9月
Taribavirin hydrochloride；化合物 T16992Taribavirin hydrochloride (2024/9/1)
简介：taribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. taribavirin hydrochloride is designed to concentrate within the liver to target hcv-infected hepatocytes while minimizing distribution within red blood cells and the development of hemolytic anemia [2].
VMRC-RCZ 人肾细胞癌 (2024/9/1)
简介：细胞特性种属: 人源组织来源: 肾疾病: 肾癌细胞类型: 表皮样细胞生长特性: 贴壁生长含量：>1x10^6 细胞数规格：t25瓶或者1ml冻存管包装用途：仅供科研使用。
Tarafenacin；化合物 T16990SVT-40776；SVT-40776 (2024/9/1)
简介：tarafenacin is a highly selective m3 muscarinic receptor antagonist (ki= 0.19 nm), ~200 fold selectivity over the m2 receptor.
resorufin galactopyranoside；试卤灵Β-D-半乳糖吡喃糖苷resorufin galactopyranoside (2024/9/1)
简介：resorufin galactopyranoside is a fluorescent substrate for β-galactosidase.after cleavage by β-galactosidase, the fluorescent portion of resorufin is released and its fluorescence can be used to quantify β-galactosidase activity. it has an excitation light of 570 and an emission light of 580 nm.
Tarafenacin D-tartrate；Tarafenacin D-酒石酸盐SVT-40776 D-tartrate；SVT-40776 D-tartrate (2024/9/1)
简介：tarafenacin d-tartrate (svt-40776 d-tartrate) is a selective and potent muscarinic acetylcholine m3 receptor antagonist used in the study of overactive bladder and bronchial disorders.
Taprenepag isopropyl；化合物 T16988PF-04217329；PF-04217329 (2024/9/1)
简介：taprenepag isopropyl is a highly selective agonist of the ep2 receptor.
TAO Kinase inhibitor 1；化合物TAO Kinase inhibitor 1TAO Kinase inhibitor 1 (2024/9/1)
简介：tao kinase inhibitor 1 delays mitosis and induces mitotic cell death. tao kinase inhibitor 1 is a selective and atp-competitive thousand-and-one amino acid kinases inhibitor (ic50s: 11 to 15 nm for taok1 and 2, respectively).
Tanomastat；化合物 T16986BAY 12-9566；BAY 12-9566 (2024/9/1)
简介：tanomastat is an orally bioavailable and non-peptidic biphenyl matrix metalloproteinases inhibitor. for mmp-2, mmp-3, mmp-9, mmp-13 the ki values are 11, 143, 301, and 1470 nm respectively.
Tanaproget；化合物 T16985NSP-989；NSP-989 (2024/9/1)
简介：tanaproget is a novel nonsteroidal progesterone receptor agonist which can bind to the pr from various species with a higher relative affinity than reference steroidal progestins (ic50: 0.1 nm),
TAMRA-PEG4-Alkyne；化合物 T16984TAMRA-PEG4-Alkyne (2024/9/1)
简介：tamra-peg4-alkyne 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.
VMRC-RCZ +LUC人肾细胞癌 +LUC (2024/9/1)
简介： 细胞特性种属: 人源组织来源: 肾疾病: 肾癌细胞类型: 表皮样细胞生长特性: 贴壁生长含量：>1x10^6 细胞数规格：t25瓶或者1ml冻存管包装用途：仅供科研使用。
TAMRA-PEG4-acid；化合物 T16983TAMRA-PEG4-acid (2024/9/1)
简介：tamra-peg4-acid 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.
TAMRA-PEG3-Azide；化合物 T16982TAMRA-PEG3-Azide (2024/9/1)
简介：tamra-peg3-azide 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.
TAMRA-Azide-PEG-biotin；化合物 T16981TAMRA-Azide-PEG-biotin (2024/9/1)
简介：tamra-azide-peg-biotin 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.
Taminadenant；化合物TaminadenantTaminadenant (2024/9/1)
简介：taminadenant is an adenosine receptor antagonist.
Carvedilol EP IMpurity E；卡维地洛杂质Carvedilol USP E|||Carvedilol Impurity E；Carvedilol USP E|||Carvedilo (2024/9/1)
简介：carvedilol ep impurity e (carvedilol usp e) is used as a pharmaceutical intermediate.
