p 63

P3FI-63 是一种选择性 KDM3B 抑制剂（IC50：7 μM），具有抗肿瘤活性，可用于研究融合阳性横纹肌肉瘤和其他转录成瘾癌症。

Exp 631 is a centrally-acting non-opioid analgesic; exhibits serotonin and norepinephrine reuptake inhibiting activities.

lunresertib (RP-6306) 是有效的、选择性的、口服活性的 PKMYT1 抑制剂 ，其IC50值为 14 nM。lunresertib (RP-6306) 在几种临床前异种移植模型中抑制 CCNE1 扩增的肿瘤细胞生长。

Pep63 (VFQVRARTVA) 是一种具有神经保护功能的肽。它能促进突触可塑性及增强记忆力，并且可与 Aβ1-42 寡聚体进行竞争性结合，从而阻断 Aβ 纤维的形成。该化合物可用于阿尔茨海默病 (AD) 的相关研究。

BDZ-h is a potent inhibitor of both the closed-channel and the open-channel conformations of all four homomeric AMPA receptor channels and two GluA2R containing complex AMPA receptor channels.

PACAP (6-38), human, ovine, rat acetate 是一种有效的 PACAP 受体拮抗剂。PACAP (6-38) 作用于 PACAP I 型受体，PACAP II 型受体 VIP1 和 PACAP II 型受体 VIP2，IC50 分别为 30 nM，600 nM 和 40 nM。

PACAP (6-38), human, ovine, rat TFA is a potent PACAP receptor antagonist with IC50 values of 30 nM, 600 nM, and 40 nM for the PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively.

(Trp63,Trp64)-C3a(63-77) 是一种合成的 C3a 类似肽，在人中性粒细胞和表达 hC3aR 或 mC3aR 的 RBL-2H3 细胞中刺激 Ca2+通量，EC50 分别为 9.5、2.0 和 0.8 nM。

PACAP (6-38), human, ovine, rat, is a potent and selective antagonist of PACAP 38, outperforming PACAP (6-27) in inhibiting PACAP-27-stimulated pituitary adenylate cyclase.

BOS-172722 是一种单极纺锤体 1 (MPS1) 检查点抑制剂，对MPS1 (1 mM ATP) 和P-MPS1 的IC50值分别为 11 nM 和 63 nM。它可研究多种乳腺癌。

Substance P acetate 是一种主要由神经元分泌的肽，参与包括伤害感受和炎症在内的许多生物过程。Substance P acetate 是一种神经炎症因子，可在中枢神经系统中作为神经递质和神经调节剂，可用于研究心血管疾病和神经系统疾病。

Gliovirin is a fungal metabolite that has been found inT. harzianumand has fungicidal, antimicrobial and anti-inflammatory activities.1It is active against the plant pathogenic fungusP. ultimum(MIC = 60 ng/ml) and the parasiteT. brucei brucei(IC50= 90 ng/ml), but has no effect on the plant pathogenic fungiR. solani,P. omnivorum,T. basicola,R. arrhizus, andV. dahliaeor the bacteriaB. thuringiensis,P. fluorescens, andX. malvacearumwhen used at concentrations up to 1,000 ng/ml.2,3Gliovirin decreases phorbol 12-myristate 13-acetate (TPA)- and ionomycin-induced increased expression of COX-2 (IC50= 1 μM) and protein levels of IL-2 in Jurkat cells (IC50= 5.2 μM).1 1.Rether, J., Serwe, A., Anke, T., et al.Inhibition of inducible tumor necrosis factor-α expression by the fungal epipolythiodiketopiperazine gliovirinBiol. Chem.388(6)627-637(2007) 2.Howell, C.R., and Stipanovic, R.D.Gliovirin, a new antibiotic from Gliocladium virens, and its role in the biological control of Pythium ultimumCan. J. Microbiol.29(3)321-324(1983) 3.Iwatsuki, M., Otoguro, K., Ishiyama, A., et al.In vitro antitrypanosomal activity of 12 low-molecular-weight antibiotics and observations of structure/activity relationshipsJ. Antibiot. (Tokyo)63(10)619-622(2010)

1,6,2',3',6'-O-Pentaacetyl-3-O-trans-p-coumaroylsucrose 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN5842，CAS号为 138213-63-5。

CAY10771 is a dual agonist of farnesoid X receptor (FXR) and peroxisome proliferator-activated receptor δ (PPARδ).1It activates FXR and PPARδ in reporter assays using HEK293T cells (EC50s = 0.94 and 1.5 μM, respectively) and is selective for these receptors over retinoic acid receptor α (RARα), retinoid X receptor α (RXRα), PPARα, PPARγ, and liver X receptor α (LXRα) at 10 μM. 1.Schierle, S., Neumann, S., Heitel, P., et al.Design and structural optimization of dual FXR/PPARδ activatorsJ. Med. Chem.63(15)8369-8379(2020)

3-Deoxy-1,2-O-isopropylidene-5-O-(p-toluoyl)- α-D-glycero-pent-3-enofuranose 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 TNU1040，CAS号为 75096-63-8。