Others

S-14671 is a 5-HT1A receptor agonist (pKi = 9.3) with high efficacy and exceptional in vivo potency. S-14671 also acts as a 5-HT2A and 5-HT2C receptor antagonist (both are pKi = 7.8).

Isocytidine derivative; fluoro-modified nucleoside

5'-Deoxy-5'-N-(2-chloroethyl)aminothymidine is a Nucleoside Derivative - 5'-Modified nucleoside.

TRPV2-selective blocker 1 (compound IV2-1) 为选择性TRPV2通道阻断剂，具有6.3 μM IC50，不对TRPV1、TRPV3和TRPV4通道产生影响。该化合物能够抑制巨噬细胞中TRPV2介导的Ca2+流入，进而抑制其吞噬功能。

SARM1-IN-2 是一种有效的 SARM1 抑制剂，可用于研究代谢系统和神经系统相关疾病。

Stepronin (TTPG) 具有祛痰活性并抑制气道分泌。

5-Methyl-2(5H)-furanone是一种呋喃酮，对多种ASPERGILLUS具有抗真菌活性，可用于生物化学实验和药物合成研究。

Lactyl-CoA是一种酰基辅酶A，其辅酶A的巯基与乳酸的羧基发生了缩合反应，可用于合成乳酸基共聚物的生物材料。

NAV-2729 是有效的Arf1/Arf6活化抑制剂。

allosteric potentiator of mGlu5

GPR40 agonist 1 is an effective new GPR40 agonist (EC50s: 17 nM and 2 nM for rGPR40 and hGPR40).

Propylene carbonate是一种常用的极性非质子溶剂，广泛应用于生物化学实验和药物合成研究。

GOAT-IN-1 is an inhibitor of ghrelin O-acyltransferase (GOAT), which could be useful for the prophylaxis or treatment of diabetes, hyperlipidemia, non-alcoholic fatty liver, Alzheimer’s disease, Parkinson’s disease, cerebrovascular dementia, cerebral infa

DNA-PK-IN-2 is a highly effective inhibitor of DNA-dependent protein kinase (DNA-PK), which is a complex enzyme composed of Ku70/Ku80 heterodimer and DNA-PK catalytic subunit (DNA-PKcs). With its potential applications in cancer research, DNA-PK-IN-2 demonstrates promise as a valuable tool for studying cancer diseases [1].

Baxdrostat 是一种醛固酮合成酶抑制剂。

Tussilagone 是Tussilago farfara 的主要活性成分，具有抗炎作用。它抑制盲肠结扎和穿刺导致脓毒症的小鼠的炎症反应，提高其生存率。它改善葡聚糖硫酸钠诱导的小鼠结肠炎的炎症反应。

Indacrinone is an investigational diuretic.

Mal-amido-PEG4-TFP ester, a PEG-based PROTAC linker, finds utility in the synthesis of PROTACs[1].

GKA-22 is a human glucokinase allosteric activator in the absence of glucose.

INO5042 is an anti-inflammatory agent.

USP1-IN-3 是 USPI 的选择性抑制剂，能够抑制 USPI-UAFI (IC50<30 nM)。USP1-IN-3 可用于研究癌症。

Dual AChE-MAO B-IN-2 是一种有效的、双重的 AChE (IC50: 0.12 μM) 和 MAO B (IC50: 0.01 μM) 抑制剂。Dual AChE-MAO B-IN-2 具有潜力进行阿尔茨海默病的研究。

CDK7-IN-16 (compound 9) 是一种 CDK 7 的有效抑制剂 (IC50: 1-10 nM)。CDK7-IN-16 能够用于研究抗癌，特别是转录异常的癌症。

Z-DEVD-AFC 在生命科学相关研究中具有广泛的应用。

Azido-PEG10-Boc 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.

AST 7062601 是一种高效 Ucp1 诱导剂，在原代小鼠棕色脂肪细胞中促使内源性 Ucp1 表达。AST 7062601 可能用于研究肥胖。

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.

γ-Glu-Tyr (gamma-Glutamyltyrosine) 是一种对二肽基肽酶-IV (DPP-IV) 具有竞争性抑制作用的 kokumi 肽，可用于研究糖尿病。

Boc-NH-PEG10-CH2CH2COOH is a polyethylene glycol (PEG)-based PROTAC linker utilized for PROTAC synthesis[1].

7-Methoxyflavone 是一种分离自 Zornia brasiliensis 的化合物。它能够抑制福尔马林疼痛反应神经源期的舔爪时间 (65.6%)，有外周镇痛活性，但不影响炎症期的伤害性反映。

RET-IN-5 是 RET 的有效抑制剂 (IC50: 4.57 nM)。

RTIL 13 is a highly effective inhibitor of dynamin GTPase, exhibiting an IC50 value of 2.3 μM for dynamin I GTPase. Furthermore, it selectively interacts with the pleckstrin homology lipid binding domain. This compound effectively suppresses both receptor-mediated and synaptic vesicle endocytosis, demonstrating IC50 values of 9.3 μM and 7.1 μM, respectively.

Alexidine 是一种双双胍，对多种真菌病原体具有抗真菌 (antifungal) 和抗生物膜作用。Alexidine 靶向哺乳动物细胞中的线粒体酪氨酸磷酸酶PTPMT1，能够导致线粒体凋亡 (apoptosis)，表现出抗肿瘤作用。

(S)-Sitagliptin phosphate, the less active S-enantiomer of Sitagliptin phosphate, is a high-potency inhibitor of DPP4. It exhibits an IC50 of 19 nM in Caco-2 cell extracts.

Nigakinone 是一种苦木中含量丰富的生物碱，具有重要的药理活性。

AChE/MAO-IN-1 是一种有效的AChE、MAO-A 和MAO-B 抑制剂，对人 AChE、MAO-B 和MAO-A 的IC50分别为 0.0248、0.0409 和 0.1108 μM。