T23209 |
Qc1
|
403718-45-6
|
100%
|
|
Qc1 is an inhibitor of threonine dehydrogenase (TDH) inhibitor and can be used in studies about metabolic diseases.
|
T72814 |
11β-HSD1-IN-12
|
872506-67-7
|
100%
|
|
11β-HSD1-IN-12 is an 11β-HSD1 inhibitor.11β-HSD1-IN-12 is implicated in the conversion of glucocorticoids in vivo and can be used to study metabolic syndrome and...
|
T9333 |
Perfluorooctanoic acid
|
335-67-1
|
100%
|
|
Perfluorooctanoic acid (PFOA) (PFOA) is a persistent and widespread industry-made chemical.
|
T1473 |
Trilostane
|
13647-35-3
|
100%
|
|
Trilostane (Win 24540) is a synthetic derivative of androstane with adrenocortical suppressive properties. Trilostane reversibly inhibits 3 beta-hydroxysteroid d...
|
T8480 |
Tenovin-6 Hydrochloride
|
1011301-29-3
|
100%
|
|
Tenovin-6 Hydrochloride is an SIRT1, SIRT2 and HDAC8 inhibitor(IC50s of 21 μM, 10 μM, and 67 μM for SirT1, SirT2, and SirT3, respectively), and is also a potent ...
|
T68664 |
Epostane
|
80471-63-2
|
100%
|
|
Epostane (Win-32729) is a 3β-hydroxysteroid dehydrogenase inhibitor that acts by inhibiting the enzyme 3β-hydroxysteroid dehydrogenase, blocking progesterone pro...
|
T4515 |
A939572
|
1032229-33-6
|
100%
|
|
A939572 is stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50 values of <4 nM for mSCD1 and 37 nM for hSCD1.
|
T2346 |
Enasidenib
|
1446502-11-9
|
100%
|
|
Enasidenib (AG-221) is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential ...
|
T7741 |
DS-1001b
|
1898207-64-1
|
100%
|
|
DS-1001b is an inhibitor of mutant IDH-1 (Isocitrate Dehydrogenase-1)
|
T11021 |
DHODH-IN-12
|
1263303-93-0
|
100%
|
|
DHODH-IN-12 is a leflunomide derivative and a weak dihydrorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.07.
|
T19831 |
Sodium Oxamate
|
565-73-1
|
|
|
Sodium Oxamate (Oxamic acid sodium salt) is an LDH inhibitor that specifically inhibits LDHA. Sodium Oxamate has antitumor activity and induces cell cycle arrest...
|
T10140 |
4-Diethylaminobenzaldehyde
|
120-21-8
|
|
|
4-Diethylaminobenzaldehyde is a reversible aldehyde dehydrogenase (ALDH) inhibitor (Ki: 4 nM for ALDH1). It displays a potent anti-androgenic effect (IC50: 1.71μ...
|
T12196 |
NCT-505
|
2231079-74-4
|
|
|
NCT-505 is a potent and selective inhibitor of aldehyde dehydrogenase (ALDH1A1, IC50 = 7 nM) and a weak inhibitor of hALDH1A2, hALDH1A3, hALDH2, hALDH3A1 with IC...
|
T12438 |
PfDHODH-IN-1
|
183945-55-3
|
|
|
PfDHODH-IN-1 is an analogue of the active Leflunomide metabolite, has antimalarial activity.
|
TJS1382 |
Taraxerone
|
514-07-8
|
|
|
Taraxerone has allelopathic and antifungal effects.Taraxerone prevents catalase, superoxide dismutase, and reduces glutathione concentrations from the decrease i...
|
T15551 |
IDH889
|
1429179-07-6
|
|
|
IDH889 is a brain penetrant, an allosteric and mutant specific IDH1 inhibitor. IDH889 has effective selectivity for IDH1 R132* mutations (IC50s: 0.02 μM, 0.072 μ...
|
T14388 |
AZD 4017
|
1024033-43-9
|
|
|
AZD 4017 is an inhibitor of 11β-Hydroxysteroid Dehydrogenase Type 1(11β-HSD1) (IC50: 7 nM).
|
T4173 |
R162
|
64302-87-0
|
98%
|
|
R162 is an effective glutamate dehydrogenase 1 (GDH1) inhibitor.
|
T9494 |
Imidazole-5-propionic acid
|
1074-59-5
|
98%
|
|
Imidazole-5-propionic acid (Imidazolylpropionic acid) is a product of histidine metabolism and may involve oxidation or transamination. Imidazole-5-propionic aci...
|
T10146 |
4-Hydroxyderricin
|
55912-03-3
|
98%
|
|
4-Hydroxyderricin, a potent and selective MAO-B inhibitor (IC50: 3.43 μM), is the main active ingredient of Angelica sinensis, which mildly inhibits dopamine β-h...
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