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| Product | Description | |
|---|---|---|
| Ta-5.5W Alloy Powder | Ta-5.5W alloy powder is composed of tantalum (Ta) and tungsten (W). |  |
| Ta-7.5W Alloy Powder | Ta-7.5W spherical tantalum alloy powder is commonly used in powder metallurgy applications and has high strength at room temperature due to its high interstitial element content. | |
| Ta-7.5W Alloy Powder | Ta-7.5W Alloy Powder. | |
| TAA; N,N-diphenyl-2,4,6-trimethylaniline, >99%(HPLC), Sublimed | TAA; N,N-diphenyl-2,4,6-trimethylaniline, >99%(HPLC), Sublimed. CAS No. 603134-65-2. Molecular formula: C21H21N. Mole weight: 287.4g/mol. IUPAC Name: 2,4,6-trimethyl-N,N-diphenylaniline. SMILES: CC1=CC(=C(C(=C1)C)N(C2=CC=CC=C2)C3=CC=CC=C3)C. InChI: InChI=1S/C21H21N/c1-16-14-17(2)21(18(3)15-16)22(19-10-6-4-7-11-19)20-12-8-5-9-13-20/h4-15H,1-3H3. | |
| Tabalumab | Tabalumab (LY2127399) is a human anti-BAFF (B-cell activating factor) monoclonal antibody (IgG4 type) with neutralising activity against membrane bound and soluble BAFF. Tabalumab can be used in studies of autoimmune diseases such as rheumatoid arthritis, renal failure and systemic lupus erythematosus[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LY2127399. CAS No. 1143503-67-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99220. |  |
| Tabanon | Tabanon. CAS No. 13215-88-8. FEMA No. 4663. VIGON Item # 502538. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Tabernanthine | Tabernanthine is an alkaloid isolated from Tabernaemontana hilariana. Tabernanthine can reduce the self-administration of cocaine and morphine in rats. Tabernanthine acts as a benzodiazepine receptor inverse agonist in a discriminant in vitro binding assay. Synonyms: 13-Methoxyibogamine. Grade: 97.0%. CAS No. 83-94-3. Molecular formula: C20H26N2O. Mole weight: 310.441. |  |
| Tabersonine | Tabersonine. Group: Biochemicals. Grades: Plant Grade. CAS No. 4429-63-4. Pack Sizes: 20mg. Molecular Formula: C21H24N2O2, Molecular Weight: 336.43. US Biological Life Sciences. |  Worldwide |
| Tabersonine | Tabersonine is a monoterpenoid indole alkaloid found in the beans of Voacanga africana, a plant traditionally used for religious purposes in Africa. Synonyms: (-)-Tabersonine; Tabersonin; Aspidospermidine-3-carboxylic acid, 2,3,6,7-tetradehydro-, methyl ester, (5α,12R,19α)-; 1H-Indolizino[8,1-cd]carbazole-5-carboxylic acid, 3a-ethyl-3a,4,6,11,12,13a-hexahydro-, methyl ester. Grade: 98%. CAS No. 4429-63-4. Molecular formula: C21H24N2O2. Mole weight: 336.43. | |
| Tabersonine | Tabersonine is a selective, orally active NLRP3 inhibitor. Tabersonine directly binds to the NACHT domain of NLRP3, inhibiting its ATPase activity and oligomerization, thereby blocking ASC spot formation and caspase-1 activation, and reducing the release of pro-inflammatory cytokines such as IL-1β. Tabersonine also inhibits K63-linked ubiquitination of TRAF6, blocking NF-κB, PI3K/Akt, and p38 MAPK signaling pathways. Tabersonine can inhibit inflammatory responses, induce apoptosis of liver cancer cells through mitochondrial pathways and death receptor pathways, reduce mitochondrial membrane potential, promote cytochrome c release, and activate caspase proteins. Tabersonine is mainly used in the study of NLRP3-driven inflammatory diseases (such as acute lung injury, sepsis, peritonitis) and tumors such as liver cancer[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 4429-63-4. Pack Sizes: 10 mM * 1 mL in DMSO; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1431. | |
