Ubiquitination/ Proteasome(泛素化/蛋白酶体)
- Autophagy(1114)
- DUB(17)
- E1 Activating(1)
- E2 conjugating(1)
- E3 Ligase(7)
- Proteasome(69)
- p97(12)
- Mitophagy(82)
- ULK(9)
- Cat.No. 产品名称 Information
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GC32468
Lanatoside C
毛花甙丙
Lanatoside C is a cardiac glycoside with antiviral and anti-tumor activity. Lanatoside C induces G2/M cell cycle arrest and induces autophagy and apoptosis via attenuating MAPK, Wnt, JAK-STAT, and PI3K/AKT/mTOR signaling pathways.
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GC32411
FR 167653 (FR 167653 sulfate)
FR 167653 sulfate
FR 167653 (FR 167653硫酸盐) (FR 167653 (FR 167653硫酸盐)),一种具有口服活性和选择性的p38 MAPK抑制剂,是TNF-α的强效抑制剂;和 IL-1β;通过特异性抑制 p38 MAPK 活性产生。 -
GC32407
Rpn11-IN-1
Capzimin intermediate
Rpn11-IN-1是一种有效的选择性蛋白酶体亚基Rpn11抑制剂,IC50为390nM。 -
GC32232
Pyriproxyfen (S-31183)
吡丙醚; S-31183
A pyridine insecticide - GC32209 ITX5061 ITX5061是一个II型p38MAPK抑制剂,也是清道夫受体B1(SR-B1)的拮抗剂。
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GC32152
Lumefantrine (Benflumetol)
苯芴醇; Benflumetol
An antimalarial drug -
GC32107
Peretinoin (NIK333)
NIK333
Peretinoin (NIK333) 是一种具有维生素 A 样结构的口服无环类维生素 A,可靶向类维生素 A 核受体,如类维生素 X 受体 (RXR) 和视黄酸受体 (RAR)。 -
GC32078
Clioquinol (Iodochlorhydroxyquin)
氯碘羟喹,Iodochlorhydroxyquin
A metal-chelating antimicrobial agent
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GC32048
Emetine dihydrochloride hydrate
吐根碱盐酸盐水合物
An alkaloid with diverse biological activities
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GC31988
p38α inhibitor 1
p38αinhibitor1是p38α的抑制剂,来自专利WO2008076265A1。
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GC31964
Sulfosuccinimidyl oleate
Sulfo-N-succinimidyl oleate
An irreversible inhibitor of CD36
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GC31935
Trifarotene (CD5789)
曲法罗汀; CD5789
Trifarotene (CD5789) (CD5789) 是一种有效的选择性 RARγ;激动剂。 - GC31924 AZD7624 AZD7624是一种可吸入的p38抑制剂,具有高效的抗炎活性。
- GC31899 KZR-504 KZR-504是具有口服活性的、高度选择性的免疫原体低分子质量多肽2(LMP2)的抑制剂、其对LMP2和LMP7的IC50值分别为51nM,4.274μM。
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GC31809
Yangonin
甲氧醉椒素
A kavalactone with affinity for the CB1 receptor -
GC31717
Ginkgetin
银杏双黄酮
A biflavonoid with diverse biological activities -
GC31705
Sofalcone
索法酮
Gastroprotective chalcone derivative -
GC31697
Dilmapimod (SB-681323)
度马莫得; SB-681323; GW 681323
Dilmapimod (SB-681323,GW 681323) is a potent p38 MAPK inhibitor that potentially suppresses inflammation in chronic obstructive pulmonary disease. - GC31665 (R)-BPO-27 (R)-BPO-27是有效的CFTR抑制剂,IC50值为4nM。
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GC31586
Monacolin J (Antibiotic MB 530A)
辛伐他汀内酯二醇,Antibiotic MB 530A; Lovastatin diol lactone
Monacolin J (Antibiotic MB 530A) 是一种胆固醇生物合成抑制剂,可抑制 HMG-CoA 还原酶的活性。 - GC31563 FK-448 Free base FK-448Freebase是一种有效的,特异性的糜蛋白酶(chymotrypsin)抑制剂,IC50值为720nM。
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GC31395
PX20606 trans racemate (PX-102 trans racemate)
CPDD1220反式消旋体,PX-102 trans racemate
PX20606 trans racemate (PX-102 trans racemate) (PX-102 trans racemate) 是一种 FXR 激动剂,在 FRET 和 M1H 试验中对 FXR 的 EC50 分别为 32 和 34 nM。 -
GC31386
(-)-PX20606 trans isomer ((-)-PX-102 trans isomer)
PX-20606手性,(-)-PX-102 trans isomer; (-)-PX-104
(-)-PX20606 trans isomer ((-)-PX-102 trans isomer) 是一种 FXR 激动剂,在 FRET 和 M1H 试验中对 FXR 的 EC50 分别为 18 和 29 nM。 -
GC31317
Sitagliptin (MK0431)
西格列汀; MK-0431
Sitagliptin (MK-0431) is an oral and highly selective DPP-4 inhibitor with an IC50 of 18 nM. It is used for the treatment of type 2 diabetes. - GC31239 SA72 SA72是高度选择性的脂肪酸酰胺水解酶(FAAH)抑制剂。
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GC31170
Calmodulin-Dependent Protein Kinase II 290-309
A CaMKII inhibitor
