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T23860CAY10444；化合物 T23860BML-241|||CAY 10444|||CAY-10444|||BML241|||BML 241；BML-241|||CAY 10444|||CAY-1044
CAY10444 is an S1P3 specific antagonist.
价 格：￥电议型 号：T23860产 地：中国大陆
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T23843Butaperazine；化合物 T23843Butyrylyperazine|||Bayer 1362|||Butaperazina|||Butyrylperazine；Butyrylyperazi
Butaperazine is a typical antipsychotic of the phenothiazine class.
价 格：￥电议型 号：T23843产 地：中国大陆
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T23842Butaclamol free base；化合物 T23842Butaclamol|||AY 23028|||AY 23,028|||AY-23028|||AY23,028|||AY-23,028；B
Butaclamol is a typical antipsychotic which was never marketed. It also acts as a dopamine receptor antagonist.
价 格：￥电议型 号：T23842产 地：中国大陆
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T23775BAY-958；化合物 T23775BAY 958；BAY 958
BAY-958 is a potent and selective inhibitor of PTEFb/CDK9.
价 格：￥电议型 号：T23775产 地：中国大陆
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T23711WAY-260022；化合物 T23711NRI-022|||NRI022|||NRI 022|||WAY260022|||WAY 260022；NRI-022|||NRI022|||NRI 022|
WAY-260022 is the norepinephrine transporter inhibitor.
价 格：￥电议型 号：T23711产 地：中国大陆
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T23654Afeletecan free base；化合物 T23654BAY 56-3722|||BAY56-3722|||BAY-563722|||Afeletecan；BAY 56-3722|||BAY5
Afeletecan is a water-soluble camptothecin derivative. Afeletecan stabilizes the topoisomerase I-DNA covalent complex and forms an enzyme-drug-DNA ternary complex. Both the initial cleavage reaction and religation steps are inhibited and subsequent collision of the replication fork with the cleaved strand of DNA results in inhibition of DNA replication, double-strand DNA breakage, and triggering of apoptosis.
价 格：￥电议型 号：T23654产 地：中国大陆
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T23631Adatanserin；阿达色林WY-50324|||WY 50324|||WAY SEB 324|||WY50324；WY-50324|||WY 50324|||WAY SEB 324|||WY50
Adatanserin (WY 50324) is a mixed 5-HT1A receptor partial agonist and a 5-HT2A and 5-HT2C receptor antagonist with potential neuroprotective activity for the study of anxiety and depression.
价 格：￥电议型 号：T23631产 地：中国大陆
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T23531WAY 629 hydrochloride；化合物 T23531WAY 629 hydrochloride
5-HT2C agonist
价 格：￥电议型 号：T23531产 地：中国大陆
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T23529WAY 316606 HCl (915759-45-4 free base)；化合物 T23529WAY 316606 HCl；WAY 316606 HCl
WAY 316606 HCl is a selective small-molecule inhibitor of secreted frizzled-related protein-1 (EC50: 0.65 μM).
价 格：￥电议型 号：T23529产 地：中国大陆
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T23527WAY208466 dihydrochloride；化合物 T23527WAY 208466 dihydrochloride；WAY 208466 dihydrochloride
5-HT6 agonist
价 格：￥电议型 号：T23527产 地：中国大陆
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T23526WAY 161503 hydrochloride；化合物 T23526WAY 161503 hydrochloride
WAY 161503 hydrochloride is a 5-HT2C receptor agonist.
价 格：￥电议型 号：T23526产 地：中国大陆
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T2327Pelitinib；培利替尼EKB-569|||WAY-EKB 569；培利替尼|||EKB-569|||WAY-EKB 569
Pelitinib (EKB-569) (EKB-569) is an effective irreversible EGFR inhibitor (IC50: 38.5 nM).
价 格：￥电议型 号：T2327产 地：中国大陆
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T2266SantacruzaMate A；化合物SantacruzaMate ACAY-10683；CAY-10683
SantacruzaMate A (CAY-10683) is a potent and selective HDAC inhibitor.
价 格：￥电议型 号：T2266产 地：中国大陆
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T22547Acifran；阿西弗兰AY 25712；AY 25712
Acifran (AY 25712) is an HM74A/GPR109A and GPR109B agonist and displays antihyperlipidemic activity.
价 格：￥电议型 号：T22547产 地：中国大陆
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T2245CL-387785；化合物CL-387785WAY-EKI 785|||EKI-785；WAY-EKI 785|||EKI-785
CL-387785 (WAY-EKI 785)(EKI785; WAY-EKI 785) is an irreversible inhibitor of EGFR(IC50： 370+/-120 pM); is able to overcome resistance caused by the T790M mutation on a functional level.
价 格：￥电议型 号：T2245产 地：中国大陆
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T22262Ansamitocin p-3；安丝菌素 P 3Maytansinol isobutyrate|||Antibiotic C 15003P3|||NSC292222；Maytansinol isobu
Ansamitocin p-3 (Maytansinol isobutyrate) is an inhibitor of microtubule with IC50 of 3.4 μM for tubulin polymerization.
价 格：￥电议型 号：T22262产 地：中国大陆
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T21864BAY-u 9773；化合物 T21864BAY-u 9773
BAY-u 9773 is a non-selective antagonist of the CysLT receptors (cysteinyl leukotrienes receptors) with about the same IC 50 for CysLT 1 and CysLT 2. BAY-u9773 is used to the inhibit LT responses [1].
价 格：￥电议型 号：T21864产 地：中国大陆
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T21712BAY 41-8543；化合物BAY 41-8543BAY 41-8543
BAY 41-8543 is a nitric oxide (NO)-independent stimulator of soluble guanylyl cyclase (sGC).
价 格：￥电议型 号：T21712产 地：中国大陆
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T2160Suramin Sodium Salt；苏拉明钠BAY-205|||Suramin hexasodium salt|||NF-060；苏拉明钠|||BAY-205|||Suramin hexasodi
Suramin Sodium Salt (BAY-205) is a sodium salt form of suramin, a polysulphonated naphthylurea with potential antineoplastic activity. Suramin blocks the binding of various growth factors, including insulin-like growth factor I (IGF-I), epidermal growth factor (EGF), platelet-derived growth factor (PDGF), and tumor growth factor-beta (TGF-beta), to their receptors, thereby inhibiting endothelial cell proliferation and migration. This agent also inhibits vascular endothelial growth factor (VEGF)-
价 格：￥电议型 号：T2160产 地：中国大陆
