A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| Duloxetine Related Compound H | Duloxetine Related Compound H is an impurity of Duloxetine, which is a serotonin-norepinephrine reuptake inhibitor used to treat major depressive disorder, generalized anxiety disorder, fibromyalgia, neuropathic pain and central sensitization. Alternative Names: (S)-Duloxetine Succinamide; 4-[Methyl[(3S)-3-(1-naphthalenyloxy)-3-(2-thienyl)propyl]amino]-4-oxobutanoic Acid. Grades: 98%. CAS No. 199191-66-7. Molecular formula: C22H23NO4S. Mole weight: 397.49. |  |
| Dulse Seaweed Powder (Palmaria palmata) (Whole Plant) | Dulse Seaweed Powder (Palmaria palmata) (Whole Plant). Categories: furaltadone hydrochloride; furaltadone hcl. |  CA, FL & NJ |
| Dumacil 100 FG | Dumacil 100 FG. CAS No. 67762-90-7. | |
| Dunaimycin A1 | It is produced by the strain of Streptomyces diastatochromogenes AB 1691Q-321 and AB 1711J-452. It's an immunosuppressant. Alternative Names: (4E,18E)-3',4',5',6'-Tetrahydro-7,9,11-trihydroxy-6'-(2-hydroxybutyl)-5',6,8,12,27-pentamethyl-20-(2-methylpropyl)spiro[2,24-dioxabicyclo[21.3.1]heptacosa-4,18-diene-25,2'-[2H]pyran]-3,21-dione; 10-Deoxy-Dunaimycin C1. CAS No. 140221-72-3. Molecular formula: C42H72O9. Mole weight: 721.02. | |
| Dunaimycin C1 | It is produced by the strain of Streptomyces diastatochromogenes AB 1691Q-321 and AB 1711J-452. It's an immunosuppressant. Alternative Names: (4E,18E)-3',4',5',6'-Tetrahydro-7,9,11,12-tetrahydroxy-6'-(2-hydroxybutyl)-5',6,8,12,27-pentamethyl-20-(2-methylpropyl)spiro[2,24-dioxabicyclo[21.3.1]heptacosa-4,18-diene-25,2'-[2H]pyran]-3,21-dione. CAS No. 140221-73-4. Molecular formula: C42H72O10. Mole weight: 737.02. | |
| Dunaimycin D4S | It is produced by the strain of Streptomyces diastatochromogenes AB 1691Q-321 and AB 1711J-452. It has weak anti-bacterial and anti-aspergillus Niger activity, and shows immunosuppressive effect in the mouse popliteal node model. CAS No. 140221-79-0. Molecular formula: C51H89NO14. Mole weight: 940.25. | |
| Dunaliella Salina P.E. 7.5% Carotenoids HPLC | Dunaliella Salina P.E. 7.5% Carotenoids HPLC. | CA, FL & NJ |
| Dunnianol | Dunnianol isolated from the fruits of Illicium fargesii. Alternative Names: 5,5',5''-Triallyl-1,1':3',1''-terphenyl-2,2',2''-triol; Dunnial. Grades: 98%. CAS No. 139726-29-7. Molecular formula: C27H26O3. Mole weight: 398.5. | |
| Duocarmycin A | It is produced by the strain of (Pyridamycin) Streptomyces sp. DO-88. It has strong antibacterial and antitumor activity. It can inhibit gram-positive bacteria such as Staphylococcus aureus and Streptococcus faecalis (MIC is less than 0.01 μg/mL), it can also inhibit klebsiella pneumoniae (MIC is 0.032 μg/mL), other bacteria and yeast (MIC is 1-10 μg/mL). Alternative Names: Antibiotic DC 88A; methyl (6R,7bR,8aS)-6-methyl-4,7-dioxo-2-(5,6,7-trimethoxy-1H-indole-2-carbonyl)-1,2,4,5,6,7,8,8a-octahydrocyclopropa[c]pyrrolo[3,2-e]indole-6-carboxylate; Methyl (2R,3bR,4aS)-2-methyl-3,8-dioxo-6-[(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl]-1,2,3,4,4a,5,6,8-octahydrocyclopropa[c]pyrrolo[3,2-e]indole-2-carboxylate; DUMA; (+)-Dunnione; (+)-duocarmycin A. Grades: ≥95%. CAS No. 118292-34-5. Molecular formula: C26H25N3O8. Mole weight: 507.49. | |
| Duocarmycin analog | Duocarmycin analog has cytotoxicity for solid tumor cells that can be used for antibody-drug conjugates (ADCs). Duocarmycins and the analogs acts via binding to the minor groove of DNA and alkylating the nucleobase adenine at the N3 position, which leads to DNA damage and cancer cell death. | |
