84
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T17043 |
TES
|
Others | Others |
TES 可用于制备 pH 范围为 6.8-8.2 的缓冲溶液,其 pKa 值为 7.550。 | |||
T17042 |
TES-1025
|
Others | Others |
TES-1025 是一种有效且特异性的人 α-氨基-β-羧基粘康酸-ε-半醛脱羧酶 (ACMSD, IC50 = 13 nM) 抑制剂。 | |||
T13132 | TES-991 | Others | Others |
TES-991 is a potent and selective inhibitor of human α Amino-β-carboxymuconate-ε-semialdehyde Decarboxylase (ACMSD)(IC50 of 3 nM). | |||
T2544 |
Bazedoxifene acetate
醋酸巴多昔芬,WAY-TES 424,TSE 424,WAY-140424 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Bazedoxifene acetate (WAY-TES 424) 是一种非甾体的、有口服活性的、选择性的雌激素受体调节剂,能够作用于 ERα (IC50:26 nM) 和 ERβ (IC50:99 nM) ,可用于研究骨质疏松症。它也是一种IL-6/GP130蛋白相互作用抑制剂,可用于研究胰腺癌。 | |||
T73082 |
TES sodium
|
||
TES sodium,作为Good's缓冲剂之一,具有pH 6.8-8.2的缓冲范围,其在25°C时的pKa值为7.550。 | |||
T76831 |
Tesidolumab
LFG316 |
Complement System | Immunology/Inflammation |
Tesidolumab (LFG316) 是一种全人IgG1/λ抗c5单克隆抗体。Tesidolumab (LFG316)对crovalimab和C5有抑制作用, 阻断C5的切割,防止膜攻击复合体的后续形成,可用于研究血管外溶血。 | |||
T17044 |
Tesaglitazar
|
PPAR | DNA Damage/DNA Repair; Metabolism |
Tesaglitazar 是一种有效且具有选择性的过氧化物 PPAR α / γ受体双重激动剂,对 PPARγ的亲和力比 PPARα更有效,对大鼠PPARα和人PPARα的EC50分别为13.4 μM 和3.6 μM,对大鼠PPARγ和人类 PPARγ的EC50都是0.2 μM。Tesaglitazar 诱导大鼠皮下组织间质间充质细胞DNA 合成和纤维肉瘤形成。 | |||
T16994 |
Pimitespib
TAS-116 |
HSP | Cytoskeletal Signaling; Metabolism |
Pimitespib (TAS-116) 是一种 ATP 竞争性和高度特异性的 HSP90α/HSP90β 抑制剂,Ki 值分别为 34.7 nM 和 21.3 nM。 | |||
T2288L |
Motesanib Diphosphate
Motesanib,AMG 706,二磷酸莫替沙尼 |
VEGFR; c-Kit | Angiogenesis; Tyrosine Kinase/Adaptors |
Motesanib Diphosphate (AMG 706) 是一种有效的VEGFR1/2/3的 ATP 竞争性抑制剂,IC50值为 2 nM/3 nM/6 nM,与对 Kit 的选择性相似,是 PDGFR 和 Ret 的 10 倍多。 | |||
T77404 |
Tesnatilimab
IPH-23XX,JNJ-64304500,JNJ 4500 |
Others | Others |
Tesnatilimab 是一种有效的人源化 IgG4 单克隆抗体,可与免疫激活受体 NKG2D 结合。Tesnatilimab 具有潜在的免疫调节和抗炎活性,可用于研究活动性溃疡性结肠炎 。 | |||
TP2219L |
Alytesin acetate
|
Others | Others |
Alytesin acetate 是一种两栖类铃蟾肽样肽。 | |||
TQ0166 |
Tesevatinib
KD-019,XL-647,EXEL-7647 |
EGFR; VEGFR; FLT; Ephrin Receptor | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tesevatinib (XL-647) 是一种口服的多靶点酪氨酸激酶抑制剂,对 EGFR、ErbB2、KDR、Flt4和 EphB4的 IC50值分别为 0.3、16、1.5、8.7和 1.4 nM。 | |||
T2309 |
Ganetespib
STA-9090 |
Apoptosis; HSP; HIF | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism |
Ganetespib (STA-9090) 是一种热休克蛋白 90 抑制剂,通过抑制 HIF-1α 和 STAT3 对大肠癌具有抗血管生成作用。它还具有细胞毒性。 | |||
T16412 |
Oteseconazole
VT-1161 |
P450; Antifungal | Metabolism; Microbiology/Virology |
Oteseconazole (VT-1161) 是一种口服有效的抗真菌剂,结合并抑制白色念球菌的 CYP51,Kd 值小于 39 nM。 | |||
T22746 |
Tesmilifene fumarate
DPPE fumarate |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Tesmilifene fumarate (DPPE fumarate) 是一种 H1C 受体拮抗剂,可增强化疗的细胞毒性且保护正常细胞。 | |||
T9170 |
