S4582 |
Eflornithine (DFMO) hydrochloride hydrate
|
Eflornithine (DFMO) hydrochloride hydrate通过对鸟氨酸脱羧酶的不可逆抑制作用,抑制多胺生物合成。它是一种化疗保护剂,可阻止血管生成。其生物半衰期为8小时。 |
-
Front Oncol, 2023, 13:1212604
-
mBio, 2022, 13(5):e0219422
-
iScience, 2022, 25(3):103881
|
|
S2453 |
Benserazide HCl
|
Benserazide HCl (Ro-4-4602)是一种外周性的芳香族L-氨基酸脱羧酶(AAAD)或DOPA脱羧酶抑制剂。在溶液中不稳定,请现配现用! |
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Front Pharmacol, 2024, 15:1404532
-
Elife, 2022, 11e72668
-
Front Pharmacol, 2022, 13:903235
|
|
S1891 |
Carbidopa
|
Carbidopa 是一种芳香族-L-氨基酸脱羧酶抑制剂,IC50为29±2 μM。 |
-
Signal Transduct Target Ther, 2021, 6(1):77
-
J Cell Physiol, 2021, 10.1002/jcp.30587
-
PLoS One, 2017, 12(3):e0173240
|
|
S0108 |
AZ-33
|
AZ-33 (LDHA Inhibitor 33)是一种 lactate dehydrogenase A (LDHA) 的有效抑制剂,其IC50值为0.5 μM。LDHA是参与厌氧糖酵解的关键酶,在人类恶性肿瘤中该酶经常失活。 |
-
FASEB J, 2022, 36(3):e22229
-
Front Mol Biosci, 2021, 8:806650
|
|
S3086 |
Maleic acid
|
Maleic acid 可抑制 glutamate decarboxylase (GAD) 的活性,从而增强 Listeria monocytogenes 的酸敏感性。Maleic acid 会影响细胞外 GABA 的水平。 |
|
|
E2354 |
Valepotriate
|
Valepotriate从Valeriana jatamansi Jones中分离一种不稳定的环烯醚萜,通过显著增加GABAA、谷氨酸脱羧酶65 (glutamic acid decarboxylase 65)和Bcl-2的表达,以及降低caspase-3表达发挥抗癫痫作用。 |
|
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F0074New |
GAD67 mAb
|
Anti-GAD67 Mouse mAb recognizes endogenous levels of total GAD67 protein. |
|
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S1642 |
Methyldopa
|
Methyldopa 是DOPA 脱羧酶竞争性抑制剂,ED50为21.8 mg/kg。 |
|
|
A5290 |
GAD67 Rabbit Recombinant mAb
|
|
|
|
E0654 |
D-Arginine
|
D-Arginine是精氨酸脱羧酶(arginine decarboxylase,ADC)的抑制剂,可调节腐胺的生物合成。 |
|
|
S5448 |
S(-)-Carbidopa
|
S(-)-Carbidopa is a peripheral decarboxylase inhibitor, used in combination with levodopa for treatment of Parkinsonism. |
|
|
E1189 |
TES-1025
|
TES-1025是一种高效、选择性的人α-氨基-β-羧酸-ε-半醛脱羧酶(human α-amino-β-carboxymuconate-ε-semialdehyde decarboxylase, ACMSD)抑制剂,其IC50为13 nM。 |
|
|
S5444 |
4-Bromo-3-hydroxybenzoic acid
|
4-bromo-3-hydroxybenzoic acid is a potent inhibitor of the enzyme histidine decarboxylase with resultant inhibition of histamine formation in mammals. |
|
|
S5579 |
Chelidonic acid
|
Chelidonic acid (Jerva acid, Jervaic acid, γ-Pyrone-2,6-dicarboxylic acid) 是在几种植物中发现的次级代谢产物,对实验动物的过敏性疾病具有治疗潜力。Chelidonic acid 通过阻断HMC-1细胞中的 NF-κB 和 caspase-1 来抑制 IL-6 的产生。Chelidonic acid 也是 glutamate decarboxylase 的抑制剂,其Ki值为1.2 μM。 |
|
|
S5409 |
Chelidamic acid hydrate
|
