np 2

2-NP 是选择性的STAT1转录增强剂。它能够增强 IFN-γ 的功能，提高对人乳腺癌和纤维肉瘤细胞增殖的抑制能力。

2-NP-AMOZ is a 2-nitrophenyl derivative of AMOZ, which is a metabolite of the antibiotic Furaltadone. This chemical compound specifically serves as a reliable tool for protein bound AMOZ detection.

2-NP-AOZ is a chemical compound that is a 2-nitrophenyl derivative of AOZ, which is a tissue-bound metabolite of Furazolidone. 2-NP-AOZ is specifically used for the determination of AOZ residues.

2-NP-AHD is a 2-nitrophenyl derivative of AHD, which is a metabolite of nitrofurans, a class of antibiotics. It serves as an indicator for the detection of illicit use of nitrofuran drugs.

NP-G2-044 是fascin 蛋白抑制剂，具有口服活性，IC50值约为 2 μM。它可阻断肿瘤转移并增强抗肿瘤免疫应答。

2-NP-AOZ-d4 是 2-NP-AOZ 的氘代化合物。2-NP-AOZ 的 CAS 号为 19687-73-1。2-NP-AOZ 是 AOZ 的 2-硝基苯基衍生物的一种化合物，AOZ 是呋喃唑酮的组织结合代谢产物。2-NP-AOZ 专门用于 AOZ 残留物的测定。

2-NP-AMOZ-d5 是 2-NP-AMOZ 的氘代化合物。2-NP-AMOZ 的 CAS 号为 183193-59-1。2-NP-AMOZ 是 AMOZ 的 2-硝基苯基衍生物，AMOZ 是抗生素呋喃他酮的代谢产物。2-NP-AMOZ 专门作为蛋白质结合 AMOZ 检测的可靠工具。

P2X3 antagonist 34 是一种对P2X3同型三聚体受体具有高效性、选择性和口服活性的拮抗剂，其IC50值针对人类P2X3、大鼠P2X3及豚鼠P2X3分别为25 nM、92 nM和126 nM。相比之下，该化合物对人类、大鼠和豚鼠的P2X2 3异三聚体受体展现低活性。P2X3 antagonist 34 显著具有抗咳功效，同时不会影响味觉。

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

Clofexamide (ANP 246) 具有抗抑郁和抗炎活性，可用于研究关节炎和神经系统疾病。

NP-252 is a calcium channel antagonist potentially for the treatment of angina pectoris and congestive heart failure.

Caged Raseglurant . Releases raseglurant upon exposure to 405 nm (violet) light. Inhibits the effects of Quisqualate in cultured neurons when exposed to 405 nm light. Exhibits analgesic activity in pain models in vivo on photoactivation. Quantum yield = 0.18. Font et al (2017) Optical control of pain in vivo with a photoactive mGlu5 receptor negative allosteric modulator. eLIFE 6 e23545 PMID:28395733

Bovine Peripheral Myelin Protein P2 (53-78) is a derivative composed of amino acid residues 53 to 78 from the peripheral myelin P2 protein of bovine origin. It acts as a T cell epitope and is used to induce experimental autoimmune neuritis (EAN) in Lewis rats.

Defensin HNP-2 is a naturally occurring antibiotic and monocyte chemotactic peptide synthesized by human neutrophils.

SENP2-IN-1 是一种选择性的 SENP2 抑制剂。SENP2-IN-1 能够抑制 SENP1 (IC50: 1.3 μM)、SENP2 (IC50: 0.69 μM) 和 SENP5 (IC50: 22.7 μM)。SENP2-IN-1 能够用于研究癌症。

Azurin p28 peptide是一种具有肿瘤穿透能力和抗肿瘤活性的肽。它通过与p53结合形成p28:p53复合物，从而降低p53在蛋白酶体中的降解，进而诱导细胞凋亡(apoptosis)或使细胞周期停滞。此外，Azurin p28 peptide通过抑制VEGFR-2、FAK和Akt的磷酸化表现出抗血管生成效果，抑制p53阳性肿瘤的生长。

BNP (22-46), Pro (Human) 为多肽类化合物，主要应用于心功能障碍研究领域。

NP213 TFA is a rapidly acting and first-in-class synthetic antimicrobial peptide (AMP) with anti-fungal activity. It targets the fungal cytoplasmic membrane via membrane perturbation and disruption.

NP213 is a rapidly acting synthetic antimicrobial peptide (AMP). NP213 is effective and well-tolerated in resolving nail fungal infections. NP213 has anti-fungal activities. NP213 targets the fungal cytoplasmic membrane and plays its role via membrane perturbation and disruption.

A-317491 (ABT 202) 是选择性和非核苷酸的 P2X3和 P2X2 3受体的拮抗剂，通过阻断 P2X3和 P2X2 3受体介导的钙通量减轻炎性和神经性疼痛。它对其他 P2 受体和神经递质受体，离子通道以及酶具有高度选择性，IC50大于10 μM。

NP-313 (NSC-4264) 是一种有效的抗血栓剂，对血栓素 A 2 合成和选择性抑制由 SOCC 介导的 Ca 2+ 内流有抑制作用，可以抑制血小板的聚集和活化。

Pogostone (DHELWANGIN) 是从薄荷中分离出，对革兰氏阴性菌、革兰氏阳性菌、大肠埃希菌等具有强效抗菌、抗真菌活性。它诱导细胞凋亡和自噬。

TDZD-8 (NP 01139) 是抑制GSK-3β的抑制剂，其 IC50=2 μM。它对 Cdk-1 cyclin B，CK-II，PKA 和 PKC 的作用较弱，IC50值均 >100 μM。

Apelin-36(rat, mouse) TFA 是一种内源性孤儿 G 蛋白偶联受体 APJ 激动剂。Apelin-36(rat, mouse) TFA 与 APJ 受体结合，IC50为 5.4 nM，显著抑制 cAMP 的产生，EC50为 0.52 nM。Apelin-36(rat, mouse) TFA 阻断 HIV-1和 HIV-2毒株进入表达 APJ 的 NP-2 CD4 细胞。