| Duocarmycin B1 | It is produced by the strain of (Pyridamycin) Streptomyces sp. DO-88. It has anti-gram-positive bacteria, gram-negative bacteria and tumor activity. Alternative Names: Antibiotic DC 89B1; 1H-Pyrrolo3,2-fquinoline-2-carboxylic acid, 8-bromo-2,3,6,7,8,9-hexahydro-4-hydroxy-2-methyl-1-oxo-6-(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl-, methyl ester, (2R,8S)-; Duocarmycin B(sub 1). Grades: ≥95%. CAS No. 124325-93-5. Molecular formula: C26H26BrN3O8. Mole weight: 588.40. | |
| Duocarmycin B2 | It is produced by the strain of (Pyridamycin) Streptomyces sp. DO-88. It has anti-tumor activity. Alternative Names: DUMB2; Benzo1,2-b:4,3-bdipyrrole-2-carboxylic acid, 8-(bromomethyl)-1,2,3,6,7,8-hexahydro-4-hydroxy-2-methyl-1-oxo-6-(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl-, methyl ester, (2R,8S)-. CAS No. 124325-94-6. Molecular formula: C26H26BrN3O8. Mole weight: 588.40. | |
| Duocarmycin DM free base | Duocarmycin DM free base, a DNA minor-groove alkylator, is an antibody agent conjugates (ADCs) toxin. Duocarmycin DM free base is based on its characteristic curved indole structure and a spirocyclopropylcyclohexadienone electrophile to act anticancer activity[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1116745-06-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-128915. |  |
| Duocarmycin SA | Duocarmycin SA is an orally active antitumor antibiotic with an IC50 of 10 pM[1]. Duocarmycin SA is an extremely potent cytotoxic agent capable of inducing a sequence-selective alkylation of duplex DNA. Duocarmycin SA demonstrates synergistic cytotoxicity against glioblastoma multiforme (GBM) cells treated with proton radiation in vitro[2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 130288-24-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-12456. | |
| Duocarmycin TM | Duocarmycin TM (CBI-TMI) is a potent antitumor antibiotic. Duocarmycin TM induces a sequence-selective alkylation of duplex DNA. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CBI-TMI. CAS No. 157922-77-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107769. | |
| Duolite a-7 ion-exchange resin | Duolite a-7 ion-exchange resin. CAS No. 32610-77-8. Molecular formula: C13H26N4O2. Mole weight: 270.37g/mol. IUPAC Name: N'-[2-(2-aminoethylamino)ethyl]ethane-1,2-diamine;formaldehyde;phenol. SMILES: C=O.C1=CC=C(C=C1)O.C(CNCCNCCN)N. InChI: InChI=1S/C6H18N4.C6H6O.CH2O/c7-1-3-9-5-6-10-4-2-8;7-6-4-2-1-3-5-6;1-2/h9-10H,1-8H2;1-5,7H;1H2. |  |
| duolite c-26 ion-exchange resin | duolite c-26 ion-exchange resin. CAS No. 68441-33-8. | |
| Duostatin 5 | Duostatin 5 is a ADC Cytotoxin designed based on MMAF (HY-15579) and can be used to synthesize ADCs. The preparation of Duostatin 5 has the advantages of fewer synthetic steps, simple operation, less difficulty in quality control, and more stable chemical synthesis process. Duostatin 5 can be linked to the antibody targeting 5T4 (ZV05) by cross-linking with interchain cysteines through a disubstituted C-Lock linker. Duostatin 5 is a click chemistry reagent. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-driven alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2124210-34-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145149. | |
| Duoxitasai Liposome | Duoxitasai is a paclitaxel derivative with 2 times the affinity and 10 times the activity of paclitaxel, with broad-spectrum antitumor effects. This product is a PEGylated pre-formulated liposome with duoxitasai. It is only for research purposes. Group: Drug-loaded liposome. |  |
