asp-2

ASP-2205，作为一种5-HT2C受体激动剂，具有针对性的激活效果（人5-HT2C受体，EC50=0.85 nM; 大鼠5-HT2C受体，EC50=2.5 nM）。该化合物通过增强通过5-HT2C受体介导的阴部神经尿道闭合反射，有效地用于预防尿失禁。

MASP-2-IN-1 (Compound 77) 是一种甘露聚糖结合凝集素相关丝氨酸蛋白酶 (mannan-binding lectin-associated serine protease，MASP) 抑制剂，能够抑制MASP2和MASP3，其IC50分别为11.4 nM和13.2 µM。该化合物对hERG通道的抑制作用较弱，IC50为175 µM。在小鼠血浆中稳定性较差，半衰期为4.4小时。

Gilteritinib (ASP2215) 是一种 FLT3 抑制剂 (IC50=0.29 nM)，也是一种 AXL 抑制剂 (IC50=0.73 nM)，具有 ATP 竞争性、选择性和口服活性。Gilteritinib 具有抗肿瘤活性，可以用于治疗 FLT3 突变阳性的 AML。

ASP-2905 是一种有效且选择性的钾通道 Kv12.2抑制剂。ASP2905 (ASP-2905) 可以穿越血脑屏障并具有抗精神病活性。

(Asp)2-Rhodamine 110 (D2R) 属于高荧光性的半胱天冬酶底物。

ASP2535 is a potent, selective, orally bioavailable, brain permeable and centrally-active glycine transporter-1 (GlyT1) inhibitor.ASP2535 can improve cognitive impairment in animal models of schizophrenia and Alzheimer's disease[1].

ASP2453是选择性的KRAS G12C 共价抑制剂，抑制Son of Sevenless 介导的KRAS G12C 和Raf 之间的相互作用，IC50为40 nM。

Amenamevir (ASP2151) 是一种新型解旋酶引发酶抑制剂，对水痘带状疱疹病毒和 1 型和 2 型单纯疱疹病毒具有活性，EC50值为 14 ng mL。

AZD-5248 is a potent, selective, first generation, oral inhibitor of dipeptidyl peptidase 1 (DPP1).

(Asp28)-Exenatide 是艾塞那肽 的降解产物。(Asp28)-Exenatide 可用作GLP-1R 激动剂。

'(Asp28)-Glucagon (1-29) (human, rat, porcine)' 为胰高血糖素的一种改良型结构，在第28位氨基酸残基上天冬氨酸（Asp）替换原有残基，显著提高了该化合物在生理pH条件下的溶解性，且保持了与天然胰高血糖素相同的生物活性。

Fmoc-Asp-NH2 是一种可切割的 ADC 接头，用于合成抗体-药物偶联物。

Z-Asp-CH2-DCB 是广谱半胱天冬酶的不可逆抑制剂。

R 396 (Acleu-asp-gln-trp-phe-glynh2) 是一种线性六肽，也是一种 NK-2 速激肽受体拮抗剂。

Antiflammin P2 is a nonapeptide fragment of lipocortin I which has no phospholipase A2 inhibitory and anti-inflammatory activity.

H-Arg-Gly-Asp-Cys-OH is a tetrapeptide that contains the arginine-glycine-aspartate (RGD) motif, a sequence that acts as a recognition site for various adhesion proteins.1It inhibits the binding of fibrinogen to endothelial cells and ADP-stimulated platelets with IC50values of 320 and 35 μM, respectively.2Implantation of titanium rods coated with H-Arg-Gly-Asp-Cys-OH increases bone formation in rat femurs.3H-Arg-Gly-Asp-Cys-OH has been conjugated to polyethylenimine to improve gene transfection efficiency.4 1.Park, H.S., Kim, C., and Kang, Y.K.Preferred conformations of RGDX tetrapeptides to inhibit the binding of fibrinogen to plateletsBiopolymers63(5)298-313(2002) 2.Tranqui, L., Andrieux, A., Hudry-Clergeon, G., et al.Differential structural requirements for fibrinogen binding to platelets and to endothelial cellsJ. Cell Biol.108(6)2519-2527(1989) 3.Ferris, D.M., Moodie, G.D., Dimond, P.M., et al.RGD-coated titanium implants stimulate increased bone formation in vivoBiomaterials20(23-24)2323-2331(1999) 4.Kunath, K., Merdan, T., Hegener, O., et al.Integrin targeting using RGD-PEI conjugates for in vitro gene transferJ. Gene Med.5(7)588-599(2003)

Z-VDVA-(DL-Asp)-FMK is a derivative compound of Z-VDVAD-FMK specifically designed as an inhibitor targeting caspase-2.

Arg-Gly-Asp TFA (99896-85-2(free base)) (RGD Trifluoroacetate) 是一种三肽，可有效触发细胞粘附、定位某些细胞系并引发特定的细胞反应；与整合素结合。

Fmoc-Asp(ODMAB)-OH 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 T65179，CAS号为 269066-08-2。

H-Asp(OcHx)-OH 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 T65684，CAS号为 112259-66-2。

Z-Asp(OMe)-OH 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 T65922，CAS号为 3160-47-2。

Boc-Asp(OAll)-OH 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 T66689，CAS号为 132286-77-2。

Fmoc-Asp(OcHex)-OH 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 T67551，CAS号为 130304-80-2。

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.