15:1

Ginkgolic Acid (Romanicardic acid) 是一种天然化合物， 在体外实验中抑制SUMOylation，IC50=3.0 μM。

Tunicamycin 15:1 is a mixture of tunicamycin structural isomers that contain a 15-carbon N-acyl chain with variable branching patterns. The N-acyl chain incorporated into tunicamycins, like tunicamycin 15:1, is derived from the same pool of cellular branched-chain fatty acids (BCFAs) inStreptomycesand directly impacts the biological activity of each individual tunicamycin variant.1,2,3Purified tunicamycin 15:1 withiso,anteiso, or a mixture ofisoandanteisobranching configurations inhibit bacterial phospho-MurNAc-pentapeptide transferase (MraY) with IC50values of 0.05, 0.36, and 0.09 μM, respectively.2 1.Price, N.P.J., Jackson, M.A., Hartman, T.M., et al.Branched chain lipid metabolism as a determinant of the N-Acyl variation of Streptomyces natural productsACS Chem. Biol.16(1)116-124(2021) 2.Hering, J., Dunevall, E., Snijder, A., et al.Exploring the active site of the antibacterial target MraY by modified tunicamycinsACS Chem Biol.15(11)2885-2895(2020) 3.Duksin, D., and Mahoney, W.C.Relationship of the structure and biological activity of the natural homologues of tunicamycinJ. Biol. Chem.257(6)3105-3109(1982)

Cardanol (C15:1) 存在于腰果壳液中，可诱导人黑色素瘤细胞线粒体相关的细胞凋亡。

Sphingosine (d18:1), an amino alcohol, is chiefly recognized for its 18-carbon unsaturated hydrocarbon chain. Nevertheless, in mammalian tissues, both sphingosine and its variant, dihydrosphingosine, feature hydrocarbon chains ranging from 12 to 26 carbons. Sphingosine (d15:1) represents a naturally rare variant, serving as an internal standard for chromatographic or spectrometric analyses of sphingoid compounds.

Ginkgolic Acids(C13:0,C15:1,C17:2,C15:0,C17:1) 是一种天然产物，可用作天然产物对照品，用于生命科学相关领域的研究，其产品编号为 TN8870。

H-151 是一种 STING 拮抗剂，具有高效性和选择性。H-151 与 STING 的 Cys91 共价结合，抑制 Cys91 的棕榈酰化，从而抑制 STING 的活性。H-151 可用于体内外自身炎症性疾病的研究。

MW01-2-151SRM 是一种新型可穿过血脑屏障的小分子小胶质细胞活化抑制剂，具有抗神经炎作用，可减弱神经炎症模型中的神经胶质细胞因子上调，可用研究创伤性脑损伤、阿尔茨海默病和海藻氨酸毒性。

(S)-5-chloro-N-(1-((4-chlorophenyl)amino)-1-oxo-3-phenylpropan-2-yl)-2-hydroxybenzamide 具有抗真菌和抗结核活性。

MV151 是一种具有细胞渗透性的荧光广谱蛋白酶体抑制剂，特异性靶向活细胞中蛋白酶体和免疫蛋白酶体的所有活性亚基，可用于体外和体内标记蛋白酶体。

7-Amino-4-(trifluoromethyl)coumarin (Coumarin 151) 是一种荧光标记物，其激发和发射波长分别为400和500 nm，可用来灵敏的检测蛋白酶。

I-BET151 (GSK1210151A) 是 BRD2 3 4 的特异性 BET 抑制剂，IC50值分别为0.5、0.25、0.79 μM。

4(15),11-Oppositadien-1-ol 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN2996，CAS号为 70389-96-7。

E3 Ligase Ligand-linker Conjugate 151 是一种由E3连接酶配体和连接子组成的偶联物。E3 Ligase Ligand-linker Conjugate 151 可用于合成PROTACSMARCA2 4 degrader-36。

ZZ151是一种高效、协同且选择性的SOS1 PROTAC，针对KRAS突变癌症展示出体内抗肿瘤活性。该化合物能够快速且特异性地诱导SOS1降解，并在多种KRAS突变驱动的癌细胞中表现出强大的抗增殖效果。此外，在具KRASG12D和G12V突变的小鼠异种移植模型中展现出卓越的抗癌效果。ZZ151是一种有前景的先导化合物，适合开发用于KRAS突变治疗的新型化疗药物。

I-BET 151 dihydrochloride is a BET bromodomain inhibitor that prevents BET from recruiting to chromatin.

Potent and selective CLK inhibitor (IC50 values are 28, 88 and 510 nM for CLK4, 1 and 2, respectively). Exhibits no significant activity at CLK3, DYRK, CDK or GSK3 at a concentration of 10 μM. Inhibits growth of a range of cancer cell lines in vitro at subnanomolar concentrations. Walter et al (2018) Molecular structures of cdc2-like kinases in complex with a new inhibitor chemotype. PLoS One 13 e0196761 PMID:29723265

Plp(139-151) trifluoroacetate 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 T64674。

(3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl (Z)-octadec-9-en-1-yl carbonate 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 T65075，CAS号为 17110-51-9。

(8S,9S,10R,14S)-13-Ethyl-11-methylene-2,3,7,8,9,10,11,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(6H)-one 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 T66298，CAS号为 54024-21-4。

YM-543, also known as ASP-543, is a selective SGLT2 inhibitor. Sodium-glucose cotransporter 2 (SGLT2) is a specifically expressed transporter in the kidney that plays an important role in renal glucose reabsorption, and its inhibition may present a novel therapeutic strategy for treating diabetes. YM543 potently and selectively inhibited mouse and human SGLT2 activities at nanomolar ranges. In vivo single oral administration of YM543 dose-dependently and significantly reduced blood glucose levels and improved glucose tolerance with a concomitant increase in urinary glucose excretion in KK Ay type 2 diabetic mice, effects that were sustained even after 12 h.

AM4299 A is a novel thiol protease inhibitor.

JTE 151A is a novel RORγ inverse agonist.

HBVSeq1 aa:141-151 是一种肽。HBVSeq1 aa:141-151 可用于慢性乙型肝炎病毒（HBV）的研究。

Clenoliximab (IDEC-151)为一种猕猴-人嵌合型单克隆抗体（immunoglobulin G4），特异性结合于T淋巴细胞表面CD4分子。该化合物主要用于类风湿性关节炎的科研领域。