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Bis-T-23是一种肌动蛋白依赖性达纳敏低聚物的促进剂，是一种 HIV-I 整合酶抑制剂，是泰尔普斯丁衍生物。Bis-T-23可以促进肌动蛋白依赖性的dynamin 寡聚化。Bis-T-23可用于HIV 和慢性肾脏疾病（CKD）的研究。

T-1105 是 T-705 的结构类似物，是一种广谱病毒聚合酶抑制剂，在转化为核糖核苷三磷酸代谢物后抑制 RNA 病毒的聚合酶，有抗病毒活性。

Chloramine-T (Chloralone) 是一种 N-氯化和 N-去质子化磺胺，用作杀生物剂和温和消毒剂。

T-0509 是一种选择性 beta 1 受体激动剂，可增加犬心室肌的肌力，选择性下调大鼠心脏 β 1-肾上腺素受体。

C15AlkOPP Tetrabutylamine salt 是一种 可点击 的farnesyl diphosphate (FPP)的炔烃修饰类似物。

T-900607是一种新型微管蛋白活性剂，通过独特的作用机制破坏微管聚合。t-900607具有心脏毒性。

Peptide T acetate(106362-32-7 free base) 是一种来自 HIV-1 gp120 V2 区域的八肽。它是一种合成八肽，其可能的作用机制是 gp120 对 CD4 受体的竞争性抑制以及与血管肠肽受体的结合和抑制细胞因子作用。

SV40 T-Ag-derived NLS peptide acetate (SV40 T-Ag-derived NLS peptide acetate)(105425-98-7 free base) 是一种核定位信号肽。用这种肽标记的 DNA 可以有效地转移到细胞核中。

(S)-GNA-T-phosphoramidite 是一种核苷类化合物，常用于和成其他有活性的化合物。

T-0156 是一种新型高效且具有选择性的 5 型磷酸二酯酶抑制剂，抑制环磷酸鸟苷 (cGMP) 的水解，对 PDE6、PDE1、PDE2、PDE3 和 PDE4 较低的亲和力。

T-1095 是一种口服有活性的Na+-葡萄糖协同转运蛋白选择性抑制剂，能够抑制 SGLT1 (IC50:22.8 µm) 及 SGLT2 (IC50:2.3 µm) 。它可用于研究糖尿病。

(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl dihydrogen diphosphate,tetrabutylammonium(1:1.5) 是紫杉二烯，如紫杉醇，的常见前体。

Geranylgeranyl pyrophosphate tetrabutylammonium(1：2)是甲羟戊酸途径产生内源性胆固醇和中间体之一。Geranylgeranyl pyrophosphate tetrabutylammonium(1：2) 香叶基香叶基焦磷酸三铵是二萜类化合物的常见前体，例如紫杉醇，可用于癌症研究。

inhibitor of phosphodiesterase type 5 (PDE5).This compound is unstable in powder form and other related salt forms are recommended.

T-1840383 is an inhibitor of VEGF-induced VEGFR-2 phosphorylation and HGF-induced c-Met phosphorylation in vascular endothelial cells and cancer epithelial cells.

T-448 是一种可口服且具有高效性的赖氨酸特异性去甲基化酶1 抑制剂（IC50：22 nM），可改善小鼠的学习功能。T-448 可用于研究记忆缺陷。

T-5224 是选择性的转录因子c-Fos activator protein (AP)-1抑制剂，具有抗炎作用，能够特异性抑制 c-Fos c-Jun 的 DNA 结合活性，但对其他转录因子的结合活性无影响。它抑制 IL-1β 诱导的 Mmp-3、Mmp-13、Adamts-5 转录上调。

T-3364366 是一种噻吩并嘧啶酮 delta-5 去饱和酶 (Δ5D) 抑制剂，在 HepG2 和 RLN-10 细胞中的 IC50 分别为 1.9 nM 和 2.1 nM。

T-00127_HEV1 是有效的phosphatidylinositol 4-kinase III beta 抑制剂，IC50为 60 nM。

T-1101 tosylate (TAI-95 tosylate) 是一种具有抗肿瘤活性的 Hec1 Nek2抑制剂。

T-kinin (Ile-Ser-bradykinin) 是一种涉及炎症研究的缓激肽类肽。

MC-VA-T-moiety(CH2-NH-CH3)–Exatecan (化合物 11-5) 作为一种Drug-Linker Conjugates for ADC，主要应用于合成抗癌活性的ADC。

FmocNH-PEG4-t-butyl ester 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.

