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| Product | Description | |
|---|---|---|
| Temporin H | Temporin H is an antibacterial peptide isolated from Rana temporaria. It has activity against gram-positive bacteria. Synonyms: Leu-Ser-Pro-Asn-Leu-Leu-Lys-Ser-Leu-Leu-NH2. Grade: >97%. Molecular formula: C51H93N13O13. Mole weight: 1096.38. |  |
| Temporin-HN1 | Temporin-HN1 is an antibacterial peptide isolated from Odorrana hainanensis. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Ala-Ile-Leu-Thr-Thr-Leu-Ala-Asn-Trp-Ala-Arg-Lys-Phe-Leu-NH2. Grade: >96%. Molecular formula: C77H125N21O17. Mole weight: 1616.98. | |
| Temporin-HN2 | Temporin-HN2 is an antibacterial peptide isolated from Odorrana hainanensis. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Asn-Ile-Leu-Asn-Thr-Ile-Ile-Asn-Leu-Ala-Lys-Lys-Ile-Leu-NH2. Grade: >97%. Molecular formula: C73H134N20O18. Mole weight: 1580.00. | |
| Temporin-K | Temporin-K is an antibacterial peptide isolated from Rana temporaria. It has activity against gram-positive bacteria. Synonyms: Leu-Leu-Pro-Asn-Leu-Leu-Lys-Ser-Leu-Leu-NH2. Grade: >98%. Molecular formula: C54H99N13O12. Mole weight: 1122.47. | |
| Temporin L | Temporin L is a potent antimicrobial peptide and is active against Gram-negative bacteria and yeast strains. Temporin L also has antiendotoxin properties [1] [2]. Uses: Scientific research. Group: Peptides. CAS No. 188713-81-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2523. |  |
| Temporin-L | Temporin-L is an antibacterial peptide isolated from Rana temporaria. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. It has hemolytic and cytotoxic activity. Synonyms: Phe-Val-Gln-Trp-Phe-Ser-Lys-Phe-Leu-Gly-Arg-Ile-Leu-NH2. Grade: >97%. CAS No. 188713-81-7. Molecular formula: C83H122N20O15. Mole weight: 1640.0. | |
| Temporin-La | Temporin-La is an antibacterial peptide isolated from Lithobates catesbeiana. It has activity against gram-positive bacteria. Synonyms: Leu-Leu-Arg-His-Val-Val-Lys-Ile-Leu-Glu-Lys-Tyr-Leu-NH2. Grade: >96%. Molecular formula: C78H135N21O16. Mole weight: 1623.07. | |
| Temporin-LF4 antimicrobial peptide precursor | Temporin-LF4 antimicrobial peptide precursor is an antibacterial peptide isolated from Amolops lifanensis. Synonyms: Thr-Ser-Lys-Lys-Pro-Leu-Leu-Leu-Phe-Phe-Phe-Leu-Gly-Thr-Ile-Asn-Leu-Ser-Leu-Cys-Glu-Gln-NH2. Grade: >95%. Molecular formula: C119H191N27O30S. Mole weight: 2512.06. | |
| Temporin-LK1 | Temporin-LK1 is an antibacterial peptide isolated from Limnonectes kuhlii. Synonyms: Phe-Phe-Pro-Leu-Leu-Phe-Gly-Ala-Leu-Ser-Ser-Met-Met-Pro-Lys-Leu-Phe-NH2. Grade: >96%. Molecular formula: C97H145N19O19S2. Mole weight: 1945.46. | |
| Temporin-LT1 | Temporin-LT1 is an antibacterial peptide isolated from Hylarana latouchii. It has activity against gram-positive bacteria. Synonyms: Phe-Leu-Pro-Gly-Leu-Ile-Ala-Gly-Ile-Ala-Lys-Met-Leu-NH2. Grade: >96%. Molecular formula: C65H111N15O13S. Mole weight: 1342.76. | |
| Temporin-LT2 | Temporin-LT2 is an antibacterial peptide isolated from Hylarana latouchii. It has activity against gram-positive bacteria. Synonyms: Phe-Leu-Pro-Ile-Ala-Leu-Lys-Ala-Leu-Gly-Ser-Ile-Phe-Pro-Lys-Ile-Leu-NH2. Grade: >96%. Molecular formula: C93H154N20O18. Mole weight: 1840.38. | |
| Temporin-LTa | Temporin-LTa is an antibacterial peptide isolated from Hylarana latouchii. It has activity against gram-positive bacteria. Synonyms: Phe-Phe-Pro-Leu-Val-Leu-Gly-Ala-Leu-Gly-Ser-Ile-Leu-Pro-Lys-Ile-Phe-NH2. Molecular formula: C94H147N19O18. Mole weight: 1831.33. | |
