德尔塔
您当前所在位置:首页 > 材料科学
[抗氧化小分子]Nisoldipine

[抗氧化小分子]Nisoldipine

作者:德尔塔生物 日期:2023-04-04

Binding experiments of electrophysiologyCHO cells expressing the subunit of the voltage-dependent L-type Ca2+ channel were cultrured in medium without serum in the presence of different concentrations of Nisoldipine. Then Ca2+ channel current elicited from a holding potential of -100 mV or -50 mV was recorded at room temperature with the whole-cell configuration of the patch-clamp method using the List EPC-7 patch-clamp amplifer and pClamp software. The IC50 values were calculated.Cell experiment [2]:Cell linesGuinea-pig ventricular myocytesPreparation methodThe solubility of this compound in DMSO is > 11.6 mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below - 20 °C for several months.Reacting condition10 ~ 100 μM; 8 ~ 10 minsApplicationsIn guinea-pig ventricular myocytes, Nisoldipine inhibited rapidly activating delayed-rectifier K+ current (I(Kr) ) with an IC50 value of 23 μM, as well as slowly activating delayed-rectifier K+ current (I(Ks) ) with an IC50 value of 40 μM. It was estimated that Nisoldipine is approximately 30 times more selective for L-type Ca2+ channels than for delayed-rectifier K+ channels.Animal experiment [3]:Animal modelsA dog model of coronary ischemia-reperfusionDosage form6.6 μg/kg/min; i.v.ApplicationsCompared with the control group, the Nisoldipine treatment group showed similar hemodynamic measurements. However, mass of necrosis and mass at risk was obviously lower in the Nisoldipine group. In a dog model of c

[抗氧化抑制剂]Nerol

[抗氧化抑制剂]Nerol

作者:德尔塔生物 日期:2023-04-04

Nerol is a monoterpene and isomer of geraniol that has been found in a variety of plants, including Cannabis. It increases production of reactive oxygen species (ROS) and intracellular calcium levels and induces mitochondrial dysfunction, cytochrome C release, and apoptosis in A. flavus. Nerol (30-300 mg/kg) reduces weight loss, production of the inflammatory cytokines IL-13 and TNF-α, gastric damage, and hyperalgesia in a mouse model of oxazolone-induced colitis.Cas No.106-25-2别名:橙花醇Canonical SMILES: C/C(C)=C/CC/C(C)=C\CO分子式: C10H18O 分子量: 154.3溶解度: Chloroform: Slightly Soluble,Methanol: Slightly Soluble 储存条件: Store at -20°C General tips: For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. Shipping Condition Evaluation sample solution : ship with blue iceAll other available size: ship with RT , or blue ice upon request热门文章:活性氧(reactive oxygen species , ROS)Reactive Oxygen Species Assay Kit 活性氧(ROS)检测试剂盒活性氧(reactive oxygen species , ROS)与线粒体凋亡通路活性(reactive oxygen species , ROS)氧作用的靶标简单介绍活性氧(reactive oxygen species , ROS)的产生活性氧(reactive oxygen species , ROS)简介活性氧分子 Cas号:25696-21-3 ACTH 1-14 Reactive Oxygen Species ROS活性氧小分子,蟾蜍灵Bufotalin,471-95-4/CAS:520-26-3,橙皮苷/己唑醇活性氧与活性硫荧光探针的设计、合成及生物成像应用的研究

