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3-Acetoxy-24-hydroxydammara-20,25-diene | CAS:143519-04-4
3-Acetoxy-24-hydroxydammara-20,25-diene
  • Name:3-Acetoxy-24-hydroxydammara-20,25-diene
  • CAS:143519-04-4
  • Synonyms:
  • Molecular Formula:C32H52O3
  • Molecular Weight:484.77
  • EINESC:

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Peer-Reviewed Papers
Design, synthesis and biochemical evaluation of novel multi-target inhibitors as potential anti-Parkinson agents.Carradori S, et al. European Journal of Medicinal Chemistry, 143, 1543-1552 (2018) 1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors.Jinbing Liu et al.Bioorganic & medicinal chemistry, 16(3), 1096-1102 (2008-03-08) Synthesis and structure-activity relationship studies of 4-arylthiosemicarbazides as topoisomerase IV inhibitors with Gram-positive antibacterial activity. Search for molecular basis of antibacterial activity of thiosemicarbazides.Agata Siwek et al.European journal of medicinal chemistry, 46(11), 5717-5726 (2011-10-08) Removal of cations using ion-binding terpolymer involving 2-amino-6-nitro-benzothiazole and thiosemicarbazide with formaldehyde by batch equilibrium technique.Mohamed A Riswan Ahamed et al.Journal of hazardous materials, 248-249, 59-68 (2013-01-29) A highly selective colorimetric sensor for Hg²⁺ based on nitrophenyl-aminothiourea.Juan Liu et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 93, 245-249 (2012-04-10) Neutral gold complexes with tridentate SNS thiosemicarbazide ligands.Pedro I da S Maia et al.Inorganic chemistry, 51(3), 1604-1613 (2012-01-12) Design and synthesis of thienopyrimidine urea derivatives with potential cytotoxic and pro-apoptotic activity against breast cancer cell line MCF-7.Abdelhaleem EF, et al. European Journal of Medicinal Chemistry, 143, 1807-1825 (2018) 3-mercapto-1,2,4-triazoles and N-acylated thiosemicarbazides as metallo-β-lactamase inhibitors.Faridoon et al.Bioorganic & medicinal chemistry letters, 22(1), 380-386 (2011-11-26) Cytotoxic effect and molecular docking of 4-ethoxycarbonylmethyl-1-(piperidin-4-ylcarbonyl)-thiosemicarbazide--a novel topoisomerase II inhibitor.Agata Siwek et al.Journal of molecular modeling, 19(3), 1319-1324 (2012-11-29) Single-fluorophore-based fluorescent probes enable dual-channel detection of Ag⁺ and Hg²⁺ with high selectivity and sensitivity.Yanlin Lv et al.Analytica chimica acta, 839, 74-82 (2014-07-30) Rhenium mixed-ligand complexes with S,N,S-tridentate thiosemicarbazone/thiosemicarbazide ligands.Pedro I da S Maia et al.Dalton transactions (Cambridge, England : 2003), 42(14), 5111-5121 (2013-02-13) A metal-organic tetrahedron as a redox vehicle to encapsulate organic dyes for photocatalytic proton reduction.Xu Jing et al.Journal of the American Chemical Society, 137(11), 3967-3974 (2015-03-05) Carbamylation of immunoglobulin abrogates activation of the classical complement pathway.Catalin Koro et al.European journal of immunology, 44(11), 3403-3412 (2014-08-19) Exploiting the 2-Amino-1, 3, 4-thiadiazole Scaffold To Inhibit Trypanosoma brucei Pteridine Reductase in Support of Early-Stage Drug Discovery.Linciano P, et al. ACS Omega, 2(9), 5666-5683 (2017) Novel bis-C,N-cyclometalated iridium(III) thiosemicarbazide antitumor complexes: interactions with human serum albumin and DNA, and inhibition of cathepsin B.José Ruiz et al.Inorganic chemistry, 52(2), 974-982 (2013-01-11) Impedimetric and electrochemical evaluation of a new redox active steroid derivative for hormone immunosensing.Jessica Kelch et al.Biosensors & bioelectronics, 150, 111876-111876 (2019-11-22) Synthesis, molecular modeling and biological evaluation of chalcone thiosemicarbazide derivatives as novel anticancer agents.Hong-Jia Zhang et al.European journal of medicinal chemistry, 46(9), 4702-4708 (2011-08-06) Preparation, characterization and application of thiosemicarbazide grafted multiwalled carbon nanotubes for solid-phase extraction of Cd(II), Cu(II) and Pb(II) in environmental samples.Jie Zhang Journal of environmental sciences (China), 25(11), 2331-2337 (2014-02-21) Photochemical isomerizations of thiosemicarbazide, a