| Temporin-LTb | Temporin-LTb is an antibacterial peptide isolated from Hylarana latouchii. It has activity against gram-positive bacteria. Synonyms: Phe-Ile-Ile-Thr-Gly-Leu-Val-Arg-Gly-Leu-Thr-Lys-Leu-Phe-NH2. Molecular formula: C77H129N19O16. Mole weight: 1577.00. | |
| Temporin-LTc | Temporin-LTc is an antibacterial peptide isolated from Hylarana latouchii. It has activity against gram-positive bacteria. Synonyms: Ser-Leu-Ser-Arg-Phe-Leu-Ser-Phe-Leu-Lys-Ile-Val-Tyr-Pro-Pro-Ala-Phe-NH2. Grade: >95%. Molecular formula: C99H150N22O21. Mole weight: 1984.42. | |
| Temporin-LTe | Temporin-LTe is an antibacterial peptide isolated from Hylarana latouchii (broad-folded frog). Synonyms: Phe-Leu-Ala-Gly-Leu-Ile-Gly-Gly-Leu-Ala-Lys-Met-Leu-NH2. Grade: >97%. Molecular formula: C62H107N15O13S. Mole weight: 1302.69. | |
| Temporin-MT1 antimicrobial peptide precursor | Temporin-MT1 antimicrobial peptide precursor is an antibacterial peptide isolated from Amolops mantzorum. Synonyms: Thr-Leu-Lys-Lys-Ser-Leu-Leu-Leu-Phe-Phe-Phe-Leu-Gly-Thr-Ile-Asn-Leu-Ser-Leu-Cys-Glu-Gln-NH2. Grade: >98%. Molecular formula: C120H195N27O30S. Mole weight: 2528.10. | |
| Temporin-MT3 antimicrobial peptide precursor | Temporin-MT3 antimicrobial peptide precursor is an antibacterial peptide isolated from Amolops mantzorum. Synonyms: Thr-Met-Lys-Lys-Ser-Leu-Leu-Leu-Leu-Phe-Phe-Leu-Gly-Thr-Ile-Asn-Leu-Ser-Leu-Cys-Glu-Gln-Glu-Arg-Asn-Ala-Glu-Glu-Glu-Arg-Arg-Asp-Asp-Leu-Gly-Glu-Arg-Gln-Ala-Glu-Val-Glu-Lys-Arg-NH2. Molecular formula: C223H373N67O72S2. Mole weight: 5208.95. | |
| Temporin-PRa | Temporin-PRa is an antibacterial peptide isolated from Rana pretiosa. It has activity against gram-positive bacteria. Synonyms: Phe-Leu-Pro-Ile-Leu-Gly-Asn-Leu-Leu-Ser-Gly-Leu-Leu-NH2. Grade: >97%. Molecular formula: C67H113N15O15. Mole weight: 1368.73. | |
| Temporin-PRb | Temporin-PRb is an antibacterial peptide isolated from Rana pretiosa. It has activity against gram-positive bacteria. Synonyms: Phe-Leu-Pro-Ile-Ile-Thr-Asn-Leu-Leu-Gly-Lys-Leu-Leu-NH2. Grade: >97%. Molecular formula: C72H124N16O15. Mole weight: 1453.88. | |
| Temporin-PRc | Temporin-PRc is an antibacterial peptide isolated from Rana pretiosa. It has activity against gram-positive bacteria. Synonyms: Asn-Phe-Leu-Asp-Thr-Leu-Ile-Asn-Leu-Ala-Lys-Lys-Phe-Ile-NH2. Grade: >95%. Molecular formula: C79H129N19O19. Mole weight: 1649.02. | |
| Temporin-PTa | Temporin-PTa is an antibacterial peptide isolated from Rana picturata, which has activity against gram-positive bacteria and gram-negative bacteria. Synonyms: Phe-Phe-Gly-Ser-Val-Leu-Lys-Leu-Ile-Pro-Lys-Ile-Leu-NH2. Grade: >96%. Molecular formula: C75H124N16O14. Mole weight: 1473.92. | |
| Temporin-Ra | Temporin-Ra is an antibacterial peptide isolated from Rana ridibunda, which has activity against gram-positive bacteria and gram-negative bacteria. Synonyms: Phe-Leu-Lys-Pro-Leu-Phe-Asn-Ala-Ala-Leu-Lys-Leu-Leu-Pro-NH2. Grade: >96%. Molecular formula: C80H130N18O15. Mole weight: 1584.03. | |
| Temporin-Rb | Temporin-Rb is an antibacterial peptide isolated from Rana ridibunda, which has activity against gram-positive bacteria and gram-negative bacteria. Synonyms: Phe-Leu-Pro-Val-Leu-Ala-Gly-Val-Leu-Ser-Arg-Ala-NH2. Grade: >97%. Molecular formula: C59H100N16O13. Mole weight: 1241.55. | |
