Metabolism
Research Areas
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Products Related to Metabolism(2997)
- GC74700DSPE-succinic acidCAS: 248253-94-3Purity: >98.00%
DSPE-succinic acid ist ein Phophalipid, das mit einem Carbonsäureanteil bedeckt ist.
- GC74728Butylated hydroxytoluene-d3CAS: 86819-59-2Purity: >98.00%
Butylated hydroxytoluene-d3 ist das Deuterium markierte butylierte Droxytoluol.
- GC78560GlycerophosphoglycerolCAS: 6418-92-4Purity: >99.50%
Glycerophosphoglycerol is a precursor for complex phospholipids, including the cardiolipins in mitochondria, which can form abundant negative ions.
- GC78942UH15-38 TFAPurity: >99.50%
UH15-38 TFA is a potent RIPK3 inhibitor with an IC 50 value of 20 nM.
- GC789442',4-DihydroxychalconeCAS: 13323-66-5Purity: >98.00%
2',4-Dihydroxychalcone is an orally active natural chalcone flavonoid.
- GC78965ACT001 hydrochlorideCAS: 1403357-80-1Purity: >98.00%
ACT001 (Dimethylaminomicheliolide; DMAMCL) hydrochloride is an orally active, blood-brain barrier-permeable anti-inflammatory and anti-tumor agent.
- GC78976NFE2L1 activator-1CAS: 3070514-51-8Purity: >98.50%
NFE2L1 activator-1 (Compound 5b) is a potent nuclear factor erythroid 2-related factor 1 ( NFE2L1 ) activator ( EC 50 = 2.4 µM).
- GC78978(rac)-MitiperstatCAS: 1933460-18-4Purity: >98.00%
(rac)-Mitiperstat ((rac)-AZD4831) is the racemic form of Mitiperstat.
- GC78979Ferfluor-1CAS: 3030473-59-4Purity: >99.00%
Ferfluor-1 is a Ferroptosis inhibitor ( EC 50 of 57 nM in HT108 cells; EC 50 of 75 nM in OS-RC-2 cells; EC 50 of 2.3 nM in SH-SY5Y neuroblastoma cells), and ratiometric photoluminescent probe with blood-brain barrier permeability.
- GC79067ADAR1i-124Purity: >98.50%
ADAR1i-124 is an A-to-I RNA editing inhibitor by inhibiting the catalytic activities of both ADAR1p150 and ADAR1p110.
- GC79074HSP70/DnaK substrate peptide TFAPurity: >98.00%
HSP70/DnaK substrate peptide TFA is a short peptide that the HSP70/DnaK molecular chaperone can bind and act on.
- GC79118Hydrangeic acidCAS: 491-79-2Purity: >96.00%
Hydrangeic acid is an orally effective stilbene-type glycolipid metabolism regulator that lowers blood glucose and lipids.
- GC79119PPARα agonist 6CAS: 959699-23-1Purity: >99.50%
PPARα agonist 6 (Compound 15) is a PPARα agonist.
