HIF
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Hypoxia inducible factors (HIFs) are heterodimeric proteins belonging to the basic helix-loop-helix-PAS (bHLH/PAS) family of transcription factors that mediate the primary transcriptional response to stress caused by hypoxia (accessible O2 level < 2%). HIFs are characterized by containing two subunits, including O2-labile α subunit (HIFα) and constitutively expressed β subnit (HIFβ). Mammalian HIFα consists of three isoforms, including HIF1α, HIF2α and HIF3α, which play an essential role in the regulation of HIF activity by O2 availability. Under normal O2 tension, HIFα is hydroxylated at the two conserved proline residues within the O2-dependent degradation (ODD) domain by prolylhydroxylase domain proteins (PHDs) and undergoes proteosomal degradation catalyzed by a complex formed by E3 ubiquitin ligase and the von Hippel-Lindau protein (pVHL); while, under hypoxia, HIFα stabilizes with PHDs being deactivated and hence induce transcription of genes with adaptive functions.
Products Related to HIF(118)
- GC30263Glucosamine (D-Glucosamine)CAS: 3416-24-8Purity: >98.00%
Glucosamine (D-Glucosamine) (D-Glucosamine (D-Glucosamine)) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement.
- GC31230Dencichin (Dencichine)CAS: 5302-45-4Purity: >98.00%
Dencichin is a non-protein amino acid originally extracted from Panax notoginseng, and can inhibit HIF-prolyl hydroxylase-2 (PHD-2) activity.
- GC31358HIF-2α-IN-1CAS: 1799948-06-3Purity: >99.50%
HIF-2α-IN-1 is a HIF-2α inhibitor has an IC50 of less than 500 nM in HIF-2α scintillation proximity assay.
- GC32083AcriflavineCAS: 8048-52-0Purity: >98.00%
Acriflavine is a fluorescent dye for labeling high molecular weight RNA.
- GC32724LW6 (HIF-1α inhibitor)CAS: 934593-90-5Purity: >98.00%
LW6 is a hypoxia-inducing factor 1(HIF) inhibitor, which effectively inhibits HIF-1α accumulation by degrading HIF-1α, but does not affect HIF-1A mRNA level during hypoxia.
- GC33170ENMD-119 (ENMD 1198)CAS: 864668-87-1Purity: >98.50%
ENMD-119 (ENMD 1198) (IRC-110160), an orally active microtubule destabilizing agent, is a 2-methoxyestradiol analogue with antiproliferative and antiangiogenic activity. ENMD-119 (ENMD 1198) is suitable for inhibiting HIF-1alpha and STAT3 in human HCC cells and leads to reduced tumor growth and vascularization.
- GC33634Enarodustat (JTZ-951)CAS: 1262132-81-9Purity: >98.00%
Enarodustat (JTZ-951) is a potent and orally active hypoxia-inducible factor prolyl hydroxylase inhibitor, with an EC50 of 0.22 μM.
- GC35230AcetylarenobufaginCAS: 184673-79-8Purity: >98%
Acetylarenobufagin is a steroidal hypoxia inducible factor-1 (HIF-I) modulator.