| DuP 697 | DuP 697. Group: Biochemicals. Grades: Purified. CAS No. 88149-94-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| DuP-697 | DuP-697 is a member of the vicinal diaryl heterocycles and a potent, irreversible, selective and orally active COX-2 inhibitor (IC50 of 10 nM and 800 nM for human COX-2 and COX-1, respectively). DuP-697 exerts antiproliferative (IC50 of 42.8 nM), antiangiogenic and apoptotic effects on HT29 colorectal cancer cells. DuP-697 inhibits prostaglandin synthesis and has anti-inflammatory, anticancer and antipyretic effects[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 88149-94-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-103387. | |
| DUPA | DUPA, belongs to a class of glutamate ureas, is used as the targeting moiety in agent conjugate to selectively deliver cytotoxic agents to prostate cancer cells[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 302941-52-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111606. | |
| DUPA(OtBu)-OH | DUPA(OtBu)-OH is a PEG linker for antibody-drug-conjugation (ADC). DUPA(OtBu)-OH is a DUPA precursor. DUPA is used as the targeting moiety to actively deliver Docetaxel (DTX) for treatment of Prostate-Specific Membrane Antigen (PSMA) expressing prostate cancer. Alternative Names: (S)-5-tert-Butoxy-4-(3-((s)-1,5-di-tert-butoxy-1,5-dioxopentan-2-yl)ureido)-5-oxopentanoic Acid; L-Glutamic acid, N-[[[(1S)-3-carboxy-1-[(1,1-dimethylethoxy)carbonyl]propyl]amino]carbonyl]-, 1,5-bis(1,1-dimethylethyl) ester; 2-[3-(1,3-bis-tert-butoxycarbonylpropyl)ureido]pentanedioic acid 1-tert-butyl ester. Grades: 95%. CAS No. 1026987-94-9. Molecular formula: C23H40N2O9. Mole weight: 488.57. | |
| dUpCp | dUpCp, a nucleoside analogue hailed for its therapeutic potential in treating viral infections such as hepatitis C and HIV, has garnered attention for its capacity to inhibit viral replication and to stymie further infection. What's more, this potent analogous substance holds great promise in fighting cancer, with studies demonstrating its propensity to selectively trigger apoptosis in cancer cells. Although the ramifications of its usage as an antitumor agent call for further inquiry into its efficacy, it's an exciting prospect indeed. Alternative Names: dUMPCP; 2'-Deoxyuridine-5'-[(α,β)-methyleno]diphosphate, Sodium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C10H16N2O10P2(free acid). Mole weight: 386.19 (free acid). | |
| dUpCpp | dUpCpp - a chemical compound utilized in the field of biomedical research - holds promising potential as an enzyme activator which facilitates DNA and RNA replication. By augmenting the function of polymerases essential for viral replication, this unique substance presents a promising target for antiviral drug development. Furthermore, dUpCpp has been utilized to probe and unravel the mechanisms underlying the polymerization of DNA and RNA in a spectrum of systems. Alternative Names: dUMPCPP; 2'-Deoxyuridine-5'-[(α,β)-methyleno]triphosphate, Sodium salt. Grades: ≥ 95 % by HPLC. CAS No. 170428-84-9. Molecular formula: C10H17N2O13P3.xNa. Mole weight: 466.17 (free acid). | |
| Dupical | Dupical. CAS No. 30168-23-1. VIGON Item # 503212. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, muguet butanal. |  America & Internationally |
| Dupilumab | Dupilumab, marketed under the brand name Dupixent, is a monoclonal antibody used to treat several chronic inflammatory conditions. It works by inhibiting the signaling of interleukin-4 (IL-4) and interleukin-13 (IL-13), which are cytokines involved in the inflammatory response. Dupilumab is approved for the treatment of several conditions, including, atopic dermatitis, asthma, chronic rhinosinusitis with nasal polyps (CRSwNP), and eosinophilic esophagitis. Alternative Names: Immunoglobulin, anti-(human interleukin 4 receptor α) (human REGN668 heavy chain), disulfide with human REGN668 κ-chain, dimer; Dupixent; REGN 668; SAR 231893. CAS No. 1190264-60-8. | |
