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| Product | Description | |
|---|---|---|
| D-Aspartic acid dimethyl ester hydrochloride | D-Aspartic acid dimethyl ester hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 69630-50-8. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. |  Worldwide |
| D-Aspartic acid dimethyl ester hydrochloride 99+% (HPLC) | D-Aspartic acid dimethyl ester hydrochloride 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| D-Aspartic acid,N-[(1S)-1,2-dicarboxyethyl]-, rel- | D-Aspartic acid,N-[(1S)-1,2-dicarboxyethyl]-, rel-. Alternative Names: 2-(1,2-dicarboxyethylamino)butanedioicacid; Iminodisuccinicacid; 131669-35-7; D-Asparticacid,N-[(1S)-1,2-dicarboxyethyl]-,rel-; iminodisuccinicacid; imidodisuccinicacid. Grades: 95%. CAS No. 131669-35-7. Molecular formula: C8H11NO8. Mole weight: 249.17484. |  |
| D-Aspartic acid sodium salt | D-Aspartic acid sodium salt. Group: Biochemicals. Alternative Names: Sodium D-aspartate. Grades: Highly Purified. CAS No. 10329-81-4. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. Molecular Formula: C4H6NO4·Na. US Biological Life Sciences. | Worldwide |
| DATEM-E472e | Diacetyl tartaric acid esters of mono- and diglycerides of fatty acids, or simply DATEM, is an emulsifier used in breadmaking to strengthen the dough structure so that it can successfully expand during proofing and baking. Synonyms: DATEM---E472e;Diacetyl tartaric acid monodiglyceride;Acetylated single (double) glycerol fatty acid ester. CAS No. 977051-29-8. Product ID: CDF4-0258. Category: It is used in bread, buns and many other yeast-leavened bakery products at levels of 0.2-0.6% (based on flour weight). DATEM possesses excellent dough strengthening properties due to its ability to adsorb at the gas/liquid interface of dough and stabilize the foam structure trapped by the gluten matrix and prevent gas bubble coalescence.1,2 So, DATEM enhances gas (CO3) retention and improves tolerance to shocks in case of mechanical abuse during final proofing and baking. Due to its anionic nature, DATEM also has the capacity to interact with gluten proteins, promoting protein aggregation. Product Keywords: Food Emulsifiers; CDF4-0258; DATEM-E472e; 977051-29-8; DATEM---E472e;Diacetyl tartaric acid monodiglyceride;Acetylated single (double) glycerol fatty acid ester. Chemical Name: Diacety Tartaric Acid Esters of Mono & Diglycerides. Grade: Food grade. Stability and Storage Conditions: Prevent from moisture and caking. Sealed and stored in the low temperature, dry, cool and well-ventilated place. Forbid storing and transporting with |  |
| Date Palm Fruit (Phoenix Dactylifera) Powder | Date Palm Fruit (Phoenix Dactylifera) Powder. |  CA, FL & NJ |
| Date Palm Pollen P.E. 4:1 | Date Palm Pollen P.E. 4:1. | CA, FL & NJ |
| Date Palm Seed P.E. 4:1 | Date Palm Seed P.E. 4:1. | CA, FL & NJ |
| dA-Thiophosphoramidite | dA-Thiophosphoramidite, a widely utilized chemical compound in the biomedical sector, is an imperative tool employed to fabricate chemically modified oligonucleotides and investigate the complexities of nucleic acids structure and biology. Furthermore, it holds significant value in designing therapeutic medications that selectively target genes responsible for the onset of malignant neoplasms and viral infections. Alternative Names: 5'-Dimethoxytrityl-N-benzoyl-2'-deoxyAdenosine, 3'-[(ß-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C51H51N6O7PS2. Mole weight: 955.09. | |