Talazoparib tosylate化合物 T16979BMN 673ts (2024/9/1)
简介：talazoparib tosylate is a novel and potent parp1/2 (n ic50: 0.57 nm for parp1).
Talaporfin sodium；他拉泊芬钠ME2906|||NPe6|||Mono-L-aspartyl chlorin e6；ME2906|||他拉泊芬钠|||NPe6|||Mono-L-asp (2024/9/1)
简介：talaporfin is a photosensitizer used in photodynamic therapy.
VMRC-RCZ +LUC+RFP人肾细胞癌 +LUC+RFP (2024/9/1)
简介：细胞特性种属: 人源组织来源: 肾疾病: 肾癌细胞类型: 表皮样细胞生长特性: 贴壁生长含量：>1x10^6 细胞数规格：t25瓶或者1ml冻存管包装用途：仅供科研使用。
Talampanel；化合物TalampanelGYKI-53773|||LY-300164；GYKI-53773|||LY-300164 (2024/9/1)
简介：talampanel (ly-300164) is an orally and selective α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor antagonist with anti-seizure activity. talampanel (ivax) has neuroprotective effects in rodent stroke models.
TAK-915；化合物 T16976TAK-915 (2024/9/1)
简介：tak-915 is a potent, selective, and brain-penetrant phosphodiesterase 2a (pde2a) inhibitor (ic50: 0.61 nm). tak-915 is >4100-fold more selectivity for pde2a than pde1a.
TAK-593；化合物TAK-593TAK-593 (2024/9/1)
简介：tak-593 is an effective vegfr and pdgfr family inhibitor (ic50s: 3.2, 0.95, 1.1, 4.3, and 13 nm for vegfr1, vegfr2, vegfr3, pdfgrα, and pdfgrβ, respectively).
TAK-243；化合物TAK-243MLN7243；MLN7243 (2024/9/1)
简介：tak-243 (mln7243) is a selective inhibitor of the ubiquitin-activating enzyme uae (ic50=1 nm). tak-243 blocks ubiquitin binding and disrupts mono-ubiquitin signaling as well as overall protein ubiquitination. tak-243 exhibits antitumor activity and promotes apoptosis.
TAK-220；化合物 T16973TAK-220 (2024/9/1)
简介：tak-220 is a selective and orally bioavailable ccr5 antagonist (ic50s: 3.5 nm and 1.4 nm for inhibition on the binding of rantes and mip-1α to ccr5, respectively).
TA 0910 acid-type；化合物 T16972TA 0910 acid-type (2024/9/1)
简介：ta 0910 acid-type is a metabolite of ta 0910. ta-0910 is a metabolically stable analog of thyrotropin-releasing hormone.
VMRC-RCZ +LUC+GFP人肾细胞癌 +LUC+GFP (2024/9/1)
简介：细胞特性种属: 人源组织来源: 肾疾病: 肾癌细胞类型: 表皮样细胞生长特性: 贴壁生长含量：>1x10^6 细胞数规格：t25瓶或者1ml冻存管包装用途：仅供科研使用。
t-Boc-Aminooxy-PEG7-methane；化合物 T16971t-Boc-Aminooxy-PEG7-methane (2024/9/1)
简介：t-boc-aminooxy-peg7-methane is a polyethylene glycol (peg)-based linker, which finds application in the synthesis of proteolysis targeting chimeras (protacs)[1].
t-Boc-aminooxy-PEG6-propargyl；化合物 T16970t-Boc-aminooxy-PEG6-propargyl (2024/9/1)
简介：t-boc-aminooxy-peg6-propargyl is a peg-based protac linker utilized for protac synthesis[1].
t-Boc-Aminooxy-PEG3-alcohol；化合物 T16969t-Boc-Aminooxy-PEG3-alcohol (2024/9/1)
简介：t-boc-aminooxy-peg3-alcohol is a polyethylene glycol (peg)-based linker compound commonly employed for the synthesis of proteolysis targeting chimeras (protacs)[1].
t-Boc-Aminooxy-PEG2-azide；化合物 T16968t-Boc-Aminooxy-PEG2-azide (2024/9/1)
简介：t-boc-aminooxy-peg2-azide is a polyethylene glycol (peg) derived linker compound employed for the synthesis of proteolysis targeting chimeras (protacs)[1].
MSN交谈
