KEAP1-Nrf2
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The KEAP1-Nrf2 pathway is the major regulator of cytoprotective responses to chemical and/or oxidative stresses caused by reactive oxygen species (ROS) and electrophiles. Nrf2 (nuclear factor erythroid 2-related factor 2) is a transcription factor that binds together with small Maf proteins to the antioxidant response element (ARE) in the regulatory regions of cellular defense enzyme genes leading to the activation of a wide rang of cell defense processes; while KEAP1 (Kelch ECH associating protein 1), a negative repressor of Nrf2, is an adaptor protein for a Cul3-based ubiqutitin E3 ligase that binds to Nrf2 and promotes its degradation by the ubiquitin proteasome pathway.
Products Related to KEAP1-Nrf2(56)
- GC16590Dimethyl FumarateCAS: 624-49-7Purity: >97.00%
nuclear factor (erythroid-derived)-like 2 (Nrf2) pathway activator
- GB10587Gingerenone ACAS: 128700-97-0Purity: >98.00%
Gingerenone A is an orally active Nrf2-Gpx4 activator with an EC 50 value of 24μM.
- GC11302HinokitiolCAS: 499-44-5Purity: >98.00%
Hinokitiol is a naturally occurring tropolone compound from the Formosan cypress with antibacterial and anticancer properties.
- GC13693Omaveloxolone (RTA-408)CAS: 1474034-05-3Purity: >98.00%
Omaveloxolone (RTA-408) is an antioxidant inflammation modulator (AIM), which activates Nrf2 and suppresses nitric oxide (NO).
- GC17393Pyridoxine HClCAS: 58-56-0Purity: >99.50%
Pyridoxine HCl is the hydrochloride form of vitamin B6 that functions as an antioxidant.
- GC316484-Octyl ItaconateCAS: 3133-16-2Purity: >98.00%
4-Octyl Itaconate (4-OI) is a cell-permeable itaconate derivative.
- GC31783Methyl 3,4-dihydroxybenzoate (Protocatechuic acid methyl ester)CAS: 2150-43-8Purity: >98.00%
Methyl 3,4-dihydroxybenzoate (Protocatechuic acid methyl ester) (Protocatechuic acid methyl ester; Methyl protocatechuate) is a major metabolite of antioxidant polyphenols found in green tea.
- GC32723CDDO-Im (RTA-403)CAS: 443104-02-7Purity: >98.00%
CDDO-Im (RTA-403) is a synthetic triterpenoid that activates Nuclear factor erythroid 2–related factor 2 (Nrf2) signaling by binding to Kelch-like ECH-associated protein 1 (Keap1), thereby inhibiting Nrf2 degradation and increasing its protein levels.
- GC338154-Hydroxyphenylacetic acidCAS: 156-38-7Purity: >99.00%
A phenolic acid with anti-inflammatory activity
- GC34057TBHQ (tert-Butylhydroquinone)CAS: 1948-33-0Purity: >99.50%
TBHQ(tert-Butylhydroquinone) is a powerful phenolic antioxidant capable of reducing oxidative stress and inflammatory reactions.