- GC79167METTL1-WDR4-IN-1 TFAPurity: >99.50%
METTL1-WDR4-IN-1 (Compound 1) TFA is a selective competitive inhibitor of the methyltransferase complex METTL1-WDR4 ( IC 50 =144 μM).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC74700 | DSPE-succinic acid | 248253-94-3 | >98.00% | |
DSPE-succinic acid ist ein Phophalipid, das mit einem Carbonsäureanteil bedeckt ist. | ||||
| GC74728 | Butylated hydroxytoluene-d3 | 86819-59-2 | >98.00% | |
Butylated hydroxytoluene-d3 ist das Deuterium markierte butylierte Droxytoluol. | ||||
| GC78560 | Glycerophosphoglycerol | 6418-92-4 | >99.50% | |
Glycerophosphoglycerol is a precursor for complex phospholipids, including the cardiolipins in mitochondria, which can form abundant negative ions. | ||||
| GC78942 | UH15-38 TFA | - | >99.50% | |
UH15-38 TFA is a potent RIPK3 inhibitor with an IC 50 value of 20 nM. | ||||
| GC78944 | 2',4-Dihydroxychalcone | 13323-66-5 | >98.00% | |
2',4-Dihydroxychalcone is an orally active natural chalcone flavonoid. | ||||
| GC78965 | ACT001 hydrochloride | 1403357-80-1 | >98.00% | |
ACT001 (Dimethylaminomicheliolide; DMAMCL) hydrochloride is an orally active, blood-brain barrier-permeable anti-inflammatory and anti-tumor agent. | ||||
| GC78976 | NFE2L1 activator-1 | 3070514-51-8 | >98.50% | |
NFE2L1 activator-1 (Compound 5b) is a potent nuclear factor erythroid 2-related factor 1 ( NFE2L1 ) activator ( EC 50 = 2.4 µM). | ||||
| GC78978 | (rac)-Mitiperstat | 1933460-18-4 | >98.00% | |
(rac)-Mitiperstat ((rac)-AZD4831) is the racemic form of Mitiperstat. | ||||
| GC78979 | Ferfluor-1 | 3030473-59-4 | >99.00% | |
Ferfluor-1 is a Ferroptosis inhibitor ( EC 50 of 57 nM in HT108 cells; EC 50 of 75 nM in OS-RC-2 cells; EC 50 of 2.3 nM in SH-SY5Y neuroblastoma cells), and ratiometric photoluminescent probe with blood-brain barrier permeability. | ||||
| GC79057 | BF-175 | 1333375-02-2 | >98% | |
BF-175 is a selective SIRT1 agonist. | ||||
| GC79067 | ADAR1i-124 | - | >98.50% | |
ADAR1i-124 is an A-to-I RNA editing inhibitor by inhibiting the catalytic activities of both ADAR1p150 and ADAR1p110. | ||||
| GC79071 | Apidaecin IA acetate | - | >98.00% | |
Apidaecin IA acetate is a basic peptide. | ||||
| GC79073 | HSF1-IN-2 | 304453-52-9 | >98.00% | |
HSF1-IN-2 (Compound 0048) is a HSF1 inhibitor. | ||||
| GC79074 | HSP70/DnaK substrate peptide TFA | - | >98.00% | |
HSP70/DnaK substrate peptide TFA is a short peptide that the HSP70/DnaK molecular chaperone can bind and act on. | ||||
| GC79077 | DDO-6600 | 2640292-37-9 | >98.00% | |
DDO-6600 is a covalent Hsp90 inhibitor. | ||||
| GC79118 | Hydrangeic acid | 491-79-2 | >96.00% | |
Hydrangeic acid is an orally effective stilbene-type glycolipid metabolism regulator that lowers blood glucose and lipids. | ||||
| GC79119 | PPARα agonist 6 | 959699-23-1 | >99.50% | |
PPARα agonist 6 (Compound 15) is a PPARα agonist. | ||||
| GC79120 | EL244 | 3047548-70-6 | >99.50% | |
EL244 is a dua Autotaxin ( ATX ) ( IC 50 = 50 nM) inhibitor and PPARγ ( IC 50 = 1.3 μM; K d = 1.3 μM) agonist. | ||||
| GC79167 | METTL1-WDR4-IN-1 TFA | - | >99.50% | |
METTL1-WDR4-IN-1 (Compound 1) TFA is a selective competitive inhibitor of the methyltransferase complex METTL1-WDR4 ( IC 50 =144 μM). | ||||
| GC79168 | EP102 | 3050818-07-7 | >98% | |
EP102 is an orally active, selective inhibitor of the METTL3/METTL14 complex with an IC 50 of 2 nM. | ||||
| GC79251 | PBF-999 | 1620909-95-6 | >98.50% | |
PBF-999 is a phosphodiesterase10A (PDE-10A) and adenosine A2A receptor (A2AR) dual antagonist. | ||||
| GC79293 | PIPE-791 | 2901868-37-7 | >98% | |
PIPE-791 is an orally active, blood-brain barrier-permeable selective antagonist of LPAR1. | ||||
| GC79301 | GS-5759 | 1346653-91-5 | >99.00% | |
GS-5759 is both a β₂-adrenergic receptor agonist and a PDE4 inhibitor. | ||||
| GC79337 | ZSTK3744 | - | >98.00% | |
ZSTK3744 is an aryl hydrocarbon receptor ( AhR ) agonist. | ||||