Metabolism(代谢)
- PPAR(215)
- 5-alpha Reductase(11)
- 5-Lipoxygenase(11)
- Adenosine Deaminase(10)
- Aminopeptidase(15)
- C14ɑ demethylase(2)
- Carbonic Anhydrase(55)
- CETP(9)
- Cholesterol absorption(1)
- CPT1(2)
- CYP3A/CYP450(18)
- Dehydrogenase(39)
- DHFR(7)
- DGAT(7)
- Dopamine β-hydroxylase(10)
- Enolase(5)
- FAAH(36)
- Factor Xa(59)
- Ferroptosis(193)
- Folate Analogue(2)
- Glucokinase(17)
- HMG-CoA Reductase(37)
- HSP(97)
- IDO(45)
- KRAS-PDEδ(3)
- MAO(6)
- Metabolic Enzymes(6)
- Neuronal Metabolism(8)
- Oxidative Phosphorylation(25)
- P450(441)
- PDE(242)
- Phospholipase(129)
- Procollagen C Proteinase(1)
- Saccharometabolism(1)
- SCD(19)
- SGLT(29)
- TPH(4)
- Transferase(26)
- ALP(1)
- Carbohydrates(33)
- Transaminase(3)
- Glutathione Reductase(1)
- Catalase(11)
- monooxygenase(1)
- PKM2(1)
- Aldehyde dehydrogenase(1)
- Squalene synthase(1)
- Hydrolase(17)
- ornithine decarboxylase(1)
- Amino acid metabolism(3)
- phosphatases(101)
- Pyruvate kinase(13)
- Others(64)
- MGL(1)
- Galactosidase(2)
- 12-Lipoxygenase(1)
- Fatty Acid Synthase (FASN)(8)
- Dihydroorotate Dehydrogenase(13)
- Bile Acids & Microbiome(119)
- Bone Growth & Remodeling(53)
- Carbohydrate Metabolism(161)
- Cofactors & Vitamins(84)
- Dyslipidemias(103)
- Inborn Errors of Metabolism(97)
- Metabolic Syndrome(22)
- Necroptosis(11)
- Necrosis(16)
- Nutrient Sensing(14)
- Phosphodiesterase(33)
- Reproductive Biology(172)
- Thermogenesis(8)
- Sterol Biosynthesis(40)
- Prolyl Hydroxylation Enzymes(2)
- Biliary System(11)
- Metabolic Disease(5)
- Fat Mass and Obesity-associated Protein (FTO)(5)
- SHIP(1)
- Furin(1)
- Liposome(8)
- PI5P4K(1)
- Metabolic Diseases(2)
- Cat.No. 产品名称 Information
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GC13948
GPi 688
GPi 688 是一种有效且具有口服活性的糖原磷酸化酶 (GPa) 抑制剂,对人肝 GPa、大鼠肝 GPa 和人骨骼肌 GPa 的 IC50 分别为 19 nM、61 nM 和 12 nM。
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GC15877
CP 316819
GPi 819
An inhibitor of glycogen phosphorylase A -
GC16777
YM 511
YM 511 是一种高度特异性的非甾体芳香酶抑制剂。
-
GC12481
TCS PrP Inhibitor 13
3(4Nitrophenyl)1phenyl2pyrazolin5one
An antiprion compound -
GC13611
CGP 3466B maleate
CGP3466B maleate
A GAPDH ligand -
GC11789
T 0156 hydrochloride
T 0156 hydrochloride 是一种有效的选择性 5 型磷酸二酯酶 (PDE5) 抑制剂。
-
GC16451
L-690330
L-690,330 是一种肌醇单磷酸酶 (IMPase) 的竞争性抑制剂,对重组人和牛 IMPase 的 Kis 分别为 0.27 和 0.19 μM,对人和牛额叶皮层 IMPase 的 Kis 分别为 0.30 和 0.42 μM。
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GC14328
FCCP
碳酰氰-4-三氟甲氧基苯腙,Carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone
FCCP是一种质子载体(H+离子载体),也是一种强磷酸化解偶联剂,促进质膜和线粒体膜的去极化。 -
GC10554
3-Cyano-7-ethoxycoumarin
3-氰基-7-乙氧基香豆素
A fluorogenic CYP450 substrate -
GC12693
JZL 195
4-硝基苯基4-(3-苯氧基苄基)哌嗪-1-甲酸叔丁酯
A potent inhibitor of both FAAH and MAGL -
GC10652
ONO 2506
(R)-(-)-2-丙基辛酸,ONO-2506; (R)-2-Propyloctanoic acid
An inhibitor of astrocyte activation -
GC16048
BC 11-38
A potent and selective PDE11 inhibitor
-
GC14697
HA 130
A reversible autotaxin inhibitor
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GC15673
CP 775146
A PPARα agonist
-
GC17684
VU 0364739 hydrochloride
phospholipase D2 (PLD2) inhibitor