| tabersonine 16-hydroxylase | A heme-thiolate protein (P-450). Group: Enzymes. Synonyms: tabersonine-11-hydroxylase; T11H. Enzyme Commission Number: EC 1.14.13.73. CAS No. 250378-34-8. 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-0880; tabersonine 16-hydroxylase; EC 1.14.13.73; 250378-34-8; tabersonine-11-hydroxylase; T11H. Cat No: EXWM-0880. |  |
| tabersonine 16-O-methyltransferase | Involved in the biosynthesis of vindoline from tabersonine in the Madagascar periwinkle, Catharanthus roseus. Group: Enzymes. Synonyms: 11-demethyl-17-deacetylvindoline 11-methyltransferase; 11-O-demethyl-17-O-deacetylvindoline O-methyltransferase; S-adenosyl-L-methionine:11-O-demethyl-17-O-deacetylvindoline 11-O-methyltransferase. Enzyme Commission Number: EC 2.1.1.94. CAS No. 100984-95-0. 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-1994; tabersonine 16-O-methyltransferase; EC 2.1.1.94; 100984-95-0; 11-demethyl-17-deacetylvindoline 11-methyltransferase; 11-O-demethyl-17-O-deacetylvindoline O-methyltransferase; S-adenosyl-L-methionine:11-O-demethyl-17-O-deacetylvindoline 11-O-methyltransferase. Cat No: EXWM-1994. | |
| Tabimorelin hemifumarate | Tabimorelin hemifumarate. Group: Biochemicals. Grades: Purified. CAS No. 242143-80-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Tabimorelin impurity 1 | Tabimorelin impurity 1. Uses: For analytical and research use. CAS No. 193085-20-0. Molecular formula: C37H48N4O5. Mole weight: 628.81. Catalog: APB193085200. |  |
| TABPT;4'-[4,6-bis(4'-formyl[1,1'-biphenyl]-4-yl)-1,3, 5-triazin-2-yl]-[1,1'-Biphenyl]-4-carboxaldehyde; 4',4''',4'''''-(1,3 ,5-triazine-2,4,6-triyl)tris(([1,1'-biphenyl]-4-carbaldehyde)) | TABPT;4'-[4,6-bis(4'-formyl[1,1'-biphenyl]-4-yl)-1,3, 5-triazin-2-yl]-[1,1'-Biphenyl]-4-carboxaldehyde; 4',4''',4'''''-(1,3 ,5-triazine-2,4,6-triyl)tris(([1,1'-biphenyl]-4-carbaldehyde)). CAS No. 1221509-80-3. | |
| TABS Buffer | TABS Buffer. Uses: For analytical and research use. Alternative Names: N-tris(Hydroxymethyl)methyl-4-aminobutanesulfonic acid. CAS No. 54960-65-5. Molecular formula: C8H19NO6S. Mole weight: 257.30. Purity: ≥98%. Catalog: APB54960655. | |
| Tabular Alumina Balls | Tabular Alumina Balls. Products can be packaged according to specific requirements and as per international standards for export shipments. |  Worldwide |
| TAC1_CARRO Tachyplesin-1 | TAC1_CARRO Tachyplesin-1 is an antibacterial peptide isolated from Carcinoscorpius rotundicauda. Synonyms: Tachyplesin I; Lys-Trp-Cys-Phe-Arg-Val-Cys-Tyr-Arg-Gly-Ile-Cys-Tyr-Arg-Arg-Cys-Arg. Molecular formula: C99H151N35O19S4. Mole weight: 2263.8. | |
| TACA | TACA. Group: Biochemicals. Grades: Purified. CAS No. 38090-53-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Tacalcitol | Tacalcitol. Group: Biochemicals. Grades: Purified. CAS No. 57333-96-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tacalcitol | Tacalcitol (1,24(R)-Dihydroxyvitamin D3; 1.alpha.,24R-Dihydroxyvitamin D3) can promote normal bone growth by regulating calcium ions. Tacalcitol inhibits cancer cell proliferation and migration. Tacalcitol can be used in the research of inflammation, cancer, and skin diseases[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 1,24(R)-Dihydroxyvitamin D3; 1.alpha.,24R-Dihydroxyvitamin D3. CAS No. 57333-96-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-32337. | |
| Tacalcitol EP Impurity A | Tacalcitol EP Impurity A. Uses: For analytical and research use. CAS No. 1294517-97-7. Molecular formula: C27H44O3. Mole weight: 416.65. Catalog: APB1294517977. | |
