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Teneligliptin-d8 is labeled Teneligliptin which is a dipeptidyl peptidase-4 (DPP-4) inhibitor that is used to treat type 2 diabetes. Tenegliptin is eliminated from the via excretion, with a half-life of 24.2 hours in the human body. Group: 2h labeled compounds. CAS No. 1391012-95-5. Molecular formula: C22H22D8N6OS. Mole weight: 434.63. Catalog: ACM1391012955.
Teneligliptin HBr
Teneligliptin hydrobromide is a novel, potent, and long-lasting dipeptidyl peptidase-4 inhibitor. It competitively inhibited human plasma, rat plasma, and human recombinant DPP-4 in vitro. Synonyms: [(2S,4S)-4-[4-(3-Methyl-1-phenyl-1H-pyrazol-5-yl)-1-piperazinyl]-2-pyrrolidinyl]-3-thiazolidinylmethanone Hydrobromide (2:5); Teneligliptin Hydrobromide (2:5). Grades: >98%. CAS No. 906093-29-6. Molecular formula: C44H65Br5N12O2S2. Mole weight: 1257.72.
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.
Teneligliptin hydrobromide hydrate
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 hydrobromide hydrate. CAS No. 1572583-29-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-14806B.
Teneligliptin Impurity 1
One impurity of Teneligliptin, which is a DPP-4 inhibitor and has been found to be effective in the treatment of type 2 diabetes. Grades: > 95%. Molecular formula: C42H58N12O2S2. Mole weight: 827.14.
Teneligliptin impurity 10
Teneligliptin impurity 10. Uses: For analytical and research use. Group: Impurity standards. CAS No. 401566-80-1. Molecular Formula: C27H38N6O3S. Mole Weight: 526.7. Catalog: APB401566801.
Teneligliptin impurity 13
Teneligliptin impurity 13. Uses: For analytical and research use. Group: Impurity standards. CAS No. 401564-30-5. Molecular Formula: C13H22N2O4S. Mole Weight: 302.39. Catalog: APB401564305.
Teneligliptin impurity 14
Teneligliptin impurity 14. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1453906-29-0. Molecular Formula: C16H20N4O. Mole Weight: 284.36. Catalog: APB1453906290.
Teneligliptin Impurity 2
One impurity of Teneligliptin, which is a DPP-4 inhibitor and has been found to be effective in the treatment of type 2 diabetes. Grades: > 95%. Molecular formula: C44H60N12O2S2. Mole weight: 853.18.
Teneligliptin impurity 3
Teneligliptin impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1404559-15-4. Molecular Formula: C22H30N6OS. Mole Weight: 426.58. Catalog: APB1404559154.
Teneligliptin Impurity 3
One impurity of Teneligliptin, which is a DPP-4 inhibitor and has been found to be effective in the treatment of type 2 diabetes. Grades: > 95%. Molecular formula: C20H28N6OS. Mole weight: 400.55.
Teneligliptin impurity 4
Teneligliptin impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1404559-22-3. Molecular Formula: C27H38N6O3S. Mole Weight: 526.7. Catalog: APB1404559223.
Teneligliptin Impurity 4
One impurity of Teneligliptin, which is a DPP-4 inhibitor and has been found to be effective in the treatment of type 2 diabetes. Grades: > 95%. Molecular formula: C45H60N12O2S2. Mole weight: 865.19.
Teneligliptin impurity 5
Teneligliptin impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1415908-67-6. Molecular Formula: C13H20N2O4S. Mole Weight: 300.37. Catalog: APB1415908676.
Teneligliptin Impurity 5
One impurity of Teneligliptin, which is a DPP-4 inhibitor and has been found to be effective in the treatment of type 2 diabetes. Grades: > 95%. Molecular formula: C22H29BrN6OS. Mole weight: 505.48.
Teneligliptin impurity 6
Teneligliptin impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1404559-17-6. Molecular Formula: C22H30N6OS. Mole Weight: 426.58. Catalog: APB1404559176.
Teneligliptin impurity 7 (saxagliptin impurity 11). Uses: For analytical and research use. Group: Impurity standards. CAS No. 2407632-38-4. Molecular Formula: C19H25N5O2. Mole Weight: 355.4. Catalog: APB2407632384.
