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Search Results for " lysosomal "

77

抑制剂 & 化合物

7

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T41160	Lalistat 2	Lipase	Metabolism
	Lalistat 2 是一种溶酶体酸性脂肪酶的特异性抑制剂，IC50 为 152 nM，对人胰脂肪酶或牛乳脂蛋白脂肪酶没有抑制作用（高达 10 μM）。
T23004	ML-SA1 Mucolipin synthetic agonist 1	Others; TRP/TRPV Channel	Membrane transporter/Ion channel; Others
	ML-SA1 (Mucolipin synthetic agonist 1) 是一种选择性的TRPML 激动剂，通过促进溶酶体的酸化和蛋白酶活性抑制登格病毒 2 和寨卡病毒，抗 DENV2 RNA 和 ZIKV RNA 的IC50分别为 8.3 μM 和 52.99 μM。ML SA1可诱发自噬。ML SA1可用于广谱抗病毒研究。
T71126	Allixin
	Allixin is a phytoallexin found in garlic (Allium sativum) bulbs. Allixin has weak antimicrobial activity and exerts an anti-promoting activity against skin tumors induced by the chemical 12-O-tetradecanoylphorbol-13-acetate (TPA). Allixin also demonstrates an inhibitory effect on aflatoxin B1-induced mutagenesis.
T7944	VPS34 inhibitor 1 (Compound 19, PIK-III analogue) PIK-III analogue	PI3K	PI3K/Akt/mTOR signaling
	VPS34 inhibitor 1 (Compound 19, PIK-III analogue) (PIK-III analogue) 是一种有效的选择性 VPS34抑制剂( IC50 : 15 nM)。
T40542	Sinbaglustat ACT-519276,Sinbaglustat,OGT2378	Transferase	Metabolism
	Sinbaglustat (OGT2378) (OGT2378) 是葡萄糖神经酰胺合成酶 (GCS) 和非溶酶体葡萄糖神经酰胺酶 (GBA2) 的双重抑制剂。Sinbaglustat 是一种可透过血脑屏障的的口服N-烷基亚氨基糖。Sinbaglustat 可用于治疗溶酶体贮积症和研究溶酶体功能障碍相关的中枢神经退行性疾病。
T3436	LYS01 lys05 (free base)	Autophagy	Autophagy
	LYS01 是一种新型溶酶体自噬抑制剂。
T37986	D-Mannose-6-Phosphate sodium salt hydrate	Others	Others
	D-Mannose-6-Phosphate sodium salt hydrate 是一种多功能单糖，可用于研究代谢、溶酶体传递和癌症。
T38344	Lalistat 1 ZINC795230	Antibacterial	Microbiology/Virology
	Lalistat 1是溶酶体酸性脂肪酶（LAL）抑制剂（IC50 = 68 nM）和流感病毒IgA1蛋白酶的抑制剂。Lalistat 1可用于有关尼曼-皮克C 型疾病的研究。
T27730	KGP94 KGP-94,KGP 94	Cysteine Protease	Proteases/Proteasome
	KGP94 是一种有效的、选择性的和竞争性的溶酶体内肽酶抑制剂。
T20626	Esomeprazole	Proton pump; Cysteine Protease	Membrane transporter/Ion channel; Proteases/Proteasome
	Esomeprazole 是奥美拉唑(omeprazole) 的S-异构体，抑制溶酶体半胱氨酸蛋白酶legumain，防止癌症转移。它是一种质子泵抑制剂（PPI）。
T6583	MG-101 ALLN,Ac-LLnL-CHO,Calpain inhibitor I,Calpain inhibitor-1,MG101,钙蛋白酶抑制剂I	Cysteine Protease; Proteasome	Proteases/Proteasome; Ubiquitination
	MG-101 (Calpain inhibitor I) 是一种有效的半胱氨酸蛋白酶抑制剂，能够抑制钙蛋白酶I (Ki:190 pM)，钙蛋白酶II (Ki:220 pM)，组织蛋白酶B (Ki:150 pM)和组织蛋白酶L (Ki:500 pM)。
T11191	EN6	Proton pump; Autophagy	Autophagy; Membrane transporter/Ion channel
	EN6 是一种小分子体内自噬激活剂，其共价靶向溶酶体v-ATP 酶的 ATP6V1A 亚基中的半胱氨酸 277。它以溶酶体依赖性方式清除 TDP-43 聚集体，这是额颞叶痴呆的病原体。它介导的 ATP6V1A 修饰使 v-ATP 酶与 Rags 分离，从而抑制 mTORC1 信号传导、增加溶酶体酸化和激活自噬。
T21992	Vacuolin-1	PI3K; Autophagy	Autophagy; PI3K/Akt/mTOR signaling
	Vacuolin-1 是一种细胞渗透性抑制剂，可抑制 Ca2+ 依赖性溶酶体与细胞膜的融合。它通过抑制溶酶体内容物的释放起作用。它是一种有效的选择性 PIKfyve 抑制剂，通过损害溶酶体成熟来抑制晚期自噬。