- GC35629CDDO-dhTFEACAS: 1191265-33-4Purity: >99.50%
CDDO-dhTFEA (RTA dh404) is a synthetic oleanane triterpenoid compound which potently activates Nrf2 and inhibits the pro-inflammatory transcription factor NF-κB.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC14352 | TAT 14 | 1362661-34-4 | >98.00% | |
Nrf2 activator | ||||
| GC16120 | AI-3 | 882288-28-0 | >98% | |
Nrf2/Keap1 and Keap1/Cul3 interaction inhibitor | ||||
| GC16590 | Dimethyl Fumarate | 624-49-7 | >97.00% | |
nuclear factor (erythroid-derived)-like 2 (Nrf2) pathway activator | ||||
| GB10587 | Gingerenone A | 128700-97-0 | >98.00% | |
Gingerenone A is an orally active Nrf2-Gpx4 activator with an EC 50 value of 24μM. | ||||
| GC11302 | Hinokitiol | 499-44-5 | >98.00% | |
Hinokitiol is a naturally occurring tropolone compound from the Formosan cypress with antibacterial and anticancer properties. | ||||
| GC12821 | Oltipraz | 64224-21-1 | >99.50% | |
Oltipraz is an HIF-1α inhibitor (IC 50 =10μM) and an Nrf2 activator. | ||||
| GC13058 | NK 252 | 1414963-82-8 | >98.00% | |
NK 252 is an Nrf2 activator. | ||||
| GC13693 | Omaveloxolone (RTA-408) | 1474034-05-3 | >98.00% | |
Omaveloxolone (RTA-408) is an antioxidant inflammation modulator (AIM), which activates Nrf2 and suppresses nitric oxide (NO). | ||||
| GC15355 | 2-Trifluoromethyl-2'-methoxychalcone | 1309371-03-6 | >98.00% | |
Nrf2 activator | ||||
| GC15457 | Pyridoxine | 65-23-6 | >99.50% | |
A 4-methanol form of vitamin B 6 | ||||
| GC15605 | Ezetimibe | 163222-33-1 | >99.00% | |
Ezetimibe is a selective cholesterol absorption inhibitor with IC 50 values of 50μM for lung cancer cell (A549), human embryonic kidney cells (HEK293) and 30μM for melanoma cell (A375) for 48h. | ||||
| GC17393 | Pyridoxine HCl | 58-56-0 | >99.50% | |
Pyridoxine HCl is the hydrochloride form of vitamin B6 that functions as an antioxidant. | ||||
| GC19254 | ML385 | 846557-71-9 | >98.00% | |
ML385 is a cell-active NRF2 inhibitor (IC 50 =1.9μM). | ||||
| GC31321 | KI696 | 1799974-70-1 | >99.00% | |
KI696 is a high affinity probe that disrupts the Keap1/NRF2 interaction. | ||||
| GC31648 | 4-Octyl Itaconate | 3133-16-2 | >98.00% | |
4-Octyl Itaconate (4-OI) is a cell-permeable itaconate derivative. | ||||
| GC31691 | (+)-DHMEQ | 287194-41-6 | >99.50% | |
(+)-DHMEQ is an activator of antioxidant transcription factor Nrf2. | ||||
| GC31783 | Methyl 3,4-dihydroxybenzoate (Protocatechuic acid methyl ester) | 2150-43-8 | >98.00% | |
Methyl 3,4-dihydroxybenzoate (Protocatechuic acid methyl ester) (Protocatechuic acid methyl ester; Methyl protocatechuate) is a major metabolite of antioxidant polyphenols found in green tea. | ||||
| GC32723 | CDDO-Im (RTA-403) | 443104-02-7 | >98.00% | |
CDDO-Im (RTA-403) is a synthetic triterpenoid that activates Nuclear factor erythroid 2–related factor 2 (Nrf2) signaling by binding to Kelch-like ECH-associated protein 1 (Keap1), thereby inhibiting Nrf2 degradation and increasing its protein levels. | ||||
| GC33092 | Hesperin | 4430-35-7 | >98.00% | |
An isothiocyanate with diverse biological activities | ||||
| GC33815 | 4-Hydroxyphenylacetic acid | 156-38-7 | >99.00% | |
A phenolic acid with anti-inflammatory activity | ||||
| GC34057 | TBHQ (tert-Butylhydroquinone) | 1948-33-0 | >99.50% | |
TBHQ(tert-Butylhydroquinone) is a powerful phenolic antioxidant capable of reducing oxidative stress and inflammatory reactions. | ||||
| GC34070 | Brusatol | 14907-98-3 | >98.00% | |
Brusatol is an Nrf2 inhibitor isolated from Brucea javanica and exhibits significant tumor inhibition in multiple cancers through decreased resistance to cancer oxidative stress injury. | ||||
| GC34642 | KI696 isomer | 1799974-69-8 | >99.00% | |
KI696 isomer is the less active isomer of KI696. | ||||
| GC35629 | CDDO-dhTFEA | 1191265-33-4 | >99.50% | |
CDDO-dhTFEA (RTA dh404) is a synthetic oleanane triterpenoid compound which potently activates Nrf2 and inhibits the pro-inflammatory transcription factor NF-κB. | ||||