| Temporin-RN1 | Temporin-RN1 is an antibacterial peptide isolated from Rana nigrovittata. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Phe-Leu-Pro-Leu-Val-Leu-Gly-Ala-Leu-Ser-Gly-Ile-Leu-Pro-Lys-Ile-Leu-NH2. Grade: >96%. Molecular formula: C88H151N19O18. Mole weight: 1763.29. | |
| Temporin-RN3 | Temporin-RN3 is an antibacterial peptide isolated from Rana nigrovittata. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Phe-Phe-Pro-Leu-Leu-Phe-Gly-Ala-Leu-Ser-Ser-His-Leu-Pro-Lys-Leu-Phe-NH2. Grade: >97%. Molecular formula: C99H145N21O19. Mole weight: 1933.38. | |
| Temporin-SHd | Temporin-SHd is an antibacterial peptide isolated from Pelophylax saharicus (Sahara frog). It has activity against gram-positive bacteria, gram-positive bacteria and parasites. Synonyms: Phe-Leu-Pro-Ala-Ala-Leu-Ala-Gly-Ile-Gly-Gly-Ile-Leu-Gly-Lys-Leu-Phe-NH2. Grade: >95%. Molecular formula: C82H133N19O17. Mole weight: 1657.08. | |
| Temporin-SHe precursor | Temporin-SHe precursor is an antibacterial peptide isolated from Pelophylax saharicus. It has activity against gram-positive bacteria. Synonyms: Leu-Pro-Ala-Leu-Ala-Gly-Ile-Ala-Gly-Leu-Leu-Gly-Lys-Ile-Phe-Gly-Lys-NH2. Grade: >95%. Molecular formula: C79H136N20O17. Mole weight: 1638.08. | |
| Temporin-SHf | Temporin-SHf is an antibacterial peptide isolated from Pelophylax saharica. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Phe-Phe-Phe-Leu-Ser-Arg-Ile-Phe-NH2. Grade: >95%. Molecular formula: C57H78N12O9. Mole weight: 1075.33. | |
| Temporin-SHf precursor, partial | Temporin-SHf precursor, partial is an antibacterial peptide isolated from Pelophylax saharicus, which has activity against gram-positive bacteria and gram-negative bacteria. Synonyms: Phe-Phe-Leu-Ser-Arg-Ile-Phe-Gly-Lys-NH2. Grade: >98%. Molecular formula: C56H84N14O10. Mole weight: 1113.38. | |
| Temporin-SN1 | Temporin-SN1 is an antibacterial peptide isolated from Hylarana spinulosa. It has activity against gram-positive bacteria. Synonyms: Phe-Phe-Pro-Phe-Leu-Leu-Gly-Ala-Leu-Gly-Ser-Leu-Leu-Pro-Lys-Ile-Phe-NH2. Grade: >96%. Molecular formula: C98H147N19O18. Mole weight: 1879.37. | |
| Temporin-SN2 | Temporin-SN2 is an antibacterial peptide isolated from Hylarana spinulosa. It has activity against gram-positive bacteria. Synonyms: Phe-Ile-Thr-Gly-Leu-Ile-Gly-Gly-Leu-Met-Lys-Ala-Leu-NH2. Grade: >95%. Molecular formula: C63H109N15O14S. Mole weight: 1332.72. | |
| Temporin-SN3 | Temporin-SN3 is an antibacterial peptide isolated from Hylarana spinulosa, which has activity against gram-positive bacteria and fungi. Synonyms: Phe-Ile-Ser-Gly-Leu-Ile-Gly-Gly-Leu-Met-Lys-Ala-Leu-NH2. Grade: >95%. Molecular formula: C62H107N15O14S. Mole weight: 1318.69. | |
| Temporin-SN4 | Temporin-SN4 is an antibacterial peptide isolated from Hylarana spinulosa, which has activity against gram-positive bacteria and fungi. Synonyms: Phe-Ile-Thr-Gly-Leu-Ile-Ser-Gly-Leu-Met-Lys-Ala-Leu-NH2. Grade: >96%. Molecular formula: C64H111N15O15S. Mole weight: 1362.74. | |
| Temporin-TR3_2 antimicrobial peptide precursor | Temporin-TR3_2 antimicrobial peptide precursor is an antibacterial peptide isolated from Amolops torrentis. Synonyms: Thr-Leu-Lys-Lys-Pro-Met-Leu-Leu-Leu-Phe-Phe-Leu-Gly-Thr-Ile-Asn-Leu-Ser-Leu-Cys-NH2. Grade: >95%. Molecular formula: C108H182N24O24S2. Mole weight: 2264.91. | |
| Temsavir | Temsavir (BMS-626529) is a novel attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4 + T cells. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMS-626529. CAS No. 701213-36-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15440. | |