Teneligliptin impurity 8
Teneligliptin impurity 8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 401566-79-8. Molecular Formula: C14H18N4. Mole Weight: 242.33. Catalog: APB401566798.
Teneligliptin impurity 9
Teneligliptin impurity 9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2131105-24-1. Molecular Formula: C25H35N5O4. Mole Weight: 469.59. Catalog: APB2131105241.
Teneligliptin Impurity G
One impurity of Teneligliptin, which is a DPP-4 inhibitor and has been found to be effective in the treatment of type 2 diabetes. Synonyms: N4-DesPyrazolo N4-Acetoacetyl Teneligliptin; 1-(4-((3S,5S)-5-(thiazolidine-3-carbonyl)pyrrolidin-3-yl)piperazin-1-yl)butane-1,3-dione. Grades: > 95%. Molecular formula: C16H26N4O3S. Mole weight: 354.47.
Teneligliptin Sulfoxide (Mixture of Diastereomers)
Teneligliptin Sulfoxide (Mixture of Diastereomers). Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 3-[[(2S,4S)-4-[4-(3-Methyl-1-phenyl-1H-pyrazol-5-yl)-1-piperazinyl]-2-pyrrolidinyl]carbonyl]thiazolidine Sulfoxide,[(2S,4S)-4-[4-(3-Methyl-1-phenyl-1H-pyrazol-5-yl)-1-piperazinyl]-2-pyrrolidinyl]-3-thiazolidinylmethanone Sulfoxide, Tenelia Sulfoxide. IUPAC Name: [(2S,4S)-4-[4-(5-methyl-2-phenyl-pyrazol-3-yl)piperazin-1-yl]pyrrolidin-2-yl]-(1-oxo-1,3-thiazolidin-3-yl)methanone. Molecular Formula: C22H30N6O2S. Mole Weight: 442.58. Catalog: APS003276. SMILES: Cc1cc (N2CCN (CC2)[C@@H]3CN[C@@H] (C3)C (=O)N4CCS (=O)C4)n (n1)c5ccccc5. Format: Neat.
Tenellin
Tenellin is a yellow pigment produced by species of the genus Beauveria, isolated and reported by Canadian researchers in 1968. Structure elucidation in 1977 showed that tenellin belongs to the rare 4-hydroxypyridone class containing a dienone side chain. Little has been published on the biological activity of tenellin despite the extensive use of Beauveria species, capable of producing tenellin, as biocontrol agents for agrochemical pests. Group: Pheromone ingredients. CAS No. 53823-15-7. Molecular formula: C21H23NO5. Mole weight: 369.4. Appearance: yellow solid. Purity: 0.95. Catalog: ACM53823157.
Tenellin
It is a yellow pigment produced by species of the genus beauveria. It belongs to the rare 4-hydroxypyridone class containing a dienone side chain. Synonyms: 2(1H)-Pyridinone, 3-[(2E,4E,6R)-4,6-dimethyl-1-oxo-2,4-octadien-1-yl]-1,4-dihydroxy-5-(4-hydroxyphenyl)-. Grades: >95% by HPLC. CAS No. 53823-15-7. Molecular formula: C21H23NO5. Mole weight: 369.41.
Tenidap
Tenidap is one of the nonsteroidal antiinflammatory drugs. It is a COX1/2 and 5-lipoxygenase inhibitor. Tenidap preferentially inhibits COX-1 and IC50 value is 30 Nm. It has less inhibitory activity towards COX-2 and 5-lipoxygenase with IC50 values is 1.2μM for COX-2 and and > 30μM for 5-lipoxygenase. It was developed by Pfizer for treatment of rheumatoid arthritis. Because of the liver and kidney toxicity, the development was discontinued. In 1998, Tenidap for HIV infections treatment was also discontinued. Uses: Rheumatoid arthritis. Synonyms: TENIDAP;AKOS 91367; AKOS91367; AKOS-91367; 5-Chloro-2,3-dihydro-2-oxo-3-(2-thenoyl)-1H-indole-1-carboxamide;CP66248,CP-66248-2. Grades: 96%. CAS No. 120210-48-2. Molecular formula: C14H9ClN2O3S. Mole weight: 320.75.
