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货号 产品名 纯度
A1604091 M1002

98%
A786637 Deoxyshikonin/去氧紫草素

95%
A333509 Ciclopirox/环吡酮

Ciclopirox inhibits iron-dependent enzymes PHD2 (pIC50 = 5.8) and deoxyhypusine hydroxylase. It is an antifungal and iron-chelating agent.

97%
A654411 THS-044

THS-044 binding stabilizes the HIF2α PAS-B folded state, for regulating HIF2 activity in endogenous and clinical settings.

98%
A1176736 M1001

M1001 is the first HIF-2 allosteric agonist, capable of altering the conformation of Tyr281 of the HIF-2α PAS-B domain and enhancing the affinity of HIF-2α and ARNT for transcriptional activation.

99%+
A615450 Ononin/芒柄花苷

Ononin is an isoflavonoid isolated and purified from the herb of Ononis natrix L., can inhibit the growth of pathogen such as Enterococcus sp., Enterobacter sp.

98+%
A460721 MK-8617

MK-8617 is a potent, selective, orally bioavailabl pan-inhibitor of hypoxia-inducible factor prolyl hydroxylase 1−3 (HIF PHD1−3), inhibiting PHD1, 2, 3 with IC50s of 1.0, 1.0 and 14 nM, respectively.

99%+
A103226 IDF-11774

IDF-11774 is a hypoxia-inducible factor (HIF)-1α inhibitor which regulates cancer metabolism, thereby suppressing tumor growth.

99%+
A100621 HIF-2α-IN-1

HIF-2α-IN-1 is a HIF-2α inhibitor has an IC50 of less than 500 nM in HIF-2α scintillation proximity assay.

97%
A171766 SYP-5

SYP-5 is a HIF-1 inhibitor, suppresses tumor cells invasion and angiogenesis.

98%
A174113 Lificiguat/利非西呱

Lificiguat is an acivator of guanylyl cyclase (sGC) and can bind to the heme-containing domain of the β subunit with Kd of 0.6 μM - 1.1 μM.

99%+
A1154544 FM19G11

97%
A1176416 ZINC13466751

99%+
A1209379 Adaptaquin

97%
A1216748 Belzutifan

99%+
A1227222 HIF-1 inhibitor-4

99%+
A1227413 HIF1-IN-3

99%+
A1340294 1,4-DPCA

98%
A1475625 Acriflavine/吖啶黄素

Cl,13.3-15.8%
A227990 Dimethyl-bisphenol A/双酚A二甲醚

95%
产品名 HIF HIF1 PHD1 PHD2 PHD3 其他靶点 纯度
KC7F2 +

HIF-1α, IC50: 20 μM

+

HIF-1α, IC50: 20 μM

99%+
Lificiguat 99%+
BAY 87-2243 99%+
PX-478 98%+
2-Methoxyestradiol 98%
CAY10585 ++

HIF, IC50: 4.4 μM

BCRP 97%
DMOG 98%
FG-2216 ++

PHD2, IC50: 3.9 μM

99%+
MK-8617 ++++

PHD1, IC50: 1 nM

++++

PHD2, IC50: 1 nM

++++

PHD3, IC50: 14 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
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