| Temsirolimus | Temsirolimus is an inhibitor of mTOR with an IC 50 of 1.76 μM. Temsirolimus activates autophagy and prevents deterioration of cardiac function in animal model [8]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CCI-779. CAS No. 162635-04-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-50910. | |
| Temsirolimus | Temsirolimus is an mTOR inhibitor produced by Streptomyces. Temsirolimus potently inhibits mTOR kinase activity with IC50 of 1.76 μM, similar to that of rapamycin with IC50 of 1.74 μM. Synonyms: CCI779; CCI-779; CCI 779. Grade: >98%. CAS No. 162635-04-3. Molecular formula: C56H87NO16. Mole weight: 1030.29. | |
| Temsirolimus | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Temsirolimus Acetonide | Rapamycin 42-ester derivative. Group: Biochemicals. Alternative Names: Rapamycin 42-(2,2,5-Trimethyl-1,3-dioxane-5-carboxylate). Grades: Highly Purified. CAS No. 162635-03-2. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Temsirolimus-d3 | Labeled ester analog of Rapamycin. Group: Biochemicals. Alternative Names: Rapamycin 42-[3-Hydroxy-2-(hydroxymethyl)-2-(methyl-d3)-propanoate; CCL-779-d3. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Temsirolimus-d7 | Labelled ester analog of Rapamycin. Group: Biochemicals. Alternative Names: Rapamycin 42-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoate-d7; CCL-779-d7. Grades: Highly Purified. CAS No. 1132660-51-5. Pack Sizes: 1mg. Molecular Formula: C56H80D7NO16, Molecular Weight: 1037.33. US Biological Life Sciences. | Worldwide |
| Temsirolimus isomer C | Temsirolimus isomer C. Uses: For analytical and research use. Group: Impurity standards. CAS No. 150821-39-9. Molecular formula: C51H79NO13. Mole weight: 914.17. Catalog: APB150821399. | |
| Temsirolimus (Rapamycin 42-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoate, CCL-779) | Ester analog of rapamycin. Group: Biochemicals. Alternative Names: Rapamycin 42-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoate; CCL-779. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Temtokibart | Temtokibart is a humanized IgG1 λ2 antibody targeting IL22RA1. Expressed by cells lacking the glutamine synthetase gene. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ARGX-112. CAS No. 2639874-57-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990016. | |
| Temuterkib | Temuterkib (LY3214996) is a highly selective inhibitor of ERK1 and ERK2, with IC50 of 5 nM for both enzymes in biochemical assays. Temuterkib potently inhibits cellular p-RSK1 in BRAF and RAS mutant cancer cell lines. Temuterkib shows potent antitumor activities in cancer models with MAPK pathway alterations. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY3214996. CAS No. 1951483-29-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101494. | |
| Tenacigenin B, 3-O- β-Allopyranosyl-(1?4)- β-oleandropyranosyl-11-O-isobutyryl-12-O-acetyl- | Tenacigenin B, 3-O- β-Allopyranosyl-(1?4)- β-oleandropyranosyl-11-O-isobutyryl-12-O-acetyl-. Group: Biochemicals. Grades: Plant Grade. CAS No. 1260252-18-3. Pack Sizes: 10mg. Molecular Formula: C41H64O14, Molecular Weight: 780.95. US Biological Life Sciences. | Worldwide |
| Tenacissoside G | Tenacissoside G. Group: Biochemicals. Alternative Names: Tenacissimoside A. Grades: Plant Grade. CAS No. 191729-43-8. Pack Sizes: 10mg. Molecular Formula: C42H64O14, Molecular Weight: 792.948999999999. US Biological Life Sciences. | Worldwide |