Testosterone decanoate
|
Others | Others |
Testosterone decanoate 是天然存在的雄激素睾酮酯,具有长效男性抗生育活性。 | |||
T2288 |
Motesanib
AMG 706,莫特塞尼,莫替沙尼 |
VEGFR; c-Kit | Angiogenesis; Tyrosine Kinase/Adaptors |
Motesanib (AMG 706) 是有效的、ATP 竞争性的 VEGFR1/2/3 的抑制剂,其IC50值为 2 nM/3 nM/6 nM,与对 Kit 的选择性相似,是 PDGFR 和 Ret 的 10 倍多。 | |||
T38565 |
Testosterone glucuronide
|
Others | Others |
Testosterone glucuronide 是睾酮的主要尿液代谢物,是一种潜在的尿液生物标记物。 | |||
T9035 |
Testosterone undecanoate
|
Others; Androgen Receptor | Endocrinology/Hormones; Others |
Testosterone undecanoate 是一种睾酮酯,是睾酮的代谢产物,睾酮是很有前途的男性激素避孕雄激素。 | |||
T81135 |
Sodium caseinates
Casein sodium salt from bovine milk |
Others | Others |
Sodium caseinates (CasNa) 是一种可溶性酪蛋白,也是一种食品添加剂和乳化剂,广泛应用于食品工业。 Sodium caseinates (CasNa) 在体外诱导小鼠带粒细胞的分化和 M-CSF 产生,诱导功能性粒细胞的粒细胞生成。 | |||
TP2058L |
Catestatin acetate
Catestatin acetate(142211-96-9 free base) |
Endogenous Metabolite; AChR | Metabolism; Neuroscience |
Catestatin acetate 是 nAChR 的非竞争性拮抗剂,可抑制儿茶酚胺的释放。 Catestatin acetate 调节心脏功能和血压。 | |||
T6791 |
BPTES
|
transporter; Glutaminase | Metabolism; Proteases/Proteasome |
BPTES 是一种特异性 GlutamiN/Ase GLS1 (KGA) 抑制剂,IC50=0.16 μM。 | |||
T62684 |
Lartesertib
ATM Inhibitor-5,M4076 |
ATM/ATR | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
Lartesertib (ATM Inhibitor-5) 是一种丝氨酸/苏氨酸蛋白激酶 ATM 的抑制剂,具有潜在的抗癌活性,可用于研究肺癌。 | |||
T18873 |
VHL Ligand-Linker Conjugates 17
|
Others | Others |
VHL Ligand-Linker Conjugates 17 are chemical compounds that consist of a VHL ligand specialized for the E3 ubiquitin ligase, as well as a PROTAC linker. These conjugates are utilized in the synthesis of various PROTACs, including the notable ARD-266. ARD-266 is an exceptionally effective androgen receptor (AR) PROTAC degrader[1]. | |||
T17895 |
cIAP1 Ligand-Linker Conjugates 1
E3 ligase Ligand-Linker Conjugates 41 |
Others | Others |
cIAP1 Ligand-Linker Conjugates 1 is composed of an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 1, is particularly useful in the development of SNIPERs[1]. | |||
T39609 |
cIAP1 Ligand-Linker Conjugates 16
cIAP1 Ligand-Linker Conjugates 16 |
||
cIAP1 Ligand-Linker Conjugates 16 refers to a specific type of ligase ligand-linker conjugate, possessing the ability to engage with E3 ligases, which finds application in the synthesis of PROTACs. | |||
T17364 |
AhR Ligand-Linker Conjugates 1
E3 Ligase Ligand-Linker Conjugates 57 |
Others | Others |
AhR Ligand-Linker Conjugates 1, also known as E3 Ligase Ligand-Linker Conjugates 57, is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a SNIPER linker. It is specifically designed to be used in the development of SNIPER[1]. | |||
T17884 |
cIAP1 Ligand-Linker Conjugates 11 Hydrochloride
E3 ligase Ligand-Linker Conjugates 33 Hydrochloride |