| Datilat | Datilat. CAS No. 68039-69-0. VIGON Item # 502493. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Datiscetin | Datiscetin (compound 5) is a natural compound isolated from the cultivar Roland, and shows fungitoxic activity towards F. oxysporum f. sp. dianthi.[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 480-15-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N8722. |  |
| Datopotamab | Datopotamab (CDP7657) is a humanized anti trophoblast cell surface antigen 2 (TROP2) antibody. Datopotamab can generate antibody drug conjugates (ADC) (HY-141598) with DNA topoisomerase I inhibitor Deruxtecan (HY-13631E). Datopotamab can be used in the study of triple negative breast cancer and non-small cell lung cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2267989-53-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P99843. | |
| Datopotamab deruxtecan | Datopotamab deruxtecan is an antibody-drug conjugate consisting of a humanized anti-TROP2 IgG1 monoclonal antibody conjugated to a potent topoisomerase I inhibitor payload via a stable tetrapeptide-based cleavable linker. Alternative Names: DS-1062; DS-1062A; Dato-DXd. CAS No. 2238831-60-0. | |
| Datopotamab deruxtecan | Datopotamab deruxtecan (DS-1062, DS-1062A, Anti-TRP2/dxd) is an antibody-drug conjugate (ADC) composed of a humanized anti-TROP2 monoclonal antibody, conjugated to topoisomerase I inhibitor, via a tetrapeptide-based linker. Datopotamab deruxtecan has the potential for use in solid tumors mainly in advanced unresectable advanced NSCLC. Alternative Names: DS-1062, DS-1062A, Anti-TRP2/dxd. CAS No. 2238831-60-0. Pack Sizes: 1mg. Product ID: D4050. Formula: 4.2. Storage Conditions: Store the undiluted solution at -20°C in the dark to avoid freeze-thaw cycles. |  United States; Europe |
| Datopotamab deruxtecan (solution) | Datopotamab deruxtecan (DS-1062) solution is a TROP2-targeted antibody-drug conjugate (ADC) with human TROP2 Kd of 0.74 nmol/L. Datopotamab deruxtecan solution consists of the antibody Datopotamab (HY-P99843) and the toxic molecule-linker conjugate Deruxtecan (HY-13631E). Datopotamab deruxtecan solution binds TROP2, triggers internalization and lysosomal trafficking and releases DXd topoisomerase I inhibitor payload. Datopotamab deruxtecan solution disrupts DNA function, induces DNA damage, apoptosis, and bystander killing of tumor microenvironment cells. Datopotamab deruxtecan solution can be used in research related to triple-negative breast cancer, gastric cancer, and non-small cell lung cancer[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: DS-1062 (solution); Dato-DXd (solution). CAS No. 2238831-60-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-141598. | |
| dATP | dATP is a purine nucleoside triphosphate used in the synthesis of DNA by being incorporated into DNA. Alternative Names: 2'-Deoxyadenosine-5'-Triphosphate. Grades: ≥ 95% by HPLC. CAS No. 1927-31-7. Molecular formula: C10H16N5O12P3. Mole weight: 491.18. | |
| dATPαS | dATPαS is a modified nucleotide analog that is widely used as a substrate for various DNA polymerases. It is commonly used in DNA labeling experiments due to its incorporation into target DNA by polymerases during DNA synthesis. It has also been used to generate non-cleavable modified DNA for studying DNA repair mechanisms. Alternative Names: 2'-Deoxyadenosine-5'-(α-thio)-triphosphate, Sodium salt (1 : 1 Mixture of Rp and Sp isomers). Grades: ≥ 95% by HPLC. CAS No. 64145-28-4. Molecular formula: C10H16N5O11P3S (free acid). Mole weight: 507.24 (free acid). | |