| Tacalcitol EP Impurity B | Tacalcitol EP Impurity B. Uses: For analytical and research use. Molecular formula: C27H44O3. Mole weight: 416.65. Catalog: APB10872. | |
| Tacalcitol EP Impurity C | Tacalcitol EP Impurity C. Uses: For analytical and research use. Molecular formula: C27H44O3. Mole weight: 416.65. Catalog: APB10871. | |
| Tacalcitol Impurity 1 | Tacalcitol Impurity 1. Uses: For analytical and research use. CAS No. 57333-95-6. Molecular formula: C27H44O3. Mole weight: 416.65. Catalog: APB57333956. | |
| Tacalcitol Monohydrate | Tacalcitol Monohydrate. Group: Biochemicals. Alternative Names: (1α,3 β,5Z,7E,24R)-9,10-Secocholesta-5,7,10(19)-triene-1,3,24-triol Monohydrate; 1α,24(R)-Dihydroxy-vitamin D3 Monohydrate; 1 α , 24 (R) -Di hydroxycholecalciferol Monohydrate. Grades: Highly Purified. CAS No. 93129-94-3. Pack Sizes: 1mg. Molecular Formula: C27H44O3 H2O, Molecular Weight: 434.65. US Biological Life Sciences. | Worldwide |
| Taccalonolide A | Taccalonolide A is a microtubule stabilizer, which is a steroid isolated from Tacca chantrieri, with cytotoxic and antimalarial activities[1][2]. Taccalonolide A causes G2-M accumulation, Bcl-2 phosphorylation and initiation of apoptosis[1]. Taccalonolide A is effective in vitro against cell lines that overexpress P-glycoprotein (Pgp) and multidrug resistance protein 7 (MRP7), with an IC50 of 622 nM for SK-OV-3 cells[3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 108885-68-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-N2416. | |
| Taccalonolide A | Taccalonolide A. Group: Biochemicals. Grades: Plant Grade. CAS No. 108885-68-3. Pack Sizes: 20mg. Molecular Formula: C36H46O14, Molecular Weight: 702.75. US Biological Life Sciences. | Worldwide |
| taccalonolide B | taccalonolide B. Group: Biochemicals. Grades: Plant Grade. CAS No. 108885-69-4. Pack Sizes: 20mg. Molecular Formula: C34H44O13, Molecular Weight: 660.71. US Biological Life Sciences. | Worldwide |
| Tacedinaline | Tacedinaline is a histone deacetylase (HDAC) inhibitor. Tacedinaline is an anti-cancer agent as HDAC inhibitors block angiogenesis, arrest cell growth, and lead to differentiation and apoptosis in tumor cells. Studies show Tacedinaline to be effective against acute myeloid leukemia in vitro and in vivo when used in combination with conventional anti-cancer agents. Group: Biochemicals. Alternative Names: 4-(Acetylamino)-N-(2-aminophenyl)benzamide; Acetyldinaline; CI 994; Goe 5549; PD 123654. Grades: Highly Purified. CAS No. 112522-64-2. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Tacedinaline | Tacedinaline (N-acetyldinaline) is an inhibitor of the histone deacetylase (HDAC) with IC50s of 0.9, 0.9, 1.2 μM for recombinant HDAC 1, 2 and 3 respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: N-acetyldinaline; CI-994; Goe-5549. CAS No. 112522-64-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-50934. | |
| T Acetic acid | A nucleobase for PNA synthesis. Uses: T-acetic acid, also known as trichloroacetic acid, is a potent compound with a wide range of applications in various fields including medicine, research, and industry. in the field of drug discovery, t-acetic acid plays a vital role in several key processes that facilitate the development of new drugs. this versatile compound is used in various stages of drug discovery, from target identification. Synonyms: Thymine-1-acetic acid; 2-(5-Methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetic acid; (5-Methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)acetic acid. Grade: 98%. CAS No. 20924-05-4. Molecular formula: C7H8N2O4. Mole weight: 184.15. | |