| Dupilumab | Dupilumab (REGN-668) is a fully human mAb to IL-4 receptor α (IL-4Rα) that inhibits both IL-4 and IL-13 signaling, markedly improved moderate-to-severe atopic dermatitis[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: REGN-668; SAR-231893. CAS No. 1190264-60-8. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P9926. | |
| Dupilumab (anti-IL-4Rα) | Dupilumab (anti-IL-4Rα) is a fully human anti-interleukin-4 receptor α monoclonal antibody that inhibits both interleukin-4 (IL-4) and interleukin-13 (IL-13) signaling through blockade of the shared IL-4α subunit. Group: Antibodies. Alternative Names: REGN-668, SAR-231893. CAS No. 1190264-60-8. Pack Sizes: 1mg. Product ID: A2038. Storage Conditions: Store the undiluted solution at 4°C in the dark to avoid freeze-thaw cycles. |  United States; Europe |
| Duplex 2209, 20 mesh woven from 0.3mm (0.012mm) dia wire | Duplex 2209, 20 mesh woven from 0.3mm (0.012mm) dia wire. | |
| Duplex 2209, 40 mesh woven from 0.2mm (0.008mm) dia wire | Duplex 2209, 40 mesh woven from 0.2mm (0.008mm) dia wire. | |
| Duplex 2209, 60 mesh woven from 0.15mm (0.006mm) dia wire | Duplex 2209, 60 mesh woven from 0.15mm (0.006mm) dia wire. | |
| dUpNHp | dUpNHp, a noteworthy biochemical research instrument, exhibits extensive applicability in the modification and examination of enzymatic activity within cells. Remarkably, its specificity in targeting and altering the activity of protein kinases and G proteins has proven invaluable within the realm of biomedicine, aiding in the study of prevalent diseases such as diabetes, cancer, and Alzheimer's whilst facilitating the development of new drugs targeted to combat them. Alternative Names: dUMPNP;2'-Deoxyuridine-5'-[(α,β)-imido]diphosphate, Sodium salt. Grades: ≥ 95 % by HPLC. CAS No. 178809-71-7. Molecular formula: C9H15N3O10P2.xNa. Mole weight: 387.17 (free acid). | |
| dUpNHpp | dUpNHpp, a formidable small molecule inhibitor with potential therapeutic benefits, is a contender in the battle against cancer. Its mode of action rests on disrupting protein-protein interactions, resulting in the arrest of tumor growth. Ovarian and breast cancer, both notorious for their lethality, have been subject to clinical trials with auspicious outcomes. Alternative Names: dUMPNPP;2'-Deoxyuridine-5'-[(α,β)-imido]triphosphate, Sodium salt. Grades: ≥ 95 % by HPLC. CAS No. 170428-86-1. Molecular formula: C9H16N3O13P3.xNa. Mole weight: 467.15 (free acid). | |
| Duponol G (9CI) | Duponol G (9CI). CAS No. 12626-51-6. Molecular formula: C22H47NO4S. Mole weight: 421.70. | |
| DuPont Mask USA | DuPont Mask USA. Product ID: CDC10-0625. Category: Silk Mask Series. Product Keywords: Cosmetic Ingredients; Cosmetic packaging material; DuPont Mask USA; CDC10-0625; Silk Mask series; Lyocell fibers. |  |
| DuPont Mask USA | DuPont Mask USA. Product ID: CDC10-0686. Category: Cosmetic Packaging Material. Product Keywords: Cosmetic Ingredients; Mask; CDC10-0686; DuPont Mask USA; Cosmetic Packaging Material;. | |
| DuPont Three Generations Mask | DuPont Three Generations Mask. Product ID: CDC10-0685. Category: Cosmetic Packaging Material. Product Keywords: Cosmetic Ingredients; Mask; CDC10-0685; DuPont Three Generations Mask; Cosmetic Packaging Material;. | |