| dATP(dGTP)-DNA purinetransferase | The purine residue is transferred on to the apurinic site forming a normal glycosylic bond. dATP reacts at sites of the double-stranded depurinated DNA that lack adenine, and dGTP at sites that lack guanine. Group: Enzymes. Enzyme Commission Number: EC 2.6.99.1. 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-2942; dATP(dGTP)-DNA purinetransferase; EC 2.6.99.1. Cat No: EXWM-2942. |  |
| dATP solution - Lithium Salt | The lithium salt solution form of dATP. dATP is a purine nucleoside triphosphate used in the synthesis of DNA by being incorporated into DNA. Grades: ≥ 99% by HPLC. Molecular formula: C10H16N5O12P3 (free acid). Mole weight: 491.18 (free acid). | |
| dATP solution - Sodium Salt | The sodium salt solution form of dATP. dATP is a purine nucleoside triphosphate used in the synthesis of DNA by being incorporated into DNA. Grades: ≥ 99% by HPLC. Molecular formula: C10H16N5O12P3 (free acid). Mole weight: 491.18 (free acid). | |
| Datucin | Datucin is an antibacterial peptide isolated from Datura stramonium. It has activity against fungi. Alternative Names: Thr-Phe-Pro-Lys-Cys-Ala-Pro-Thr-Arg-Pro-Pro-Gly-Pro-Lys-Pro-Cys-Asp-Ile-Asn-Asn-Phe-Lys-Ser-Lys-Phe-Trp-His-Ile-Trp-Arg-Ala. Grades: 96.7%. | |
| Daturabietatriene | Daturabietatriene is isolated from the heartwoods of Pinus yunnanensis. Alternative Names: Abieta-8,11,13-triene-15,18-diol. Grades: 96.5%. CAS No. 65894-41-9. Molecular formula: C20H30O2. Mole weight: 302.5. | |
| DAU 5884 hydrochloride | DAU 5884 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 131780-48-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Daucosterol | Daucosterol is an orally active natural sterol compound, which has anti-inflammatory, anticancer and immunomodulatory activities. Daucosterol inhibits cancer cell proliferation by inducing autophagy through ROS-dependent manner. Daucosterol also inhibits colon cancer growth by inducing apoptosis, inhibiting cell migration and invasion and targeting caspase signalling pathway[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Eleutheroside A; β-Sitosterol β-D-glucoside. CAS No. 474-58-8. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-N0410. | |
| DAUDA | DAUDA (11-(dansylamino) undecanoic acid) is an environment-sensitive fluorescent fatty acid analogue. DAUDA alters its intensities and fluorescent emission spectra on entry into binding proteins. DAUDA is used to determine the relative affinity of natural fatty acids for polymorphs of the Schistosoma mansoni Sm14 fatty acid-binding protein[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 73025-02-2. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg. Product ID: HY-120959. | |
| Daun02 | Daun02 is a proagent of the topoisomerase inhibitor Daunorubicin. Uses: Scientific research. Category: Signaling pathways. CAS No. 290304-24-4. Pack Sizes: 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13061. | |
| Daunchinain-B1 antimicrobial peptide precursor | Daunchinain-B1 antimicrobial peptide precursor is an antibacterial peptide isolated from Babina daunchina. Alternative Names: Thr-Ser-Lys-Lys-Pro-Leu-Leu-Leu-Leu-Phe-Phe-Leu-Gly-Thr-Ile-Asn-Leu-Ser-Leu-Cys-Glu-Gln-Glu-Arg-Asn-Ala-Glu-Glu-Glu-Thr-Gly-Asp-Tyr-Pro-Asp-Gln-Arg-Asp-Val-Glu-Val-Glu-Lys-Arg. | |
| Daunchinain-D1 antimicrobial peptide precursor | Daunchinain-D1 antimicrobial peptide precursor is an antibacterial peptide isolated from Babina daunchina. Alternative Names: Thr-Met-Lys-Lys-Ser-Leu-Leu-Leu-Leu-Phe-Phe-Leu-Gly-Thr-Ile-Asn-Leu-Ser-Leu-Cys-Glu-Gln-Glu-Gly-Asn-Ala-Glu-Glu-Glu-Thr-Gly-Asp-Asn-Pro-Asp-Gln-Arg-Glu-Asp-Glu-Val-Glu-Lys-Arg. | |
