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59

抑制剂 & 化合物

4

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T5036	cangrelor tetrasodium	GPR; P2Y Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Cangrelor tetrasodium 是三磷酸腺苷类似物，是可逆的选择性血小板P2Y12拮抗剂，也是非特异性的GPR17拮抗剂。它直接阻断腺苷二磷酸诱导的血小板活化和聚集，具有迅速有效的抗血小板作用。
T19332	Gadopentetic acid gadolinium complex,钆喷酸,Gd-DTPA	Others	Others
	Gadopentetic acid (gadolinium complex) 是一种顺磁性造影剂，通常通过静脉内注射 (i.v.) 的方式用于 DCE-MRI 研究。
T8316	1V209 TLR7 agonist T7	TLR	Immunology/Inflammation
	1V209 (TLR7 agonist T7) 是一种 Toll 样受体 7 (TLR7) 激动剂，可与各种多糖缀合，以改善其水溶性，增强功效并保持低毒性，具有抗肿瘤作用。
T6322	Copanlisib BAY 80-6946,可泮利塞,库潘尼西	Apoptosis; PI3K	Apoptosis; PI3K/Akt/mTOR signaling
	Copanlisib (BAY 80-6946) 是一种选择性的和 ATP 竞争性的泛 I 类PI3K 抑制剂，具有抗肿瘤活性，对PI3Kα，PI3Kδ，PI3Kβ和PI3Kγ的IC50分别为 0.5 nM、0.7 nM、3.7 nM 和 6.4 nM。
T8132	Iron sucrose Iron saccharate,蔗糖铁,Sucroferric oxyhydroxide	Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB
	Iron sucrose (Sucroferric oxyhydroxide) 是一种静脉注射铁制剂，也是一种促氧化剂，可用于研究缺铁性贫血。
T14998	Copanlisib dihydrochloride 库潘尼西盐酸,BAY 80-6946 dihydrochloride	Apoptosis; PI3K; mTOR	Apoptosis; PI3K/Akt/mTOR signaling
	Copanlisib dihydrochloride (BAY 80-6946 dihydrochloride) 是一种选择性和 ATP 竞争性的泛 I 类 PI3K 抑制剂。它具有优越的抗肿瘤活性，对除 mTOR 以外的其他脂质和蛋白激酶的选择性也超过 2,000 倍。
T61354	Fosphenytoin	Others	Others
	Fosphenytoin 是一种磷酸酯前药，可替代静脉注射苯妥英，用于急性干预癫痫发作。Fosphenytoin 在肠胃外给药可水解成具有抗惊厥作用的苯妥英。Fosphenytoin 可用于多种给药方式，如静脉注射和腹腔注射。
T3557	GAL-021 GAL 021	Potassium Channel	Membrane transporter/Ion channel
	GAL-021新型静脉内BKCa-channel 阻滞剂。
T5467	SAR125844 SAR125884	Apoptosis; c-Met/HGFR	Apoptosis; Tyrosine Kinase/Adaptors
	SAR125844 是高度选择性可逆ATP 竞争性的MET 受体酪氨酸激酶抑制剂，其IC50值为4.2 nM。能抑制细胞中MET 的自磷酸化。
T34146	Propanidid FBA 1420,Epontol,Sombrevin,Fabontal,Fabantol	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Propanidid (Sombrevin) 是一种 γ-氨基丁酸 A 型受体 (GABAA) 激动剂，也是一种可快速发挥作用的静脉注射麻醉剂,可以降低动脉血压。
T0271	Iodipamide Iodipamic acid,胆影酸,Adipiodone	Others	Others
	Iodipamide (Iodipamic acid) 是一种三碘苯甲酸酯衍生物，也是一种离子二聚剂，可用于诊断成像。
T0344	Miconazole R18134,咪康唑	Potassium Channel; NOS; Antibacterial; Antibiotic; Antifection; Antifungal	Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology
	Miconazole (R18134) 是一种具有抗菌作用的咪唑类抗真菌剂。
T1459	Cisatracurium besylate 顺苯磺酸阿曲库铵,顺苯磺阿曲库铵,51W89	Adrenergic Receptor; AChR; Autophagy	Autophagy; GPCR/G Protein; Neuroscience
	Cisatracurium besylate (51W89) 是一种用于静脉内给药的非去极化骨骼肌松弛剂。
T36506	Tempone 4-Oxo-tempo
	Tempone 是一种氨基氧烷，具有自由基清除剂的作用，会与活性氧（ROS）发生反应。静脉注射 Tempone 可降低自发性高血压大鼠的平均动脉。
T4506	Gadopentetate dimeglumine Meglumine gadopentetate,SH-L-451A,Gd-DTPA,Gadopentetic acid dimeglumine,钆喷酸葡胺,Gadopentetic acid dimeglumine salt	Others	Others
	Gadopentetate dimeglumine (Gd-DTPA) 可用于核磁共振成像 (MRI) 中，使血管、器官和其他非骨组织能够更清晰地被看到。
T1790	Fosaprepitant dimeglumine 福沙匹坦二甲葡胺,L785298,福沙吡坦二甲葡胺,MK-0517,Fosaprepitant dimeglumine salt	Neurokinin receptor	GPCR/G Protein; Neuroscience
	Fosaprepitant dimeglumine (MK-0517) 是 Aprepitant 的前药。它是一种神经激肽 1 受体拮抗剂，可用于预防化疗引起的恶心呕吐。
T28466	PSMA-11 HBED-CC-PSMA,Psma-hbed-CC,PSMA11
	PSMA-11 (HBED-CC-PSMA)通过与前列腺特异性膜抗原(PSMA)的细胞外结构域结合来检测前列腺癌的复发和转移。PSMA-11常被用作正电子发射断层扫描(PET)中用作表达PSMA 的肿瘤的示踪剂，通过静脉注射镓Ga 68标记的PSMA-11，Glu-urea-Lys(Ahx)分子靶向并结合表达PSMA 的肿瘤细胞。内化后，PSMA 表达的肿瘤细胞可在PET 成像中被检测到。
T4996	Atosiban 阿托西班,RWJ22164,RW22164	Oxytocin Receptor; Vasopressin Receptor	Endocrinology/Hormones; GPCR/G Protein
	Atosiban (RW22164) 是一种脱氨基催产素类似物，是一种九肽，也是竞争性的催产素受体拮抗剂。它是一种宫缩抑制剂，可用于自发早产的研究。
T5148	Atosiban acetate RW22164,Atosiban acetate (90779-69-4 free base),RWJ22164,醋酸阿托西班	Oxytocin Receptor; Vasopressin Receptor	Endocrinology/Hormones; GPCR/G Protein
