21H22N2O7. Mole weight: 414.41. Catalog: APB906364485. | |
| Sancycline Impurity 5 | Sancycline Impurity 5. Uses: For analytical and research use. CAS No. 113164-67-3. Molecular formula: C21H21IN2O7. Mole weight: 540.31. Catalog: APB113164673. | |
| Sancycline Impurity 6 | Sancycline Impurity 6. Uses: For analytical and research use. CAS No. 1035655-10-7. Molecular formula: C22H22N2O8. Mole weight: 442.42. Catalog: APB1035655107. | |
| Sancycline Impurity 7 | Sancycline Impurity 7. Uses: For analytical and research use. CAS No. 5585-59-1. Molecular formula: C21H21N3O9. Mole weight: 459.41. Catalog: APB5585591. | |
| Sandalore ® | Sandalore ®. CAS No. 65113-99-7. VIGON Item # 500931. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Sandalwood 77125 B | Sandalwood 77125 B. CAS No. MIXTURE. VIGON Item # 502839. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Sandalwood Essential Oil (Natural) | Sandalwood Essential Oil (Natural). |  CA, FL & NJ |
| Sandalwood oil | Sandalwood oil. Alternative Names: Essential oils,sandalwood. CAS No. 8006-87-9. Purity: 0.98. Product ID: CI-EO-0081. Molecular formula: C30H48O2. Mole weight: 440.7 g/mol. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Sandalwood Powder | Sandalwood Powder. | CA, FL & NJ |
| Sandaracopimaric acid | Sandaracopimaric acid. Alternative Names: 13-Methyl-17-norabieta-8(14),15-diene-18-oic acid. CAS No. 471-74-9. Purity: >95.0%. Product ID: FFC-AR-471749. Molecular formula: C20H30O2. Mole weight: 302.45. IUPAC Name: (1R,4aR,4bS,7R,10aR)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Sandaxol | Sandaxol (Sandalmysore). CAS No. 28219-60-5. VIGON Item # 503560. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Sandela ® | Sandela ®. CAS No. MIXTURE. VIGON Item # 501149. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Sandenol | 5g Pack Size. Group: Analytical Reagents, Aroma Chemicals, Biochemicals, Building Blocks, Flavours and Fragrance Materials, Organics. Formula: C16H28O. CAS No. 3407-42-9. Prepack ID 90028841-5g. Molecular Weight 236.39. See USA prepack pricing. |  |
| Sanderol RH | Sanderol RH (Bacdanol). CAS No. 28219-61-6. Kosher: Y. VIGON Item # 503492. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Sandospace R | Sandospace R can be utilized for technical or engineered material use in for the manufacture of textile products, including fabrics, towels and knitted garments in different shades and hues. It is also an anti-bacteria material. Group: Biochemicals. Grades: Highly Purified. CAS No. 4156-21-2. Pack Sizes: 100mg, 250mg. Molecular Formula: C9H5Cl2N4NaO3S, Molecular Weight: 343.12. US Biological Life Sciences. | Worldwide |
| Sandoz 58-035 | Sandoz 58-035 is a selective acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. Sandoz 58-035 inhibits this enzyme in intact cells and isolated microsomal fractions. Sandoz 58-035 blocks the esterification of exogenous vesicle-derived cholesterol and the incorporation of oleic acid into cellular cholesterol esters, reducing the formation and accumulation of cholesterol esters. Sandoz 58-035 causes a slight increase in cellular free cholesterol, and at high concentrations, it also causes a slight reduction in overall cellular protein synthesis. Sandoz 58-035 can be used in studies related to cellular cholesterol regulation[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 78934-83-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-112487. | |
| Sandoz FK 33-824 | Sandoz FK 33-824 is a stable synthetic analog of methionine enkephalin. Synonyms: D-Ala(2); MePhe(4); Met(0)-ol-enkephalin; FK 33-824; FK-33-824; FK-33824; CID11758339; DAMME. Grade: ≥95% by HPLC. CAS No. 64854-64-4. Molecular formula: C29H41N5O7S. Mole weight: 603.73. | |
| Sandramycin | Sandramycin is a high molecular weight, symmetric, cyclic depsipeptide belonging to the quinomycin class produced by Kribbella sp. Sandramycin has potent antitumor and antibacterial activity and is thought to act by bis-intercalation of DNA. Group: Biochemicals. Grades: Highly Purified. CAS No. 100940-65-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Sanggenol L | Sanggenol L. Group: Biochemicals. CAS No. 329319-20-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Sanggenol P | Sanggenol P is a natural flavonoid found in the root bark of Morus alba L. Synonyms: Sanggenol P; 1351931-30-0; 2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one; HY-N1323; AKOS040762295; FS-9426; DA-57654; CS-0016727. Grade: >95%. CAS No. 1351931-30-0. Molecular formula: C30H36O6. Mole weight: 492.60. | |
| Sanggenon C | Sanggenon C. Group: Biochemicals. Grades: Plant Grade. CAS No. 80651-76-9. Pack Sizes: 20mg. Molecular Formula: C40H36O12, Molecular Weight: 708.71. US Biological Life Sciences. | Worldwide |