| DuPont Three Generations Mask | DuPont Three Generations Mask. Product ID: CDC10-0624. Category: Silk Mask Series. Product Keywords: Cosmetic Ingredients; Cosmetic packaging material; DuPont Three Generations Mask; CDC10-0624; Silk Mask series; Lyocell fibers. | |
| Duralink HTS | Duralink HTS. Molecular formula: C6H12Na2O6S4. Mole weight: 354.4g/mol. IUPAC Name: disodium;1,6-bis(sulfonatosulfanyl)hexane. SMILES: C(CCCSS(=O)(=O)[O-])CCSS(=O)(=O)[O-].[Na+].[Na+]. InChI: InChI=1S/C6H14O6S4.2Na/c7-15(8,9)13-5-3-1-2-4-6-14-16(10,11)12;;/h1-6H2,(H,7,8,9)(H,10,11,12);;/q;2*+1/p-2. | |
| Duramycin | Duramycin. Alternative Names: Ancovenin,2-L-lysine-6-(3-aminoalanine)-10-L-phenylalanine-12-L-phenylalanine-13-L-valine-15-(erythro-3-hydroxy-L-aspartic acid)-,cyclic 6-19)-imine; LANCOVUTIDE; Leucopeptin; UNII-BPR0F3X56H; Lancovutide [INN]. CAS No. 1391-36-2. Purity: 90+%. Product ID: ACM1391362. Molecular formula: C89H125N23O25S3. Mole weight: 2013.28. IUPAC Name: Duramycin. Canonical SMILES: CC1C2C(=O)NC(C(=O)NC(C(=O)NC3CSCC4C(=O)NC(CS1)C(=O)NC(CNCCCCC(NC(=O)C(CSCC(C(=O)NC(C(=O)NC(C(=O)N4)CCC(=O)N)CCCCN)N)NC(=O)C(NC(=O)CNC(=O)C(NC3=O)C(C(=O)O)O)CC(=O)N)C(=O)O)C(=O)NC(C(=O)NCC(=O)N5CCCC5C(=O)NC(C(=O)N2)CC6=CC=CC=C6)CC7=CC=CC=C7)C(C)C)CC8=CC=CC=C8. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Duramycin | Duramycin (Moli1901) is a lantibiotic derived from Streptomyces cinnamoneuma. Duramycin also is a antimicrobial peptide. Duramycin can be used for the research of cystic fibrosis (CF)[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Moli1901; Lancovutide. CAS No. 1391-36-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-106302. | |
| Duramycin | It is produced by the strain of Streptomyces cinnamomeus. It has activity against gram-positive bacteria, gram-negative bacteria (individual, weak), Mycobacterium and Candida albicans. Alternative Names: 27,46-(Methaniminopentaniminomethano)-6,43:15,40-bis(methanothiomethano)pyrrolo[2,1-d1][1,4,7,10,13,16,19,22,25,28,31,34,37,40,43,46,49,52]thiaheptadecaazacyclopentapentacontine, cyclic peptide deriv.; Antibiotic PA 48009; Lancovutide; Leucopeptin; Ancovenin, 2-L-lysine-6-(3-aminoalanine)-10-L-phenylalanine-12-L-phenylalanine-13-L-valine-15-(erythro-3-hydroxy-L-aspartic acid)-, cyclic 6-19)-imine; Duramycin A. Grades: ≥90%. CAS No. 1391-36-2. Molecular formula: C88H123N23O25S3. Mole weight: 1999.25. | |
| Duramycin B | Duramycins B is a new lanthionine containing antibiotic, has been isolated from Streptoverticillium strain R2075. Duramycins B is a potent inhibitor of human phospholipase A2. It exhibits only a weak antibacterial activity against B.subtilis, and does not display antimicrobial activity against S.aureus, S.mitis, E.coli, K.pneumoniae, P.vulgaris and C.albicans. Grades: ≥98%. CAS No. 132246-31-2. Molecular formula: C86H127N25O25S3. Mole weight: 2007.27. | |
| Duramycin C | Duramycin C is a new lanthionine containing antibiotic, has been isolated from Streptomyces griseoluteus (R2107). Duramycin C is a potent inhibitor of human phospholipase A2. It exhibits only a weak antibacterial activity against B.subtilis, and does not display antimicrobial activity against S.aureus, S.mitis, E.coli, K.pneumoniae, P.vulgaris and C.albicans. Grades: ≥98%. CAS No. 132268-38-3. Molecular formula: C82H115N23O27S3. Mole weight: 1951.12. | |