[活性氧抑制剂]Neosperidin dihydrochalcone

[活性氧抑制剂]Neosperidin dihydrochalcone

作者:德尔塔生物 日期:2023-04-04

Cell experiment:WST-8 dye is used in the cell viability assay. HIT-T15 and HUVEC cells are grown and maintained in Dulbecco’s modified Eagle’s medium, supplemented with 10% fetal bovine calf serum. 1000 cells in each well are incubated with various concentrations of neohesperidin dihydrochalcone (50, 100, 500 μM, 1 mM) and other compounds. After treating HIT-T15 and HUVEC cells with 500 μM HOCl, WST-8 dye is added to each well, and the absorbance is detected at 420 nm with microplate reader[1].Animal experiment:Rats: The embryotoxicity/teratogenicity of neohesperidin dihydrochalcone is examined in Wistar Crl:(WI)WU BR rats. The study is comprised of four groups of 28 mated female rats each, i.e., a control group (0% neohesperidin dihydrochalcone) and three treatment groups (1.25, 2.5, and 5% neohesperidin dihydrochalcone). The general condition and behavior of the animals are observed twice daily. Body weight is determined on days 0, 7, 14, and 21 of gestation. Food consumption is determined during three consecutive periods (days 0-7, 7-14, and 14-21 of gestation)[4]. [3]Mice: Neohesperidin dihydrochalcone is dissolved in a 0.5% CMC vehicle. Mice are randomized into four groups. The control group receives equal volume of vehicles throughout. The PQ group receives saline once daily for 6 consecutive days. One hour after final saline treatment, mice are injected with PQ (75 mg/kg body weight). The neohesperidin dihydrochalcone group receives a daily dose of 200 mg/kg body weight by oral gavage for 6 consecutive days. One hour after final neohesperidin dihydrochalcone treatmen

[活性氧物种]Naringenin

[活性氧物种]Naringenin

作者:德尔塔生物 日期:2023-04-04

Cell experiment:Naringenin is dissolved in DMSO and diluted in cell culture medium. The cells are rinsed with PBS and grown in a medium containing various concentrations of naringenin (50, 100, 150, 200, 250, 300 μM). The solvent DMSO treated cells are served as control. After 24 hrs of treatment, the medium is removed and replaced by another medium containing MTT. Cell viability is measured using the MTT assay[1].Animal experiment:Rats: Semi-purified, powdered diets are prepared for concentrations of naringenin: 0, 0.003, 0.006, and 0.012% of diet. After 7 days of acclimatization, rats are assigned to one of four groups, with six animals per group, and fed semi-purified experimental diets for 6 weeks. The experimental diets contain 16% fat, 45.5% sucrose, and different naringenin concentration (0, 0.003, 0.006, or 0.012%) (Table 1). Rats have ad libitum access to food and water during the study period. Food intake and body weight are measured throughout the experiment[3]. Mouse: Eight- to 12-week-old mice are fed ad libitum a rodent standard diet or a high-fat diet containing 42% of calories from fat plus cholesterol (0.05% wt/wt). Naringenin is added to the Western diet at 1 or 3% (wt/wt). Ldlr−/− mice are fed for 4 weeks and C57BL/6J mice for 30 weeks. Food intake is measured daily, and body weight is measured biweekly. Mice are fasted for 6 h before intervention[4].Cell experiment:Naringenin is dissolved in DMSO and diluted in cell culture medium. The cells are rinsed with PBS and grown in a medium containing various concentrations of naringenin (50, 100, 150, 200, 250,

[活性氧簇]N-hydroxylamine Dapsone

[活性氧簇]N-hydroxylamine Dapsone

作者:德尔塔生物 日期:2023-04-04

N-hydroxylamine Dapsone is an active metabolite of dapsone .1 It is formed via N-hydroxylation of dapsone by the cytochrome P450 (CYP) isoforms CYP2C8, CYP2C9, CYP2C18, and CYP2C19 in the liver.2 N-hydroxylamine Dapsone is cytotoxic to rat hepatocytes (LC50 = 3.6 mM).3 It induces hemolysis in isolated human erythrocytes at a concentration of 100 µM.1 N-hydroxylamine Dapsone induces phosphatidylserine (PS) exposure on the outer membrane, a marker of apoptosis and platelet activation, and increases the production of reactive oxygen species (ROS) in a concentration-dependent manner in isolated human erythrocytes. It increases thrombus weight in a rat model of surgically induced thrombosis when administered at a single dose of 50 mg/kg or at a dose of 10 mg/kg per day for four days.1.Bian, Y., Kim, K., An, G.-J., et al.Dapsone hydroxylamine, an active metabolite of dapsone, can promote the procoagulant activity of red blood cells and thrombosisToxicol. Sci.172(2)435-444(2019)2.Winter, H.R., Wang, Y., and Unadkat, J.D.CYP2C8/9 mediate dapsone N-hydroxylation at clinical concentrations of dapsoneDrug Metab. Dispos.28(8)865-868(2000)3.Veggi, L.M., Pretto, L., Ochoa, E.J., et al.Dapsone induces oxidative stress and impairs antioxidant defenses in rat liverLife Sci.83(5-6)155-163(2008)Cas No.32695-27-5 SDF Download SDF 别名:羟胺氨苯砜Canonical SMILES: O=S(C1=CC=C(C=C1)N)(C2=CC=C(NO)C=C2)=O分子式: C12H12N2O3S 分子量: 264.3溶解度: DMSO: soluble 储存条件: -20°C General tips: For obtaining a higher solubility , ple

