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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GC47735
N-acetyl Desethylchloroquine-d4
N-acetyl-(mono) Desethylchloroquine
An internal standard for the quantification of N-acetyl desethylchloroquine -
GC47470
Isovaleryl-L-carnitine-d3 (chloride)
CAR 5:0-d3, C5:0 Carnitine-d3, L-Carnitine isovaleryl ester-d3, L-Isovalerylcarnitine-d3
A neuropeptide with diverse biological activities -
GC47445
Hydroxychloroquine-d4 (sulfate)
HCQ-d4 sulfate
An internal standard for the quantification of hydroxychloroquine -
GC47436
HT-2 Toxin-13C22
HT-2毒素-13C22溶液
An internal standard for the quantification of HT-2 toxin -
GC47408
Glycochenodeoxycholic Acid-d4
甘氨鹅脱氧胆酸-D4,Chenodeoxycholylglycine-d4
An internal standard for the quantification of glycochenodeoxycholic acid -
GC47407
Glycochenodeoxycholic Acid (sodium salt hydrate)
GCDCA, NSC 681056
A neuropeptide with diverse biological activities -
GC47303
Erlotinib-d6 (hydrochloride)
埃罗替尼-D6盐酸盐,CP-358774-d6 hydrochloride; NSC 718781-d6 hydrochloride; OSI-774-d6 hydrochloride
An internal standard for the quantification of erlotinib -
GC47284
Elaidic Acid-d17
C18:1(9E)-d17, 9(E)-Oleic Acid-d17, trans-Oleic Acid-d17
A neuropeptide with diverse biological activities -
GC47271
D-Pyrohomoglutamic Acid
D-6-氧代哌啶-2-甲酸
A building block -
GC47195
Desethylchloroquine-d4
N-Desethylchloroquine-d4
An internal standard for the quantification of desethylchloroquine -
GC47194
Desethylchloroquine
羟基氯喹EP杂质D-d5二盐酸
An active metabolite of chloroquine -
GC47193
Desethyl Hydroxychloroquine-d4
Desethylhydroxychloroquine-d4
An internal standard for the quantification of desethyl hydroxychloroquine - GC47065 CAY10773 A derivative of sorafenib
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GC47042
Carfilzomib-d8
来那度胺-D8
An internal standard for the quantification of carfilzomib -
GC47016
Cabergoline-d6
FCE-21336-d6
A neuropeptide with diverse biological activities -
GC46989
C18 dihydro Ceramide-d3 (d18:0/18:0-d3)
N-octadecanoyl-D-erythro-Dihydrosphingosine-d3
An internal standard for the quantification of C18 dihydro ceramide -
GC46942
Bortezomib-d15
LDP-341-d15, MG-341-d15, PS-341-d15
A neuropeptide with diverse biological activities -
GC46923
Bexarotene-d4
LGD1069 D4
A neuropeptide with diverse biological activities -
GC46897
AUTEN-99
Autophagy enhancer-99 hydrobromide
An inhibitor of MRMR14/Jumpy -
GC46792
Ac-Nle-Pro-Nle-Asp-AMC (trifluoroacetate salt)
Ac-Nle-Pro-Nle-Asp-7-amido-4-Methylcoumarin, Ac-nLPnLD-AMC
A neuropeptide with diverse biological activities -
