Autophagy(自噬)
Autophagy is a catabolic process which degrades and recycles long-lived proteins and cytoplasmic organelles through lysosome. It plays an important role in growth regulation and maintenance of homeostasis.
Products for Autophagy
- Cat.No. 产品名称 Information
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GC62626
ICCB-19 hydrochloride
ICCB-19 hydrochloride is an inhibitor of TNFRSF1A Associated Via Death Domain (TRADD) with IC50 of 1.12 μM and 2.01 μM for protecting Velcade-induced apoptosis in Jurkat cells and protecting RDA in MEFs, respectively. ICCB-19 indirectly inhibits Receptor-interacting serine/threonine-protein kinase 1 (RIPK1). ICCB-19 effectively induces autophagy.
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GC14969
Idarubicin HCl
盐酸伊达比星; 4-Demethoxydaunorubicin hydrochloride
Antitumor antibiotic used in treatment of leukemia -
GC62465
Idelalisib D5
CAL-101 D5; GS-1101 D5
Idelalisib D5 (CAL-101 D) 是 Idelalisib 的一种氘代化合物。Idelalisib 是一种口服有效的高选择性 p110δ 抑制剂。 -
GC19411
IITZ-01
IITZ-01 是一种有效的溶酶体自噬抑制剂,具有单剂抗肿瘤活性,对 PI3Kγ 的 IC50 为 2.62 μM。
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GC10314
Imatinib (STI571)
伊马替尼; STI571; CGP-57148B
伊马替尼 (STI571) (STI571) 是一种口服生物可利用的酪氨酸激酶抑制剂,可选择性抑制 BCR/ABL、v-Abl、PDGFR 和 c-kit 激酶活性。伊马替尼 (STI571) (STI571) 通过在 ATP 结合位点附近结合而起作用,将其锁定在封闭或自我抑制的构象中,从而半竞争性地抑制蛋白质的酶活性。伊马替尼 (STI571) 也是 SARS-CoV 和 MERS-CoV 的抑制剂。 -
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。 -
GC39612
Imatinib D8
伊马替尼D8,STI571-d8; CGP-57148B-d8
Imatinib D8 (STI571 D8) 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。 -
GC11759
Imatinib Mesylate (STI571)
甲磺酸伊马替尼; STI571 Mesylate; CGP-57148B Mesylate
Imatinib Mesylate (STI571)是一种口服生物有效的多靶点抑制剂,对Bcr-Abl,c-Kit和PDGFR的IC50分别为0.6μM,0.1μM 和0.1μM。 -
GC16407
Imiquimod
咪喹莫特; R 837
A TLR7 agonist
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GC10712
Imiquimod hydrochloride
盐酸咪喹莫特; R 837 hydrochloride
A TLR7 agonist
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GC12645
Imiquimod maleate
马来酸咪喹莫特; R 837 maleate
A TLR7 agonist
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GC49670
Indium (III) thiosemicarbazone 5b
An anticancer agent
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GC17556
Indomethacin
吲哚美辛; Indometacin
Indomethacin(吲哚美辛)是一种有效的口服活性 COX1/2 抑制剂,COX-1 和 COX-2 的IC50 值分别为 18 nM 和 26 nM。 -
GC60935
Indomethacin sodium hydrate
吲哚美辛钠盐三水合物; Indometacin sodium hydrate
A non-selective COX inhibitor -
GC40227
Indomethacin-d4
吲哚美辛-D4; Indometacin-d4
An internal standard for the quantification of indomethacin -
GC61565
Indophagolin
5-溴-N-(4-氯-3-(三氟甲基)苯基)-1-(环丙烷羰基)吲哚啉-6-磺酰胺
Indophagolin, a potent indoline-containing autophagy inhibitor with IC50 of 140 nM, antagonizes the purinergic receptor P2X4 as well as P2X1 and P2X3 with IC50s of 2.71, 2.40 and 3.49 μM, respectively, also has a strong antagonistic effect on serotonin receptor 5-HT6 with IC50 of 1.0 μM. -
GC10969
INK 128 (MLN0128)
沙帕色替; INK-128; MLN0128; TAK-228
Inhibitor of TORC1/2 -
GC32742
INT-767
INT-767是法尼醇X受体/TGR5双激动剂,平均EC50分别为30和630nM。
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GC16105
Iohexol
碘海醇
A contrast reagent -
GC11229
IOWH-032
3-(3,5-二溴-4-羟基苯基)-N-(4-苯氧基苄基)-1,2,4-恶二唑-5-甲酰胺
A modulator of CFTR -
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。
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GC11473
Irinotecan
伊立替康; (+)-Irinotecan; CPT-11
Irinotecan是一种拓扑异构酶抑制剂,主要用于治疗结直肠癌。Irinotecan可通过与拓扑异构酶 I-DNA 复合物结合,阻止 DNA 链的再连接,并导致 DNA 双链断裂和细胞死亡 。 -
GC11048
Irinotecan HCl Trihydrate