| daunomycin-arachidonic acid complex | daunomycin-arachidonic acid complex. CAS No. 86589-37-9. Product ID: ACM86589379. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Daunomycinone | Daunomycinone is the aglycone core structure of the anthracycline antibiotics daunorubicin and doxorubicin, lacking their sugar moiety. As a key pharmacophore, it contributes to the DNA-intercalating and topoisomerase II inhibition properties of these drugs, enabling anticancer activity. While less potent than the glycosylated forms, daunomycinone retains cytotoxic effects by generating reactive oxygen species (ROS) and disrupting DNA replication. Alternative Names: Daunorubicin Impurity A; (8S,10S)-8-Acetyl-6,8,10,11-tetrahydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione; Daunorubicin EP Impurity A; (+)-Daunomycinone; NSC 109531; (8S,10S)-8-Acetyl-7,8,9,10-tetrahydro-6,8,10,11-tetrahydroxy-1-methoxy-5,12-naphthacenedione; Daunomycin Aglicone; Daunomycinon; Daunorubicin Aglycone; Leukaemomycinone C; Daunorubicinone; 5,12-Naphthacenedione, 8-acetyl-7,8,9,10-tetrahydro-6,8,10,11-tetrahydroxy-1-methoxy-, (8S,10S)-; Epirubicin EP Impurity B. Grades: ≥95%. CAS No. 21794-55-8. Molecular formula: C21H18O8. Mole weight: 398.37. | |
| Daunomycinone | Daunomycinone. Group: Biochemicals. Alternative Names: (8S,10S)-8-Acetyl-7,8,9,10-tetrahydro-6,8,10,11-tetrahydroxy-1-methoxy- -5,12-naphthacenedione; (+)-Daunomycinone; Daunomycin aglicone; Daunorubicinone. Grades: Highly Purified. CAS No. 21794-55-8. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C21H18O8. US Biological Life Sciences. | Worldwide |
| Daunomycinone | Daunomycinone (NSC-109351) is a metabolite of Daunomycin (HY-13062A) and anticancer intermediate. Daunomycinone binds to nucleic acids synergistically with metal ions. Daunomycinone can be used in the research of leukemia[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NSC-109351. CAS No. 21794-55-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114658. | |
| Daunomycinone-d3 | The main metabolite of labeled Daunorubicin (DNR). Group: Biochemicals. Alternative Names: (8S,10S)-8-Acetyl-7,8,9,10-tetrahydro-6,8,10,11-tetrahydroxy-1-methoxy- -5,12-naphthacenedione-d3; (+)-Daunomycinone-d3; Daunomycin Aglicone-d3; Daunomycinon-d3; Daunorubicin Aglycone-d3; Daunorubicinone-d3; Leukaemomycinone C-d3; NSC 109351-d3. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Daunorubicin | Daunomycin is an anthracycline antibiotic produced by Streptomyces peucetius. The mechanism of action is the same as that of doxorubicin, which is inserted into DNA and inhibits RNA and DNA synthesis. It is mainly used for the treatment of acute myeloid and lymphocytic leukemia, with adverse reactions such as cardiotoxicity and bone marrow suppression. It has anti-gram-positive bacteria, negative bacteria and tumor activity. Uses: Adcs cytotoxin. Alternative Names: Doxorubicin EP Impurity A; (8S,10S)-8-Acetyl-10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione; Daunomycin; Acetyladriamycin; Leukaemomycin C; Cerubidine; Rubidomycin; (1S,3S)-3-Acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-tetracenyl-3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranoside; NSC 82151; (8S-cis)-8-Acetyl-10-((3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyrannosyl)oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-napthacenedione; Epirubicin EP Impurity D; Rubomycin C. Grades: 95%. CAS No. 20830-81-3. Molecular formula: C27H29NO10. Mole weight: 527.52. | |
