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T10221Abeprazan hydrochloride；非苏拉赞盐酸盐Fexuprazan Hydrochloride|||Abeprazan hydrochloride|||Abeprazan Hydroc
Abeprazan hydrochloride (Fexuprazan hydrochloride) is an effective reversible potassium-competitive acid blocker with oral activity, inhibiting H+, K+ -atPase by competitive binding to potassium ions without acid activation. Abeprazan hydrochloride is a proton pump inhibitor (PPI) that acts by reducing gastric acid production and is used to treat gastric acid-related disorders, such as gastroesophageal reflux disease (GERD) and peptic ulcers.
价 格：￥电议型 号：T10221产 地：中国大陆
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T10219ABBV-4083；化合物 T10219ABBV-4083
ABBV-4083 is a Tylosin A analog that has potent anti-Wolbachia and anti-filarial activity.
价 格：￥电议型 号：T10219产 地：中国大陆
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T10218Abatacept；化合物 T10218CTLA4lg；CTLA4lg
Abatacept (CTLA4lg) is a soluble fusion protein consisting of the extracellular domain of human CTLA4 and a fragment of the Fc portion of human IgG1 (hinge and CH2 and 3 domains). It is a selective T-cell co-stimulation modulator and a protein drug for autoimmune diseases.
价 格：￥电议型 号：T10218产 地：中国大陆
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T10217LAbarelix；阿巴瑞克R3827|||PPI 149；R3827|||阿巴瑞克|||PPI 149
Abarelix (PPI 149) is a potent gonadotrophin-releasing hormone (GnRH) antagonist, which is used for prostate cancer treatment.
价 格：￥电议型 号：T10217L产 地：中国大陆
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T10217Abarelix Acetate (183552-38-7 free base)；化合物 T10217PPI 149 Acetate|||Abarelix Acetate；PPI 149 Acetat
Abarelix (PPI 149; R 3827) Acetate is a potent gonadotrophin-releasing hormone (GnRH) antagonist, used for prostate cancer research.
价 格：￥电议型 号：T10217产 地：中国大陆
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T10215AAPK-25；化合物AAPK-25AAPK-25
AAPK-25, a potent and selective dual inhibitor of Aurora/PLK, causes mitotic delay and cell arrest in prometaphase, via phosphorylation of the biomarker histone H3Ser10, followed by a surge in apoptosis. AAPK-25 targets Aurora A, Aurora B, and Aurora C with Kd values ??ranging from 23-289 nM, and PLK1, PLK2, and PLK3 with Kd values ??ranging from 55-456 nM. AAPK-25 has antitumor activity.
价 格：￥电议型 号：T10215产 地：中国大陆
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T10214A7132；化合物A7132A7132
A7132 is an antibacterial agent and possesses broad and potent antibacterial activity.
价 格：￥电议型 号：T10214产 地：中国大陆
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T10213A-437203；化合物A-437203ABT-925|||A37203|||Lu201640；ABT-925|||A37203|||Lu201640
A-437203 (Lu201640) is A kind of based on 1 h - pyrimidin - 2 - one sca ? old, selective, new powerful d3 receptor antagonist, on D2, d3, and D4 receptor, Ki value 71, respectively 1.6 and 6220 nM.
价 格：￥电议型 号：T10213产 地：中国大陆
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T10212A2AR-agonist-1；化合物A2AR-agonist-1N-(2-(1H-Indol-3-yl)ethyl)adenosine；N-(2-(1H-Indol-3-yl)ethyl)adenos
A2AR-agonist-1 (N-(2-(1H-Indol-3-yl)ethyl)adenosine) is a potent A2AR and ENT1 agonist (Ki: 4.39 and 3.47 for A2AR and ENT1. It targets the Adenosine A2A Receptor and Adenosine Transporter for Neuroprotection.
价 格：￥电议型 号：T10212产 地：中国大陆
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T10211Aβ42-IN-1；化合物 T10211Aβ42-IN-1
Aβ42-IN-1, compound 1v, is a novel, potent and orally active γ-secretase modulator (GSM). Aβ42-IN-1 potently reduced Aβ42 levels with an IC 50 value of 0.091 μM in cultured cells without inhibiting CYP3A4. Aβ42-IN-1 shows a sustained pharmacokinetic profile.