Eriochrome Black T is a complexometric indicator. Eriochrome Black T is used in complexometric titrations.

Hydroxy-PEG12-t-butyl ester is a PEG derivative containing a hydroxyl group and a t-butyl ester. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. Under acidic conditions, the t-butyl protected carbox

3'-O-(t-Butyldiphenylsilyl)thymidine is a Nucleoside Derivative - Protected nucleoside w/NH2/OH open.

3'-O-t-Butyldimethylsilyl adenosine is a Nucleoside; Used for special nucleoside modification.

T-Type calcium channel inhibitor 2 (compound 6g) 是一种 T 型钙通道的有效抑制剂，能够作用于 Cav3.1 (α1G) (IC50: 31.0 μM)、Cav3.2 (α1H) (IC50: 83.1 μM)、Cav3.3 (α1I) (α1H) (IC50: 69.3 μM)。T-Type calcium channel inhibitor 2 对 A549、HCT-116 细胞表现出细胞毒性，IC50s 分别为5.0、6.4 μM。

N-Trityl-morpholino-T-5'-O-phosphoramidite is a Nucleoside Derivative - Morpholino nucleoside; Phosphoramidite.

5-(t-Butyloxycarbonylmethoxy)uridine is a Nucleoside Derivative - 5-Modified pyrimidine nucleoside.

T-611, a cytomegalovirus replication inhibitor, is used potentially for the treatment of cytomegalovirus infections.

(R)-GNA-T phosphoramidite is a Nucleoside Phosphoramidite.

N-DMTr-morpholino-T-5'-O-phosphoramidite is a Nucleoside Phosphoramidite.

T-3861174 is a prolyl tRNA synthetase (PRS) inhibitor, exhibiting significant in vitro anti-tumor activity with GCN2-ATF4 pathway activation.

T 82 is an antagonist of 5-HT3 and inhibitor of acetylcholinesterase (AChE) and used for the treatment of Alzheimer's Disease.

Ir[p-F(t-Bu)-ppy]3 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T64556。

T-1095A is an active metabolite of T-1095, a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs). Chronic administration of T-1095 (0.1% w w(-1) pellet chow, for 12 weeks) decreased blood glucose and haemoglobin A(1C) levels, and improved

Morpholino T subunit 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T64595。

T-226296 is a antagonist of melanin concentrating hormone receptor 1 (MCHR1).

t-Butyl acetate-PEG3-CH2COOH is a polyethylene glycol-derived PROteolysis TArgeting Chimera (PROTAC) linker, specifically designed for incorporation into the synthesis of PROTAC molecules.

SV40 large T antigen NLS, originating from Large T antigen residue 47 to 55, facilitates protein import into the cell nucleus. This peptide is specifically generated from Large T antigen residue 47 to 55.

Peptide T (TFA) is an octapeptide derived from the V2 region of HIV-1 gp120. It serves as a ligand for the CD4 receptor, effectively inhibiting the binding of HIV to the CD4 receptor.

Peptide T is an octapeptide from the V2 region of HIV-1 gp120. This synthetic octapeptide potentially functions through competitive inhibition of gp120 binding to the CD4 receptor, as well as interaction with vasointestinal peptide (VIP) receptors.

t-Boc-Aminooxy-PEG7-methane is a polyethylene glycol (PEG)-based linker, which finds application in the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Tos-PEG4-t-butyl ester (Tos-PEG4-Boc) is a PROTAC linker characterized by its PEG composition. This compound plays a crucial role in the synthesis of a range of PROTACs, including BI-3663, a highly selective PTK2 FAK PROTAC. It employs cereblon ligands to target E3 ligases for the degradation of PTK2, exhibiting potent inhibitory activity with an IC50 of 18 nM[1].

t-Boc-Aminooxy-PEG5-azide is a polyethylene glycol (PEG) derivative that serves as a linker for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Azido-PEG3-S-PEG4-t-butyl ester is a PEG-based PROTAC linker employed for PROTAC synthesis[1].

N-(Propargyl-PEG2)-N-Boc-PEG3-t-butyl ester is a polyethylene glycol (PEG)-based linker employed for the synthesis of proteolysis-targeting chimeras (PROTACs) [1].