Tenidap
Tenidap. Group: Biochemicals. Grades: Purified. CAS No. 120210-48-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
Tenidap
Tenidap, a non-steroidal anti-inflammatory drug, is a selective COX-1 inhibitor, with IC 50 values of 0.03 μM and 1.2 μM for COX-1 and COX-2, respectively. Tenidap has anti-inflammatory and antirheumatic properties [1] [2]. Tenidap is also a specific SLC26A3 inhibitor [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP-66248. CAS No. 120210-48-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105028.
Tenifatecan, also known as SN2310, is an injectable emulsion composed of 7-ethyl-10-hydroxycamptothecin (SN-38) conjugate with vitamin E through a succinate linker. SN-38 is the active metabolite of irinotecan. SN-38 binds to and inhibits topoisomerase I by stabilizing the cleavable complex between topoisomerase I and DNA, resulting in DNA breaks, inhibition of DNA replication, and apoptosis. SN-38 has been reported to exhibit up to 1,000-fold more cytotoxic activity against various cancer cells in vitro than irinotecan. SN2310 Injectable Emulsion is being developed with the objective of demonstrating improved anti-tumor activity as a result of increased exposure to SN-38 based on a longer half-life. Synonyms: SN 2300; SN2300; SN-2300; BEL2310; BEL 2310; BEL-2310. CAS No. 850728-17-5. Molecular formula: C53H68N2O8. Mole weight: 861.12.
Tenilsetam
Tenilsetam is an endonuclease modulator, also a nootropic agent and advanced glycation end product (AGE) inhibitor with the potential to treat Alzheimer's disease (AD). Preclinical studies indicated that tenilsetam may have an inhibitory effect on diabetic retinopathy, without amelioration of pericyte loss. Uses: Potential treatment of alzheimer's disease. Synonyms: 3-(thiophen-2-yl)piperazin-2-one; 3-thiophen-2-ylpiperazin-2-one; 3-(2-thienyl)piperazin-2-one. Grades: 99%. CAS No. 86696-86-8. Molecular formula: C8H10N2OS. Mole weight: 182.24.
Teniposide
Teniposide is a podophyllotoxin derivative, acts as a topoisomerase II inhibitor, and used as a chemotherapeutic agent. Uses: Scientific research. Group: Signaling pathways. Alternative Names: VM26. CAS No. 29767-20-2. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-13761.
Teniposide
Teniposide is a chemotherapeutic medication mainly used in the treatment of childhood acute lymphocytic leukemia (ALL).It is in a class of drugs known as podophyllotoxin derivatives and slows the growth of cancer cells in the body. Uses: Antineoplastic agents; enzyme inhibitors; nucleic acid synthesis inhibitors. Synonyms: NSC-122819; NSC 122819; NSC122819; VM26; VM-26; VM 26; HSDB 6546; HSDB6546; HSDB-6546; CCRIS 2058. Brand name: Vumon; Vehem. Abbreviations: EPT; PTG. Grades: >98%. CAS No. 29767-20-2. Molecular formula: C32H32O13S. Mole weight: 656.65.
Tenivastatin impurity 1
Tenivastatin impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 530112-57-3. Molecular Formula: C25H44CaO7. Mole Weight: 496.7. Catalog: APB530112573.
Tennis courts
Tennis courts. Group: Polymers.
Tenocyclidine hydrochloride
Tenocyclidine hydrochloride. Group: Biochemicals. Alternative Names: 1-[1- (2-Thienyl) cyclohexyl]piperidine hydrochloride; GK 0; N-[1- (2-Thienyl) cyclohexyl]piperidine. Grades: Highly Purified. CAS No. 1867-65-8. Pack Sizes: 50mg, 100mg. Molecular Formula: C15H24ClNS. US Biological Life Sciences.
Worldwide
Tenofovir
Tenofovir (GS 1278) is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B ( HBV ) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS 1278; PMPA. CAS No. 147127-20-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13910.
Tenofovir
Acyclic phosphonate nucleotide analogue. Used as an anti-HIV agent. Group: Biochemicals. Alternative Names: [ [ (1R) -2 (6-Amino-9H-purin-9-yl) -1-methylethoxy] methyl] phosphonic Acid; (R) -9- (2-Phosphonomethoxypropyl ) adenine. Grades: Highly Purified. CAS No. 147127-20-6. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Tenofovir alafenamide
Tenofovir alafenamide (GS-7340) is an investigational oral proagent of Tenofovir. Tenofovir is a HIV-1 nucleotide reverse transcriptase inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-7340. CAS No. 379270-37-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15232.