| Durlobactam | Durlobactam is a novel β-lactamase inhibitor. It is designed to combat antibiotic resistance by inhibiting β-lactamase enzymes produced by certain bacteria, which can degrade β-lactam antibiotics. By inhibiting these enzymes, durlobactam allows β-lactam antibiotics to remain effective against resistant bacterial strains. Durlobactam is often combined with other antibiotics to enhance their efficacy, particularly in treating infections caused by multidrug-resistant organisms. Alternative Names: Sulfuric acid, mono[(1R,2S,5R)-2-(aminocarbonyl)-3-methyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-3-en-6-yl] ester; ETX 2514; ETX2514; ETX-2514; (1R,2S,5R)-2-(Aminocarbonyl)-3-methyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-3-en-6-yl hydrogen sulfate; (1R,2S,5R)-2-carbamoyl-3-methyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-3-en-6-yl hydrogen sulfate. Grades: ≥95%. CAS No. 1467829-71-5. Molecular formula: C8H11N3O6S. Mole weight: 277.25. | |
| Durlobactam sodium | Durlobactam, also known as ETX2514, is a beta-lactamase inhibitor drug candidate. Durlobactam sodium can be used in studies about drug-resistant Gram-negative bacteria including Acinetobacter baumannii. Alternative Names: ETX 2514 sodium; ETX-2514 sodium; ETX2514 sodium; (1R,2S,5R)-2-Carbamoyl-3-methyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-3-en-6-yl sodium sulfate; Sulfuric acid, mono[(1R,2S,5R)-2-(aminocarbonyl)-3-methyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-3-en-6-yl] ester, sodium salt (1:1); Durlobactam sodium salt; ETX 2514 Sodium salt. Grades: ≥95%. CAS No. 1467157-21-6. Molecular formula: C8H10N3NaO6S. Mole weight: 299.24. | |
| Durlobactam sodium | Durlobactam sodium salt (ETX2514) is a broad-spectrum β-lactamase inhibitor with IC50s of 4, 14 and 190 nM for Class A KPC-2, Class C AmpC and Class D OXA-24, respectively. For the treatment of drug-resistant Gram-negative bacteria including Acinetobacter baumannii[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ETX2514. CAS No. 1467157-21-6. Pack Sizes: 10 mM * 1 mL in Water; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-117974. | |
| Durvalumab | Durvalumab (MEDI 4736) is an human anti-PD-L1 monoclonal antibody[1]. Durvalumab (MEDI4736) completely blocks the binding of PD-L1 to both PD-1 and CD80, with IC50s of 0.1 and 0.04 nM, respectively[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MEDI 4736. CAS No. 1428935-60-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P9919. | |
| Durvalumab (anti-PD-L1) | Durvalumab (anti-PD-L1)(MEDI 4736) is a human anti-PD-L1 protein monoclonal antibody. Durvalumab (anti-PD-L1) completely blocks PD-L1 binding to PD-1 and CD80, IC 50 are 0.1 and 0.04 nM respectively, has anti-tumor activity[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MEDI 4736 (anti-PD-L1). CAS No. 1428935-60-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P9919A. | |
| Durvalumab (anti-PD-L1) | Durvalumab (anti-PD-L1) is a selective, high affinity human IgG1 mAb that blocks programmed cell death ligand-1 (PD-L1) binding to PD-1 (IC50=0.1 nM) and CD80 (IC50=0.04 nM). MW=146.3 kDa. Group: Antibodies. Alternative Names: MEDI4736. CAS No. 1428935-60-7. Pack Sizes: 5mg. Product ID: A2013. Storage Conditions: Store the undiluted solution at 4°C in the dark to avoid freeze-thaw cycles. | United States; Europe |
| Dusigitumab | Dusigitumab is a fully human IgG2λ monoclonal antibody that targets IGF-1 and IGF-2 with picomolar binding affinity. Dusigitumab blocks IGF-1 and IGF-2-induced phosphorylation of IGF-1R as well as activation of IR-A, thereby inhibiting the activation of downstream signaling pathways. Dusigitumab is applicable to research related to advanced solid tumors and hormone receptor-positive metastatic breast cancer[1][2]. Uses: Scientific research. Category: Inhibitory antibodies. Alternative Names: MEDI 573. CAS No. 1204390-13-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99867. | |