matrix isolation study.Hanna Rostkowska et al.The journal of physical chemistry. A, 116(40), 9863-9871 (2012-09-13) Synthesis, Characterization, Catalytic Activity, and DFT Calculations of Zn(II) Hydrazone Complexes.Temiloluwa T Adejumo et al.Molecules (Basel, Switzerland), 25(18) (2020-09-10) Ethyl thiosemicarbazide intercalated organophilic calcined hydrotalcite as a potential sorbent for the removal of uranium(VI) and thorium(IV) ions from aqueous solutions.T S Anirudhan et al.Journal of environmental sciences (China), 25(4), 717-725 (2013-08-09) Cobalt Complex with Thiazole-Based Ligand as New Pseudomonas aeruginosa Quorum Quencher, Biofilm Inhibitor and Virulence Attenuator.Anabela Borges et al.Molecules (Basel, Switzerland), 23(6) (2018-06-13) Antimicrobial activity and SAR study of some novel thiosemicarbazide derivatives bearing piperidine moiety.Agata Siwek et al.Medicinal chemistry (Shariqah (United Arab Emirates)), 7(6), 690-696 (2012-02-09) Hybrid immobilization of galactosyl lactose and cellobiose on a gold substrate to modulate biological responses.Takuya Kitaoka et al.Carbohydrate polymers, 92(1), 374-379 (2012-12-12) Structural, spectral, DFT, pH-metric and biological studies on Cr(III), Mn(II) and Fe(III) complexes of dithione heterocyclic thiosemicarbazide ligand.Gaber M Abu El-Reash et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 383-393 (2013-01-01) 2:1 multiplexing function in a simple molecular system.Sha Xu et al.Sensors (Basel, Switzerland), 12(4), 4421-4430 (2012-06-06) Antifungal effect of 4-arylthiosemicarbazides against Candida species. Search for molecular basis of antifungal activity of thiosemicarbazide derivatives.Agata Siwek et al.Journal of molecular modeling, 18(9), 4159-4170 (2012-04-27) The use of umbelliferone in the synthesis of new heterocyclic compounds.Ahmed A Al-Amiery et al.Molecules (Basel, Switzerland), 16(8), 6833-6843 (2011-08-13) Rhodamine-modified upconversion nanophosphors for ratiometric detection of hypochlorous acid in aqueous solution and living cells.Yi Zhou et al.Small (Weinheim an der Bergstrasse, Germany), 10(17), 3560-3567 (2014-02-06) Regioselective synthesis of 2-amino-substituted 1,3,4-oxadiazole and 1,3,4-thiadiazole derivatives via reagent-based cyclization of thiosemicarbazide intermediate.Seung-Ju Yang et al.The Journal of organic chemistry, 78(2), 438-444 (2012-12-12) Synthesis and antityrosinase mechanism of benzaldehyde thiosemicarbazones: novel tyrosinase inhibitors.Liang-Hua Chen et al.Journal of agricultural and food chemistry, 60(6), 1542-1547 (2012-01-19) Synthesis and antitumor activity of novel quinazoline derivatives containing thiosemicarbazide moiety.Junbo He et al.European journal of medicinal chemistry, 54, 925-930 (2012-07-04) Synthesis, crystal structures, and biological evaluation of manganese(II) and nickel(II) complexes of 4-cyclohexyl-1-(1-(pyrazin-2-yl)ethylidene)thiosemicarbazide.Ming Xue Li et al.European journal of medicinal chemistry, 46(9), 4383-4390 (2011-07-26) Spectroscopic evaluation for VO(II), Ni(II), Pd(II) and Cu(II) complexes derived from thiosemicarbazide: a special emphasis on EPR study and DNA cleavage.Nashwa M El-Metwally et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 107, 289-295 (2013-02-26) 2-Acetylpyridine thiosemicarbazones. 1. A new class of potential antimalarial agents.Klayman DL, et al. Journal of Medicinal Chemistry, 22(7), 855-862 (1979) Thiosemicarbazides: synthesis and reactions.Metwally MA, et al. Journal of Sulfur Chemistry, 32(5), 489-519 (2011) Cytotoxicity of new 5-phenyl-4,5-dihydro-1,3,4-thiadiazole analogues.Mohammad Sayed Alam et al.Chemical & pharmaceutical bulletin, 59(11), 1413-1416 (2011-11-02) Growth and characterization of thiosemicarbazide hydrochloride: a semiorganic NLO material.R Santhakumari et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 82(1), 102-107 (2011-08-09) Spectral, thermal and biological studies of Mn(II) and Cu(II) complexes with two thiosemicarbazide derivatives.Moamen S Refat et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 92, 336-346 (2012-03-27)
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