GC61267
SAR439859
SAR439859
Amcenestrant (SAR439859, compound 43d) is an orally available and nonsteroidal selective estrogen receptor degrader (SERD) with potential antineoplastic activity. SAR439859 is a potent estrogen receptor (ER) antagonist with EC50 of 0.2 nM for ERα degradation. -
GC61263
Salvigenin
三裂鼠尾草素
A polyphenol flavonoid with diverse biological activities -
GC61256
Rupatadine D4 fumarate
UR-12592 D4 fumarate
RupatadineD4fumarate(UR-12592D4fumarate)是Rupatadinefumarate的氘代标记物。RupatadineFumarate(UR-12592Fumarate)富马酸盐是PAF/H1受体双抑制剂,Ki值分别为0.55μM和0.1μM。 -
GC61251
Rosuvastatin D3
ZD 4522 D3
RosuvastatinD3(ZD4522D3)是Rosuvastatin的一种氘代化合物。Rosuvastatin(ZD4522)是一种竞争性HMG-CoA还原酶抑制剂,IC50为11nM。Rosuvastatin有效阻断人类醚-a-go-go相关基因(hERG)电流,IC50为195nM,延迟心脏复极化,从而延长动作电位持续时间(APDs)和校正QT间期(QTc)间隔。 -
GC61229
Quinacrine dihydrochloride
阿的平; Mepacrine dihydrochloride; SN-390 dihydrochloride
Quinacrine 2HCl(Quinacrine dihydrochloride) is a lipophilic cationic drug with multiple actions that is commonly used as an anti-protozoal agent. Quinacrine is an effective phospholipase A2 inhibitor. -
GC61227
Quercetin D5
槲皮素 d5
QuercetinD5是Quercetin的一种氘代化合物。Quercetin是一种天然黄酮类化合物,可激活或抑制许多蛋白质的活性。Quercetin可激活SIRT1,也可抑制PI3K,抑制PI3Kγ,PI3Kδ,PI3Kβ的IC50分别为2.4μM,3.0μM,5.4μM。 -
GC61221
PTP1B-IN-9
NSC 638643
An inhibitor of the ubiquitin-proteasome system -
GC61183
Physalin B
酸浆苦味B
PhysalinB是Capegooseberry中主要的甾体活性成分之一,通过调节p53依赖的凋亡途径,诱导乳腺癌细胞周期阻滞和诱导凋亡(apoptosis)。PhysalinB抑制人结肠癌细胞泛素-蛋白酶体通路并诱导不完全自噬反应。 -
GC61155
Omeprazole sodium
奥美拉唑钠,H 16868 sodium
An irreversible inhibitor of the gastric proton pump - GC61093 MSAB MSAB is a selective inhibitor of Wnt/β-catenin signaling that binds to β-catenin, promoting its degradation, and specifically downregulates Wnt/β-catenin target genes. MSAB shows potent anti-tumor effects.
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GC61045
Metformin D6 hydrochloride
二甲双胍盐酸,1,1-Dimethylbiguanide-d6 hydrochloride
An internal standard for the quantification of metformin -
GC61003
Loperamide D6 hydrochloride
4-[4-(4-氯苯基)-4-羟基哌啶-1-基]-2,2-二苯基-N,N-二(三氘甲基)丁酰胺盐酸盐,R-18553-d6 hydrochloride
LoperamideD6hydrochloride(R-18553D6hydrochloride)是Loperamidehydrochloride的氘代化合物。Loperamidehydrochloride是一种阿片受体(opioidreceptor)的激动剂,可用于腹泻的研究。 -
GC60935
Indomethacin sodium hydrate
吲哚美辛钠盐三水合物; Indometacin sodium hydrate
A non-selective COX inhibitor -
GC60930
Imatinib D4
[2H4]-伊马替尼,STI571 D4; CGP-57148B D4
ImatinibD4(STI571D4)是Imatinib(STI571)的氘代物。Imatinib是一种口服生物可用的酪氨酸激酶抑制剂,可选择性抑制BCR/ABL,v-Abl,PDGFR,c-kit激酶活性。 -
GC60891
GW406108X
