yingweiwo

HIF HIF Prolyl-Hydroxylase

HIF HIF Prolyl-Hydroxylase

HIFs (Hypoxia-inducible factors) are transcription factors that react to variations in the amount of oxygen available to cells, more specifically, to reductions in oxygen, or hypoxia. The effects of hypoxia, a condition of low oxygen concentration, on the cell are mediated by the HIF signaling cascade. Oftentimes, hypoxia prevents cells from differentiating. However, hypoxia encourages the growth of blood vessels and is crucial for the development of a vascular system in both cancer tumors and embryos.Additionally, the hypoxia in wounds encourages keratinocyte migration and epithelium repair. HIFs are essential to development in general. HIF-1 gene deletion in mammals causes perinatal death. It has been demonstrated that HIF-1 is essential for chondrocyte survival and enables the cells to adapt to low oxygen environments in the growth plates of bones. Human metabolism is controlled in large part by HIF. A number of medications that function as selective HIF prolyl hydroxylase inhibitors have recently been created.

HIF HIF Prolyl-Hydroxylase related products

Structure Cat No. Product Name CAS No. Product Description
(Rac)-Arnebin 1 ((Rac)-β,β-Dimethylacrylalkannin; (Rac)-β,β-Dimethylacrylshikonin) V73834 (Rac)-Arnebin 1 ((Rac)-β,β-Dimethylacrylalkannin; (Rac)-β,β-Dimethylacrylshikonin) 5162-01-6 (Rac)-Arnebin 1 ((Rac)-β,β-Dimethylacrylalkannin) is the racemate of β,β-Dimethylacrylalkannin and/or β,β-Dimethylacrylshikonin.
1,4-DPCA V3952 1,4-DPCA 331830-20-7 1,4-DPCA is a novel, potent and competitive inhibitor of prolyl 4-hydroxylase with IC50 value of 3.6 μM.
1,4-DPCA ethyl ester V51644 1,4-DPCA ethyl ester 86443-19-8 1,4-DPCA ethyl ester is the ethyl ester form of 1,4-DPCA and can inhibit FIH.
2’,4’,5,7-四羟基黄烷酮 V51634 Steppogenin 56486-94-3 Steppogenin is a potent HIF-1α and DLL4 replacement with IC50s of 0.56 and 8.46 μM, respectively.
5,3',4',3'',4'',5''-6-O-Ethyl-EGCG V85084 5,3',4',3'',4'',5''-6-O-Ethyl-EGCG 1613308-63-6
7-Hydroxyneolamellarin A V51627 7-Hydroxyneolamellarin A 959662-26-1 7-Hydroxyneolamellarin A is a naturally occurring compound that can be found in the sponge Dendrilla nigra.
Adaptaquin V10310 Adaptaquin 385786-48-1 Adaptaquin is a novel and potent hydroxyquinoline inhibitor of HIF-PHD (hypoxia-inducible factor prolyl hydroxylase 2) with an IC50 of 2 μM.
AFP464 dihydrochloride (NSC710464 dihydrochloride) V86307 AFP464 dihydrochloride (NSC710464 dihydrochloride)
AJM 290 V87508 AJM 290 840474-95-5 AJM 290 is a Trx-1 inhibitor.
Angiogenesis agent 1 V51635 Angiogenesis agent 1 2765218-28-6 Angiogenic agent 1 (compound C-31) is a glycoside analog of a Rhodiola rosean analogue.
Anti-inflammatory agent 79 V87491 Anti-inflammatory agent 79 Anti-inflammatory agent 79 (compound 17q) is an isoquinolinone derivative-based HIF-1 inhibitor (IC50: 0.55 μM), which can effectively block HIF-1 signaling and increase HIF-1α degradation.
Antiproliferative agent-57 V96811 Antiproliferative agent-57 Antiproliferative agent-57 (Compound M2) is a tumor angiogenesis inhibitor.
Arylsulfonamide 64B (HIF inhibitor 64B) V86107 Arylsulfonamide 64B (HIF inhibitor 64B) 1342890-83-8
Axl-IN-16 V78298 Axl-IN-16 Axl-IN-16 is a dual (bifunctional) inhibitor of Axl and HIF.
Casdatifan V99680 Casdatifan 2709069-30-5 Casdatifan (AB521) is an oral HIF-2α (hypoxia-inducible factor 2α) inhibitor.
Cyclo(CKLIIF) TFA V87498 Cyclo(CKLIIF) TFA Cyclo CKLIIF is a dual inhibitor of hypoxia-inducible factors HIF1 and HIF2, disrupts the interaction of HIF1-α and HIF2-α with HIF1-β, and has KD of 2.6 and 2.2 μM for the PAS-B domains of HIF1-α and HIF2-α, respectively.
cyclo(CLLFVY) V87488 cyclo(CLLFVY) 1446322-73-1 cyclo(CLLFVY) is an inhibitor of hypoxia-inducible factor-1 (HIF-1) with IC50 of 19 μM (in U2OS) and 16 μM (in MCF-7).
Cyclo(CRLLIF) V87494 Cyclo(CRLLIF) Cyclo CRLLIF is a dual inhibitor of hypoxia-inducible factors HIF1 and HIF2, disrupts the interaction of HIF1-α and HIF2-α with HIF1-β, and has KD of 14.5 and 10.2 μM for the PAS-B domains of HIF1-α and HIF2-α, respectively.
Cyclo(CRVIIF) V87503 Cyclo(CRVIIF) Cyclo CRVIIF is a dual inhibitor of hypoxia-inducible factors HIF1 and HIF2, disrupts the interaction of HIF1-α and HIF2-α with HIF1-β, and has KD of 65 and 123 μM for the PAS-B domains of HIF1-α and HIF2-α, respectively.
D-01 V87502 D-01 D-01 is a dual-targeted HIF-1α and EZH2 inhibitor (IC50 of 4.86 μM and 0.99 μM, respectively).
Contact Us