Tenofovir Alafenamide
Tenofovir Alafenamide is a prodrug of Tenofovir, which is a reverse transcriptase inhibitor used to treat HIV and Hepatitis B. Antiviral. Synonyms: (S)-isopropyl 2- ( ( (S) - ( ( ( (R) -1- (6-amino-9H-purin-9-yl) propan-2-yl) oxy) methyl) (phenoxy) phosphoryl) amino) propanoate; GS7340; GS-7340; GS 7340; Tenofovir alafenamide. Grades: >98%. CAS No. 379270-37-8. Molecular formula: C21H29N6O5P. Mole weight: 476.47.
Tenofovir Alafenamide
Tenofovir Alafenamide is a prodrug of Tenofovir (T018500), which is a reverse transcriptase inhibitor used to treat HIV and Hepatitis B. Antiviral. Group: Biochemicals. Grades: Highly Purified. CAS No. 379270-37-8. Pack Sizes: 5mg, 25mg. Molecular Formula: C21H29N6O5P. US Biological Life Sciences.
Worldwide
Tenofovir alafenamide fumarate
Tenofovir alafenamide fumarate (GS-7340 fumarate) is an investigational oral proagent of Tenofovir. Tenofovir is a HIV-1 nucleotide reverse transcriptase inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-7340 fumarate. CAS No. 379270-38-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15232A.
Tenofovir alafenamide hemifumarate
Tenofovir alafenamide hemifumarate, also known as Tenofovir alafenamide fumarate (2:1), is a nucleotide reverse transcriptase inhibitor (NRTIs) and a novel prodrug of tenofovir. By blocking reverse transcriptase, TAF prevents HIV from multiplying and can reduce the amount of HIV in the body. Synonyms: Isopropyl ((S)-((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)(phenoxy)phosphoryl)-L-alaninate hemifumarate; TAF; GS734; GS-734; GS 734; GS 7340; GS-7340; GS7340; Tenofovir alafenamide fumarate (2:1). Grades: > 98%. CAS No. 1392275-56-7. Molecular formula: C46H62N12O14P2. Mole weight: 1069.02.
Tenofovir Alafenamide PMPA Impurity
One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: Tenofovir Dimer; Bis((((R)-1-(6-Amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)diphosphonic Acid. CAS No. 1607007-18-0. Molecular formula: C18H26N10O7P2. Mole weight: 556.41.
Tenofovir-d6
2H Labeled Compounds. Alternative Names: ((1R)-2(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]-d6-phosphonic Acid. CAS No. 1020719-94-1. Molecular formula: C9H8D6N5O4P. Mole weight: 293.25. Catalog: ACM1020719941.
Tenofovir Dibenzyloxy Isopropyl Carbamate
Protected Tenofovir. Acyclic phosphonate nucleotide analogue; reverse transcriptase inhibitor. Used as an anti-HIV agent. Antiviral. Group: Biochemicals. Alternative Names: [ [ (1R) -2 (6-Isopropyl aminocarbamate-9H-purin-9-yl) -1-methylethoxy] methyl] phosphonic Acid Dibenzyl Ester. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences.
Worldwide
Tenofovir Dimer Triethylammonium Salt
It could be used as an anti-HIV agent. Synonyms: Bis((((R)-1-(6-Amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)diphosphonic Acid Triethylammonium Salt. Grades: 98%. Molecular formula: C30H56N12O7P2. Mole weight: 758.79.
Tenofovir Diphosphate
The diphosphate salt form of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: PMPApp; Diphosphoric Acid, Anhydride with [[(1R)-2-(6-Amino-9H-purin-9-yl)-1-methylethoxy]. Grades: > 95%. CAS No. 166403-66-3. Molecular formula: C9H16N5O10P3. Mole weight: 447.18.
Tenofovir diphosphate triethylamine salt
Tenofovir diphosphate triethylamine salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 2122333-63-3. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C9H16N5O10P3·x (C6H15N). US Biological Life Sciences.