[ROS小分子]N-formyl-2-Aminophenol

[ROS小分子]N-formyl-2-Aminophenol

作者:德尔塔生物 日期:2023-04-04

N-formyl-2-Aminophenol is a bacterial secondary metabolite that has been found in P. chrysogenum and has antioxidant activity.1,2 It scavenges DPPH radicals in a cell-free assay with an IC50 value of 3.23 µg/ml.2 N-formyl-2-Aminophenol has also been used in the synthesis of compounds with antibacterial and antifungal activities.31.Frisvad, J.C., Smedsgaard, J., Larsen, T.O., et al.Mycotoxins, drugs and other extrolites produced by species in Penicillium subgenus PenicilliumStud. Mycol.49201-241(2004)2.Deepali, A., Akansha, A., Anamika, B., et al.Hydroxylamine hydrochloride as an effective catalyst for form amide derivative synthesis and their DPPH scavenging activityRes. J. Chem. Sci.4(10)54-57(2014)3.Gupta, S., Verma, P., and Singh, V.Synthesis and antimicrobial study of 2-amino-imidazole derivativesIndian J. Chem. 57B679-686(2018)Cas No.2843-27-8Canonical SMILES: O=CNC1=C(O)C=CC=C1分子式: C7H7NO2 分子量: 137.1溶解度: DMF: 1 mg/mL,DMSO: 1 mg/mL,PBS (pH 7.2): 0.16 mg/mL 储存条件: -20°C General tips: For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. Shipping Condition Evaluation sample solution : ship with blue iceAll other available size: ship with RT , or blue ice upon request热门文章:活性氧(reactive oxygen species , ROS)Reactive Oxygen Species Assay Kit 活性氧(ROS)检测试剂盒活性氧(reactive oxygen species , ROS)与线粒体凋亡通路活性(reactive oxygen species , ROS)氧作用的靶标简单介绍活性氧(reactive oxygen species , ROS)的产生活性氧(reactive oxyg

[活性氧分子]N-acetyl-L-Cysteine amide

[活性氧分子]N-acetyl-L-Cysteine amide

作者:德尔塔生物 日期:2023-04-04

Cell linesPC12 cellsPreparation MethodPC12 cells were plated at a density of 25 × 103 cells/well in a 24-well collagen-coated plate for morphological assessment. The plate was divided into five groups in triplicate: (1) control: no glutamate, no N-acetyl-L-Cysteine amide (NACA); (2) Nerve growth factor (NGF) control: NGF (100 ng/ml), no glutamate, no NACA; (3) NACA only: NGF (100 ng/ml), no glutamate, NACA (750 µM); (4) glutamate only: NGF (100 ng/ml), glutamate (10 mM), no NACA; and (5) Glu + NACA: NGF (100 ng/ml), glutamate (10 mM), NACA (750 µM). All wells received 100 ng/ml NGF every other day, except Group I. After 1 week, cells were treated or not (control) with 10 mM glutamate, with or without NACA, for 24 h. Twenty-four hours later, the cells were fixed with 0.5% (v/v) glutaraldehyde in PBS and micropictures were taken.Reaction Conditions750 µM for 24 hApplicationsThe addition of N-acetyl-L-Cysteine amide protected the PC12 cells from glutamate toxicity by slightly decreasing the bleb formation on neurites.Animal experiment [2]:Animal modelsAdult male Sprague-Dawley ratsPreparation MethodIn order to access tissue sparing following Traumatic brain injury (TBI), rats were randomly divided into three groups: (I.) N-acetyl-L-Cysteine amide (NACA) loaded pump (18.5 mg/kg/hr) and a single 150 mg/kg bolus intraperitoneal (IP) injection of NACA given (30 min post-injury) (II.) N-acetylcysteine (NAC) (18.5 mg/kg/hr) loaded pump and a single 150 mg/kg bolus injection of NAC given IP (30 min post-injury) (III.) Vehicle loaded pump and single vehicle bolus injection given IP (3

