Gardiquimod trifluoroacetate

产品编号: DC26031
Gardiquimod trifluoroacetate
结构式
1159840-61-5
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
Gardiquimod trifluoroacetate 是一个特异的 TLR7 激动剂,也能抑制 HIV-1 逆转录酶。
Cas No.: 1159840-61-5
名称: 1-(4-amino-2-((ethylamino)methyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol 2,2,2-trifluoroacetate
别名:
SMILES: CC(O)(C)CN1C(CNCC)=NC2=C1C3=CC=CC=C3N=C2N.O=C(O)C(F)(F)F
分子式: C19H24F3N5O3
分子量: 427.43
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: Gardiquimod is a chemical compound which acts selectively at both mouse and human forms of toll-like receptor 7 (TLR7). It functions as an immune response modifier. The core structure is 1H-imidazo[4,5-c]quinoline, as found in related drugs such as imiquimod and resiquimod. It is structurally very similar to resiquimod differing only by an oxygen for nitrogen switch.
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.