T15635	JZP-430	Lipase; MAGL	Metabolism
	JZP-430 是不可逆的、高度选择性的 α/β 水解酶结构域 6 抑制剂，能够靶向抑制人类 ABHD6 ，其 IC50=44 nM。
T5538	DC661	Apoptosis; Autophagy	Apoptosis; Autophagy
	DC661 是一种棕榈酰蛋白硫酯酶 1 抑制剂，抑制自噬，可作为抗溶酶体剂，具有抗肿瘤活性。
T60122	Aldometanib Compound IA-47 (Br- base 2246625-81-8)	Others; AMPK	Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling
	Aldometanib (LXY-05-029) 是一种具有口服活性的醛缩酶抑制剂，可以阻止FBP 与v-ATPase 相关的醛缩酶结合，并激活溶酶体 AMPK 。Aldometanib 可用于代谢稳态的研究。
T6056	Thiamet G TMG	Others; Autophagy	Autophagy; Others
	Thiamet G 是一种有效选择性O-GlcNAcase 抑制剂，抑制人 OGA 的Ki 值为 20 nM。O-GlcNAcase 的作用是从修饰的蛋白质中去除 O-GlcNAc。
T72072	2-benzylsulfanyl-6-methoxy-4-methylquinazoline	ROS	Immunology/Inflammation
	2-benzylsulfanyl-6-methoxy-4-methylquinazoline 可作为TRPML 调节剂，可用于治疗与TRPML 活性相关的疾病，如溶酶体储存病、肌肉萎缩症、氧化应激或活性氧(ROS)相关疾病和衰老。
T41308L	Gly-Phe β-naphthylamide acetate Gly-Phe β-naphthylamide acetate(21438-66-4 Free base)	Others	Others
	Gly-Phe β-naphthylamide acetate 是 Cathepsin C 的底物，可用于研究组织蛋白酶 C 的功能、溶酶体内水解和溶酶体膜通透性。
T3437	Lys05 Lys01 trihydrochloride	lysosomal autophagy; Autophagy	Autophagy
	Lys05 是一种有效的水溶性溶酶体自噬抑制剂，具有抗肿瘤活性。在 MTT 试验中，对1205Lu、c8161、LN229 和 HT-29细胞系的IC50值分别为3.6、3.8、6 和7.9 μM。
T39518	PFB-FDGlu	Others	Others
	PFB-FDGlu 是一种溶酶体葡糖脑苷脂酶（GCase）底物，具有细胞渗透特异性，裂解后产生荧光素。PFB-FDGlu 通常与流式细胞仪结合使用，以单个细胞为基础测量活细胞中 GCase 的活性。
T72073	AKOS037652256
	AKOS037652256可作为 TRPML 调节剂，可用于治疗如溶酶体积存病、肌肉萎缩症、与年龄相关的常见神经退行性疾病、氧化应激或活性氧(ROS)相关疾病以及衰老等与 TRPML 活性相关的疾病。
T7739	L-Leucyl-L-Leucine methyl ester hydrochloride Leu-Leu-ome hydrochloride	Others; Endogenous Metabolite	Metabolism; Others
	L-Leucyl-L-Leucine methyl ester hydrochloride (Leu-Leu-ome hydrochloride) 是一种人单核细胞或多形核白细胞产生的 L-亮氨酸甲酯的二肽缩合产物，能够选择性消除具有细胞毒性潜能的淋巴细胞，也能够诱导溶酶体途径应激。
T6040	Aloxistatin E64d,Loxistatin,阿洛司他丁,E64c ethyl ester	SARS-CoV; Cysteine Protease	Microbiology/Virology; Proteases/Proteasome
	Aloxistatin (E64d) 是一种不可逆的、可透过膜的溶酶体和细胞溶质半胱氨酸蛋白酶抑制剂，能够抑制完整血小板中的钙蛋白酶活性。它是一种半胱氨酸蛋白酶抑制剂，具有血小板聚集抑制活性。
T4473	Ibiglustat Venglustat,SAR402671,GZ402671	Transferase	Metabolism
	Ibiglustat (GZ402671) 是一种可透过血脑屏障的、具有口服活性的葡萄糖神经酰胺合成酶(GCS)抑制剂。它可用于戈谢病 3 型、法布瑞氏症、与 GBA 突变相关的帕金森病、GM2 神经节苷脂病和常染色体显性多囊肾病的研究。
T37885	1-Dodecylimidazole	Antifungal	Microbiology/Virology
	1-Dodecylimidazole 是溶酶体活性洗涤剂。1-Dodecylimidazole 通过在溶酶体中的酸依赖性积累、溶酶体膜的破坏和半胱氨酸蛋白酶释放到细胞质中而导致细胞死亡。它显示出降胆固醇和广谱抗真菌活性。
T60202	MMRi62 7-[(2,3-dichlorophenyl)-(pyridin-2-ylamino)methyl]quinolin-8-ol	Ferroptosis	Apoptosis
	MMRi62 (7-[(2,3-dichlorophenyl)-(pyridin-2-ylamino)methyl]quinolin-8-ol) 是一种铁死亡 (ferroptosis) 诱导剂，靶向 MDM2-MDM4 (抑癌基因 p53 负调控因子)。MMRi62 对胰腺导管腺癌 (PDAC) 细胞显示出 p53 独立的促凋亡 (apoptosis) 活性，并诱导其自噬 (autophagy)。MMRi62 诱导铁死亡，伴随着活性氧增加和铁蛋白重链 (FTH1) 溶酶体降解。MMRi62 还可导致突变型 p53 的蛋白酶体降解，并对具有 KRAS 和 TP53 高频突变特征的原位异种移植 PDAC 小鼠模型具有体内药效。