| Daunorubicin | Daunorubicin (Daunomycin) is a topoisomerase II inhibitor with potent anti-tumor activity. Daunorubicin inhibits DNA and RNA synthesis. Daunorubicin is a cytotoxin that inhibits cancer cell viability and induces apoptosis and necrosis. Daunorubicin is also an anthracycline antibiotic. Daunorubicin can be used in the research of infection and variety of cancers, including leukemia, non-Hodgkin lymphomas, Ewing's sarcoma, Wilms' tumor[1][2][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Daunomycin; RP 13057; Rubidomycin. CAS No. 20830-81-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13062A. | |
| Daunorubicin-13C,d3 | Daunorubicin-13C,d3. Group: Biochemicals. Alternative Names: (8S-cis)-8-Acetyl-10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-naphthacenedione-13C,d3. Grades: Purified. CAS No. 20830-81-3 unlabeled. Pack Sizes: 250ug. Molecular Formula: C2613CH26D3NO10, Molecular Weight: 531.53. US Biological Life Sciences. | Worldwide |
| Daunorubicin Citrate | Daunorubicin Citrate is the citrate salt of daunorubicin, a naturally occurring anthracycline antibiotic isolated from Streptomyces peucetius. It possesses antineoplastic properties and is structurally characterized by a tetracyclic aglycone (daunomycinone) glycosidically linked to the aminosugar daunosamine. Applications: Indicated for the treatment of acute myeloid leukemia (aml), acute lymphoblastic leukemia (all), and other hematologic malignancies. daunorubicin citrate is an anthracycline antibiotic that intercalates dna and inhibits topoisomerase ii, triggering apoptotic cell death in rapidly dividing cells. it is also used in hiv-related kaposi sarcoma therapy. Category: Active pharmaceutical ingredients. Synonyms: Daunorubicin citrate liposome. CAS No. 371770-68-2. Product ID: API371770682. Molecular formula: C33H37NO17. Mole weight: 719.6. InChIKey: VNTHYLVDGVBPOU-QQYBVWGSSA-N. |  |
| Daunorubicin EP Impurity B (Mixture of Diastereomers) | Daunorubicin EP Impurity B (Mixture of Diastereomers). Uses: For analytical and research use. Alternative Names: 28008-55-1 ((S)-Isomer); 28008-53-9 ((S)-Isomer, HCl salt); (8S,10S)-10-(((2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-6,8,11-trihydroxy-8-(1-hydroxyethyl)-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione. Molecular formula: C27H31NO10. Mole weight: 529.54. Catalog: APB02226. |  |
| Daunorubicin EP Impurity E (Mixture of Diastereomers) | Daunorubicin EP Impurity E (Mixture of Diastereomers). Uses: For analytical and research use. Alternative Names: (8S,10S)-6,8,10,11-tetrahydroxy-8-((R)-1-hydroxyethyl)-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione. Molecular formula: C21H20O8. Mole weight: 400.38. Catalog: APB05535. | |
| Daunorubicin EP Impurity F | Daunorubicin EP Impurity F. Uses: For analytical and research use. Category: Impurity standards. Alternative Names: (8S,10S)-10-(((2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-6,8,11-trihydroxy-1-methoxy-8-propionyl-7,8,9,10-tetrahydrotetracene-5,12-dione. CAS No. 771423-67-7. Molecular formula: C28H31NO10. Mole weight: 541.55. Catalog: APB771423677. | |
| Daunorubicin hydrochloride | 10mg Pack Size. Group: Antibiotics, Research Organics & Inorganics. Formula: C27H29NO10 · HCl. CAS No. 23541-50-6. Prepack ID 11269897-10mg. Molecular Weight 563.98. See USA prepack pricing. |  |
| Daunorubicin hydrochloride | 25mg Pack Size. Group: Antibiotics, Research Organics & Inorganics. Formula: C27H29NO10 · HCl. CAS No. 23541-50-6. Prepack ID 11269897-25mg. Molecular Weight 563.98. See USA prepack pricing. | |