	Atosiban acetate (RW22164) 是一种脱氨基催产素类似物，是一种九肽，也是竞争性的催产素受体拮抗剂。它是一种宫缩抑制剂，可用于自发早产的研究。
T31759	Felbinac Trometamol L141,Felbinac,L-141,L 141
	Felbinac Trometamol is an intravenous preparation used to treat severe postoperative pain.
T33322	Methiodal sodium Abrodan,Abrodil,Diagnorenol,Conturex,Iodomethanesulfonic acid sodium salt,Abroden
	Methiodal sodium is a crystalline salt used as a radiopaque contrast medium in intravenous urography.
T35064	Viquidacin NXL101,NXL-101,NXL 101
	Viquidacin ( NXL-101) is an oral/intravenous antibiotic that targets Gram-positive bacteria such as MRSA. In 2008, Novexel announced it had discontinued the development of Viquidacin (NXL 101).
T28378	PF-0713 PF 0713,PF713
	PF 0713, a GABAA receptor agonist, is used as an intravenous sedative-hypnotic for general anaesthesia, ICU sedation, procedural sedation, chemotherapy.
T26230	Stilbamidine dihydrochloride NSC 35605,NCI 174
	Stilbamidine dihydrochloride is a blocker of neuromuscular transmission and axonal conduction used to study the distribution of the drug in the organs and tissues of rats following intravenous injection.
T24517	Nafiverine UNII-WLT400RC9Q,Nafiverina,Nafiverinum,EINECS 225-766-5
	Nafiverine is a new antispasmodic. The effectiveness of an intramuscular administration of nafiverine was comparable to that of an intravenous administration.
T39603	Mn(II) protoporphyrin IX
	Mn(II) protoporphyrin IX is a potent intravenous paramagnetic magnetic resonance contrast agent, known for its strong paramagnetic properties.
T27540	Hexoprenaline Sulfate ST-1512,Argocian,Gynipral
	Hexoprenaline Sulfate is a selective beta2-adrenoreceptor agonist. Hexoprenaline Sulfate is active in man as a bronchodilator by the oral or intravenous routes and by inhalation. Hexoprenaline Sulfate is indicated for use in the treatment of bronchospasm
T25380	Epipropidine Lilly28002,Epoxypropidine,Eponate,Lilly 28002,Lilly-28002
	Epipropidine 是环氧化物，它是一种烷基化剂，具有抗肿瘤活性，小鼠静脉注射LD50：74mg/kg。由于其不稳定的性质而未在临床上使用。
T61232	(Rac)-Upacicalcet
	(Rac)-Upacicalcet is a racemate of Upacicalcet, which serves as an intravenous calcimimetic agent. Upacicalcet acts by directly targeting calcium-sensing receptors on parathyroid cell membranes, effectively suppressing the release of excessive parathyroid hormone (PTH) and reducing blood PTH levels. This compound holds the potential for researching secondary hyperparathyroidism (SHPT) [1].
T35865	Telmisartan Acyl-β-D-Glucuronide
	Telmisartan acyl-β-D-glucuronide is a major metabolite of the angiotensin II receptor antagonist telmisartan . It does not bind human serum albumin and is cleared from rat plasma with a clearance rate of 180 ml/min/kg following intravenous administration.
T39444	Upacicalcet sodium
	Upacicalcet (sodium) is an intravenous calcimimetic agent that acts directly on parathyroid cell membrane calcium-sensing receptors to suppress excessive parathyroid hormone (PTH) secretion, thereby lowering blood PTH levels. It is indicated for the research of secondary hyperparathyroidism (SHPT).
T29213	Zelandopam free base YM-435,YM435,MYD-37,MYD37,Zelandopam
	Zelandopam is a dopamine D1 agonist. Zelandopam is a potent stimulant of pancreatic exocrine secretion by acting on DA D1 receptors of the pancreas in dogs. Intravenous administration of Zelandopam produces renal vasodilating and diuretic/natriuretic effe
T37027	MHAPC-Chol