[活性氧抑制剂]Berberine

[活性氧抑制剂]Berberine

作者:德尔塔生物 日期:2023-04-04

Cell lineshuman hepatoma cell lines (HepG2 cells)Preparation methodGeneral tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.Reacting condition0.5, 2.5, 5, 7.5, 10, 15 μg/ml, 24 hApplicationsBerberine as a new upregulator of liver LDLR (low-density lipoprotein receptor) expression. In HepG2 cells, the effect of berberine was also dose dependent. Northern blot showed a 50% increase in LDLR mRNA in cells treated with 2.5 μg/ml of berberine and a maximal increase of four fold of control was seen with a concentration of 15 μg/ml. The effect of BBR on LDLR was further confirmed in another human hepatoma cell line, Bel-7402. BBR at 2.5 μg/ml increased the LDLR mRNA in these cells by 2.3-fold.Animal experiment [2]:Animal modelsfemale golden hamstersDosage formorally twice a day at 50 mg/kg/d or 100 mg/kg/d for 10 d.ApplicationIn hamsters, treatment of these hyperlipidemic animals with berberine by oral administration for 10 d resulted in dose-dependent decreases in both serum total cholesterol and LDL-c. After the 10-d treatment, berberine at a dose of 50 mg/kg/d reduced LDL-c by 26%, and at a dose of 100 mg/kg/d, reduced LDL-c by 42% as compared to the control animals on the same HFHC (high-fat and high-cholesterol) diet. The berberine effect was also time dependent. LDLR mRNA and protein levels were elevated in all berberine -treated hamsters in a dose-dependent manner. A 3.5-fold increase in mRNA and a 2.6-fold increase in protein in

[活性氧物种]AZT triphosphate TEA

[活性氧物种]AZT triphosphate TEA

作者:德尔塔生物 日期:2023-04-04

Cas No.别名:3'-Azido-3'-deoxythymidine-5'-triphosphate TEACanonical SMILES: O=C(NC(C(C)=C1)=O)N1[C@H](O2)C[C@H](N=[N+]=[N-])[C@H]2COP(O)(OP(OP(O)(O)=O)(O)=O)=O.CCN(CC)CC.[x]分子式: C10H16N5O13P3.xC6H15N 分子量: 溶解度: 储存条件: Store at -20°C General tips: For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. Shipping Condition Evaluation sample solution : ship with blue iceAll other available size: ship with RT , or blue ice upon request热门文章:活性氧(reactive oxygen species , ROS)Reactive Oxygen Species Assay Kit 活性氧(ROS)检测试剂盒活性氧(reactive oxygen species , ROS)与线粒体凋亡通路活性(reactive oxygen species , ROS)氧作用的靶标简单介绍活性氧(reactive oxygen species , ROS)的产生活性氧(reactive oxygen species , ROS)简介活性氧分子 Cas号:25696-21-3 ACTH 1-14 Reactive Oxygen Species ROS活性氧小分子,蟾蜍灵Bufotalin,471-95-4/CAS:520-26-3,橙皮苷/己唑醇活性氧与活性硫荧光探针的设计、合成及生物成像应用的研究

[活性氧簇]Asiaticoside

[活性氧簇]Asiaticoside

作者:德尔塔生物 日期:2023-04-04

Cell experiment:Cells are seeded at a density of 2-9 × 104 cells/mL into 24-well plates for cell viability, 60-mm plates for RNA and protein analysis in DMEM containing 10% FBS (DMEM/10% FBS). After 24 h, medium is removed and cells are placed in serum-free DMEM. After 48 h, different concentrations of Asiaticoside in DMEM/10% FBS are added simultaneously to cells. Control cells are grown in DMEM/10% FBS without the addition of Asiaticoside. At different time points, the fibroblasts are harvested for analysis[1].Animal experiment:Rats[3]Sprague-Dawley rats are used to establish the Alzheimer's disease (AD) model. Asiaticoside is administered orally at 5, 15 or 45 mg/kg body weight per day for 7 days. The learning and memory function of the rats are evaluated by the MWM test 7 days after surgery. The swimming pool (180 cm in diameter) is maintained at 22-24°C, and divided into four quadrants with equal size. A hidden platform is placed in the center of one quadrant. Each of the cardinal points of these four quadrants is randomLy selected as the start location. On the pre-test day, rats are allowed to swim freely for 120 sec. During the test (days 1-4), each rat is subjected to 8 trials each day. The trial begins when a rat is placed in the pool, and ended when the rat finds the platform. The escape latency is recorded. If a rat fails to find the platform within 120 sec, the trial is terminated and the escape latency is recorded as 120 sec, and the rat is guided to the platform. On day 5, the swimming path is recorded by a video recording system, and the digital images are an