| Tenacissoside H | Tenacissoside H. Group: Biochemicals. Alternative Names: Tenacissimoside C. Grades: Plant Grade. CAS No. 191729-45-0. Pack Sizes: 20mg. Molecular Formula: C42H66O14, Molecular Weight: 794.965. US Biological Life Sciences. | Worldwide |
| Tenacissoside I | Tenacissoside I. Group: Biochemicals. Alternative Names: Tenacissimoside B. Grades: Plant Grade. CAS No. 191729-44-9. Pack Sizes: 10mg. Molecular Formula: C44H62O14, Molecular Weight: 814.955. US Biological Life Sciences. | Worldwide |
| Tenacity No. 125 Flux Powder, working range 750-1200°C (1382-2102°F) | Tenacity No. 125 Flux Powder, working range 750-1200°C (1382-2102°F). Group: Alloys. |  |
| Tenacity No. 125 Paste, a high temperature flux paste, working range 800-1100°C (1472-2012°F) | Tenacity No. 125 Paste, a high temperature flux paste, working range 800-1100°C (1472-2012°F). Group: Alloys. | |
| Tenacity No. 6 Flux Powder | Tenacity No. 6 Flux Powder. Group: Alloys. | |
| Tenalisib | Tenalisib, also known as RP6530, is a potent and selective dual PI3Kδ/γ inhibitor that inhibited growth of B-cell lymphoma cell lines with a concomitant reduction in the downstream biomarker, pAKT. Additionally, the compound showed cytotoxicity in a panel of lymphoma primary cells. Findings provide a rationale for future clinical trials in B-cell malignancies. Uses: Designed for use in research and industrial production. Additional or Alternative Names: RP6530; RP-6530; RP 6530; Tenalisib. Product Category: Inhibitors. Appearance: White solid powder. CAS No. 1639417-53-0. Molecular formula: C23H18FN5O2. Mole weight: 415.43. Purity: >98%. IUPACName: (S)-2-(1-((7H-purin-6-yl)amino)propyl)-3-(3-fluorophenyl)-4H-chromen-4-one. Canonical SMILES: O=C1C(C2=CC=CC(F)=C2)=C([C@@H](NC3=C4NC=NC4=NC=N3)CC)OC5=C1C=CC=C5. Product ID: ACM1639417530. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Te Nanowires | Grayish-white, lustrous, brittle, crystalline solid; dark-gray to brown, amorphous powder with metallic characteristics. Used as a coloring agent in chinaware, porcelains, enamels, glass; producing black finish on silverware; semiconductor devices and research; manufacturing special alloys of marked electrical resistance. Improves mechanical properties of lead; powerful carbide stabilizer in cast iron, tellurium vapor in "daylight" lamps, vulcanization of rubber. Blasting caps. Semiconductor research. (EPA, 1998);DARK GREY-TO-BROWN AMORPHOUS POWDER, WITH METAL CHARACTERISTICS OR SILVERY-WHITE, LUSTROUS CRYSTALLINE SOLID.;Odorless, dark-gray to brown, amorphous powder or grayish-white, brittle solid.;Odorless, dark-gray to brown, amorphous powder or grayish-white, brittle solid. Group: Thermoelectric materials. CAS No. 13494-80-9. Product ID: tellurium. Molecular formula: 127.6g/mol. Mole weight: Te. [Te]. InChI=1S/Te. PORWMNRCUJJQNO-UHFFFAOYSA-N. 99.9wt%. | |
| Tenapanor | Tenapanor. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 17-[[[3-[(4S)-6,8-Dichloro-1,2,3,4-tetrahydro-2-methyl-4-isoquinolinyl]phenyl]sulfonyl]amino]-N-[2-[2-[2-[[[3-[(4S)-6,8-dichloro-1,2,3,4-tetrahydro-2-methyl-4-isoquinolinyl]phenyl]sulfonyl]amino]ethoxy]ethoxy]ethyl]-8-oxo-12,15-dioxa-2,7,9-triazaheptadecanamide. Appearance: Solid. CAS No. 1234423-95-0. Molecular formula: C50H66Cl4N8O10S2. Mole weight: 1145.04. IUPACName: 1-[2-[2-[2-[[3-[(4S)-6,8-dichloro-2-methyl-3,4-dihydro-1H-isoquinolin-4-yl]phenyl]sulfonylamino]ethoxy]ethoxy]ethyl]-3-[4-[2-[2-[2-[[3-[(4S)-6,8-dichloro-2-methyl-3,4-dihydro-1H-isoquinolin-4-yl]phenyl]sulfonylamino]ethoxy]ethoxy]ethylcarbamoylamino]butyl]urea. Canonical SMILES: CN1C[C@H](C2=C(C1)C(=CC(=C2)Cl)Cl)C3=CC(=CC=C3)S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)C4=CC=CC(=C4)[C@@H]5CN(CC6=C5C=C(C=C6Cl)Cl)C. Product ID: ACM1234423950. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tenapanor | Tenapanor (AZD1722) is a potent and orally active sodium/hydrogen exchanger isoform 3 (NHE3) inhibitor. Tenapanor reduces intestinal phosphate absorption predominantly through reduction of passive paracellular phosphate flux. Tenapanor has the potential for the research of hyperphosphatemia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD1722; RDX5791. CAS No. 1234423-95-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15991. | |
| Tenapanor hydrochloride | Tenapanor (AZD1722) hydrochloride is a potent and orally active sodium/hydrogen exchanger isoform 3 (NHE3) inhibitor. Tenapanor hydrochloride reduces intestinal phosphate absorption predominantly through reduction of passive paracellular phosphate flux. Tenapanor hydrochloride has the potential for the research of hyperphosphatemia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD1722 hydrochloride; RDX5791 hydrochloride. CAS No. 1234365-97-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15991A. | |
| Tenatoprazole | Tenatoprazole (TU-199) is an orally active imidazopyridine-based proton pump inhibitor with a prolonged plasma half-life. Tenatoprazole inhibits hog gastric H+/K+-ATPase activity with an IC50 of 6.2 ?M. Tenatoprazole blocks the interaction of ubiquitin with the ESCRT-1 factor Tsg101, inhibits production of several enveloped viruses, including EBV[1][2][3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TU-199. CAS No. 113712-98-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-17421. | |
| Tenatoprazole | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyenzyme activators, inhibitors & substrates. | |
| Tenatoprazole | A proton pump inhibitor for reduction and/or prevention of gastrointestinal disorders. Group: Biochemicals. Alternative Names: 5-Methoxy-2-[[ (4-methoxy-3, 5-dimethyl-2-pyridinyl) methyl]sulfinyl]-1H-imidazo[4, 5-b]pyridine; 5-Methoxy-2-[[ (4-methoxy-3, 5-dimethyl-2-pyridyl) methyl]sulfinyl]-1H-imidazo[4, 5-b]pyridine; TU 199. Grades: Highly Purified. CAS No. 113712-98-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Tenax PC-ABS 3D Printing Filament | Tenax PC-ABS 3D Printing Filament. Group: 3d printing materials. | |
| TENAX®-TA | It is a TENAX Porous Polymer Resin for thermal desorption analysis of VOC. It is widely used as an adsorbent in both air collection and purge trap applications. Its unique structure provides alternate and desirable adsorption/desorption characteristics compared to other porous polymers. Synonyms: Tenax® Porous Polymer Adsorbent; matrix Tenax TA, 60-80 mesh, bottle of 10 g; TENAX®-TA 60/80 MESH. Molecular formula: (C18H12O)n. | |
| Tenecin-1 | Tenecin-1 is an inducible antibacterial protein secreted in the larvae of Tenebrio molitor. Synonyms: Tenicin-1; Val-Thr-Cys-Asp-Ile-Leu-Ser-Val-Glu-Ala-Lys-Gly-Val-Lys-Leu-Asn-Asp-Ala-Ala-Cys-Ala-Ala-His-Cys-Leu-Phe-Arg-Gly-Arg-Ser-Gly-Gly-Tyr-Cys-Asn-Gly-Lys-Arg-Val-Cys-Val-Cys-Arg. | |
| Tenecteplase | Tenecteplase (TNK-tPA) is a modified tissue plasminogen activator. Tenecteplase is a recombinant human tissue plasminogen activator (rt-PA) that has been bioengineered to produce mutations in three gene loci. Tenecteplase (TNK-tPA) can be used in the study of acute ischemic stroke [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TNK-tPA. CAS No. 191588-94-0. Pack Sizes: 100 μg. Product ID: HY-108845. | |