盐酸伊立替康三水合物; (+)-Irinotecan hydrochloride trihydrate; CPT-11 hydrochloride trihydrate
A potent inhibitor of DNA topoisomerase I -
GC36329
Irinotecan hydrochloride
伊立替康盐酸盐; (+)-Irinotecan hydrochloride; CPT-11 hydrochloride
A potent inhibitor of DNA topoisomerase I -
GN10666
Isoalantolactone
异土木香内酯; (+)-Isoalantolactone; Isohelenin
A sesquiterpene lactone with diverse biological activities -
GC13795
Isobavachalcone
补骨脂乙素; Corylifolinin; Isobacachalcone
A chalcone and flavonoid with diverse biological activities -
GC39109
Isodeoxyelephantopin
异去氧苦地胆苦素
Isodeoxyelephantopin 是一种倍半萜烯内酯,可从Elephantopus scaber 中分离得到。Isodeoxyelephantopin 可诱导活性氧的生成,抑制NF-κB 的激活。Isodeoxyelephantopin 还能调节LncRNA 的表达,有抗乳腺癌的作用。 -
GN10088
Isoliquiritigenin
异甘草素; GU17; ISL; Isoliquiritigen; SJ000286237
A flavonoid with diverse biological activities -
GC12017
Isoniazid
异烟肼; INH; Isonicotinic acid hydrazide; Isonicotinic hydrazide
An inhibitor of mycolic acid synthesis -
GC64098
Isoniazid-d4
异烟肼-D4,INH-d4; Isonicotinic acid hydrazide-d4; Isonicotinic hydrazide-d4
Isoniazid-d4 (INH-d4) 是 Isoniazid 的氘代物。Isoniazid (INH) 是一种前药,必须被细菌过氧化氢酶 KatG 激活。Isoniazid 对快速分裂的分枝杆菌具有杀菌作用,并具有抗菌活性。 -
GC36339
Isorhapontigenin
异丹叶大黄素
Isorhapontigenin (ISOR), isolated from Belamcanda chinensis, is a derivative of stilbene. Isorhapontigenin possessed potent antioxidative activity. Isorhapontigenin suppresses interleukin-1β-induced inflammation and cartilage matrix damage in rat chondrocytes. -
GC15826
Isosorbide
异山梨酯; D-Isosorbide; Dianhydro-D-glucitol
A dianhydrohexitol -
GC36346
Isosorbide mononitrate
单硝酸异山梨酯; Isosorbide-5-mononitrate
A nitric oxide donor with cardioprotective activity -
GC15382
Isotretinoin
异维A酸; 13-cis-Retinoic acid
A retinoid -
GC43922
Isovaleryl-L-carnitine (chloride)
L-异戊酰基肉碱
An acylcarnitine -
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 -
GC10447
Isradipine (Dynacirc)
伊拉地平,PN 200-110
An L-type calcium channel blocker -
GC15462
ISRIB (trans-isomer)
ISRIB(TRANS-ISOMER)抑制剂
ISRIB (trans-isomer)是一种选择性抑制整合应激反应(ISR)通路的小分子化合物。ISRIB (trans-isomer)是PERK的一种高度选择性抑制剂,IC50为5nM。 -
GC11056
Itraconazole
伊曲康唑 ; R51211
An antifungal agent and hedgehog pathway inhibitor -
GC74091
Itraconazole-d9
R51211-d9
Itraconazole-d9是氘标记的伊曲康唑。 -
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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GC14797
IU1
Usp14 inhibitor
IU1是一种细胞可渗透的、可逆的选择性蛋白酶体抑制剂,对USP14的 IC50 为 4.7μM。 -
GC10296
Ivacaftor (VX-770)
依伐卡托; VX-770
A CFTR potentiator -
GC12489
Ivacaftor benzenesulfonate
VX-770 benzenesulfonate;VX 770 benzenesulfonate;VX770 benzenesulfonate;Kalydeco benzenesulfonate
A CFTR potentiator -
GC13316
Ivacaftor hydrate
VX-770 hydrate;VX 770 hydrate;VX770 hydrate;Kalydeco hydrate
A CFTR potentiator -
GC12339
Ivermectin
伊维菌素; MK-933
A mixture of ivermectin B1a and ivermectin B1b -
GC36356
Ixazomib citrate
枸橼酸艾沙佐米; MLN9708
Ixazomib citrate (MLN9708, Ninlaro) is a prodrug of Ixazomib (MLN2238), which is a selective, orally bioavailable inhibitor of 20S proteasome that inhibits the chymotrypsin-like proteolytic (β5) site with IC50 of 3.4 nM and Ki of 0.93 nM, respectively. Ixazomib (MLN2238) also inhibits caspase-like (β1) and trypsin-like (β2) proteolytic sites with IC50 of 31 nM and 3500 nM, respectively. -
GC65331
IZCZ-3
IZCZ-3 是有效的 c-MYC 转录抑制剂,具有抗肿瘤活性。
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GC10133
JNJ-42165279
N-(4-氯-3-吡啶基)-4-[(2,2-二氟-1,3-苯并二恶茂-5-基)甲基]-1-哌嗪甲酰胺
An irreversible FAAH inhibitor -
GC32690
JPH203 (KYT-0353)
KYT-0353
JPH203 (KYT-0353) 是一种选择性 L 型氨基酸转运蛋白 1 抑制剂,显着抑制 HT-29 YD-38 和白血病细胞的亮氨酸摄取和细胞生长,IC50 值分别为 0.06 μM 和 4.1 μM 。