[ROS小分子]Acetylcysteine

[ROS小分子]Acetylcysteine

作者:德尔塔生物 日期:2023-04-04

Kinase experiment [1]:Preparation MethodPRP was preincubated at 37°C for 4 min with Acetylcysteine or with nitroglycerin, or first with Acetylcysteine and then nitroglycerin, and sodium nitroprusside, sodium azide, sodium nitrite, or S-nitroso-N-acetylcysteine for 1 min before addition of agonist.Reaction Conditions5.5 mM Acetylcysteine for 4 minApplicationsMillimolar concentrations of Acetylcysteine potentiated markedly the inhibitory effect of nitroglycerin on platelet aggregation induced by ADP, epinephrine, collagen, and arachidonate, decreasing the 50% inhibitory concentration (IC50) approximately 50-fold for each of these agents.Cell experiment [2]:Cell linesPC12 cell linePreparation MethodCells were treated with 100 ng/ml NGF or 60 mm Acetylcysteine in serum-containing medium for the indicated times.Reaction Conditions60 mm Acetylcysteine for 15min-4hApplicationsAcetylcysteine activates the Ras-ERK pathwayAnimal experiment [3]:Animal modelsThirty-five male Wistar ratsPreparation MethodGroup control underwent IIR without Acetylcysteine. In the other groups, Acetylcysteine was administered intraperitoneally with different regimens: 150 mg/kg before ischemia, 300 mg/kg before ischemia, and 150 mg/kg before ischemia plus 150 mg/kg 5 min before reperfusion.Dosage form150-300 mg/kg Acetylcysteine(Intraperitoneal administration)ApplicationsAcetylcysteine exerts a significant protective role in liver injury following IIR, which seems to be independent of an intestinal protective effect. Additional administration of Acetylcysteine before reperfusion was of no furthe

[活性氧分子](E/Z)-GSK5182

[活性氧分子](E/Z)-GSK5182

作者:德尔塔生物 日期:2023-04-04

Cas No.Canonical SMILES: OCCC/C(C1=CC=CC=C1)=C(C2=CC=C(C=C2)OCCN(C)C)\C3=CC=C(C=C3)O分子式: C27H31NO3 分子量: 417.54溶解度: DMSO: 100 mg/mL (239.50 mM); Water: < 0.1 mg/mL (insoluble) 储存条件: Store at -20°C General tips: For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. Shipping Condition Evaluation sample solution : ship with blue iceAll other available size: ship with RT , or blue ice upon request热门文章:活性氧(reactive oxygen species , ROS)Reactive Oxygen Species Assay Kit 活性氧(ROS)检测试剂盒活性氧(reactive oxygen species , ROS)与线粒体凋亡通路活性(reactive oxygen species , ROS)氧作用的靶标简单介绍活性氧(reactive oxygen species , ROS)的产生活性氧(reactive oxygen species , ROS)简介活性氧分子 Cas号:25696-21-3 ACTH 1-14 Reactive Oxygen Species ROS活性氧小分子,蟾蜍灵Bufotalin,471-95-4/CAS:520-26-3,橙皮苷/己唑醇活性氧与活性硫荧光探针的设计、合成及生物成像应用的研究

[Reactive Oxygen Species](-)-Epigallocatechin gallate (EGCG)

[Reactive Oxygen Species](-)-Epigallocatechin gallate (EGCG)