| Tachyplesin I | Tachyplesin I is a β-hairpin antimicrobial peptide that contains 17 amino acid residues. Tachyplesin I exhibits cytotoxic properties against various human tumor cell lines acting primarily by impairing the integrity of the outer cell membrane[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 118231-04-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1632. | |
| Tachyplesin I | Tachyplesin I, an antimicrobial peptide originally found in the extract of hemocytes from the Japanese horseshoe crab, has antiviral activity against vesicular stomatitis virus, influenza A virus and HIV-1. It belongs to arthropodous peptide antibiotics, and can inhibit the growth of Gram-negative bacteria and positive bacteria, and form a complex with bacterial lipopolysaccharides. Synonyms: H-Lys-Trp-Cys-Phe-Arg-Val-Cys-Tyr-Arg-Gly-Ile-Cys-Tyr-Arg-Arg-Cys-Arg-NH2 (Disulfide bridge: Cys3-Cys16, Cys7-Cys12); L-lysyl-L-tryptophyl-L-cysteinyl-L-phenylalanyl-L-arginyl-L-valyl-L-cysteinyl-L-tyrosyl-L-arginyl-glycyl-L-isoleucyl-L-cysteinyl-L-tyrosyl-L-arginyl-L-arginyl-L-cysteinyl-L-argininamide (3->16),(7->12)-bis(disulfide); Lipopolysaccharide-binding peptide; Tachyplesin I (Tachypleus tridentatus); Tachyplesin. Grade: 95%. CAS No. 118231-04-2. Molecular formula: C99H151N35O19S4. Mole weight: 2263.74. | |
| Tachystatin A | Tachystatin A is an antibacterial peptide isolated from Tachypleus tridentatus. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. | |
| Tachystatin-A1 | Tachystatin-A1 is an antibacterial peptide isolated from Tachypleus tridentatus. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Tyr-Ser-Arg-Cys-Gln-Leu-Gln-Gly-Phe-Asn-Cys-Val-Val-Arg-Ser-Tyr-Gly-Leu-Pro-Thr-Ile-Pro-Cys-Cys-Arg-Gly-Leu-Thr-Cys-Arg-Ser-Tyr-Phe-Pro-Gly-Ser-Thr-Tyr-Gly-Arg-Cys-Gln-Arg-Phe. | |
| Tachystatin C | Tachystatin C is an antibacterial peptide isolated from Tachypleus tridentatus. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Asp-Tyr-Asp-Trp-Ser-Leu-Arg-Gly-Pro-Pro-Lys-Cys-Ala-Thr-Tyr-Gly-Gln-Lys-Cys-Arg-Thr-Trp-Ser-Pro-Arg-Asn-Cys-Cys-Trp-Asn-Leu-Arg-Cys-Lys-Ala-Phe-Arg-Cys-Arg-Pro-Arg. | |
| Tachystatin-C | Tachystatin-C is an antibacterial peptide isolated from Tachypleus tridentatus. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Tachystatin C also showed sequence similarity to several insecticidal neurotoxins of spider venoms. Synonyms: Asp-Tyr-Asp-Trp-Ser-Leu-Arg-Gly-Pro-Pro-Lys-Cys-Ala-Thr-Tyr-Gly-Gln-Lys-Cys-Arg-Thr-Trp-Ser-Pro-Pro-Asn-Cys-Cys-Trp-Asn-Leu-Arg-Cys-Lys-Ala-Phe-Arg-Cys-Arg-Pro-Arg. | |
| Tachysterol | Bioactive, synthetic vitamin D3 analog; exhibits anti-proliferative effect on keratinocytes. Anti-psoriatic. Group: Biochemicals. Alternative Names: (1S)-3-[(1E)-2-[(1R,3aR,7aR)-2,3,3a,6,7,7a-Hexahydro-7a-methyl-1-[(1R,2E,4R)-1,4,5-trimethyl-2-hexen-1-yl]-1H-inden-4-yl]ethenyl]-4-methyl-3-cyclohexen-1-ol; (3 β,6E,22E)-9,10-Secoergosta-5(10),6,8,22-tetraen-3-ol; Provitamin D; Tachysterin2; Tachysterol2. Grades: Highly Purified. CAS No. 115-61-7. Pack Sizes: 1mg. Molecular Formula: C??H??O, Molecular Weight: 396.65. US Biological Life Sciences. | Worldwide |
| Tachysterol 3 | Tachysterol3 (Cholecalciferol EP Impurity E) is a bioactive, synthetic vitamin D3 analog. Group: Biochemicals. Alternative Names: (1S)-3-[(1E)-2-[(1R,3aR,7aR)-1-[(1R)-1,5-Dimethylhexyl]-2,3,3a,6,7,7a-hexahydro-7a-methyl-1H-inden-4-yl]ethenyl]-4-methyl-3-cyclohexen-1-ol; (3 β,6E)-9,10-Secocholesta-5(10),6,8-trien-3-ol; Cholecalciferol EP Impurity E. Grades: Highly Purified. CAS No. 17592-07-3. Pack Sizes: 1mg, 5mg. Molecular Formula: C27H44O, Molecular Weight: 384.64. US Biological Life Sciences. | Worldwide |