价 格：￥电议型 号：T10211产 地：中国大陆
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T10210A-9758；化合物 T10210A-9758
A-9758 is a RORγ ligand and a selective RORγt inverse agonist (IC50: 5 nM) and exhibits robust potency against IL-17A release. It is effective in suppressing both Th17 differentiation and Th17 effector function. A-9758 significantly attenuates IL-23 driven psoriasiform dermatitis.
价 格：￥电议型 号：T10210产 地：中国大陆
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T1021(R)-Lansoprazole；右旋兰索拉唑Dexlansoprazole|||T 168390|||TAK 390|||R-(+)-Lansoprazole；Dexlansoprazole|||右
(R)-Lansoprazole (T 168390) is the R-isomer of lansoprazole and a substituted benzimidazole prodrug with selective and irreversible proton pump inhibitor activity.Lansoprazole (AG 1749) is a potent brain penetrant neutral sphingomyelinase (N-SMase) inhibitor (exosome inhibitor)
价 格：￥电议型 号：T1021产 地：中国大陆
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T10121Substance P Receptor Antagonist 1；化合物 T10121Substance P Receptor Antagonist 1
Substance P Receptor Antagonist 1 has the potential function in gastrointestinal disorders, inflammatory diseases, respiratory, and central nervous system disorders.
价 格：￥电议型 号：T10121产 地：中国大陆
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T1011Itraconazole；伊曲康唑R51211；伊曲康唑|||R51211
Itraconazole (R51211) belongs to the triazole group of natural products and is an antifungal agent with oral activity. Itraconazole is a Hedgehog signaling pathway antagonist, an oxysterol-binding protein (OSBP) inhibitor, and an inhibitor of cytochrome P-450-dependent enzymes.
价 格：￥电议型 号：T1011产 地：中国大陆
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T10062(-)-GSK598809；化合物 T100621S,5R-GSK598809；1S,5R-GSK598809
(-)-GSK598809 is an isomer of GSK598809 that is a potent and selective antagonist of dopamine D3 Receptor.
价 格：￥电议型 号：T10062产 地：中国大陆
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T1004211-Oxomogroside IIa；化合物 T1004211-Oxomogroside IIa
11-Oxomogroside IIa is a cucurbitane glycoside extracted from the fruits of Siraitia grosVenorii. It has inhibitory effects against the EBV-EA activation induced by TPA, shows weak inhibitory effects on activation of NOR 1, a nitric oxide (NO) donor.
价 格：￥电议型 号：T10042产 地：中国大陆
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T100221-Myristoyl-2-stearoyl-sn-glycero-3-phosphocholine；化合物T100221-Myristoyl-2-stearoyl-sn-glycero-3-phos
1-Myristoyl-2-stearoyl-sn-glycero-3-phosphocholine is an endogenous metabolite. 1-Myristoyl-2-stearoyl-sn-glycero-3-phosphocholine is a non-limiting exemplary phosphatidyl choline.
价 格：￥电议型 号：T10022产 地：中国大陆
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T100211-Methylxanthine；1-甲基黄嘌呤1-Methylxanthine
1-Methylxanthine is a caffeine derivative. 1-Methylxanthine is an essential human urinary metabolite of caffeine and theophylline (1,3-dimethylxanthine, TP). 1-Methylxanthine enhances the radiosensitivity of tumor cells.
价 格：￥电议型 号：T10021产 地：中国大陆
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T0971Dirithromycin；地红霉素Dirithromycinum|||ASE 136|||LY237216|||Diritromicina|||Dirithromycine；Dirithromyci
Dirithromycin (LY237216) is a macrolide glycopeptide antibiotic. It is used to treat many different types of bacterial infections, such as bronchitis, pneumonia, tonsillitis, and even skin infections.
价 格：￥电议型 号：T0971产 地：中国大陆
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T0947Dexamethasone acetate；醋酸地塞米松Dexamethasone 21-acetate|||Dexamethason acetate|||NSC 39471；Dexamethason
Dexamethasone acetate (NSC 39471) is the acetate salt form of Dexamethasone, a synthetic adrenal corticosteroid with potent anti-inflammatory properties. In addition to binding to specific nuclear steroid receptors, dexamethasone also interferes with NF-kB activation and apoptotic pathways. This agent lacks the salt-retaining properties of other related adrenal hormones.
价 格：￥电议型 号：T0947产 地：中国大陆