| Teneligliptin | Teneligliptin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Teneligliptin (hydrobroMide);Teneligliptin HydrobroMide Hydrate;3-[[(2S,4S)-4-[4-(3-Methyl-1-phenyl-1H-pyrazol-5-yl)-1-piperazinyl]-2-pyrrolidinyl]carbonyl]-thiazolidine hydrobromide (2:5);Teneligliptin HydrobroMide (2:5);Teneligliptin HBr. Appearance: off-white to brown solid. CAS No. 906093-29-6. Molecular formula: 2(C22H30N6OS).5(HBr). Mole weight: 0. Purity: 98%+. IUPACName: [(2S,4S)-4-[4-(5-methyl-2-phenylpyrazol-3-yl)piperazin-1-yl]pyrrolidin-2-yl]-(1,3-thiazolidin-3-yl)methanone;pentahydrobromide. Canonical SMILES: CC1=NN(C(=C1)N2CCN(CC2)C3CC(NC3)C(=O)N4CCSC4)C5=CC=CC=C5.CC1=NN(C(=C1)N2CCN(CC2)C3CC(NC3)C(=O)N4CCSC4)C5=CC=CC=C5.Br.Br.Br.Br.Br. Product ID: ACM906093296. Alfa Chemistry ISO 9001:2015 Certified. | |
| Teneligliptin | Teneligliptin, is a dipeptidyl peptidase-4 (DPP-4) inhibitor that is used to treat type 2 diabetes. It is eliminated via excretion, and has a half-life of 24.2 hours in the human body. Group: Biochemicals. Grades: Highly Purified. CAS No. 760937-92-6. Pack Sizes: 10mg, 25mg. Molecular Formula: C22H30N6OS. US Biological Life Sciences. | Worldwide |
| Teneligliptin | Teneligliptin (MP-513) hydrobromide hydrate is an orally active and selective dipeptidyl peptidase 4 (DPP-4) inhibitor ( IC 50 s: 0.37 and 0.29 nM for the human and rat DPP-4, respectively). Teneligliptin hydrobromide hydrate improves blood glucose levels and can be used in researches related to type 2 diabetes mellitus [1] [2] [3] [4] [5] [6] [7] [8]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MP-513. CAS No. 760937-92-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-14806. | |
| Teneligliptin-[2,2,6,6-d4] | Teneligliptin-[2,2,6,6-d4] is the labelled analogue of Teneligliptin, which is a DPP-4 inhibitor and has been found to be effective in the treatment of type 2 diabetes. Synonyms: Teneligliptin d4; ((2S,4S)-4-(4-(3-Methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl-2,2,6,6-d4)pyrrolidin-2-yl)(thiazolidin-3-yl)methanone. Grade: 95% by HPLC; 98% atom D. CAS No. 1391012-98-8. Molecular formula: C22H26D4N6OS. Mole weight: 430.61. | |
| Teneligliptin-[d8] | Teneligliptin-[d8] is the labelled analogue of Teneligliptin, which is a DPP-4 inhibitor and has been found to be effective in the treatment of type 2 diabetes. Synonyms: Teneligliptin D8; [(2S,4S)-4-[4-(3-Methyl-1-phenyl-1H-pyrazol-5-yl)-1-piperazinyl]-2-pyrrolidinyl]-3-thiazolidinylmethanone-d8; 3-[[(2S,4S)-4-[4-(3-Methyl-1-phenyl-1H-pyrazol-5-yl)-1-piperazinyl]-2-pyrrolidinyl]carbonyl]thiazolidine-d8. Grade: 95% by HPLC; 95% atom D. CAS No. 1391012-95-5. Molecular formula: C22H22D8N6OS. Mole weight: 434.63. | |
| Teneligliptin hydrobromide | Teneligliptin (MP-513) hydrobromide is an orally active and selective dipeptidyl peptidase 4 (DPP-4) inhibitor ( IC 50 s: 0.37 and 0.29 nM for the human and rat DPP-4, respectively). Teneligliptin hydrobromide improves blood glucose levels and can be used in researches related to type 2 diabetes mellitus [1] [2] [3] [4] [5] [6] [7] [8]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MP-513 hydrobromide. CAS No. 906093-29-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14806A. | |
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