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T10529BF-168化合物 T10529BF168|||BF 168
BF-168 is a candidate probe for PET and specifically recognizes both neuritic and diffuse plaques (Ki: 6.4 nM for Aβ1-42).
价 格：￥电议型 号：T10529产 地：中国大陆
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T10516Beperidium iodide；化合物 T10516SX 810；SX 810
Beperidium iodide is a competitive antagonist of the acetylcholine receptor (pA2: 7.93).
价 格：￥电议型 号：T10516产 地：中国大陆
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T10467BAY-1816032；化合物BAY-1816032BAY-1816032
BAY-1816032 is a potent and orally available inhibitor of bidding uninhibited by benzimidazoles 1 ( BUB1) kinase (IC50: 7 nM).
价 格：￥电议型 号：T10467产 地：中国大陆
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T10416Autotaxin-IN-4；化合物 T10416Autotaxin-IN-4
Autotaxin-IN-4 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis.
价 格：￥电议型 号：T10416产 地：中国大陆
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T10398ATN-161；化合物 T10398ATN-161
ATN-161 is a novel integrin α5β1 antagonist that inhibits angiogenesis and growth of liver metastases in a murine model.
价 格：￥电议型 号：T10398产 地：中国大陆
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T10397ATN-161 trifluoroacetate salt；化合物ATN-161 trifluoroacetate saltATN-161 TFA salt；ATN-161 TFA salt
ATN-161 trifluoroacetate salt (ATN-161 TFA salt) is a novel integrin α5β1 antagonist that inhibits angiogenesis and growth of liver metastases and improves survival in a murine model.
价 格：￥电议型 号：T10397产 地：中国大陆
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T10376ARS-1630；化合物ARS-1630ARS-1630
ARS-1630 is a mutant K-ras G12C inhibitor. It is a less active enantiomer of ARS-1620.
价 格：￥电议型 号：T10376产 地：中国大陆
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T10343AOH1160；化合物AOH1160N-(2-Oxo-2-(2-phenoxyphenylamino)ethyl)-1-naphthamide；N-(2-Oxo-2-(2-phenoxyphenyla
AOH1160 is an inhibitor of proliferating cell nuclear antigen (PCNA). AOH1160 induces apoptosis and causes cell-cycle arrest by interfering with DNA replication.
价 格：￥电议型 号：T10343产 地：中国大陆
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T10316AN3199；化合物AN3199AN3199
AN3199 is a selective inhibitor of PDE4 with an IC50 of 94.5 nM.
价 格：￥电议型 号：T10316产 地：中国大陆
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T10290LAlpertine HCl；阿尔哌汀盐酸盐Win 31665 HCl|||Alpertine HCl（27076-46-6 Free base）；Win 31665 HCl|||Alpertine H
Alpertine HCl is a small molecule compound with anti-neuropathic properties.
价 格：￥电议型 号：T10290L产 地：中国大陆
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T10290Alpertine；化合物 T10290Win 31665；Win 31665
Alpertine is an antipsychotic agent.
价 格：￥电议型 号：T10290产 地：中国大陆
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T10270BAY 2416964；化合物BAY 2416964BAY 2416964
BAY 2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist(example 192, IC50: 341 nM). It has the potential for cancer treatment.
价 格：￥电议型 号：T10270产 地：中国大陆
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T10225ABT-546；化合物 T10225A-216546；A-216546
ABT-546 (A-216546) is a potent, highly selective, and active endothelin ETA receptor antagonist with a Ki of 0.46 nM for [125I]endothelin-1 binding to cloned human endothelin ETA.
价 格：￥电议型 号：T10225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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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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T101816-beta-Naloxol D5 hydrochloride；化合物 T101816β-Naloxol D5 hydrochloride；6β-Naloxol D5 hydrochloride
6-beta-Naloxol D5 hydrochloride is a deuterium-labeled opioid antagonist, closely related to naloxone, that serves as an effective compound in the field of chemical research.
价 格：￥电议型 号：T10181产 地：中国大陆
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T101695-HT4 antagonist 1；化合物5-HT4 antagonist 15-HT4 antagonist 1
5-HT4 antagonist 1 is an antagonist of 5-HT4 (pKi = 9.6).
价 格：￥电议型 号：T10169产 地：中国大陆
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T101685-HT1A modulator 1；化合物5-HT1A modulator 15-HT1Amodulator1；5-HT1Amodulator1
5-HT1A modulator 1 displays very high affinities for the 5-HT1A, α1-adrenergic receptor, and D2 receptor (IC50s = 2 nM, 10 nM, and 40 nM).
价 格：￥电议型 号：T10168产 地：中国大陆
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T101675-Dehydroepisterol；化合物 T101675-Dehydroepisterol
5-Dehydroepisterol is an episterol derivative with anti-fungal activities. It can be formed by C-5 sterol desaturase and converted into 24-methylenecholesterol by 7-dehydrocholesterol reductase.
价 格：￥电议型 号：T10167产 地：中国大陆
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T10165L5-A-RU hydrochloride；5-A-RU 盐酸盐5-Amino-6-(D-ribitylamino)uracil hydrochloride；5-Amino-6-(D-ribitylam
5-A-RU hydrochloride (5-Amino-6-(D-ribitylamino)uracil hydrochloride) is an intermediate of bacterial riboflavin that activates mucosal-associated invariant T cells (MAIT).5-A-RU is used in the study of breast and prostate cancer.
价 格：￥电议型 号：T10165L产 地：中国大陆