Others | Others |
cIAP1 Ligand-Linker Conjugates 11 Hydrochloride is a chemical compound consisting of an IAP ligand that targets the E3 ubiquitin ligase, along with a PROTAC linker. It is primarily utilized in the development of SNIPERs, a molecular tool for targeted protein degradation[1]. | |||
T17898 |
cIAP1 Ligand-Linker Conjugates 7
E3 ligase Ligand-Linker Conjugates 44 |
Others | Others |
cIAP1 Ligand-Linker Conjugates 7 is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a PROTAC linker. It is utilized in the design of SNIPERs[1]. | |||
T28952 |
Testosterone glucoside
|
||
Testosterone glucoside is an androgen receptor agonist. | |||
T17894 |
cIAP1 Ligand-Linker Conjugates 3
E3 ligase Ligand-Linker Conjugates 40 |
Others | Others |
cIAP1 Ligand-Linker Conjugates 3 are chemical compounds comprising an IAP ligand designed specifically for the E3 ubiquitin ligase and a PROTAC linker. These conjugates, denoted as cIAP1 Ligand-Linker Conjugates 3, find utility in the design of SNIPERs, short for Specific and Non-genetic IAP-dependent Protein Erasers [1]. | |||
T81012 |
Testololactone
|
||
Testololactone,一种芳香酶抑制剂,常用于乳腺癌研究。 | |||
TP2058 |
Catestatin
|
||
Non-competitive nicotinic cholinergic antagonist; selectively inhibits nicotinic-stimulated catecholamine secretion from chromaffin cells and noradrenergic neurons (IC50 ~ 200 nM). Blocks nicotinic-induced cationic signaling (IC50 ~ 200 - 250 nM) and inhi | |||
TMIH-0560 |
Testosterone-d3
|
||
Testosterone-d3 是 Testosterone 的氘代化合物。 | |||
T24454 |
Metesind Glucuronate
AG 331,AG331,AG-331 |
||
Metesind Glucuronate is an antineoplastic. It also is a specific thymidylate synthase inhibitor. | |||
T17886 |
cIAP1 Ligand-Linker Conjugates 15 hydrochloride
E3 ligase Ligand-Linker Conjugates 34 hydrochloride |
Others | Others |
cIAP1 Ligand-Linker Conjugates 15 hydrochloride is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound is useful in the development of SNIPERs[1]. | |||
T28951 |
Tesofensine
NS 2330,NS2330,NS-2330 |
||
Tesofensine, a serotonin–noradrenaline–dopamine reuptake inhibitor, is used potentially for the treatment of obesity. | |||
T72241 |
Teslexivir hydrochloride
BTA074 hydrochloride ; AP 611074 hydrochloride,BTA074 hydrochloride,AP 611074 hydrochloride |
||
Teslexivir (BTA074) hydrochloride 是一种有效的抗病毒剂。Teslexivir hydrochloride 是两种关键病毒蛋白 (E1和 E2) 相互作用的强效选择性抑制剂,这两种蛋白的相互作用是人乳头瘤病毒 (HPV) 6 和 11 的 DNA 复制和病毒产生的重要步骤。Teslexivir hydrochloride 可用于尖锐湿疣的研究。 | |||
T76938 | Camoteskimab | ||
Camoteskimab (AVTX-007)为全人源、高亲和力抗IL-18单克隆抗体,展现于自身炎症性疾病研究潜力,包括成人斯蒂尔病(AOSD)。 | |||
T76960 | Verpasep caltespen | ||
