og 1

COH34 analog 1 是一种 COH34 氧化类似物，可用于合成具有活性的化合物。

Resveratrol analog 1 是天然产物白藜芦醇的类似物，具有比白藜芦醇更显著的抗白血病活性。

LY88074 analog 1, a benzothiophene compound with nitrogen-containing non-basic side chains, can be utilized either independently or alongside estrogen or progestin. This agent is effective for mitigating post-menopausal symptoms, including osteoporosis, cardiovascular-related pathological conditions, and estrogen-dependent cancer.

DB04760 analog 1 is an analogue of DB04760.

Thiamine diphosphate analog 1, an analog of Thiamine diphosphate (the active form of vitamin B1 and a universal cofactor in key cellular pathways), mirrors the structure and potentially the function of its prototype.

TG101209 analog 1 (Compound 8h) 是一种BUB1B的抑制剂，IC50为10.36 μM。同时，该化合物对Caki-1表现出细胞毒性，IC50为1.347 μM，并能够诱导细胞坏死和凋亡(apoptosis)。

COG 133 Acetate 是一种肽，序列为 Ac-Leu-Arg-Val-Arg-Leu-Ala-Ser-His-Leu-Arg-Lys-Leu-Arg-Lys-Arg-Leu-Leu-amide .

CE3F4 analog 1 is an analogue of CE3F4.

COG 133 TFA 是载脂蛋白 E (Apolipoprotein E, APOE) 肽的片段。COG 133 与 ApoE 全息蛋白竞争结合 LDL 受体，具有有效的抗炎和神经保护作用。COG 133 TFA 也是nAChR 拮抗剂，IC50为 445 nM。

Cryptophycin analog 1, an ADC payload, exhibits anticancer activity and demonstrates cellular potency an order of magnitude greater than the approved ADC payloads MMAE and DM1 [1].

ML120 analog 1 (compound 1) acts as a competitive inhibitor of Hematopoietic protein tyrosine phosphatase (HePTP), exhibiting a K i value of 0.69 μM [1].

HMBPP analog 1 (6e) 为 Trifluoromethyl 的类似物,其在HMBPPELISA 反应中表现出强抑制和弱激活的双重性能.

ML171 analog 1 作为NOX1抑制剂,主要应用于癌症研究领域.

Fraxinellone analog 1 (compound 2) 作为一种Nrf2介导的抗氧化防御系统激活剂,显示出高效和迅速的效应,并对谷氨酸诱导的兴奋性毒性提供保护.它通过诱导Gpx4、Sod1和Nqo1等抗氧化基因的表达来发挥作用.此外,Fraxinellone analog 1 还具备神经保护特性,可调节抗氧化应激和炎症,适用于神经退行性疾病的相关研究.

ML179 是一种有效的选择性肝受体同源物 1 (LRH1, NR5A2) 反向激动剂，IC50 为 320 nM。

Ecteinascidins is a family of tetrahydroisoquinoline alkaloids with wide range of antitumor and antimicrobial activities. Ecteinascidin-Analog-1 is a useful intermediate for chemical sythesis of Ecteinascidin analogues.

Nucleoside-Analog-1 is a 4′-Azidocytidine analogue, used to against Hepatitis C virus replication.

YT 6-2 analog-1 (compound 2-3) 是一种靶向p62 SQSTM1的自噬靶向配体 (ATL)，用于合成AR (Androgen Receptor)的AUTOTAC降解剂ATC-324。ATC-324 通过诱导 AR p62 复合物的形成，促进 AR 的自噬-溶酶体降解，并能降低核 AR 含量，抑制 AR 和 AR-v7 相关基因的表达，对前列腺癌中常见的 AR 突变体也具有降解作用。

DLPC 是LRH-1 激动剂的配体，是一种可用于生物学研究的磷脂。

COG-1410 is an apolipoprotein E (apoE) peptide mimetic.

COG-1410 acetate 是一种载脂蛋白 E 衍生肽，可用于神经系统疾病的研究。

VUN 00829, also known as N-(m-PEG4)-N'-(PEG4-acid)-Cy5 is a near infrared (NIR) fluorescent Cy 5 labeled PEG derivative containing free terminal carboxyl acid. Terminal carboxylic acid can react with primary amine groups in the presence of of activators (e.g. EDC, or DCC) to form a stable amide bond. The hydophilic PEG spacer increases solubility in aqueous media. Cy5 labeled PEG derivative can be easily traced from its blue color and strong fluorescence. This product has no formal name at the moment. For the convenience of communication, a temporary code name was therefore proposed according to MedKoo Chemical Nomenclature (see web page: https: www.medkoo.com page naming).

SKOG102 是一种有效的 OLIG2抑制剂，可直接与 OLIG2 结合并干扰 OLIG2 结合 DNA 的能力。SKOG102 可用于胶质母细胞瘤 (GBM) 的研究。

PD 173955-Analog1 is a potent c-Src inhibitor known to have activity against a variety of cancers including colon, lung, head and neck carcinoma.