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T1139LLevosalbutamol Hydrochloride化合物 T1139LR-albuterol|||R albuterol|||Xopenex|||(R)-albuterol
Levosalbutamol Hydrochloride is a β2-adrenergic receptor agonist. It is used to treat asthma and chronic obstructive pulmonary disease.
价 格:¥电议型 号:T1139L产 地:中国大陆
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T11393GET73;化合物GET73Gamma hydroxybutyric acid analogue|||GET 73;Gamma hydroxybutyric acid analogue|||GET 7
GET73 (Gamma hydroxybutyric acid analogue) is an negative allosteric modulator of mGluR5. GET73 is a naturally occurring neurotransmitter. GET73 has anti-alcohol and anxiolytic properties.
价 格:¥电议型 号:T11393产 地:中国大陆
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T11386Gemcabene calcium化合物 T11386PD-72953 calcium
Gemcabene calcium , a first-in-class lipid-lowering agent, lowers low-density lipoprotein cholesterol (LDL-C), decreases triglycerides, and raises high-density lipoprotein cholesterol (HDL-C) andexerting anti-inflammatory activity, lowers pro-inflammatory acute-phase protein, C-reactive protein (CRP).
价 格:¥电议型 号:T11386产 地:中国大陆
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T1138Taurocholic acid sodium salt hydrate;牛磺胆酸钠水合物Sodium taurocholate hydrate|||Taurocholic Acid sodium h
Taurocholic acid sodium salt hydrate (Sodium taurocholate hydrate) is the product of conjugation of taurine with cholic acid. The sodium salt, the main ingredient of the bile of carnivorous animals, is used as a detergent to solubilize fats for absorption. It is used as a cholagogue and cholerectic.
价 格:¥电议型 号:T1138产 地:中国大陆
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T11353LGallopamil hydrochloride;化合物Gallopamil hydrochlorideMethoxyverapamil hydrochloride;Methoxyverapamil
Gallopamil hydrochloride (Methoxyverapamil hydrochloride) is an antagonist of phenylalkylamine calcium. Gallopamil hydrochloride can be used in antiarrhythmic and vasodilator studies.
价 格:¥电议型 号:T11353L产 地:中国大陆
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T11353Gallopamil;戈洛帕米Methoxyverapamil;Methoxyverapamil|||戈洛帕米
Gallopamil (Methoxyverapamil) inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM. Gallopamil is a potent antiarrhythmic and vasodilator agent. Gallopamil (Methoxyverapamil), a methoxy derivative of Verapamil, is a phenylalkylamine calcium antagonist.
价 格:¥电议型 号:T11353产 地:中国大陆
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T11352Galidesivir triphosphate;化合物 T11352BCX4430-triphosphate|||Immucillin-A triphosphate|||BCX6870;BCX443
Galidesivir triphosphate is a substrate for viral RNA-dependent RNA polymerase (RDRP), resulting in termination of viral RNA replication and thus serves as an antiviral. Galidesivir triphosphate inhibits HCV NS5B RNA polymerase activity and protects mice against Ebola. Galidesivir triphosphate (Immucillin-A triphosphate) is converted by the prodrug Galidesivir.
价 格:¥电议型 号:T11352产 地:中国大陆
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T11351Galanthamine N-Oxide;加兰他明 N-氧化物Galanthamine N-Oxide
Galanthamine N-Oxide, an alkaloid extracted from Zephyranthes concolor bulbs, effectively inhibits acetylcholinesterase (AChE) from electric eel with an EC50 of 26.2 μM. It acts as a significant inhibitor of substrate accommodation within the active sites of Torpedo californica AChE (TcAChE), human AChE (hAChE), and human BChE (hBChE) enzymes.
价 格:¥电议型 号:T11351产 地:中国大陆
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T1135Vitamin D3;维生素D3Cholecalciferol|||Colecalciferol;维生素D3|||Cholecalciferol|||Colecalciferol
Vitamin D3 (Cholecalciferol) , a naturally occurring form of vitamin D, activates an H305F/H397Y mutant vitamin D receptor (VDR).
价 格:¥电议型 号:T1135产 地:中国大陆
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T11336Fumarate hydratase-IN-2 sodium salt化合物 T11336Fumarate hydrataseIN2 sodium salt|||Fumarate hydratase
Fumarate hydratase-IN-2 sodium salt (compound 3) is a cell-permeable and competitive fumarate hydratase inhibitor ( K i =4.5 μM). Fumarate hydratase-IN-2 sodium salt has nutrient-dependent cytotoxicity [1].