- GC37966ZINC13466751CAS: 117953-17-0Purity: >98.50%
ZINC13466751 is a potent inhibitor of HIF-1α/von Hippel-Lindau interaction with an IC50 of 2.0 ?M.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC30263 | Glucosamine (D-Glucosamine) | 3416-24-8 | >98.00% | |
Glucosamine (D-Glucosamine) (D-Glucosamine (D-Glucosamine)) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement. | ||||
| GC31230 | Dencichin (Dencichine) | 5302-45-4 | >98.00% | |
Dencichin is a non-protein amino acid originally extracted from Panax notoginseng, and can inhibit HIF-prolyl hydroxylase-2 (PHD-2) activity. | ||||
| GC31358 | HIF-2α-IN-1 | 1799948-06-3 | >99.50% | |
HIF-2α-IN-1 is a HIF-2α inhibitor has an IC50 of less than 500 nM in HIF-2α scintillation proximity assay. | ||||
| GC31498 | TP0463518 | 1558021-37-6 | >98.00% | |
TP0463518 is a potent hypoxia-inducible factor prolyl hydroxylases (PHDs) inhibitor | ||||
| GC32083 | Acriflavine | 8048-52-0 | >98.00% | |
Acriflavine is a fluorescent dye for labeling high molecular weight RNA. | ||||
| GC32228 | Tilorone dihydrochloride | 27591-69-1 | >99.50% | |
An interferon-inducing antiviral agent | ||||
| GC32449 | Desidustat | 1616690-16-4 | >98.00% | |
An inhibitor of HIF-PH | ||||
| GC32680 | PT-2385 | 1672665-49-4 | >99.00% | |
PT-2385 is a selective HIF-2α inhibitor with a Ki of less than 50 nM. | ||||
| GC32724 | LW6 (HIF-1α inhibitor) | 934593-90-5 | >98.00% | |
LW6 is a hypoxia-inducing factor 1(HIF) inhibitor, which effectively inhibits HIF-1α accumulation by degrading HIF-1α, but does not affect HIF-1A mRNA level during hypoxia. | ||||
| GC32876 | SYP-5 | 1384268-04-5 | >99.50% | |
A HIF-1 inhibitor | ||||
| GC32945 | THS-044 | 62054-67-5 | >98% | |
THS-044 binding stabilizes the HIF2α PAS-B folded state, for regulating HIF2 activity in endogenous and clinical settings. | ||||
| GC32948 | IDF-11774 | 1429054-28-3 | >98% | |
IDF-11774 is an orally administered HIF-1α inhibitor, with an IC 50 value of 3.65μM. | ||||
| GC33043 | EL-102 | 1233948-61-2 | >99.50% | |
EL-102 is a hypoxia-induced factor 1 (Hif1α) inhibitor. EL-102 induces apoptosis, inhibits tubulin polymerisation and shows activities against prostate cancer. EL-102 can be used for the research of cancer. | ||||
| GC33170 | ENMD-119 (ENMD 1198) | 864668-87-1 | >98.50% | |
ENMD-119 (ENMD 1198) (IRC-110160), an orally active microtubule destabilizing agent, is a 2-methoxyestradiol analogue with antiproliferative and antiangiogenic activity. ENMD-119 (ENMD 1198) is suitable for inhibiting HIF-1alpha and STAT3 in human HCC cells and leads to reduced tumor growth and vascularization. | ||||
| GC33416 | AFP464 | 468719-52-0 | >98% | |
AFP464 (NSC710464 free base), is an active HIF-1α inhibitor with an IC50 of 0.25 μM, also is a potent aryl hydrocarbon receptor (AhR) activator. | ||||
| GC33634 | Enarodustat (JTZ-951) | 1262132-81-9 | >98.00% | |
Enarodustat (JTZ-951) is a potent and orally active hypoxia-inducible factor prolyl hydroxylase inhibitor, with an EC50 of 0.22 μM. | ||||
| GC34595 | GN44028 | 1421448-26-1 | >98.00% | |
GN44028 is a hypoxia-inducible factor (HIF)-1α inhibitor with an IC₅₀ value of 14nM. | ||||
| GC35230 | Acetylarenobufagin | 184673-79-8 | >98% | |
Acetylarenobufagin is a steroidal hypoxia inducible factor-1 (HIF-I) modulator. | ||||
| GC37034 | PT2977 | 1672668-24-4 | >98.00% | |
PT2977 is an orally active and selective HIF-2α inhibitor with an IC 50 of 9nM. | ||||
| GC37066 | Rac-PT2399 | 1672662-07-5 | >99.00% | |
A potent and specific HIF-2α inhibitor | ||||
| GC37801 | TM6089 | 863421-32-3 | >98% | |
TM6089 is a unique Prolyl Hydroxylase (PHD) inhibitor which stimulates HIF activity without iron chelation and induces angiogenesis and exerts organ protection against ischemia. | ||||
| GC37889 | VCE-004.8 | 1818428-24-8 | >98.00% | |
VCE-004.8 (VCE-004.8) is an orally active, specific PPARγ and CB2 receptor dual agonist. | ||||
| GC37966 | ZINC13466751 | 117953-17-0 | >98.50% | |
ZINC13466751 is a potent inhibitor of HIF-1α/von Hippel-Lindau interaction with an IC50 of 2.0 ?M. | ||||
| GC38044 | Fraxinellone | 28808-62-0 | >99.50% | |