- GC31058 FR 167653 free base FR-167653是一种选择性的p38MAPK抑制剂。
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GC30992
Paroxetine hydrochloride hemihydrate (BRL29060 hydrochloride hemihydrate)
盐酸帕罗西汀半水合物; BRL29060 hydrochloride hemihydrate; BRL29060A hemihydrate
Paroxetine HCl (BRL-29060A, FG-7051) is an antidepressant drug of the SSRI type. -
GC30990
Calcineurin substrate
钙调神经磷酸酶底物
A synthetic peptide substrate - GC30884 LX2343 An inhibitor of BACE1 and PI3K
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GC30871
Oxidopamine hydrochloride (6-Hydroxydopamine hydrochloride)
6-羟基多巴胺盐酸盐; 6-Hydroxydopamine hydrochloride; 6-OHDA hydrochloride
Oxidopamine hydrochloride (6-Hydroxydopamine hydrochloride)(6-OHDA)是神经递质多巴胺的拮抗剂。 -
GC30842
Androsterone (5α-Androstan-3α-ol-17-one)
雄酮; 5α-Androstan-3α-ol-17-one
An androgenic steroid
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GC30790
Triflupromazine hydrochloride
盐酸三氟丙嗪
A phenothiazine with diverse biological activities -
GC30787
Sertindole (Lu 23-174)
舍吲哚; Lu 23-174
An atypical antipsychotic - GC30785 4E2RCat 4E2RCat是eIF4E-eIF4G相互作用的抑制剂,IC50值为13.5μM。
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GC30761
α-Hydroxylinoleic acid
α-羟基油酸; α-Hydroxylinoleic acid
ABTL0812 (α-Hydroxylinoleic acid, LP-10218, SCLN-0812) inhibits Akt/mTOR axis by inducing the overexpression of TRIB3 and activating autophagy in lung squamous carcinoma cell lines. ABTL0812 also induces AMPK activation and ROS accumulation. - GC30751 FAAH-IN-1 FAAH-IN-1是脂肪酸酰胺水解酶(FAAH)抑制剂,对大鼠和人FAAH的IC50值分别为145nM和650nM。
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GC30744
Norepinephrine (Adrenor)
去甲肾上腺素; Levarterenol; L-Noradrenaline
(-)-Norepinephrine (Arterenol, Levarterenol, L-Noradrenaline) is a natural neurotransmitter and hormone. It is an agonist of adrenergic receptors with Ki values of 330, 56, and 740 nM for α1, α2, and β1 adrenoceptors, respectively.
- GC30676 MAPK13-IN-1 MPAK13-IN-1是MAPK13(p38δ)的一个抑制剂,其IC50值为620nM。
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GC30646
Skatole(3-Methylindole)
粪臭素; 3-Methylindole; 3-Methyl-1H-indole
Skatole (3-methylindole, Scatole) is a mildly toxic white crystalline organic compound that occurs naturally in feces. It has a fairly broad bacteriostatic effect. - GC30609 p38 MAPK-IN-2 p38MAPK-IN-2是一种p38kinase的抑制剂。
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GC30608
Ipsalazide
伊普柳氮
Ipsalazide是一种新的柳氮磺吡啶类似物,旨在释放胃肠道中的5-氨基水杨酸和无毒载体分子。
- GC30565 BAR502 A dual agonist of GP-BAR1 and FXR
- GC30537 BPO-27 racemate BPO-27racemate是有效的CFTR抑制剂,IC50值为8nM。
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GC30366
FAAH-IN-2
4-(3-氯-4-氟苯氨基)-7-甲氧基喹唑啉-6-醇,O-Desmorpholinopropyl Gefitinib
FAAH-IN-2是摘自专利WO/2008/100977A2中的FAAH抑制剂。 - GC30360 Cresol (Cresol mixture of isomers) Cresol是一种有机化合物,是芳香族有机化合物广泛存在的天然及合成基团。
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GC30356
Metofenazate (Methophenazine)
美托奋乃酯,Methophenazine
Metofenazate (Methophenazine) 是一种选择性钙调蛋白抑制剂。 -
GC30343
Selenomethionine (Seleno-DL-methionine)
硒代蛋氨酸; Seleno-DL-methionine; DL-Selenomethionine
硒代蛋氨酸(Seleno-DL-methionine)是一种天然存在的含硒氨基酸,是硒的常见天然食物来源。
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GC30263
Glucosamine (D-Glucosamine)
氨基葡萄糖; D-Glucosamine; Chitosamine
Glucosamine (2-amino-2-deoxy-D-glucose) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids. It is commonly used as a treatment for osteoarthritis. Glucosamine(GS) treatment selectively downregulates HIF-1α at the protein level in YD-8 cells via interference of production of the citric acid cycle metabolites. -
GC30158
p38-α MAPK-IN-1
p38-α MAPK-IN-1 is an inhibitor of p38-α, with IC50 value of 2300 nM in EFC displacement assay, and 5500 nM in HTRF assay.