作者:德尔塔生物 日期:2023-04-04

Cell linesHuman and rat neural progenitor cells (NPCs)Preparation methodThe solubility of this compound in DMSO is >10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.Reaction Conditions0, 1, 2, 5 and 10 μM; 24 or 48 hrsApplications(-)-Epigallocatechin Gallate (EGCG) altered human and rat NPC development in vitro. EGCG affected migration distance, migration pattern and nuclear density of NPCs growing as neurospheres. EGCG exerted these functional impairments by binding to the extracellular matrix (ECM) glycoprotein laminin, preventing its binding to β1-integrin subunits, thereby prohibiting cell adhesion and resulting in altered glia alignment and decreased number of migrating young neurons.Animal experiment [2]:Animal modelsA rat model of partial bladder outlet obstruction (pBOO)-induced bladder injuryDosage form4.5 mg/kg/day; i.p.; 2 days or 30 daysApplicationsEGCG attenuated bladder inflammation caused by pBOO at the 48th hr. At the 30th day, EGCG attenuated endoplasmic reticulum (ER) stress-related apoptosis. In addition, EGCG improved bladder compliance, contractile frequency and inflammation at the 30th day.Other notesPlease test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.热门文章:活性氧(reactive oxygen species , ROS)Reactive Oxygen Species Assay Kit 活性氧(ROS)检测试剂盒活

CAS:2244-11-3|Alloxan (hydrate)

CAS:2244-11-3|Alloxan (hydrate)

作者:德尔塔生物 日期:2023-04-04

Cas No.2244-11-3别名:阿脲 一水合物Canonical SMILES: O=C(C(C(N1)=O)=O)NC1=O.O分子式: C4H2N2O4.H2O 分子量: 160.1溶解度: DMF: 5 mg/ml,DMSO: 5 mg/ml,PBS (pH 7.2): 10 mg/ml 储存条件: Store at -20°C General tips: For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. Shipping Condition Evaluation sample solution : ship with blue iceAll other available size: ship with RT , or blue ice upon request热门文章:活性氧(reactive oxygen species , ROS)Reactive Oxygen Species Assay Kit 活性氧(ROS)检测试剂盒活性氧(reactive oxygen species , ROS)与线粒体凋亡通路活性(reactive oxygen species , ROS)氧作用的靶标简单介绍活性氧(reactive oxygen species , ROS)的产生活性氧(reactive oxygen species , ROS)简介活性氧分子 Cas号:25696-21-3 ACTH 1-14 Reactive Oxygen Species ROS活性氧小分子,蟾蜍灵Bufotalin,471-95-4/CAS:520-26-3,橙皮苷/己唑醇活性氧与活性硫荧光探针的设计、合成及生物成像应用的研究

CAS:39011-90-0|Alibiflorin

CAS:39011-90-0|Alibiflorin

作者:德尔塔生物 日期:2023-04-04

Cas No.39011-90-0别名:芍药内酯苷化学名:((1R,3R,4R,6S,9S)-4-hydroxy-6-methyl-8-oxo-1-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-7-oxatricyclo[4.3.0.03,9]nonan-9-yl)methyl benzoateCanonical SMILES: O=C1O[C@](C2([H])[H])(C([H])([H])[H])[C@@]3([C@@]1(C([H])([H])OC(C4=C([H])C([H])=C([H])C([H])=C4[H])=O)[C@@]([C@]2([H])O[H])([H])C3([H])[H])O[C@]([C@]([C@@]5([H])O[H])([H])O[H])([H])O[C@@](C([H])([H])O[H])([H])[C@@]5([H])O[H]分子式: C23H28O11 分子量: 480.46溶解度: ≥ 48mg/mL in DMSO 储存条件: General tips: For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. Shipping Condition Evaluation sample solution : ship with blue iceAll other available size: ship with RT , or blue ice upon request热门文章:活性氧(reactive oxygen species , ROS)Reactive Oxygen Species Assay Kit 活性氧(ROS)检测试剂盒活性氧(reactive oxygen species , ROS)与线粒体凋亡通路活性(reactive oxygen species , ROS)氧作用的靶标简单介绍活性氧(reactive oxygen species , ROS)的产生活性氧(reactive oxygen species , ROS)简介活性氧分子 Cas号:25696-21-3 ACTH 1-14 Reactive Oxygen Species ROS活性氧小分子,蟾蜍灵Bufotalin,471-95-4/CAS:520-26-3,橙皮苷/己唑醇活性氧与活性硫荧光探针的设计、合成及生物成像应用的研究