T23978	Deox B 7,4 Deoxysappanone-B-7,4 dimethyl ether,Deox-B-7,4,Deoxysappanone B 7,4 dimethyl ether,DeoxB7,4
	Deox B 7,4 is a reversible microtubule inhibitor that acts by increasing lysosomal V-ATPase activity and lysosome acidity.
T11835L	LCL521 dihydrochloride 1,3DMG-B13 dihydrochloride	Others	Others
	LCL521 dihydrochloride is a compound that functions as an inhibitor of both acid ceramidase (ACDase) and lysosomal acid sphingomyelinase (ASMase).
T61883	ARN5187
	ARN5187 是一种亲溶酶体化合物，是 REV-ERBβ的配体。ARN5187抑制 REV-ERB 介导的转录调控和细胞自噬。ARN5187 显示出溶酶体效力和细胞毒性，可诱导细胞凋亡 (apoptosis)。
T63476	ARN5187 trihydrochloride
	ARN5187 trihydrochloride 是一种亲溶酶体 REV-ERBβ 配体，对 REV-ERB 介导的转录调控和细胞自噬具有抑制作用。ARN5187 trihydrochloride 具有溶酶体效力和细胞毒性，能够诱导细胞凋亡 (apoptosis)。
T11835	LCL521	Others; Phospholipase	Metabolism; Others
	LCL521 能抑制溶酶体酸性鞘磷脂酶（ASMase）。LCL521 是一种酸性神经酰胺酶(ACDase)抑制剂。
T36805	TPC2-A1-N TPC2-A1-N
	TPC2-A1-N is a novel, lipophilic, membrane permeable isoform-selective small molecule agonist of two-pore channel 2 (TPC2). TPC2-A1-N plays its role by mimicking the physiological actions of NAADP and PI(3,5)P2 through independent binding sites. TPC2-A1-N has inverse effects on key lysosomal activities and increases the pH in the lysosomal lumen in a TPC2-dependent manner[1].
T40046	UGT8-IN-1 UGT8-IN-1
	UGT8-IN-1 is a brain-permeable and orally-active inhibitor that specifically targets the ceramide galactosyltransferase enzyme (UGT8). By inhibiting UGT8, this compound has the potential to be employed in research pertaining to lysosomal storage disorders.
T36960	LysoFP-NH2 LysoFP-NH2
	LysoFP-NH2 is the fluorescent form of the lysosomal turn-on fluorescent probe for carbon monoxide (CO) lysoFP-NO2 . LysoFP-NH2 is formed when lysoFP-NO2 reacts with CO. It displays excitation/emission maxima of 440/528 nm, respectively.
T74615	NAMPT degrader-1
	NAMPTdegrader-1 (Compound A3) 是一种酰胺磷酸核糖转移酶 (NAMPT) 降解剂，IC50为 0.023 μM。NAMPTdegrader-1 通过 autophagy-lysosomal 途径显著诱导 NAMPT 降解，表现出良好的细胞抗肿瘤能力。
T69385	Baicalein monohydrate
	Baicalein monohydrate is an inhibitor of 12-lipoxygenase, leukotriene biosynthesis and release of lysosomal enzymes. It also inhibits cellular Ca2+ uptake and mobilization and adjuvant-induced arthritis.
T76010	N-CBZ-Phe-Arg-AMC TFA
	N-CBZ-Phe-Arg-AMC (Z-FR-AMC) TFA 是一种组织蛋白酶底物，可用于评估溶酶体组织蛋白酶的活性。
T26202	SP-Chymostatin B alpha-Mapi
	SP-Chymostatin B is a potent inhibitor of many proteases, including chymotrypsin, papain, chymotrypsin-like serine proteinases, chymases, and lysosomal cysteine proteinases. It weakly inhibits human leucocyte elastase. It is effective at a final concentra
T70336	Nizubaglustat