| Tachysterol 3 | Tachysterol 3 is a photoproduct of Previtamin D3 (HY-130705). Previtamin D3 is an orally active, thermolabile steroidal compound that generates vitamin D3, as well as biologically inactive lumisterol and tachysterol. Previtamin D3 is synthesized in the skin of humans and rats via the UV-B-mediated photoconversion of 7-dehydrocholesterol. Previtamin D3 lacks direct anti-rachitic activity, and its in vivo activity relies on the vitamin D3 it produces. Previtamin D3 can be used in studies related to rickets and vitamin D metabolism[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 17592-07-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-130705A. | |
| Tacrine | Tacrine is an effective oral acetylcholine (AChE) inhibitor (IC50 = 109 nM) and also acts as an active substrate for CYP1A2. Tacrine can restore cognitive dysfunction in elderly rats. Tacrine can cause liver toxicity and is used in research related to Alzheimer's disease[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 321-64-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-111338. | |
| Tacrine hydrochloride | Tacrine hydrochloride. CAS No. 1684-40-8. Purity: >99 %. Product ID: ACM1684408. Molecular formula: C13H15ClN2. Mole weight: 234.72. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Tacrine hydrochloride | Tacrine hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 1684-40-8. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tacrolimus | Tacrolimus (also FK-506 or Fujimycin) is an immunosuppressive drug whose main use is after organ transplant to reduce the activity of the patient's immune system and so the risk of organ rejection. It is also used in a topical preparation in the treatment of severe atopic dermatitis, severe refractory uveitis after bone marrow transplants, and the skin condition vitiligo. Category: Other apis. Synonyms: Fujimycin. Prograf. Tsukubaenolide. CAS No. 104987-11-3. Product ID: API104987113. Molecular formula: C44H69NO12. Mole weight: 804. EINECS: 627-021-3. SMILES: CC1CC(C2C(CC(C(O2)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C(CC(=O)C(C=C(C1)C)CC=C)O)C)C(=CC4CCC(C(C4)OC)O)C)O)C)OC)OC. Appearance: White to Off-white Solid. |  |
| Tacrolimus | FK-506 is a 23-membered macrolide lactone, it reduces peptidyl-prolyl isomerase activity by binding to the immunophilin FKBP12 (FK506 binding protein) creating a new complex. Uses: Drug. Synonyms: Prograf; Fujimycin; FK506; Protopy. Grade: >98%. CAS No. 104987-11-3. Molecular formula: C44H69NO12. Mole weight: 804.02. | |
| Tacrolimus | Tacrolimus (FK506), a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties[1]. Uses: Scientific research. Category: Induced disease models products. Alternative Names: FK506; Fujimycin; FR900506. CAS No. 104987-11-3. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-13756. | |
| Tacrolimus-[13C,d2] | Tacrolimus-[13C,d2] is the labelled analogue of Tacrolimus, which is a kind of immunosuppressant and could restrain the activity of FK-506 binding protein. Synonyms: Advagraf-13C,D2; Fujimycin-13C,D2; FK-506-13C,D2; Prograf-13C,D2; Protopic-13C,D2; TacroBell-13C,D2; Tacrolimus-13C,D2; Tsukubaenolide-13C,D2. Grade: ≥85%. CAS No. 1356841-89-8. Molecular formula: C43[13C]H67D2NO12. Mole weight: 807.02. | |
| Tacrolimus-13C,d2 | Tacrolimus-13C,d2 is a 13C-labeled and deuterium labeled Tacrolimus. Tacrolimus (FK506), a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: FK506-13C,d2; Fujimycin-13C,d2; FR900506-13C,d2. CAS No. 1356841-89-8. Pack Sizes: 1 mg. Product ID: HY-13756S. | |
