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(24)
- P450(439)
- PDE(241)
- Phospholipase(129)
- Procollagen C Proteinase(1)
- Saccharometabolism(1)
- SCD(19)
- SGLT(29)
- TPH(4)
- Transferase(26)
- ALP(1)
- Carbohydrates(32)
- 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(102)
- Pyruvate kinase(13)
- Others(63)
- MGL(1)
- Galactosidase(2)
- 12-Lipoxygenase(1)
- Fatty Acid Synthase (FASN)(8)
- Dihydroorotate Dehydrogenase(13)
- Bile Acids & Microbiome(103)
- Bone Growth & Remodeling(53)
- Carbohydrate Metabolism(157)
- Cofactors & Vitamins(82)
- Dyslipidemias(102)
- Inborn Errors of Metabolism(95)
- Metabolic Syndrome(21)
- Necroptosis(11)
- Necrosis(16)
- Nutrient Sensing(14)
- Phosphodiesterase(33)
- Reproductive Biology(171)
- Thermogenesis(8)
- Sterol Biosynthesis(41)
- 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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GC50508
PKUMDL WQ 2101
Negative allosteric modulator of 3-phosphoglycerate dehydrogenase (PHGDH)
-
GC50419
A 33
A 33 是一种具有口服活性的选择性 PDE4B 抑制剂,IC50 为 15 nM。
-
GC50357
CX08005
Competitive PTP1B inhibitor
-
GC50345
Liproxstatin-1 hydrochloride
A ferroptosis inhibitor
-
GC50321
(S)-C33
(S)-C33 是一种有效的选择性 PDE9 (phosphodiesterase-9) 抑制剂,IC50 为 11 nM。
-
GC50319
PF 04671536 hydrochloride
Potent and selective PDE8B/8A inhibitor
-
GC50285
JNJ DGAT2-A
JNJ DGAT2-A 是一种选择性二酰基甘油酰基转移酶 2 (DGAT2) 抑制剂,在表达人 DGAT2 的 Sf9 昆虫细胞膜中的 IC50 值为 0.14 μM。
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GC50279
MK 386
Potent, selective human type 1 5α-reductase inhibitor
-
GC50257
BMS 795311
BMS 795311 是一种有效的可口服生物利用的胆固醇酯转移蛋白 (CETP) 抑制剂,在基于酶的闪烁邻近试验 (SPA) 中的 IC50 为 4 nM,在人全血浆试验 (hWPA) 中的 IC50 分别为 0.22 μM。
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GC50198
Topiramate - d12
托吡酯-D12,McN 4853 D12 ; RWJ 17021 D12
An internal standard for the quantification of topiramate
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GC50196
Simvastatin - d6
六氘代辛伐他汀,MK 733-d6
An internal standard for the quantificaition of simvastatin
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GC50153
BIX
硫氰酸2-(3,4-二羟基苯基)-2-氧代乙酯
An inducer of GRP78
-
GC50074
T2AA
An inhibitor of PCNA
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GC50041
VO-OHpic
A specific inhibitor of PTEN
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GC50038
Mephenytoin
美芬妥因
Mephenytoin 是一种抗惊厥药,是 CYP2C19 和 CYP2B6 的底物。
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GC50019
GW 1929 hydrochloride
A non-thiazolidinedione activator of PPARγ
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GC39288
ent-Tadalafil
他达拉非EP杂质B(ENT-他达拉非),ent-IC-351
ent-Tadalafil (ent-IC-351) ,化合物 (6S,12aS) ,是化合物 (6R,12aS) 的无活性顺式对映异构体。化合物 (6R,12aS) 是有效的 PDE5 抑制剂,IC50 为0.090 μM,而ent-Tadalafil 在高浓度 10 µM 时仍然没有活性。
-
GC39271
(±)-Naringenin
(±)-柚皮素
A citrus-derived flavonoid
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GC39260
OR-1855
(R)-6-(4-氨基苯基)-4,5-二氢-5-甲基-3(2H)-哒嗪酮
OR-1855 是 Levosimendan 的活性代谢产物,对人体肌层收缩力有影响。Levosimendan 是一种钙敏感性药物,用于治疗急性失代偿性充血性心力衰竭。
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GC39234
DHODH-IN-2
DHODH-IN-2 是人二氢乳清酸脱氢酶 (HsDHODH) 抑制剂,可抑制麻疹病毒复制,pMIC50 值为 8.6。
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GC39221
1-Cyclohexyl-3-dodecyl urea
CDU; N-Cyclohexyl-N-dodecyl urea; NCND
1-Cyclohexyl-3-dodecyl urea (CDU, N-Cyclohexyl-N-dodecyl urea, NCND) is a highly selective inhibitor of soluble epoxide hydrolase (sEH) that increases epoxyeicosatrienoic acids (EETs) levels.