GW108X
GW406108X (GW108X) is an inhibitor of Kif15 (Kinesin-12) with an IC50 of 0.82 μM in the ATPase assay. GW406108X inhibits recombinant ULK1 kinase activity with a pIC50 of 6.37 and blocks autophagy in cells, without affecting the upstream signalling kinases mTORC1 and AMPK. -
GC60882
Glyphosate
草甘膦
An herbicide -
GC60868
Gefitinib D8
吉非替尼杂质-D8,ZD1839-d8
GefitinibD8(ZD1839D8)是Gefitinib的氘代物。Gefitinib是一种有效的(EGFR)抑制剂,在NR6wtEGFR细胞中IC50值为2-37nM。 -
GC60826
Etoposide phosphate
磷酸依托泊苷; BMY-40481
Etoposidephosphate(BMY-40481)是一种有效的抗癌(anti-cancer)化疗试剂和一种选择性拓扑异构酶II(topoisomeraseII)抑制剂,可以防止DNA链的重新连接。Etoposidephosphate是依托泊苷的磷酸酯前药,被认为与Etoposide活性相当。Etoposidephosphate诱导细胞周期阻滞、凋亡(apoptosis)和自噬(autophagy)。 -
GC60700
Chloroquine D5
氯喹 d5
An internal standard for the quantification of chloroquine -
GC60688
Cereblon modulator 1
CC-90009
A modulator of cereblon -
GC60668
Calcimycin hemimagnesium
CALIMYCIN半镁盐,A-23187 hemimagnesium; Antibiotic A-23187 hemimagnesium
Calcimycin(A-23187)hemimagnesium是一种抗生素和独特的二价阳离子离子载体(divalentcationionophore),如钙离子和镁离子。Calcimycinhemimagnesium通过增加细胞内钙浓度诱导Ca2+依赖性细胞死亡。Calcimycinhemimagnesium抑制革兰氏阳性细菌和一些真菌的生长,还抑制ATP酶的活性并解耦哺乳动物细胞的氧化磷酸化(OXPHOS),诱导细胞凋亡(apoptosis)。 - GC60567 Afatinib impurity 11 Afatinib impurity 11 is an impurity of afatinib, an EGFR family inhibitor.
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GC60395
(3S,5R)-Fluvastatin D6
(3S,5R)-XU 62-320 free acid D6
(3S,5R)-FluvastatinD6是(3S,5R)-Fluvastatinsodium的氘代物。Fluvastatin是第一个完全合成的,竞争性的HMG-CoAreductase还原酶抑制剂,IC50为8nM。Fluvastatin通过依赖Nrf2的抗氧化通路保护血管平滑肌细胞免受氧化应激。 -
GC60325
Rilmenidine
利美尼啶
An antihypertensive agent - GC60257 MSC1094308 MSC1094308 是一种可逆的、II 型 AAA ATPase (VCP)/p97 和I型 AAA ATPase VPS4B 的变构抑制剂,对VPS4B 和 p97 的IC50 值分别为 0.71 μM 和 7.2 μM。
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GC60245
Metformin
二甲双胍; 1,1-Dimethylbiguanide
二甲双胍(1,1-二甲基双胍)主要介导 AMPK 的激活,AMPK 是一种参与调节细胞能量代谢的丝氨酸/苏氨酸蛋白激酶,可导致癌细胞中 mTOR 信号传导和蛋白质合成的减少。 -
GC60241
Melatonin D5
褪黑素 D5; N-Acetyl-5-methoxytryptamine-d4
An internal standard for the quantification of melatonin -
GC60159
Ezetimibe ketone
(3R,4S)-1-(4-氟苯基)-3-[3-(4-氟苯基)-3-氧代丙基]-4-(4-羟基苯基)氮杂环丁烷-2-酮,EZM-K
Ezetimibe ketone (EZM-K) 是 Ezetimibe 的 I 期代谢产物。Ezetimibe 是一种 NPC1L1 抑制剂,是有效的 Nrf2 激活剂,Ezetimibe 还是有效的胆固醇吸收抑制剂。 -
GC60076
Bigelovin
锦菊素
Bigelovin是可从海百合中分离得到的一种倍半萜内酯,是选择性的视黄素X受体α(retinoidXreceptorα)的激动剂。Bigelovin可通过诱导凋亡和自噬来发挥抗肿瘤活性。Bigelovin通过抑制ROS的生成来调节mTOR信号通路。 - GC39708 DT2216 DT2216 是一种蛋白水解靶向嵌合体 (PROTAC),靶向 Bcl-xL 降解依赖于 Bcl-2 家族过表达蛋白(例如 Bcl-2、Bcl-xL 和 Mcl)的 T 细胞淋巴瘤-1.DT2216 抑制 G-68 细胞,IC50 值为 4.02 μM(72 小时)。