| Tacrolimus Diene | Tacrolimus Diene. Uses: For analytical and research use. Alternative Names: Tacrolimus EP Impurity I; (3S,4R,5E,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-19-hydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(prop-2-en-1-yl)-3,4,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone. CAS No. 104987-16-8. Molecular formula: C44H67NO11. Mole weight: 786.00. Catalog: APB104987168. | |
| Tacrolimus EP Impurity A | Tacrolimus EP Impurity A. Uses: For analytical and research use. Alternative Names: (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-8-Ethyl-5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-5,19-dihydroxy-3-[(1E)-2-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-15,19-epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(4H,23H)-tetrone. CAS No. 104987-12-4. Molecular formula: C43H69NO12. Mole weight: 792.01. Catalog: APB104987124. | |
| Tacrolimus EP Impurity A | Ascomycin, isolated from Streptomyces, suppresses immune response in vitro with IC50 of 0.55 nM for mouse mixed lymphocyte. Uses: Anti-bacterial agents. Synonyms: (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-8-ethyl-5,19-dihydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-3,4,5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-octadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone; FK-520; FR900520; FR-900520; FR 900520; L 683590; L-683590; L683590; Changchuanmycin; Immunomycin; Ascomycin; Tacrolimus Related Compound A USP; 15,19-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(4H,23H)-tetrone, 8-ethyl-5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-5,19-dihydroxy-3-[2-(4-hydroxy-3-methoxycyclohexyl)-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-, [3S-[3R*[E(1S*,3S*,4S*)],4S*,5R*,8S*,9E,12R*,14R*,15S*,16R*,18S*,19S*,26aR*]]-. Grade: ≥90% by HPLC. CAS No. 104987-12-4. Molecular formula: C43H69NO12. Mole weight: 792.00. | |
| Tacrolimus EP Impurity B | Tacrolimus EP Impurity B. Uses: For analytical and research use. Molecular formula: C43H69NO12. Mole weight: 792.01. Catalog: APB01983. | |
| Tacrolimus EP Impurity C | Tacrolimus EP Impurity C. Uses: For analytical and research use. Molecular formula: C43H67NO12. Mole weight: 789.99. Catalog: APB01982. | |
| Tacrolimus EP Impurity C | Tacrolimus EP Impurity C is an impurity of Tacrolimus, which is a calcineurin inhibitor used as an immunosuppressant after organ transplantation to reduce the activity of the patient's immune system, thereby reducing the risk of organ rejection. Synonyms: (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-5,19-dihydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,12,18-trimethyl-8-(prop-2-en-1-yl)-3,4,5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-octadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone; 10-Desmethyl tacrolimus; 15,19-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(4H,23H)-tetrone, 5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-5,19-dihydroxy-3-[(E)-2-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylethenyl]-14,16-dimethoxy-4,12,18-trimethyl-8-(2-propen-1-yl)-, (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-; Tacrolimus monohydrate EP impurity C; (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-8-Allyl-5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-5,19-dihydroxy-3-[(E)-2-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylvinyl]-14,16-dimethoxy-4,12,18-trimethyl-15,19-epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21-(4H,23H)-tetrone; Desmethyl tacrolimus. Grade: ≥95%. Molecular formula: C43H67NO12. Mole weight: 789.99. | |