Worldwide
Tenofovir Diphosphate Triethylamine Salt (mixture of diastereomers)
A metabolite of Tenofovir. Group: Biochemicals. Alternative Names: Diphosphoric Acid Triethylamine Salt , Anhydride with [ [ (1R) -2- (6-Amino-9H-purin-9-yl) -1-methylethoxy] methyl] phosphonic Acid Triethylamine Salt; PMPApp Triethylamine Salt. Grades: Highly Purified. CAS No. Free Acid: 166403-66-3. Pack Sizes: 500ug, 1mg. Molecular Formula: C9H16N5O10P3 x(C6H15N), Molecular Weight: 447.17. US Biological Life Sciences.
Tenofovir Disoproxil (Bis(POC)-PMPA) is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B. Group: Inhibitors. Alternative Names: Tenofovir disoproxil. CAS No. 201341-05-1. Molecular formula: C19H30N5O10P. Mole weight: 519.44. Purity: 0.9984. Density: 1.45g/cm³. Catalog: ACM201341051.
Tenofovir Disoproxil
Tenofovir dsoproxil is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B. Synonyms: 2,4,6,8-Tetraoxa-5-phosphanonanedioic acid, 5-[[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl]-, 1,9-bis(1-methylethyl) ester, 5-oxide; 2,4,6,8-Tetraoxa-5-phosphanonanedioic acid, 5-[[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl]-, bis(1-methylethyl) ester, 5-oxide; 2,4,6,8-Tetraoxa-5-phosphanonanedioic acid, 5-[[2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl]-, bis(1-methylethyl) ester, 5-oxide, (R)-; Bis-POC-PMPA; GS 4331; 5-[[(1R)-2-(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]-bis(1-methylethyl)ester-5-oxide-2,4,6,8-tetraoxa-5-phosphanonanedioic Acid; (R)-5-[[2-(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]-bis(1-methylethyl)ester-5-oxide-2,4,6,8-tetraoxa-5-phosphanonanedioic Acid. Grades: ≥95%. CAS No. 201341-05-1. Molecular formula: C19H30N5O10P. Mole weight: 519.44.
Tenofovir Disoproxil
Tenofovir Disoproxil (Bis(POC)-PMPA) is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bis(POC)-PMPA; GS 4331. CAS No. 201341-05-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-13782A.
Tenofovir Disoproxil Dimer
Atmosphere: Group: Biochemicals. Alternative Names: 5-[[ (1R) -2-[6-[[[[9-[ (2R) -2, 11-Dimethyl-5-[[[ (1-methylethoxy) carbonyl]oxy]methoxy]-5-oxido-9-oxo-3, 6, 8, 10-tetraoxa-5-phosphadodec-1-yl]-9H-purin-6-yl]amino]methyl]amino]-9H-purin-9-yl]-1-methylethoxy]methyl]-2, 4, 6, 8-tetraoxa-5-phosphanonanedioic Acid? 1,9-Bis(1-methylethyl) Ester 5-Oxide. Grades: Highly Purified. CAS No. 1093279-76-5. Pack Sizes: 5mg. US Biological Life Sciences.
Tenofovir Disoproxil fumarate is a nucleotide reverse transcriptase inhibitor used to treat HIV and chronic Hepatitis B. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Tenofovir DF; Bis(POC)-PMPA fumarate; GS 4331 fumarate. CAS No. 202138-50-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-13782.
Tenofovir Disoproxil Fumarate
Tenofovir Disoproxil Fumarate belongs to a class of antiretroviral drugs, it inhibits the activity of HIV reverse transcriptase by competing with the natural substrate deoxyadenosine 5'-triphosphate. Synonyms: GS-1278 Disoproxil Fumarate; GS 1278 Disoproxil Fumarate; GS1278 Disoproxil Fumarate. Grades: >98%. CAS No. 202138-50-9. Molecular formula: C19H30N5O10P.C4H4O4. Mole weight: 635.51.
Tenofovir Disoproxil Fumarate
Acyclic phosphonate nucleotide analogue; reverse transcriptase inhibitor. Used as an anti-HIV agent. Antiviral. Group: Biochemicals. Alternative Names: 5-[[(1R)-2-(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]-2,4,6,8-tetraoxa-5-phosphanonanedioic Acid 1,9-Bis(1-methylethyl) Ester 5-Oxide (2E)-2-Butenedioate; GS 4331-05; PMPA Prodrug. Grades: Highly Purified. CAS No. 202138-50-9. Pack Sizes: 10mg, 50mg. Molecular Formula: C23H34N5O14P, Molecular Weight: 635.51. US Biological Life Sciences.
