Others

(R)-IDO/TDO-IN-1 (化合物 25) 为一种具有优良药动学性质的吲哚胺-2,3-双加氧酶 (IDO) 抑制剂，在MC38异种移植模型中展现出抗肿瘤活性。该化合物还与抗PD-1单克隆抗体 (SHR-1210) 显示协同作用。

PF-06445974 has good selectivity for PDE4D, excellent brain permeability, and has a high level of specific binding in the "cold tracer" study.

FD-1080 free acid 是一种在 NIR-II 区域内具备激发及发射特性的荧光团（Ex=1064 nm, Em=1080 nm），适用于体内成像。

(S)-OSMI 3 (Ent-OSMI-3) 具有抗炎抗肿瘤活性，可用以研究糖尿病和神经退行性疾病。

HPK1-IN-34(Compound 143)是一种HPK1(Hematopoietic progenitor kinase 1)抑制剂，IC50< 0.1 μM，可用于研究癌症和免疫。

GNE-9278 是一种高度选择性的 NMDAR 正变构调节剂，能够作用于 GluN1 跨膜结构域 (TMD)。GNE-9278 可以作用于活化的 NMDAR，能够提高峰值电流和激动剂亲和力。

Sulfo-Cy5.5 Azide为含叠氮基团的点击化学试剂，兼具水溶性染料特性（Ex=673 nm, Em=707 nm），适用于肽、蛋白质及寡核苷酸的标记。

CNX-500 is a probe consisting of a covalent Btk inhibitor chemically linked to biotin. CNX-500 has inhibitory activity against Btk (IC50: 0.5 nM) and the ability to form a covalent bond with Btk. CNX-500 has low inhibitory effects on kinase EGFR and upstr

CRS3123 (REP-3123) dihydrochloride 是一种口服具有活力的全合成抗菌剂，能够有效抑制 Clostridioides difficile 甲硫氨酰-tRNA 合成酶 (MetRS)。CRS3123 dihydrochloride 能够用于 Clostridioides difficile 感染 (CDI) 的研究。

Phenazolam is an analytical reference standard categorized as a benzodiazepine. [1] This product is intended for research and forensic applications.

2-Acetamidofluorene 是一种强致癌物。2-Acetamidofluorene 可用于诱导肝细胞癌 (HCC) 和多原发肿瘤。

Aminobutane bisphosphonate is a powerful inhibitor of bone resorption. It can potentially be a useful measure for controlling hypercalcemia in patients with carcinoma.

Finazaflo has insecticidal and acaricidal effects.

C188 is a cell-permeable naphthol compound and a STAT3 inhibitor. C188 inhibits IL-6-stimulated STAT3 Tyr705 phosphorylation and nuclear translocation in HepG2 cells by targeting STAT3 SH2 domain peptide-binding pocket, while exhibiting little effect agai

(R)-PS210, the R enantiomer of PS210 is a substrate-selective allosteric PDK1 activator with an (AC50 of 1.8 μM).

DiZPK Hydrochloride is a structural analog of pyrrolysine (Pyl), acting as a photocrosslinker for identifying direct protein-protein interactions in living prokaryotic and eukaryotic cells.

PCSK9-IN-11 (compound 5r) 是口服有效的 PCSK9 抑制剂。 PCSK9-IN-11 在 HepG2 细胞中抑制 PCSK9 转录活性 (IC50= 5.7 μM)。 PCSK9-IN-11 可以增加 LDL 受体 (LDLR) 蛋白水平，可用于动脉粥样硬化研究。

SPiDER-βGal-2是一种有效的β-半乳糖苷酶活性探针，适合标记培养物中的活细胞。

CCG-273220 是 G 蛋白偶联受体 (GPCR) 激酶 5 (GRK5) 共价抑制剂 (IC50: 220 nM)。CCG-273220 可以共价结合GRK5亚家族特异性残基 Cys474 ，而对GRK5的选择性比 GRK2 高。

DHPS-IN-1, a chemical compound, demonstrates exceptional inhibitory potency against melanoma cells, as evidenced by its IC50 value of 0.014 μM.

Ubiquitination-IN-1 是一种有效的泛素化和Cksl-Skp2蛋白互作抑制剂 (IC50=0.17 μM) 抑制剂，增加 p27 水平，可通过阻断肿瘤抑制因子的降解发挥作用。

TDP1 Inhibitor-1 is a potent inhibitor of Tyrosyl-DNA Phosphodiesterase 1 (TDP1) (IC50 of 7 μM).

PXS-5153A monohydrochloride 是一种有效的、选择性的、具有口服活性和快速起效的赖氨酰氧化酶 2/3(LOXL2/LOXL3)的双抑制剂，对几乎所有哺乳动物物种 LOXL2的 IC50均< 40 nM，对人类 LOXL3 的 IC50为63 nM。PXS-5153A monohydrochloride 可减少交联并改善纤维化。

CGP 47656 is an agonist of GABAB receptor.

Dapagliflozin impurity is the enantiomer of Dapagliflozin, Dapagliflozin is a sodium glucose transporter 2 inhibitor.

FTO-IN-7d is the first inhibitor of the RNA demethylase FTO with anticonvulsant activity.

GSK2245035 is a highly selective intranasal TLR7 agonist with preferential Type-1 interferon (IFN)-stimulating properties (pEC50s: 9.3 and 6.5 for IFNα and TFNα). It effectively suppresses allergen-induced Th2 cytokine production in human peripheral blood

LDN-27219 是一种人组织型转谷氨酰胺酶抑制剂(IC50:600 nM)。

SOCE inhibitor 1 is a inhibitor of store-operated calcium entry (SOCE)(IC50 of 4.4 μM).

MRT-2359 是一种有效的且可口服的 GSPT1 降解剂，具有抗肿瘤活性。MRT-2359 对耐药非小细胞肺癌 (NSCLC) 和小细胞肺癌 (SCLC) 细胞的生长具有抑制作用。MRT-2359 在 MYC 驱动的细胞系中表现出优先活性。

Infigratinib monohydrate, also known as, BGJ398 monohydrate or NVP-BGJ398 monohydrate, is a pan FGFR kinase inhibitor, and is an orally bioavailable pan inhibitor of human fibroblast growth factor receptors (FGFRs) with potential antiangiogenic and antineoplastic activities. pan FGFR kinase inhibitor BGJ398 selectively binds to and inhibits the activities of FGFRs, which may result in the inhibition of tumor angiogenesis and tumor cell proliferation, and the induction of tumor cell death. Infigratinib monohydrate was approved in 2021 to treat adults with cholangiocarcinoma whose disease meets certain criteria.

S107 是一种 RyR 选择性 1, 4-苯并硫氮杂卓衍生物，通过增强 calstabin2 与突变和/或 PKA 磷酸化通道的结合亲和力来稳定 RyR2 通道。

4-Chlorokynurenine is a prodrug of 7-Cl-kynurenic acid (7-Cl-KYNA), a potent, selective antagonist of the NMDA/glycine receptor.

Melittoside (Standard) 是 Melittoside 的标准品。适用于定量分析、质量控制及生化实验等相关研究。Melittoside 是一种天然酚苷，存在于梅利藤属的花蜜中。它具有抗氧化、抗炎和抗真菌的活性，以及研究了它在治疗各种疾病中的潜在用途，包括癌症、糖尿病和心血管疾病。

1,2,3,5-Tetra-O-acetyl-D-xylofuranose is a starting material for the synthesis of nucleosides.

DGKα-IN-9 (example 298) 属于DGKα抑制剂。