| Tacrolimus EP Impurity D | Tacrolimus EP Impurity D is an impurity of Tacrolimus, which is a calcineurin inhibitor used as an immunosuppressant after organ transplantation to reduce the activity of the patient's immune system, thereby reducing the risk of organ rejection. Synonyms: (3S,4R,5S,8S,9E,12S,14S,15R,16S,18R,19R,26aS)-5,19-dihydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(prop-2-en-1-yl)-3,4,5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-octadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone; 8-epi Tacrolimus; 8-Epitacrolimus; Tacrolimus anhydrous 8-epimer; Tacrol. Grade: ≥90% by HPLC. CAS No. 129212-35-7. Molecular formula: C44H69NO12. Mole weight: 804.04. | |
| Tacrolimus EP Impurity D | Tacrolimus EP Impurity D. Uses: For analytical and research use. Alternative Names: 8-epi Tacrolimus; (3S,4R,5S,8S,12S,14S,15R,16S,18R,19R,26aS,E)-8-allyl-5,19-dihydroxy-3-((E)-1-((1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl)prop-1-en-2-yl)-14,16-dimethoxy-4,10,12,18-tetramethyl-5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-3H-15,19-epoxypyrido[2,1-c][1]oxa[4]azacyclotricosine-1,7,20,21(4H,23H)-tetraone. CAS No. 129212-35-7. Molecular formula: C44H69NO12. Mole weight: 804.02. Catalog: APB129212357. | |
| Tacrolimus EP Impurity E | Tacrolimus EP Impurity E is an impurity of Tacrolimus, which is a calcineurin inhibitor used as an immunosuppressant after organ transplantation to reduce the activity of the patient's immune system, thereby reducing the risk of organ rejection. Synonyms: (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-5,19-dihydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-propyl-3,4,5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-octadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone; Dihydro Tacrolimus; Dihydro-FK 506; 15,19-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotr. Grade: ≥90% by HPLC. CAS No. 104987-30-6. Molecular formula: C44H71NO12. Mole weight: 806.06. | |
| Tacrolimus EP Impurity E | Tacrolimus EP Impurity E. Uses: For analytical and research use. Alternative Names: (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-5,19-dihydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-propyl-3,4,5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-octadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone. CAS No. 104987-30-6. Molecular formula: C44H71NO12. Mole weight: 806.03. Catalog: APB104987306. | |
| Tacrolimus EP Impurity F | Tacrolimus EP Impurity F. Uses: For analytical and research use. Alternative Names: (3S,4R,5S,8R,12S,14S,15R,16S,18R,26aS,E)-8-allyl-5,15-dihydroxy-3-((E)-1-((1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl)prop-1-en-2-yl)-14,16-dimethoxy-4,10,12,18-tetramethyl-3,4,5,6,11,12,13,14,15,16,17,18,24,25,26,26a-hexadecahydro-1H-pyrido[2,1-c][1,4]oxaaz. CAS No. 1393890-33-9. Molecular formula: C44H69NO12. Mole weight: 804.02. Catalog: APB1393890339. | |
| Tacrolimus EP Impurity G | Tacrolimus EP Impurity G is an impurity of Tacrolimus, which is a calcineurin inhibitor used as an immunosuppressant after organ transplantation to reduce the activity of the patient's immune system, thereby reducing the risk of organ rejection. Synonyms: (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19S,26aS)-5,19-dihydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(prop-2-en-1-yl)-3,4,5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-octadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone; Tacrolimus compound II; Tacrolimus anhydrous 19-epimer; 19-Epi FK-506; 1. Grade: ≥90% by HPLC. CAS No. 144490-63-1. Molecular formula: C44H69NO12. Mole weight: 804.04. | |