	MHAPC-Chol is a cationic cholesterol. MHAPC-Chol, as part of a lipoplex with DOPE , has been used for siRNA delivery and gene silencing in MCF-7 cells in a luciferase assay without affecting cell viability. It has also been used to deliver siRNA into mice via intravenous injection, resulting in MHAPC-chol accumulation in the liver.
T37017	OH-C-Chol
	OH-C-Chol is a cationic cholesterol derivative. OH-C-Chol, as a component of lipoplexes with DOPE , has been used for siRNA delivery and gene silencing in MCF-7 cells as well as in mice via intravenous injection, resulting in lipoplex accumulation in the liver.
T72669	Loxoprofenol-SRS
	Loxoprofenol-SRS 是 Loxoprofen 活性代谢物，是可静脉注射的非甾醇抗炎药。Loxoprofenol-SRS 具有很好的抗炎和缓解疼痛活性。
T37035	HAPC-Chol
	HAPC-Chol is a cationic cholesterol. HAPC-Chol, as part of a lipoplex with DOPE , has been used for siRNA delivery and gene silencing in MCF-7 cells in a luciferase assay without affecting cell viability. It has also been used to deliver siRNA into mice via intravenous injection, resulting in HAPC-chol accumulation in the lungs.
T72146	Loxoprofenol-SRS tromethamine HR1405–01
	Loxoprofenol-SRS tromethamine (HR1405-01) 为Loxoprofen的活性代谢物，为一种可静脉注射的安全非甾体抗炎药(NSAID)，展现出良好的抗炎及镇痛效果。
T12337	Oxaquin DNV3837,MCB-3837	Others	Others
	Oxaquin 是一种有效的，具有水溶性的、可注射的前药,在体内通过静脉给药后迅速转化为活性物质MCB3681。Oxaquin 对革兰氏阳性细菌有活性，但本身没有抗菌作用。
T33785	o-Iodohippurate sodium Hippodin,NSC-63351,Sodium iodohippurate NSC 63351,NSC63351
	o-Iodohippurate sodium is an analogue of p-aminohippuric acid used to determine effective renal plasma flow. Labelled OIH has a higher clearance than other radiopharmaceutical yet developed and is extremely suitable for renography. It is eliminated mainly
T35857	Actinopyrone A
	Actinopyrone A is a pyrone isolated from S. pactum with diverse biological activities. It has selective and potent antimicrobial activity against H. pylori (MIC = 0.1 ng/mL) with no activity against other Gram-negative bacteria including E. coli, K. pneumoniae, P. aeruginosa, and B. fragilis. Actinopyrone A also mildly inhibits growth of Gram-positive bacteria and dermatophytes with MIC values ranging from <6.25 to 25 μg/mL. Intravenous administration of actinopyrone A (30 μg/kg) increases coron...
T70335	Cangrelor free acid
	Cangrelor is a P2Y12 inhibitor, and was approved in June 2015 as an antiplatelet drug for intravenous application. Cangrelor is a high-affinity, reversible inhibitor of P2Y12 receptors that causes almost complete inhibition of ADP-induced platelet aggregate. It is a modified ATP derivative stable to enzymatic degradation. It does not require metabolic conversion to an active metabolite. This allows cangrelor’s immediate effect after infusion, and the therapeutic effects can be maintained with...
T37433	Erythromycin lactobionate
	Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 50S ribosomal subunit, blocking the progression of nascent polypeptide chains.[1] It is effective against a host of bacterial genera, including Streptococcus, Staphylococcus, and Haemophilus (MIC90s range from 0.015-2.0 mg/l).[2] Erythromycin is known to potently inhibit the cytochrome P450 isoform CYP3A4, which can affect the metabolism of numerous clinically relevant medications.[3],[4] Erythromyc...
T35867	TRAP-6 Peptide (trifluoroacetate salt)
	TRAP-6 peptide is a hexapeptide corresponding to residues 42-47 of protease-activated receptor 1 (PAR1). It acts as an agonist of PAR1, inducing platelet aggregation in human platelet-rich plasma ex vivo (EC50 = 0.8 μM). TRAP-6 (0.3 and 0.6 mg/kg) has a triphasic effect on mean arterial blood pressure (MAP) in anesthetized rats with a short decrease, an increase, and then a longer decrease in MAP following intravenous administration.