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GC15189
Gisadenafil besylate
UK 369003-26
A PDE5 inhibitor -
GC18037
Tesaglitazar
(S)-2-乙氧基-3-{4-[2-(4-甲磺酰基苯基)-乙氧基-苯基]-丙酸
A PPARα/γ agonist -
GC16632
CDP 840 hydrochloride
GR259653X
CDP 840 hydrochloride (GR259653X) 是一种有效的、选择性的和口服活性的磷酸二酯酶 IV (PDE IV) 抑制剂。 -
GC13516
AS 1949490
A selective SHIP2 inhibitor
-
GC12252
S26948
A PPARγ agonist
-
GC13620
FIPI
5-Fluoro-2-indolyl deschlorohalopemide
Potent inhibitor of PLD1 and PLD2 -
GC15888
VU 0155069
CAY10593
Selective inhibitor of phospholipase D1 -
GC17824
GSK 0660
A PPARβ/δ antagonist
-
GC17046
Tris DBA
三(二亚苄基丙酮)二钯
N-myristoyltransferase-1 (NMT-1) inhibitor -
GC15475
RS 25344 hydrochloride
1-(3-硝基苯基)-3-(吡啶-4-基甲基)吡啶并[2,3-D]嘧啶-2,4(1H,3H)-二酮盐酸盐
RS 25344 hydrochloride 是一种选择性 cAMP-磷酸二酯酶 4 (PDE 4; PDE IV) 抑制剂,对人淋巴细胞的 IC50 为 0.28 nM。 -
GC15358
PF 750
N-苯基-4-(3-喹啉基甲基)-1-哌啶甲酰胺
A selective, potent FAAH inhibitor -
GC10718
PF 915275
PF 915275 是一种有效的、选择性的、具有口服活性的人 11β-羟基类固醇脱氢酶 1 型 (11βHSD1) 抑制剂,Ki 为 2.3 nM,EC50 为 15 nM(在 HEK293 细胞中)。
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GC13657
Mesopram
美索普兰-13C-D3
PDE4 inhibitor, orally active -
GC10092
SR 12813
GW 485801
A PXR agonist and cholesterol biosynthesis inhibitor -
GC14571
SIRT2-IN-8
奥司他韦杂质B(2-叠氮杂合物)
SIRT2-IN-8 是一种有效的 SIRT2 抑制剂。 -
GC12205
PD 146176
NSC168807
PD 146176 是一种有效的选择性网织红细胞 15-LOX-1 抑制剂。 -
GC10542
CP 80633
CP-80,633
Inhibitor of phosphodiesterase type 4 -
GC15472
BRL 50481
N,N,2-三甲基-5-硝基苯磺酰胺
A potent, selective inhibitor of PDE7 -
GC12062
nTZDpa
PPARγ partial agonist
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GC11586
SR 202
米福贝特,SR-202
An antagonist of agonist-induced PPARγ transcriptional activity -
GC12059
YM 976
A PDE4 inhibitor
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GC11313
ICI 63197
三氮唑嘧啶酮
A PDE3 and PDE4 inhibitor -
GC10004
Enoximone
烯氟酮
A PDE3 inhibitor -
GC18024
GW 7647
2-[[4-[2-[[环己基氨基)羰基](4-环己基丁基)氨基]乙基]苯基]硫基]-2-甲基丙酸
A selective PPARα agonist -
GC11561
NSC 95397
Cdc25 Inhibitor IV, PTP Inhibitor XXIX
An irreversible inhibitor of Cdc25 isoforms -
GC15445
TMS
2,3',4,5'-四甲氧基二苯乙烯,(E)-2,3',4,5'-tetramethoxystilbene
TMS(2,3',4,5'-tetramethoxystilbene)是一种特异性强效的CYP1B1抑制剂,IC50值为6±2nmol/L。 -
GC16103
Oleylethanolamide
油酰单乙醇胺,N-Oleoylethanolamide; Oleamide MEA; Oleic acid monoethanolamide
An endogenous, potent agonist for PPARα -
GC16115
AACOCF3
花生四烯基三氟甲酮,ATK, AATFMK
AACOCF3(花生四烯酰三氟甲基酮)是一种胞质磷脂酶A2(cPLA2)的强效抑制剂,IC50值约为10μM。AACOCF3通过不可逆烷基化酶活性位点阻断花生四烯酸释放及后续促炎性类二十烷酸生成,被广泛应用于炎症通路、神经炎症及脂质信号机制研究。 -
GC13829
BADGE
2,2-双-(4-甘胺氧苯)丙烷
A PPARγ ligand that disrupts hormone-mediated cell differentiation -
GC17135
Ciglitazone
环格列酮; ADD-3878; U-63287
A potent, selective PPARγ ligand -
GC10935
EHNA hydrochloride
外消旋-9-(2-羟基-3-壬基)腺嘌呤盐酸盐
A dual inhibitor of PDE2 and ADA -
GC14398
Siguazodan
氰胍佐旦
Siguazodan (SKF 94836) 是一种有效的、选择性的、具有口服活性的磷酸二酯酶 III (PDE-III) 抑制剂,IC50 为 117 nM。 -
GC10109
Cilostamide
OPC3689西洛酰胺,OPC3689
A selective inhibitor of PDE3 -
GC17420
OBAA
OBAA 是一种有效的磷脂酶 A2 (PLA2) 抑制剂,IC50 为 70 nM。
-
GC12878
MMPX
8-甲氧基甲基-3-异丁酰-1-甲基黄嘌呤
calmodulin-sensitive cyclic GMP phosphodiesterase inhibitor