价 格:¥电议型 号:T11336产 地:中国大陆
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T11315Fosmidomycin sodium salt膦胺霉素钠盐FR-31564 sodium salt
Fosmidomycin sodium salt (FR-31564 sodium salt) is an anti-infective antibiotic with anti-malarial activity that inhibits both Gram-negative and Gram-positive bacteria.
价 格:¥电议型 号:T11315产 地:中国大陆
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T11265Faropenem daloxate;法罗培南酯Faropenem medoxil;法罗培南酯|||Faropenem medoxil
Faropenem daloxate (Faropenem medoxil) is useful for penem and antibiotics. Faropenem medoxomil has excellent in vitro activity against Streptococcus pneumoniae, Haemophilus influenzae and other key pathogens implicated in acute bacterial rhinosinusitis.Faropenem daloxate is the first oral penem in a new class of beta-lactam antibiotics.
价 格:¥电议型 号:T11265产 地:中国大陆
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T11262Falintolol, (Z)-;化合物 T11262Falintolol, (Z)-
Falintolol, (Z)-, is a novel β-adrenergic antagonist compound distinguished by the inclusion of an oxime moiety.
价 格:¥电议型 号:T11262产 地:中国大陆
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T1126Penicillin V Potassium;青霉素V钾Penicillin V potassium salt|||Phenoxymethylpenicillin potassium salt;青霉素
Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) is a broad-spectrum penicillin antibiotic used orally in the treatment of mild to moderate infections by susceptible gram-positive organisms.
价 格:¥电议型 号:T1126产 地:中国大陆
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T11256FAAH inhibitor 1;化合物FAAH inhibitor 1Benzothiazole analog 3;Benzothiazole analog 3
FAAH inhibitor 1 (Benzothiazole analog 3) is an effective FAAH inhibitor with an IC50 of 18 nM.
价 格:¥电议型 号:T11256产 地:中国大陆
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T1125Shikonin;紫草素NSC 252844|||Isoarnebin 4|||(+)-Shikonin|||Alkanna Red|||C.I. 75535|||Anchusa acid;NSC 2
Shikonin (Anchusa acid) is a natural product, a TMEM16A chloride channel inhibitor (IC50=6.5 μM) and selective PKM2 inhibitor. Shikonin exhibits antitumor, anti-inflammatory and wound healing activities.
价 格:¥电议型 号:T1125产 地:中国大陆
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T1122Cephalothin sodium;头孢噻吩钠Cefalotin sodium|||Cephalothin|||Cefalotin;头孢噻吩钠|||Cefalotin sodium|||Cephal
Cephalothin sodium (Cefalotin) binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Cephalothin sodium (Cefalotin) is the sodium salt form of cephalothin, a semisynthetic, beta-lactam, the first-generation cephalosporin antibiotic with bactericidal activity. PBPs participate in the terminal stages of assembling the bacterial cell wall, and in reshaping the cell wall during cell division. Inactivation of PBPs interferes with the cros
价 格:¥电议型 号:T1122产 地:中国大陆
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T11207Entacapone sodium salt;恩他卡朋钠盐Entacapone sodium salt
Entacapone sodium salt inhibits catechol-O-methyltransferase(COMT) with similar IC50 in different tissues including live, duodenum, kidney and lung, but entacapone is more active than tolcapone in those tissues. Entacapone (< 100 μM) is a potent inhibitor of α-syn and β-amyloid (Aβ) oligomerization and fibrillogenesis, and also protects against extracellular toxicity induced by the aggregation of both proteins in PC12 cells.Entacapone sodium salt is a specific, potent, peripherally acting catech
价 格:¥电议型 号:T11207产 地:中国大陆
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T11206ent-Tadalafil;化合物 T11206ent-IC-351;ent-IC-351
ent-Tadalafil (ent-IC-351), compound (6S,12aS), is a inactive cis-enantiomer of compound (6R,12aS).
价 格:¥电议型 号:T11206产 地:中国大陆
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T11199Endothelial lipase inhibitor-1;内皮脂酶抑制剂-1Endothelial lipase inhibitor-1
Endothelial lipase inhibitor-1 is a potent endothelial lipase inhibitor with an IC50 of 49 nM.
价 格:¥电议型 号:T11199产 地:中国大陆