| DusQ 21 NHS ester | DusQ 21 is a dark quencher used as an acceptor in FRET applications, it has absorption maximum 656 nm, and can be used in multiplex assays due to the lack of secondary fluorescence. DusQ 21 NHS ester derivative is used for labeling with the primary amines of amine-containing molecules. It can be used for quenching of many fluorophores, including Cyanine5, Cyanine5.5, AF 647. CAS No. 304014-13-9. Molecular formula: C45H39ClN4O7S. Mole weight: 815.35. | |
| DusQ2 phosphoramidite | DusQ2 is a black quencher dye for the synthesis of dual labeled oligonucleotide probes for qPCR bearing 5'-quencher. This quencher is ideal for HEX, JOE, ROX, Cyanine5 and other dyes with the emission in orange and red part of the spectrum.,The primary phosphoramidite group couples with hydroxyls efficiently in oligonucleotide synthesis. Grades: NMR 1H, 31P, HPLC-MS (95%). CAS No. 374591-98-7. Molecular formula: C54H61N8O9P. Mole weight: 997.08. | |
| Dusquetide | Dusquetide (SGX942) is a first-in-class innate defense regulator (IDR). Dusquetide modulates the innate immune response to both PAMPs and DAMPs by binding to p62. Dusquetide shows activity in both reducing inflammation and increasing clearance of bacterial infection[1]. DAMPs: damage-associated molecular patterns; PAMPs: pathogen-associated molecular patterns. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SGX942. CAS No. 931395-42-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2076. | |
| Dustanin | Dustanin is a hopane isolated from Aschersonia. Alternative Names: 15alpha,22-dihydroxyhopane; Hopane-15α,22-diol. CAS No. 3607-96-3. Molecular formula: C30H52O2. Mole weight: 444.73. | |
| DUT-8 (Co) | Take your Metal-organic Frameworks (MOFs) Materials research to the next level by the innovative DUT-8 (Co) from CD Bioparticles Drug Delivery. Group: Cobalt-based mofs (co-mof). |  |
| DUT-8 (Ni) | Optimize your research on Ni-MOF with the cutting-edge DUT-8 (Ni) from CD Bioparticles Drug Delivery. Group: Nickel-based mofs (ni-mof). | |
| Dutasteride | 25mg Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C27H30F6N2O2. CAS No. 164656-23-9. Prepack ID 11556431-25mg. Molecular Weight 528.53. See USA prepack pricing. |  |
| Dutasteride | Dutasteride is a dual 5-α reductase inhibitor that inhibits conversion of testosterone to dihydrotestosterone (DHT). Alternative Names: 1H-Indeno[5,4-f]quinoline-7-carboxamide, N-[2,5-bis(trifluoromethyl)phenyl]-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-4a,6a-dimethyl-2-oxo-, (4aR,4bS,6aS,7S,9aS,9bS,11aR)-; (4aR,4bS,6aS,7S,9aS,9bS,11aR)-N-[2,5-Bis(trifluoromethyl)phenyl]-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-4a,6a-dimethyl-2-oxo-1H-indeno[5,4-f]quinoline-7-carboxamide; 4-Azaandrost-1-ene-17-carboxamide, N-[2,5-bis(trifluoromethyl)phenyl]-3-oxo-, (5α,17β)-; (5α,17β)-N-[(2,5-Bis(trifluoromethyl)phenyl]-3-oxo-4-aza-5-androst-1-ene-17-carboxamide; Avodart; Avolve; GG 745; GI 198745; Veltride. Grades: >98%. CAS No. 164656-23-9. Molecular formula: C27H30F6N2O2. Mole weight: 528.53. | |
| Dutasteride | Dutasteride. Uses: For analytical and research use. Category: Pharmacopoeial standards. Alternative Names: GI 206020X, GW 402836X, GI 198745X, GG 745, Dutasteride,1H-Indeno[5,4-f]quinoline-7-carboxamide, N-[2,5-bis(trifluoromethyl)phenyl]-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-4a,6a-dimethyl-2-oxo-, (4aR,4bS,6aS,7S,9aS,9bS,11aR)-, 4-Azaandrost-1-ene-17-carboxamide, N-[2,5-bis(trifluoromethyl)phenyl]-3-oxo-, (5alpha,17beta)-, Dutasteride, GW 403358X, (5alpha,17beta)-N-[(2,5-Bis(trifluoromethyl)phenyl]-3-oxo-4-aza-5-androst-1-ene-17-carboxamide, GW 504051X, Veltride, GW 402839X, Avolve, GI 246118X, Avodart, GI 198745, GW 418079X, GI 246071X. CAS No. 164656-23-9. Molecular formula: C27H30F6N2O2. Mole weight: 528.53. IUPAC Name: (1S,3aS,3bS,5aR,9aR,9bS,11aS)-N-[2,5-bis(trifluoromethyl)phenyl]-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide. Catalog: APS164656239. SMILES: C[C@]12CC[C@H]3[C@@H](CC[C@H]4NC(=O)C=C[C@]34C)[C@@H]1CC[C@@H]2C(=O)Nc5cc(ccc5C(F)(F)F)C(F)(F)F. |  |