| Sanggenon C | Sanggenon C, a flavonoid, exerts protective effects against cardiac hypertrophy and fibrosis via suppression of the calcineurin/NFAT2 pathway. Sanggenon C inhibits mitochondrial fission to induce apoptosis by blocking the ERK signaling pathway. Sanggenon C inhibits inducible nitric oxide synthase expression in RAW264.7 cells, and TNF-α-stimulated cell adhesion and VCAM-1 expression, by suppressing NF-κB activity. Sanggenon C possesses antioxidant, anti-inflammatory and antitumor activities[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 80651-76-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0617. | |
| Sanggenone D | Sanggenone D. Group: Biochemicals. Grades: Plant Grade. CAS No. 81422-93-7. Pack Sizes: 20mg. Molecular Formula: C40H36O12, Molecular Weight: 708.71. US Biological Life Sciences. | Worldwide |
| Sanggenone H | Sanggenone H. Group: Biochemicals. CAS No. 86450-80-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Sanggenon N | Sanggenon N is a natural flavonoid compound. Synonyms: (-)-5,5',7-Trihydroxy-2'-methyl-2'-(4-methyl-3-pentenyl)-2,6'-bi[2H-1-benzopyran]-4(3H)-one. Grade: >95%. CAS No. 92280-12-1. Molecular formula: C25H26O6. Mole weight: 422.5. | |
| Sangivamycin | Sangivamycin is a nucleoside (purine) antibiotic produced by the strain of Str. rimosus BA-90912. 0.02-0.05 μg/mL of Sangivamycin inhibits HeLa cells. It has weak inhibitory effect on sarcoma-180 and adenocarcinoma 755 in mice. It has obvious inhibitory effect on leukemia L-1210. When intraperitoneally administered, the drug binds to nucleic acids in tissues in mice through phosphorylation. Uses: Antibiotics, antineoplastic. Synonyms: 4-Amino-7-β-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide; 7-Deazaadenosine-7-carboxamide; NSC 65346; Antibiotic B-14437; Ara-sangivamycin. Grade: 95%. CAS No. 18417-89-5. Molecular formula: C12H15N5O5. Mole weight: 309.28. | |
| Sangivamycin | Sangivamycin (NSC 65346), a nucleoside analog, is a potent inhibitor of protein kinase C (PKC) with an Ki of 10 μM. Sangivamycin has potent antiproliferative activity against a variety of human cancers[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NSC 65346; BA-90912. CAS No. 18417-89-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-118384. | |
| Sangivamycin hydrochloride | Sangivamycin hydrochloride is a nucleoside (purine) antibiotic produced by the strain of Str. rimosus BA-90912. 0.02-0.05 μg/mL of Sangivamycin inhibits HeLa cells. It has weak inhibitory effect on sarcoma-180 and adenocarcinoma 755 in mice. It has obvious inhibitory effect on leukemia L-1210. When intraperitoneally administered, the drug binds to nucleic acids in tissues in mice through phosphorylation. Synonyms: Sangivamycin monohydrochloride; 7H-Pyrrolo(2,3-d)pyrimidine-5-carboxamide, 4-amino-7-beta-D-ribofuranosyl-, monohydrochloride; 7-Deazaadenosine-7-carboxamide hydrochloride. Grade: 95%. CAS No. 21090-35-7. Molecular formula: C12H15N5O5.HCl. Mole weight: 345.74. | |
| Sanglifehrin A | It is a cyclophilin combination produced by the strain of Streptomyces sp. A92-308110. The affinity of Sanglifehrin A to Cyclophilin is 10-20 times stronger than Cyclosporin A. The immunosuppressive effect of Sanglifehrin is lower than Cyclosporin A by mixed lymphocyte reaction assay. Synonyms: SFA; (-)-sanglifehrin A; 19-Oxa-1,4,7,25-tetraazabicyclo[19.3.1]pentacosa-13,15-diene-2,5,8,20-tetrone, 18-[(1E,3E,7S,8S)-9-[(2S,3R,4S,5S,6R,9S,11S)-9-ethyl-4-hydroxy-3,5,11-trimethyl-8-oxo-1-oxa-7-azaspiro[5.5]undec-2-yl]-8-hydroxy-1,7-dimethyl-1,3-nonadienyl]-10,12-dihydroxy-3-[(3-hydroxyphenyl)methyl]-11-methyl-6-(1-methylethyl)-9-(3-oxobutyl)-, (3S,6S,9R,10R,11S,12S,13E,15E,18S,21S)-. CAS No. 187148-13-6. Molecular formula: C60H91N5O13. Mole weight: 1090.39. | |
| Sanglifehrin B | It is a cyclophilin combination produced by the strain of Streptomyces sp. A92-308110. The affinity of Sanglifehrin B to Cyclophilin is 10-20 times stronger than Cyclosporin A. The immunosuppressive effect of Sanglifehrin is lower than Cyclosporin A by mixed lymphocyte reaction assay. Synonyms: SFB. Molecular formula: C60H89N5O12. Mole weight: 1072.37. | |
| Sanglifehrin C | It is a cyclophilin combination produced by the strain of Streptomyces sp. A92-308110. The affinity of Sanglifehrin C to Cyclophilin is similar to Cyclosporin A. The immunosuppressive effect of Sanglifehrin is lower than Cyclosporin A by mixed lymphocyte reaction assay. Synonyms: SFC. Molecular formula: C61H93N5O13. Mole weight: 1104.41. | |
| Sanglifehrin D | It is a cyclophilin combination produced by the strain of Streptomyces sp. A92-308110. The affinity of Sanglifehrin D to Cyclophilin is similar to Cyclosporin A. The immunosuppressive effect of Sanglifehrin is lower than Cyclosporin A by mixed lymphocyte reaction assay. Synonyms: SFD. Molecular formula: C61H91N5O12. Mole weight: 1086.40. | |
| Sangre de Grado Powder (Croton lechleri) | Sangre de Grado Powder (Croton lechleri). | CA, FL & NJ |
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