| Daunorubicin hydrochloride | Daunorubicin HCl inhibits both DNA and RNA synthesis and inhibits DNA synthesis with Ki of 0.02 μM. Uses: Adcs cytotoxin. Alternative Names: RP 13057 Hydrochloride; Daunomycin; RP13057 Hydrochloride; RP-13057 Hydrochloride; Rubidomycin hydrochloride. Grades: >98%. CAS No. 23541-50-6. Molecular formula: C27H30ClNO10. Mole weight: 563.98. | |
| Daunorubicin hydrochloride | Daunorubicin (Daunomycin) hydrochloride is a topoisomerase II inhibitor with potent anti-tumor activity. Daunorubicin hydrochloride inhibits DNA and RNA synthesis. Daunorubicin hydrochloride is a cytotoxin that inhibits cancer cell viability and induces apoptosis and necrosis. Daunorubicin hydrochloride is also an anthracycline antibiotic. Daunorubicin hydrochloride can be used in the research of infection and variety of cancers, including leukemia, non-Hodgkin lymphomas, Ewing's sarcoma, Wilms' tumor[1][2][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Daunomycin hydrochloride; RP 13057 hydrochloride; Rubidomycin hydrochloride. CAS No. 23541-50-6. 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-13062. | |
| Daunorubicin Hydrochloride (Daunomycin) | Daunorubicin HCl inhibits both DNA and RNA synthesis and inhibits DNA synthesis with Ki of 0.02 μM in a cell-free assay. Daunorubicin is a topoisomerase II inhibitor that induces apoptosis.Daunorubicin (RP 13057) HCl can be used to induce animal models of Kidney Disease. Group: Inhibitors. Alternative Names: Rubidomycin HCl, RP 13057 HCl. CAS No. 23541-50-6. Pack Sizes: 10mg. Product ID: S3035. Formula: C27H29NO10. HCl. Smiles: CC1C(C(CC(O1)OC2CC(CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=O)C)O)N)O.Cl. Storage Conditions: 2 years -80 in solvent. | United States; Europe |
| Daunorubicin hydrochloride impurity 1 | Daunorubicin hydrochloride impurity 1. Uses: For analytical and research use. CAS No. 126643-96-7. Molecular formula: C27H31NO10. Mole weight: 529.54. Catalog: APB126643967. | |
| Daunorubicin hydrochloride impurity 2 | Daunorubicin hydrochloride impurity 2. Uses: For analytical and research use. CAS No. 28008-55-1. Molecular formula: C27H31NO10. Mole weight: 529.54. Catalog: APB28008551. | |
| Daunorubicin hydrochloride impurity 3 | Daunorubicin hydrochloride impurity 3. Uses: For analytical and research use. Molecular formula: C27H31NO10. Mole weight: 529.54. Catalog: APB11036. | |
| Daunorubicin hydrochloride impurity 6 | Daunorubicin hydrochloride impurity 6. Uses: For analytical and research use. CAS No. 28008-51-7. Molecular formula: C21H20O8. Mole weight: 400.38. Catalog: APB28008517. | |
| Daunorubicin hydrochloride impurity 7 | Daunorubicin hydrochloride impurity 7. Uses: For analytical and research use. CAS No. 125515-17-5. Molecular formula: C21H20O8. Mole weight: 400.38. Catalog: APB125515175. | |
| Daunorubicin hydrochloride impurity 8 | Daunorubicin hydrochloride impurity 8. Uses: For analytical and research use. CAS No. 2747975-46-6. Molecular formula: C21H20O8. Mole weight: 400.38. Catalog: APB2747975466. | |
| Daunorubicin Hydrochloride (Mixture of Diastereomers) | Daunorubicin Hydrochloride (Mixture of Diastereomers). Group: Biochemicals. Alternative Names: (8S,10S)-8-Acetyl-10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-naphthacenedione Hydrochloride; (8S-cis)-Daunomycin Hydrochloride; Cerubidine; Daunoblastin; Daunomycin Chlorohydrate; ?NDC 0082-4155; Ondena; RP 13057 Hydrochloride; Rubidomycin Hydrochloride. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Daunorubicin impurity 12 | Daunorubicin impurity 12. Uses: For analytical and research use. CAS No. 76034-18-9. Molecular formula: C26H29NO9. Mole weight: 499.52. Catalog: APB76034189. | |
