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T1950PND-1186化合物PND-1186PND1186|||PND 1186|||VS-4718|||SR-2516
PND-1186 (VS-4718) is a reversible and specific FAK inhibitor (IC50: 1.5 nM).
价 格：￥电议型 号：T1950产 地：中国大陆
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T18817Thalidomide-O-amido-C8-NH2 hydrochloride；化合物 T18817Thalidomide-O-amido-C8-NH2 hydrochloride (1950635
Thalidomide-O-amido-C8-NH2 hydrochloride is a synthetic conjugate of an E3 ligase ligand-linker, which combines a cereblon ligand derived from Thalidomide and a linker. It can be utilized in the synthesis of PROTACs[1].
价 格：￥电议型 号：T18817产 地：中国大陆
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T18195m-PEG36-OH；化合物 T18195m-PEG36-OH
m-PEG36-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T18195产 地：中国大陆
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T17195UC-112；化合物UC-112UC-112
UC-112 is a novel potent IAP inhibitor and potently inhibits cell growth in two human melanoma and two human prostate cancer cell lines (IC50=0.7-3.4 uM).
价 格：￥电议型 号：T17195产 地：中国大陆
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T16546PK 11195化合物 T16546RP 52028
PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis, respectively).
价 格：￥电议型 号：T16546产 地：中国大陆
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T16195N-(Azido-PEG4)-N-bis(PEG4-acid)；化合物 T16195N-(Azido-PEG4)-N-bis(PEG4-acid)
N-(Azido-PEG4)-N-bis(PEG4-acid) is a polyethylene glycol (PEG) derived PROTAC linker, facilitating PROTAC synthesis[1].
价 格：￥电议型 号：T16195产 地：中国大陆
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T15390Glufosfamide；葡膦酰胺D 19575|||Glucosylifosfamide mustard；D 19575|||Glucosylifosfamide mustard
Glufosfamide is a novel oxazolophosphamide compound with anticancer activity for the study of advanced non-small cell lung cancer.
价 格：￥电议型 号：T15390产 地：中国大陆
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T15195Ebrotidine；乙溴替丁FI3542；FI3542|||乙溴替丁
Ebrotidine (FI3542) is a competitive H2-receptor antagonist with Ki of 127.5 nM. Ebrotidine has a potent antisecretory activity and evidenced gastroprotection.
价 格：￥电议型 号：T15195产 地：中国大陆
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T14940CGP11952；化合物 T14940CGP11952
CGP11952 is same the benzodiazepines in its pharmacological action and it also is an experimental benzodiazepine derivative.
价 格：￥电议型 号：T14940产 地：中国大陆
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T14934Cethromycin；化合物 T14934Abbott-195773|||ABT-773|||A-195773；Abbott-195773|||ABT-773|||A-195773
Cethromycin (ABT-773) is an antibiotic of ketolide.
价 格：￥电议型 号：T14934产 地：中国大陆
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T14558BI-1950；化合物 T14558BI-1950
BI-1950 is a highly potent lymphocyte function associated antigen-1 (LFA-1) inhibitor and the LFA-1 is an essential component in normal immune system function and a target for drug discovery[1].
价 格：￥电议型 号：T14558产 地：中国大陆
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T14195ALS-8112；化合物 T14195ALS-8112
ALS-8112 is a inhibitor of respiratory syncytial virus (RSV) polymerase. The 5´-triphosphate form of ALS-8112 inhibits RSV polymerase (IC50: 0.02 μM).
价 格：￥电议型 号：T14195产 地：中国大陆
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T14144AGN-195183；化合物 T14144AGN-195183
AGN 195183 is a potent and selective agonist of RARα(Kd=3 nM) with improved binding selectivity relative to AGN 193836; no activity on RARβ/γ. IC50 value: 3 nM (Kd); 200 nM (EC80, RAR Trans.) Target: RARα agonist Compound 4(AGN-195183) inhibited the growth of breast cancer cell lines, and was inactive in an in vivo model of topical irritation. Compound 4 (AGN 195183) is currently in Phase I/IIA clinical trials in cancer patients. Compound 4 and ATRA inhibit growth of the human breast cancer cell
价 格：￥电议型 号：T14144产 地：中国大陆
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T13367YKL-5-124 TFA (1957203-01-8 free base)；化合物 T13367YKL-5-124 TFA；YKL-5-124 TFA
YKL-5-124 TFA is a potent, selective, irreversible and covalent inhibitor of CDK7 (IC50s of 53.5 nM and 9.7 nM for CDK7 and CDK7/Mat1/CycH, respectively).
价 格：￥电议型 号：T13367产 地：中国大陆
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T13195Trandolapril D5；化合物 T13195RU44570 D5；RU44570 D5
Trandolapril D5 is a deuterium labeled Trandolapril. Trandolapril is an orally active inhibitor of angiotensin converting enzyme (ACE) for hypertension and congestive heart failure (CHF).
价 格：￥电议型 号：T13195产 地：中国大陆
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T131195Compound N066-0058；化合物 N066-0058Compound N066-0058
Compound N066-0058 is a useful organic compound for research related to life sciences and the catalog number is T131195.
价 格：￥电议型 号：T131195产 地：中国大陆
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T1261951-O-Caffeoyl-3,4,6-trigalloyl-?-D-glucopyranose；化合物 1-O-Caffeoyl-3,4,6-trigalloyl-?-D-glucopyranose1
1-O-Caffeoyl-3,4,6-trigalloyl-?-D-glucopyranose is a useful organic compound for research related to life sciences. The catalog number is T126195 and the CAS number is 1219501-93-5.
价 格：￥电议型 号：T126195产 地：中国大陆
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T1241957-Acetylscorpioidine；化合物 7-Acetylscorpioidine7-Acetylscorpioidine
7-Acetylscorpioidine is a useful organic compound for research related to life sciences and the catalog number is T124195.
价 格：￥电议型 号：T124195产 地：中国大陆
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T12255NS19504；化合物NS19504NS19504
NS19504 is an activator of Ca2+-activated K+ channel with EC50 of 11.0 ?M. NS19504 shows relaxing effect on bladder smooth muscle spontaneous phasic contractions[1].
价 格：￥电议型 号：T12255产 地：中国大陆