T38319	93-O17O 93-O17O
	93-O17O is a chalcogen-containing cationic lipidoid.1,2It has been used in the generation of lipid nanoparticles (LPNs). LPNs containing 93-O17O localize to the spleen after intravenous injection into mice.1LPNs containing 93-O17O have been used for the delivery of Cre recombinase and ribonucleoproteins for genome editing in mice and for the intratumoral delivery of cGAMP to enhance cross-presentation of tumor antigens.3,2 1.Zhao, X., Chen, J., Qiu, M., et al.Imidazole-based synthetic lipidoids ...
T69119	Disopyramide HCl
	Disopyramide HCl is the salt form of Disopyramide, an antiarrhythmic medication used in the treatment of ventricular tachycardia. It is a sodium channel blocker and therefore classified as a Class 1a anti-arrhythmic agent. Disopyramide has a negative inotropic effect on the ventricular myocardium, significantly decreasing the contractility. Disopyramide also has an anticholinergic effect on the heart which accounts for many adverse side effects. Disopyramide is available in both oral and intrave...
T38152	Gilvocarcin M
	Gilvocarcin M is an antibiotic originally isolated from S. gilvotanareus. It is active against S. aureus when used at a concentration of 32 μg/ml. Gilvocarcin M inhibits growth of KB cells (IC50 = 0.52 μg/ml) but has no effect on survival in a P388 mouse model of leukemia when used at doses ranging from 25 to 400 mg/kg. Gilvocarcin M intercalates into bacteriophage PM2 DNA. It is toxic to rats with an intravenous LD50 value of 450 mg/kg.
T37018	OH-Chol
	OH-Chol is a cationic cholesterol derivative.1 OH-Chol, as a component of lipoplexes with DOPE , has been used for siRNA delivery and gene silencing in MCF-7 cells, as well as in mice via intravenous injection, resulting in lipoplex accumulation in the liver. It has also been used in cationic nanoparticles in combination with Tween 80 to transfect pDNA and siRNA into PC3 mouse xenografts via intratumoral injection and with Tween 80 and folate-PEG2000-DSPE in a KB mouse xenograft model for intrat...
T71251	DS-1558
	DS-1558 is a potent and orally available GPR40 agonist.DS-1558 was found to have potent glucose lowering effects during an oral glucose tolerance test in ZDF rats. DS-1558 significantly and dose-dependently improved hyperglycemia and increased insulin secretion during the oral glucose tolerance test in Zucker fatty rats, the model of insulin resistance and glucose intolerance. DS-1558 not only increased the glucose-stimulated insulin secretion by GLP-1 but also potentiated the maximum insulinog...
T69589	PX-316
	PX-316 is a AKT inhibior. PX-316, when administered intraperitoneally to mice at 150 mg/kg, inhibits Akt activation in HT-29 human tumor xenografts up to 78% at 10 h with recovery to 34% at 48 h. PX-316 has antitumor activity against early human MCF-7 breast cancer and HT-29 colon cancer xenografts in mice. PX-316 formulated in 20% hydroxypropyl-beta-cyclodextrin for intravenous administration is well tolerated in mice and rats with no hemolysis and no hematological toxicity. Thus, PX-316 is the...
T36759	SAR 216471 hydrochloride
	Potent P2Y12 antagonist (IC50 = 17 nM). Displays antiplatelet and antithrombotic activity in vivo. Orally available. Boldron et al (2014) N-[6-(4-butanoyl-5-methyl-1H-pyrazol-1-yl)pyridazin-3-yl]-5-chloro-1-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-1H-indole-3-carboxamide (SAR216471), a novel intravenous and oral, reversible, and directly acting P2Y12 antagonist. J.Med.Chem. 57 7293 PMID:25075638