| Daunorubicin impurity 13 | Daunorubicin impurity 13. Uses: For analytical and research use. CAS No. 100992-86-7. Molecular formula: C21H20O7. Mole weight: 384.38. Catalog: APB100992867. | |
| Daunorubicin Impurity 13 | Daunorubicin Impurity 13. Uses: For analytical and research use. Alternative Names: N-((2S,3S,4S,6R)-3,6-dihydroxy-2-methyltetrahydro-2H-pyran-4-yl)-2,2,2-trifluoroacetamide. CAS No. 51996-45-3. Molecular formula: C8H12F3NO4. Mole weight: 243.18. Catalog: APB51996453. | |
| Daunorubicin Impurity 14 | Daunorubicin Impurity 14. Uses: For analytical and research use. Alternative Names: (2S,4S,5S,6S)-6-methyl-4-(2,2,2-trifluoroacetamido)tetrahydro-2H-pyran-2,5-diyl bis(4-nitrobenzoate). Molecular formula: C22H18F3N3O10. Mole weight: 541.39. Catalog: APB05531. | |
| Daunorubicin Impurity 17 | Daunorubicin Impurity 17. Uses: For analytical and research use. Alternative Names: 8-acetyl-6,11-dihydroxy-1-methoxytetracene-5,12-dione. CAS No. 32434-04-1. Molecular formula: C21H14O6. Mole weight: 362.33. Catalog: APB32434041. | |
| Daunorubicin Impurity 18 | Daunorubicin Impurity 18. Uses: For analytical and research use. Alternative Names: 8-acetyl-6,10,11-trihydroxy-1-methoxytetracene-5,12-dione. CAS No. 20982-41-6. Molecular formula: C21H14O7. Mole weight: 378.33. Catalog: APB20982416. | |
| Daunorubicin Impurity 19 | Daunorubicin Impurity 19. Uses: For analytical and research use. Alternative Names: (8S,10S)-10-(((2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-8-(2-bromo-1,1-diethoxyethyl)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione. Molecular formula: C31H38BrNO11. Mole weight: 680.54. Catalog: APB05529. | |
| Daunorubicin Impurity 20 | Daunorubicin Impurity 20. Uses: For analytical and research use. Alternative Names: (8S,10S)-8-acetyl-10-(((2R,4S,5S,6S)-4-amino-5-(benzyloxy)-6-methyltetrahydro-2H-pyran-2-yl)oxy)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione. CAS No. 1010447-40-1. Molecular formula: C34H35NO10. Mole weight: 617.64. Catalog: APB1010447401. | |
| Daunorubicin Impurity 21 | Daunorubicin Impurity 21. Uses: For analytical and research use. Alternative Names: (8S,10S)-10-(((2R,4S,5S,6S)-4-amino-5-(benzyloxy)-6-methyltetrahydro-2H-pyran-2-yl)oxy)-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione. CAS No. 677017-23-1. Molecular formula: C34H35NO11. Mole weight: 633.64. Catalog: APB677017231. | |
| Daunorubicin Impurity 24 HCl | Daunorubicin Impurity 24 HCl. Uses: For analytical and research use. Alternative Names: (8S,10S)-8-acetyl-10-(((2R,4S)-4-amino-6-methyl-3,4-dihydro-2H-pyran-2-yl)oxy)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione hydrochloride. Molecular formula: C27H27NO9·HCl. Mole weight: 545.98. Catalog: APB05528. | |
| Daunorubicin impurity 6 | Daunorubicin impurity 6. Uses: For analytical and research use. Alternative Names: 56390-08-0 (HCl Salt); (8S,10S)-8-acetyl-10-(((2R,4S,5R,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione. CAS No. 57918-24-8. Molecular formula: C27H29NO10. Mole weight: 527.52. Catalog: APB57918248. | |
| Daunorubicin impurity 9 | Daunorubicin impurity 9. Uses: For analytical and research use. Molecular formula: C27H32ClNO11. Mole weight: 582. Catalog: APB11037. | |
| Daunorubicin Impurity C (Mixture of Diastereomers) | Daunorubicin Impurity C (Mixture of Diastereomers). Uses: For analytical and research use. Alternative Names: (8S,10S)-10-(((2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-6,8,11-trihydroxy-1-methoxy-8-(2-oxopropyl)-7,8,9,10-tetrahydrotetracene-5,12-dione. CAS No. 79438-97-4. Molecular formula: C28H31NO10. Mole weight: 541.55. Catalog: APB79438974. | |