| Dutasteride | Dutasteride (GG745) is a potent inhibitor of both 5α-reductase isozymes. Dutasteride may possess off-target effects on the androgen receptor (AR) due to its structural similarity to DHT[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GG 745; GI 198745. CAS No. 164656-23-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13613. | |
| Dutasteride | Dutasteride. Group: Biochemicals. Alternative Names: (5a, 17b) -N-[2, 5-Bis (trifluoromethyl) phenyl]-3-oxo-4-azaandrost-1-ene-17-carboxamide. Grades: Highly Purified. CAS No. 164656-23-9. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C27H30F6N2O2. US Biological Life Sciences. | Worldwide |
| Dutasteride-13C6 | Labeled Dutasteride. Dutasteride is a dual inhibitor of 5α-reductase isoenzymes type 1 and 2; structurally related to Finasteride. Dutasteride is used in the treatment of benign prostatic hyperplasia. Group: Biochemicals. Alternative Names: (4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -N-[2, 5-Bis (trifluoromethyl) phenyl]-2, 4a, 4b, 5, 6, 6a, 7, 8, 9, 9a, 9b, 10, 11, 11a-tetradecahydro-4a, 6a-dimethyl-2-oxo-1H-indeno[5, 4-f]quinoline-7-carboxamide-13C6; (5α,17 β)-. Grades: Highly Purified. CAS No. 1217685-27-2. Pack Sizes: 250ug. US Biological Life Sciences. | Worldwide |
| Dutasteride EP Impurity A | Dutasteride EP Impurity A. Uses: For analytical and research use. Alternative Names: (4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid. CAS No. 104239-97-6. Molecular formula: C19H27NO3. Mole weight: 317.42. Catalog: APB104239976. | |
| Dutasteride Impurity B | Dutasteride Impurity B. Uses: For analytical and research use. Alternative Names: (4aR,4bS,6aS,7S,9aS,9bS,11aR)-N,N,4a,6a-tetramethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxamide. Molecular formula: C21H32N2O2. Mole weight: 344.49. Catalog: APB05236. | |
| Dutasteride Impurity C | Dutasteride Impurity C. Uses: For analytical and research use. Alternative Names: (4aR,4bS,6aS,7S,9aS,9bS,11aR)-ethyl 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylate. Molecular formula: C21H31NO3. Mole weight: 345.48. Catalog: APB05235. | |
| Dutasteride Impurity D | Dutasteride Impurity D. Uses: For analytical and research use. Alternative Names: (4aR,4bS,6aS,7R,9aS,9bS)-N-(2,5-bis(trifluoromethyl)phenyl)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10-dodecahydro-1H-indeno[5,4-f]quinoline-7-carboxamide. Molecular formula: C27H28F6N2O2. Mole weight: 526.51. Catalog: APB05234. | |
| Dutasteride Impurity E | Dutasteride Impurity E. Uses: For analytical and research use. Alternative Names: (4aR,4bS,6aS,7R,9aS,9bS,11aR)-N-(2,5-bis(trifluoromethyl)phenyl)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxamide. CAS No. 1796930-46-5. Molecular formula: C27H30F6N2O2. Mole weight: 528.53. Catalog: APB1796930465. | |
| Dutasteride Impurity F | Dutasteride Impurity F. Uses: For analytical and research use. Alternative Names: (4S,4aR,4bS,6aS,7S,9aS,9bS,11aR)-N-(2,5-bis(trifluoromethyl)phenyl)-4-chloro-4a,6a-dimethyl-2-oxohexadecahydro-1H-indeno[5,4-f]quinoline-7-carboxamide. Molecular formula: C27H31ClF6N2O2. Mole weight: 564.99. Catalog: APB05233. | |
Our database is helping our users find suppliers everyday.