Verpasep caltespen (HspE7) 是一种重组融合蛋白,来源于Mycobacterium bovis Calmette-Guérin 热休克蛋白 65 (Hsp65),其 C 末端与HPV16 的 E7 蛋白共价连接。Verpasep caltespen 可用于人乳头瘤病毒 (HPV)引起的癌前病变和癌性病变研究。 | |||
T126122 |
Matesaponin 1
|
||
Matesaponin 1 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 T126122,CAS号为 126622-38-6。 | |||
T70409 |
6alpha-Fluorotestosterone
|
||
6alpha-Fluorotestosterone is a synthetic nonaromatizable androgen analog of testosterone. It binds to and activates specific nuclear receptors inhibits and is equipotent to testosterone. | |||
T17045 |
Teslexivir
BTA074,AP 611074 |
Others | Others |
Teslexivir is a topical antiviral agent that is an effective and selective inhibitor of the interaction between two essential viral proteins, E1 and E2. | |||
T34812 |
Tesicam
|
||
Tesicam is a bioactive chemical. | |||
T34303 |
Retrotestosterone
Lumitestosterone |
||
Retrotestosterone, a biochemical, can affect testosterone. | |||
T18364 |
Tesirine
MP-PEG8-VA-PABC-PBD Dimer |
Others | Others |
MP-PEG8-VA-PABC-PBD Dimer is a drug-linker conjugates for ADC which is used in the treatment of several cancers. PBD Dimer is a DNA alkylating which inhibits DNA replication[1]. | |||
T17899 |
cIAP1 Ligand-Linker Conjugates 9
E3 ligase Ligand-Linker Conjugates 45 |
Others | Others |
cIAP1 Ligand-Linker Conjugates 9 feature an IAP ligand specifically targeting the E3 ubiquitin ligase, along with a PROTAC linker. It is valuable tools for developing SNIPERs[1]. | |||
T28023 |
Metesind
AG331,AG-341,AG-331,AG341 |
||
Metesind, a thymidylate synthase inhibitor, is used potentially for the treatment of brain cancer and solid tumours. | |||
TP2219 |
Alytesin
|
Others | Others |
Amphibian bombesin-like peptide | |||
T76567 |
Met-RANTES (human)
|
||
Met-RANTES (human) 为一部分CCR5拮抗剂,能够降低血液单核细胞向肝脏浸润的程度。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TC0025 |
Testosterone acetate
NSC523836,NSC-523836,NSC 523836,醋酸睾酮 |
Others | Others |
Testosterone acetate (NSC-523836) 是一种 Testosterone 前药,是一种天然存在的雄激素睾酮酯。它可用于阳痿、虚弱、疲劳和性腺机能减退的研究。 | |||
T3130 |
Testosterone phenylpropionate
Testosterone hydrocinnamate,苯丙酸睾酮,Retandrol,Testosterone 17-phenylpropionate |
Others | Others |
Testosterone phenylpropionate (Testosterone 17-phenylpropionate) 是一种长效雄激素。d3-Testosterone phenylpropionate 可用作内标物。 | |||
TC0026 |
Testosterone benzoate
|
Others | Others |
Testosterone benzoate 是一种合成的注射合成代谢雄激素类固醇 (AAS) 和一种雄激素酯。 | |||
T0433 |
Artesunate
WR-256283,青蒿琥酯 |
Virus Protease; Ferroptosis; STAT; Parasite | Apoptosis; JAK/STAT signaling; Microbiology/Virology; Stem Cells |
Artesunate (WR-256283) 是治疗疟疾的青蒿素组药物的一部分。 它是青蒿素的半合成衍生物,具有水溶性。 | |||
TN6511 |
Tessaric acid
|
||
Tessaric acid has antifeedant and allelochemical effects. Tessaric acid derivatives induce G/M cell cycle arrest in human solid tumor cell lines. |