| Daunorubicinol | Daunorubicinol, a metabolite of Daunorubicin, is an anthracycline antineoplastic antibiotic with therapeutic effects similar to those of doxorubicin. Alternative Names: Daunorubicin Impurity B ((1S)-isomer); 5,12-Naphthacenedione, 10-((3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-((1S)-1-hydroxyethyl)-1-methoxy-, (8S,10S)-; 13-Dihydrodaunorubicin; Duborimycin; Leukaemomycin D; (13S)-13-Dihydrodaunorubicin; (1S,3S)-3,5,12-Trihydroxy-3-[(1S)-1-hydroxyethyl]-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-tetracenyl-3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranoside; Daunomycinol; Dihydrodaunomycin; Antibiotic 20-798RP; 13-Dihydrodaunomycin. Grades: >95%. CAS No. 28008-55-1. Molecular formula: C27H31NO10. Mole weight: 529.54. | |
| Daunorubicinol hydrochloride | Daunorubicinol Hydrochloride is a metabolite of Daunorubicin, which is an anthracycline antibiotic used in the treatment of acute myeloid and lymphocytic leukemia, with adverse reactions such as cardiotoxicity and bone marrow suppression. Alternative Names: 5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(1-hydroxyethyl)-1-methoxy-, hydrochloride, [8S-[8α,8(R*),10α]]-; 13-Dihydrodaunorubicin Hydrochloride; Duborimycin Hydrochloride; Leukaemomycin D Hydrochloride; L-lyxo-Hexopyranoside, 1,2,3,4,6,11-hexahydro-3,5,12-trihydroxy-3-(1-hydroxyethyl)-10-methoxy-6,11-dioxo-1-naphthacenyl 3-amino-2,3,6-trideoxy-, hydrochloride, (1S,3S)-α-; 13-Dihydrodaunomycin hydrochloride; 5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-[(1S)-1-hydroxyethyl]-1-methoxy-, hydrochloride (1:1), (8S,10S)-; Antibiotic RP 20798; Antibiotic 20798 RP; Dihydrodaunomycin hydrochloride; NSC 180510. Grades: ≥95%. CAS No. 28008-53-9. Molecular formula: C27H32ClNO10. Mole weight: 566.00. | |
| dAurAB5 | dAurAB5 is a dual Aurora-A (DC50 = 8.8 nM) and Aurora-B (DC50 = 6.1 nM) PROTAC degrader. dAurAB5 induces degradation of Aurora-A and Aurora-B, reduces N-Myc levels, and decreases viability in IMR32 neuroblastoma cells. dAurAB5 downregulates the levels of AAK1, PTK2, GAK, and TTK. dAurAB5 can be used to study cancers such as neuroblastoma. (Pink: TTK ligand 2: HY-168542, Blue: Thalidomide-O-COOH: HY-103597, Black: 6-Aminocaproic acid: HY-B0236)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3115765-45-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-171770. | |
| Daurichromenic acid | Daurichromenic acid, isolated from the herbs of Rhododendron dauricum, is a terpenophenol with potent anti-HIV activity. Uses: Anti-hiv activity. Alternative Names: Daurichromenic acid;82003-90-5;(S,E)-2-(4,8-Dimethylnona-3,7-dien-1-yl)-5-hydroxy-2,7-dimethyl-2H-chromene-6-carboxylic acid;(+)-Daurichromenic acid; Dauichromenic acid;(+)-Daurichromenic acid;CHEMBL1171643;HY-N3692;BDBM50537945;AKOS040761576;FS-9068;(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-5-hydroxy-2,7-dimethylchromene-6-carboxylic acid;DA-72571;CS-0024072;(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-5-hydroxy-2,7-dimethyl-chromene-6-carboxylic acid;(S)-2-((E)-4,8-Dimethyl-nona-3,7-dienyl)-5-hydroxy-2,7-dimethyl-2H-1-benzopyran-6-carboxylic acid. Grades: 97%. CAS No. 82003-90-5. Molecular formula: C64H78N14O24. Mole weight: 1427.4. | |
| Dauricine | Dauricine. Group: Biochemicals. Alternative Names: 6,6?-Di-O-methyldauricoline. Grades: Plant Grade. CAS No. 524-17-4. Pack Sizes: 20mg. Molecular Formula: C38H44N2O6, Molecular Weight: 624.766. US Biological Life Sciences. | Worldwide |
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