| Tacrolimus EP Impurity G | Tacrolimus EP Impurity G. Uses: For analytical and research use. Alternative Names: Tacrolimus 19-epimer. CAS No. 144490-63-1. Molecular formula: C44H69NO12. Mole weight: 804.02. Catalog: APB144490631. | |
| Tacrolimus EP Impurity H | Tacrolimus EP Impurity H is an impurity of Tacrolimus, which is a calcineurin inhibitor used as an immunosuppressant after organ transplantation to reduce the activity of the patient's immune system, thereby reducing the risk of organ rejection. Synonyms: (1E,3S,4R,5S,8R,9E,12S,14S)-5-hydroxy-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-14-methoxy-14-[(2R,3S,5R)-3-methoxy-5-methyl-6-oxooxan-2-yl]-2,4,10,12-tetramethyl-7-oxo-8-(prop-2-en-1-yl)tetradeca-1,9-dien-3-yl (2S)-1-formylpiperidine-2-carboxylate; Tacrolimus monohydrate impurity H [EP]; 2-Piperidinecarboxylic acid, 1-formyl-, (1S,2R,3S,6R,7E,10S,12S)-3-hydroxy-1-[(1E)-2-[(1R,3R,4R)-4-hydroxy-. Grade: ≥95%. CAS No. 143210-33-7. Molecular formula: C43H69NO11. Mole weight: 776.01. | |
| Tacrolimus EP Impurity I | Tacrolimus EP Impurity I is an impurity of Tacrolimus, which is a calcineurin inhibitor used as an immunosuppressant after organ transplantation to reduce the activity of the patient's immune system, thereby reducing the risk of organ rejection. Synonyms: (3S,4R,5E,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-19-hydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(prop-2-en-1-yl)-3,4,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone; Tacrolimus diene; 23,24-Anhydro Tacrolimus; Δ23-FK-506; Tacrolimus Impurity I; Tacrolimus monohydrate impurity I [EP]; 15,19-Epoxy(5E,9E)-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(4H,23H)-tetrone, 8,11,12,13,14,15,16,17,18,19,24,25,26,26a-tetradecahydro-19-hydroxy-3-[(1E)-2-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(2-propen-1-yl)-, (3S,4R,8R,12S,14S,15R,16S,18R,19R,26aS)-; 15,19-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(4H,23H)-tetrone, 8,11,12,13,14,15,16,17,18,19,24,25,26,26a-tetradecahydro-19-hydroxy-3-[2-(4-hydroxy-3-methoxycyclohexyl)-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(2-propenyl)-, [3S-[3R*[E(1S*,3S*,4S*)],4S*,5E,8S*,9E,12R*,14R*,15S*,16R*,18S*,19S*,26aR*]]-. Grade: 95%. CAS No. 104987-16-8. Molecular formula: C44H67NO11. Mole w | |
| Tacrolimus hydrolyzed open-loop Impurity | Tacrolimus hydrolyzed open-loop Impurity. Uses: For analytical and research use. Molecular formula: C44H71NO13. Mole weight: 822.05. Catalog: APB09871. | |
| Tacrolimus Impurity 1 | Tacrolimus Impurity 1. Uses: For analytical and research use. Molecular formula: C43H69NO11. Mole weight: 776.02. Catalog: APB09872. | |
| Tacrolimus Impurity 10 | Tacrolimus Impurity 10. Uses: For analytical and research use. Molecular formula: C43H69NO11. Mole weight: 776.02. Catalog: APB09876. | |
| Tacrolimus Impurity 12 | Tacrolimus Impurity 12. Uses: For analytical and research use. Molecular formula: C44H69NO12. Mole weight: 804.03. Catalog: APB09875. | |
| Tacrolimus Impurity 13 | Tacrolimus Impurity 13. Uses: For analytical and research use. CAS No. 1026775-21-2. Molecular formula: C44H69NO12. Mole weight: 804.03. Catalog: APB1026775212. | |
| Tacrolimus Impurity 14 | Tacrolimus Impurity 14. Uses: For analytical and research use. CAS No. 1260758-24-4. Molecular formula: C10H15NO4S. Mole weight: 245.29. Catalog: APB1260758244. | |
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