One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Grades: > 95%. Molecular formula: C15H24N5O8P. Mole weight: 433.36.
Tenofovir Disoproxil (fumarate) (Standard)
Tenofovir Disoproxil (fumarate) (Standard) is the analytical standard of Tenofovir Disoproxil (fumarate). This product is intended for research and analytical applications. Tenofovir Disoproxil fumarate is a nucleotide reverse transcriptase inhibitor used to treat HIV and chronic Hepatitis B. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Tenofovir DF (Standard); Bis(POC)-PMPA (fumarate) (Standard); GS 4331 (fumarate) (Standard). CAS No. 202138-50-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13782R.
Tenofovir Disoproxil derivative as antiviral and antitumor agent. Group: Biochemicals. Alternative Names: 5-[[ (1R) -1-Methyl-2-[6-[ (isopropoxycarbonyl) amino]-9H-purin-9-yl]ethoxy]methyl]-2, 4, 6, 8-tetraoxa-5-phosphanonanedioic Acid Bis(1-methylethyl) Ester 5-Oxide. Grades: Highly Purified. CAS No. 1244022-54-5. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Tenofovir Disoproxil Isopropoxycarbonyl
Cas No. 1244022-54-5.
Tenofovir Disoproxil Related Compound E
Cas No. 211364-69-1.
Tenofovir Disoproxil Related Compound G Fumarate
Tenofovir Disoproxil Related Compound G Fumarate is an impurity of Tenofovir Disoproxil Fumarate, which is a potent reverse transcriptase inhibitor used to treat chronic hepatitis B and to prevent and treat HIV/AIDS. Synonyms: 2,4,7-Trioxa-5-phosphanonanoic acid, 9-(6-amino-9H-purin-9-yl)-8-methyl-5-(1-methylethoxy)-, 1-methylethyl ester, 5-oxide, (8R)-, (2E)-2-butenedioate (1:1); O-(Isopropoxycarbonyloxymethyl)-O-isopropyl-{(R)-[1-(6-amino-9H-purin-9-yl)propan-2-yloxy]}methylphosphonate fumarate salt; ( ( ( ( ( (R)-1- (6-Amino-9H-purin-9-yl)propan-2-yl)oxy)methyl) (isopropoxy)phosphoryl)oxy)methyl isopropyl carbonate fumarate; Mono-POC Isopropyl Tenofovir fumarate. Grades: ≥95%. CAS No. 1422284-15-8. Molecular formula: C17H28N5O7P.C4H4O4. Mole weight: 561.48.
Tenofovir Disoproxil USP Related Compound G Fumarate
Tenofovir Disoproxil USP Related Compound G Fumarate. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1422284-15-8. Molecular Formula: C21H32N5O11P. Mole Weight: 561.48. Catalog: APB1422284158.
Tenofovir exalidex
Tenofovir exalidex, also known as HDP-Tenofovir and CMX-157, is a highly potent prodrug of the antiviral tenofovir, appeared safe and well-tolerated in patients with hepatitis B, according to a presentation at The Liver Meeting 2017. Tenofovir exalidex results in decreased circulating levels, lowering systemic exposure and thereby reducing the potential for renal and bone side effects. Uses: Anti-hiv agents. Synonyms: 3-(hexadecyloxy)propyl hydrogen ((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonate; Tenofovir exalidex; HDP-Tenofovir; Tenofovir; CMX-157; CMX157; CMX 157. Grades: ≥98% (HPLC). CAS No. 911208-73-6. Molecular formula: C28H52N5O5P. Mole weight: 569.72.
Tenofovir hydrate
Tenofovir(GS 1278, PMPA) is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors (NRTIs), which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV. Uses: Anti-hiv agents. Synonyms: Viread hydrate; GS 1278 hydrate; GS1278 hydrate; GS-1278 hydrate; PMPA hydrate; TDF hydrate. Grades: >98%. CAS No. 206184-49-8. Molecular formula: C9H16N5O5P. Mole weight: 305.23.
Tenofovir hydrate
Tenofovir hydrate is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS 1278 hydrate; PMPA hydrate. CAS No. 206184-49-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-13910A.
Tenofovir Impurity 102
Tenofovir Impurity 102. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2615274-45-6. Molecular Formula: C5H4N6O. Mole Weight: 164.13. Catalog: APB2615274456.