FDL-169

产品编号: DC26037
FDL-169
结构式
1628416-28-3
此产品仅供科研所需,我们不出售给病人
​我们将匹配市场上最好的价格给您
Email:order@dcbio.cn
免费咨询电话:4008862077
我们的合作伙伴:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
中国地区超过5000个高品质化合物库存
应用领域
CFTR corrector 2是囊性纤维化跨膜电导调节因子 (CFTR) 的调节剂,来自专利US20140274933。
Cas No.: 1628416-28-3
名称:
别名: FDL169; FDL-169; FDL 169
SMILES: O=C(N(C)C1=CC=C2N=C(C)OC2=C1)CN(N=C(C3=CC=CC(F)=C3)C4=C5C=C(OCC)C=C4)C5=O
分子式: C27H23FN4O4
分子量: 486.17
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: FDL-169 is a novel and potent CFTR (Cystic fibrosis transmembrane conductance regulator) corrector being developed by Flatley Discovery Lab for treating cystic fibrosis (CF) patients who carry the F508del mutation, the most common mutation in this disease. Correctors are drugs designed to fix and restore the function of the defective CFTR protein. The corrected CFTR then moves to the cell surface, where it functions as a chloride channel and helps maintain the right balance of fluid in the airways.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
产品编号 产品名称 应用领域
DC20000 LR-90 LR-90 is an advanced glycation end product (AGE) inhibitor, inhibits inflammatory responses in human monocytes. LR-90 is also used in the research of diabetic animal model.
DC26231 Furin Inhibitor II Hexa-D-arginine (Furin Inhibitor II) 是一种稳定的 furin 抑制剂,对 furin,PACE4 和 PC1 的 Ki 值分别为 106 nM,580 nM 和 13.2 μM。Hexa-D-arginine 在体外和体内均可阻断假单胞菌外毒素 A 和炭疽毒素的毒性。
DC21672 SNAP-94847 hydrochloride SNAP 94847 是一种新型的,高亲和力的选择性黑色素浓缩激素受体 1 (MCHR1) 拮抗剂,其 (Ki= 2.2 nM, Kd=530 pM),它对 MCHα1A 和 MCHD2 受体分别显示出 >80 倍和 >500 倍的选择性。 SNAP 94847 以高亲和力与小鼠和大鼠 MCHR1 结合,与其他 GPCR,离子通道,酶和转运蛋白的交叉反应性很小。
DC26119 VHL ligand 2 hydrochloride E3 ligase Ligand 1是用于 PROTAC 技术中的E3连接酶配体,来自专利WO/2017/030814A1,化合物实例202。
DC26025 INCB086550 INCB086550 is an orally available, small molecule inhibitor of PD-L1 with potential immune checkpoint inhibitory and antineoplastic activities.
DC26024 GNE-8324 GNE-8324是一种有效的选择性NMDA受体PAM。
DC22207 AP1903 Rimiducid (AP1903) 是二聚化剂,其通过交联 FKBP 结构域起作用,启动 Fas 信号传导,引起凋亡。Rimiducid (AP1903) 使 Caspase 9 自杀开关二聚化,并迅速诱导细胞凋亡 (apoptosis)。
DC21242 LM11A-31 dihydrochloride LM11A-31 dihydrochloride 是一种 p75NTR (神经营养蛋白受体 p75) 配体,是有效的 proNGF 拮抗剂。LM11A-31 dihydrochloride 是一种具有高血脑屏障通透性的水溶性非肽。
DC21485 PF-05089771 PF-05089771 is a potent, state-dependent, subtype selective Nav1.7 inhibitor with IC50 of 11 nM, >1,000-fold selectivity over Nav1.3, 1.4 and Nav1.5, 1.8.
DC20928 CRT0066101 A potent, specific, orally active pan-PKD (protein kinase D) inhibitor with biochemical IC50 of 1, 2.5 and 2 nM for PKD1, 2, and 3 respectively.