化合物

cangrelor tetrasodium

Cat.No: T5036

Target: GPR, P2Y Receptor

Gadopentetic acid

Cat.No: T19332

Synonym: gadolinium complex,钆喷酸,Gd-DTPA

Target: Others

Cat.No: T8316

Synonym: TLR7 agonist T7

Target: TLR

Cat.No: T6322

Synonym: BAY 80-6946,可泮利塞,库潘尼西

Target: Apoptosis, PI3K

Cat.No: T8132

Synonym: Iron saccharate,蔗糖铁,Sucroferric oxyhydroxide

Target: Reactive Oxygen Species

Copanlisib dihydrochloride

Cat.No: T14998

Synonym: 库潘尼西盐酸,BAY 80-6946 dihydrochloride

Target: Apoptosis, PI3K, mTOR

Cat.No: T61354

Target: Others

Cat.No: T3557

Synonym: GAL 021

Target: Potassium Channel

Cat.No: T5467

Synonym: SAR125884

Target: Apoptosis, c-Met/HGFR

Cat.No: T34146

Synonym: FBA 1420,Epontol,Sombrevin,Fabontal,Fabantol

Target: GABA Receptor

Cat.No: T0271

Synonym: Iodipamic acid,胆影酸,Adipiodone

Target: Others

Cat.No: T0344

Synonym: R18134,咪康唑

Target: Potassium Channel, NOS, Antibacterial, Antibiotic, Antifection, Antifungal

Cisatracurium besylate

Cat.No: T1459

Synonym: 顺苯磺酸阿曲库铵,顺苯磺阿曲库铵,51W89

Target: Adrenergic Receptor, AChR, Autophagy

Cat.No: T36506

Synonym: 4-Oxo-tempo

Gadopentetate dimeglumine

Cat.No: T4506

Synonym: Meglumine gadopentetate,SH-L-451A,Gd-DTPA,Gadopentetic acid dimeglumine,钆喷酸葡胺,Gadopentetic acid dimeglumine salt

Target: Others

Fosaprepitant dimeglumine

Cat.No: T1790

Synonym: 福沙匹坦二甲葡胺,L785298,福沙吡坦二甲葡胺,MK-0517,Fosaprepitant dimeglumine salt

Target: Neurokinin receptor

Cat.No: T28466

Synonym: HBED-CC-PSMA,Psma-hbed-CC,PSMA11

Cat.No: T4996

Synonym: 阿托西班,RWJ22164,RW22164

Target: Oxytocin Receptor, Vasopressin Receptor

Atosiban acetate

Cat.No: T5148

Synonym: RW22164,Atosiban acetate (90779-69-4 free base),RWJ22164,醋酸阿托西班

Target: Oxytocin Receptor, Vasopressin Receptor

Felbinac Trometamol

Cat.No: T31759

Synonym: L141,Felbinac,L-141,L 141

Methiodal sodium

Cat.No: T33322

Synonym: Abrodan,Abrodil,Diagnorenol,Conturex,Iodomethanesulfonic acid sodium salt,Abroden