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GC46235
Vitamin K1-d7
维生素K1-d7
An internal standard for the quantification of vitamin K1
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GC46215
S-Acetyl-L-glutathione
S-乙酰-L-谷胱甘肽
A derivative of glutathione
-
GC46213
Ro 41-0960
A COMT inhibitor
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GC46208
Propentofylline
普罗潘非林,HWA 285
A xanthine derivative and neuroprotective agent
-
GC46192
Octanoic Acid-13C
辛酸-1-13C,Caprylic acid-13C
An internal standard for the quantification of octanoic acid
-
GC46187
Norhyodeoxycholic Acid
去甲去氧胆酸
A synthetic bile acid
-
GC46175
MOTS-c (human) (trifluoroacetate salt)
Mitochondrial open reading frame of the 12S rRNA-c
具有多种生物活性的神经肽
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GC46168
MBX-8025 (sodium salt)
A PPARδ agonist
-
GC46138
ENPP1 Inhibitor C
ENPP1 Inhibitor C是一种选择性外核苷酸焦磷酸酶/磷酸二酯酶1(ENPP1)抑制剂,对ENPP1的IC50值为10µM。
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GC46131
Diazoxide-d3
二氮嗪D3,Sch-6783-d3; SRG-95213-d3
An internal standard for the quantification of diazoxide
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GC46119
Cholic Acid anilide
A synthetic bile acid
-
GC46118
Chlothianidin
噻虫胺
A neonicotinoid insecticide
-
GC46114
CAY10761
An ENPP1 inhibitor
-
GC46105
Butyrolactone II
A fungal metabolite
-
GC46104
Butyric Acid-d7
氘代丁酸(D7),Butanoic acid-d7
An internal standard for the quantification of sodium butyrate
-
GC46101
Brinzolamide-d5
布林佐胺杂质,AL-4862-d5
An internal standard for the quantification of brinzolamide
-
GC46085
Alphitonin
A flavonoid
-
GC46083
Adenylosuccinic Acid
腺苷酸基琥珀酸,Aspartyl Adenylate
腺苷琥珀酸是一种嘌呤核苷酸,也是嘌呤核苷酸循环中的中间产物
-
GC46080
7,3',4'-Trihydroxyflavone
3',4',7-三羟基黄酮
A flavonoid with diverse biological activities
-
GC46069
4-Amino-5-(bromomethyl)-2-methylpyrimidine (hydrobromide)
A heterocyclic building block
-
GC46068
3β-OH-7-Oxocholenic Acid
3β-hydroxy-7-oxo-5-Cholenoic Acid, 3β-hydroxy-7-Oxochol-5-enoic Acid
A bile acid
-
GC46040
1,2,3-Trielaidoyl-rac-glycerol
三反油酸甘油酯9C18:1反
A triacylglycerol
-
GC39191
iRucaparib-AP6
iRucaparib-AP6 是高效且特异的 PARP1 降解剂,基于 Rucaparib (PROTAC 的方法)。 iRucaparib-AP6 是一种 "非捕获性" PARP1 降解剂,可同时阻断 PARP1 的催化活性和支架作用。
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GC39178
Canagliflozin D4
卡格列净D4,JNJ 28431754-d4
An internal standard for the quantification of canagliflozin
-
GC39168
GSK2945 hydrochloride
GSK2945 hydrochloride 是一类叔胺,是一种高度特异性的 Rev-erbα/REV-ERBα (小鼠/人反向成红细胞病病毒α) 拮抗剂, 其 EC50 值分别为 21.5 μM 和 20.8 μM。GSK2945 hydrochloride 可增强胆固醇 7α-羟化酶 (CYP7A1) 水平和胆固醇代谢。
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GC39160
BCI-215
BCI-215 是一种高效、肿瘤细胞选择性的双重特异性磷酸酶 DUSP-MKP 抑制剂。BCI-215 对肿瘤细胞有细胞毒性,但对正常细胞无毒性。
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GC39127
Palmatine
黄藤素
An alkaloid with diverse biological activities
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GC38967
Lycorine
石蒜碱
An alkaloid with diverse biological activities
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GC38921
Lirimilast
BAY 19-8004
Lirimilast (BAY 19-8004) 是一种有效的,选择性的和口服活性的磷酸二酯酶 4 (PDE4) 抑制剂,IC50 值为 49 nM。Lirimilast 可用于治疗哮喘或慢性阻塞性肺疾病 (COPD),具有强效的抗炎特性。