Chelidamic acid is a pharmaceutical intermediate as well as a cosmetic material due to its anti-inflammatory and whitening effect. Chelidamic acid is also one of the most potent inhibitors of glutamate decarboxylase, with a Ki of 33 μM. |
|
|
S4582 |
Eflornithine (DFMO) hydrochloride hydrate
|
Eflornithine (DFMO) hydrochloride hydrate通过对鸟氨酸脱羧酶的不可逆抑制作用,抑制多胺生物合成。它是一种化疗保护剂,可阻止血管生成。其生物半衰期为8小时。 |
- Front Oncol, 2023, 13:1212604
- mBio, 2022, 13(5):e0219422
- iScience, 2022, 25(3):103881
|
|
S2453 |
Benserazide HCl
|
Benserazide HCl (Ro-4-4602)是一种外周性的芳香族L-氨基酸脱羧酶(AAAD)或DOPA脱羧酶抑制剂。在溶液中不稳定,请现配现用! |
- Front Pharmacol, 2024, 15:1404532
- Elife, 2022, 11e72668
- Front Pharmacol, 2022, 13:903235
|
|
S1891 |
Carbidopa
|
Carbidopa 是一种芳香族-L-氨基酸脱羧酶抑制剂,IC50为29±2 μM。 |
- Signal Transduct Target Ther, 2021, 6(1):77
- J Cell Physiol, 2021, 10.1002/jcp.30587
- PLoS One, 2017, 12(3):e0173240
|
|
S0108 |
AZ-33
|
AZ-33 (LDHA Inhibitor 33)是一种 lactate dehydrogenase A (LDHA) 的有效抑制剂,其IC50值为0.5 μM。LDHA是参与厌氧糖酵解的关键酶,在人类恶性肿瘤中该酶经常失活。 |
- FASEB J, 2022, 36(3):e22229
- Front Mol Biosci, 2021, 8:806650
|
|
S3086 |
Maleic acid
|
Maleic acid 可抑制 glutamate decarboxylase (GAD) 的活性,从而增强 Listeria monocytogenes 的酸敏感性。Maleic acid 会影响细胞外 GABA 的水平。 |
|
|
S1642 |
Methyldopa
|
Methyldopa 是DOPA 脱羧酶竞争性抑制剂,ED50为21.8 mg/kg。 |
|
|
E0654 |
D-Arginine
|
D-Arginine是精氨酸脱羧酶(arginine decarboxylase,ADC)的抑制剂,可调节腐胺的生物合成。 |
|
|
S5448 |
S(-)-Carbidopa
|
S(-)-Carbidopa is a peripheral decarboxylase inhibitor, used in combination with levodopa for treatment of Parkinsonism. |
|
|
E1189 |
TES-1025
|
TES-1025是一种高效、选择性的人α-氨基-β-羧酸-ε-半醛脱羧酶(human α-amino-β-carboxymuconate-ε-semialdehyde decarboxylase, ACMSD)抑制剂,其IC50为13 nM。 |
|
|
S5444 |
4-Bromo-3-hydroxybenzoic acid
|
4-bromo-3-hydroxybenzoic acid is a potent inhibitor of the enzyme histidine decarboxylase with resultant inhibition of histamine formation in mammals. |
|
|
S5579 |
Chelidonic acid
|
Chelidonic acid (Jerva acid, Jervaic acid, γ-Pyrone-2,6-dicarboxylic acid) 是在几种植物中发现的次级代谢产物,对实验动物的过敏性疾病具有治疗潜力。Chelidonic acid 通过阻断HMC-1细胞中的 NF-κB 和 caspase-1 来抑制 IL-6 的产生。Chelidonic acid 也是 glutamate decarboxylase 的抑制剂,其Ki值为1.2 μM。 |
|
|
S5409 |
Chelidamic acid hydrate
|
Chelidamic acid is a pharmaceutical intermediate as well as a cosmetic material due to its anti-inflammatory and whitening effect. Chelidamic acid is also one of the most potent inhibitors of glutamate decarboxylase, with a Ki of 33 μM. |
|
|