Cat.No: T35064

Synonym: NXL101,NXL-101,NXL 101

Cat.No: T28378

Synonym: PF 0713,PF713

Stilbamidine dihydrochloride

Cat.No: T26230

Synonym: NSC 35605,NCI 174

Cat.No: T24517

Synonym: UNII-WLT400RC9Q,Nafiverina,Nafiverinum,EINECS 225-766-5

Mn(II) protoporphyrin IX

Cat.No: T39603

Hexoprenaline Sulfate

Cat.No: T27540

Synonym: ST-1512,Argocian,Gynipral

Cat.No: T25380

Synonym: Lilly28002,Epoxypropidine,Eponate,Lilly 28002,Lilly-28002

(Rac)-Upacicalcet

Cat.No: T61232

Telmisartan Acyl-β-D-Glucuronide

Cat.No: T35865

Upacicalcet sodium

Cat.No: T39444

Zelandopam free base

Cat.No: T29213

Synonym: YM-435,YM435,MYD-37,MYD37,Zelandopam

Cat.No: T37027

Cat.No: T37017

Loxoprofenol-SRS

Cat.No: T72669

Cat.No: T37035

Loxoprofenol-SRS tromethamine

Cat.No: T72146

Synonym: HR1405–01

Cat.No: T12337

Synonym: DNV3837,MCB-3837

Target: Others

o-Iodohippurate sodium

Cat.No: T33785

Synonym: Hippodin,NSC-63351,Sodium iodohippurate NSC 63351,NSC63351

Cat.No: T35857

Cangrelor free acid

Cat.No: T70335

Erythromycin lactobionate

Cat.No: T37433

TRAP-6 Peptide (trifluoroacetate salt)

Cat.No: T35867

Cat.No: T38319

Synonym: 93-O17O

Disopyramide HCl

Cat.No: T69119

Cat.No: T38152

Cat.No: T37018

Cat.No: T71251

Cat.No: T69589

SAR 216471 hydrochloride

Cat.No: T36759

Cat. No.	Product Name	Target	Signaling Pathways
T1670	Lanatoside C Cedilanid,Ceglunate,Isolanid,毛花甙丙,毛花苷C	ATPase; Virus Protease; Autophagy	Autophagy; Membrane transporter/Ion channel; Microbiology/Virology
	Lanatoside C (Ceglunate) 是一种可用于治疗充血性心力衰竭和心律失常的强心苷类药物。它作用于 HuH-7细胞，可抗登革病毒感染， IC50为0.19 μM。
TCS1704	Artemitin 艾黄素,Artemetin,Artemisetin,Erianthin	Antioxidant	oxidation-reduction
	Artemitin (Erianthin) 是一种存在于翼齿六棱菊中的天然黄酮，具有抗氧化、抗炎、抗病毒活性。
T3S2259	Methyl eugenol 4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Methyl eugenol (4-allylveratrole) 是一种苯丙类化合物，存在于植物叶子、果实、根茎中，当植物相应的部位因食草动物进食而受损时，就会释放。它可用于消灭雄性东方果蝇。
TL0018	Lobelin	AChR; Antifection	Microbiology/Virology; Neuroscience
	Inhalation challenge with capsaicin and rapid intravenous injection of Lobelin and alinamin indicated that peripheral c-fiber receptors were involved in the induction of coughing.

天然产物

Cat.No: T1670

Synonym: Cedilanid,Ceglunate,Isolanid,毛花甙丙,毛花苷C

Target: ATPase, Virus Protease, Autophagy

Cat.No: TCS1704

Synonym: 艾黄素,Artemetin,Artemisetin,Erianthin

Target: Antioxidant

Cat.No: T3S2259

Synonym: 4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚

Target: GABA Receptor

Cat.No: TL0018

Target: AChR, Antifection

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