	Nizubaglustat为一种针对神经酰胺葡萄糖基转移酶或葡萄糖神经酰胺合酶(GCS)的抑制剂，同时也能抑制GBA2，后者与神经病理学溶酶体贮积症相关。
T80055	Beta-glucuronidase (bovine liver)
	Beta-glucuronidase是一种关键溶酶体酶，主要功能是参与糖胺聚糖中含有葡萄糖醛酸成分的降解过程。
T37045	1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-Mannopyranose
	1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is an analog of N-acetylmannosamine (ManNAc) and a building block.1,2It has been used as a precursor in the synthesis of differently substituted trimers of the group AN. meningitidiscapsular polysaccharide repeating unit for use in immunological experiments.2It has also been used in the synthesis of fluorescent probes for lysosomal labeling.3
T35804	C16 Lactosylceramide (d18:1/16:0)
	C16 Lactosylceramide is an endogenous bioactive sphingolipid. It forms membrane microdomains with Lyn kinase and the αi subunits of inhibitory G protein-coupled receptors (GPCRs), suggesting a role in cell signaling. Plasma levels of C16 lactosylceramide are elevated in insulin-resistant cattle. C16 Lactosylceramide is also upregulated in a mouse model of Niemann-Pick type C1 disease, a neurodegenerative cholesterol-sphingolipid lysosomal storage disorder.
T79147	KRAS degrader-1
	KRAS degrader-1（compound 1）是通过自噬-溶酶体途径降解特定蛋白的高效KRAS降解剂。
T82340	Ganglioside GM2
	Ganglioside GM2为人类肿瘤抗原(OFA-I-1)，亦是泰-萨克斯病中主要的溶酶体贮存化合物。
T78573	Glucocerebrosidase GCase,Glucosylceramidase	Endogenous Metabolite	Metabolism
	Glucocerebrosidase (Glucosylceramidase; GBA) 是溶酶体内的酶，负责催化GC中的β-糖苷键裂解，从而生成葡萄糖和神经酰胺。
T22036	Arylquin 1
	Arylquin 1 是一种前列腺-凋亡-反应-4(Par-4)促分泌剂，靶向波形蛋白诱导 Par-4 分泌。Arylquin 1 通过诱导溶酶体膜通透性 (LMP) 诱导癌细胞非凋亡性细胞死亡。
T81713	N-4′-(p-Trifluoromethylphenyl)butyl-DAB
	N-4′-(p-Trifluoromethylphenyl)butyl-DAB (compound 5g) 作为溶酶体酸 α-葡萄糖苷酶 (GAA) 的激动剂，在携带 M519V 突变的 Pompe 病患者成纤维细胞中，能剂量依赖性地提升细胞内 GAA 的活性。
T35809	C20 Sphingomyelin (d18:1/20:0)
	C20 Sphingomyelin is a naturally occurring sphingolipid. Levels of C20 sphingomyelin are upregulated in the hippocampus of rats with diabetes induced by streptozotocin and in human plasma where it is positively correlated with insulin resistance in obese humans. C20 sphingomyelin is also upregulated in the liver of a mouse model of Niemann-Pick type C1 disease, a neurodegenerative cholesterol-sphingolipid lysosomal storage disorder. The plasma concentration of C20 sphingomyelin is decreased in m...
T73544	MPM-1
	MPM-1 是海洋生物 Eusynstyelamides 模拟物，是一种有效的抗癌剂。MPM-1 可通过诱导坏死样死亡，在体外快速杀死癌细胞。MPM-1具有诱导免疫原性细胞死亡的能力。MPM-1在癌细胞中干扰细胞自噬 (autophagy) 和溶酶体膨胀。

化合物

Cat.No: T41160

Target: Lipase

Cat.No: T23004

Synonym: Mucolipin synthetic agonist 1

Target: Others, TRP/TRPV Channel

Cat.No: T71126

VPS34 inhibitor 1 (Compound 19, PIK-III analogue)

Cat.No: T7944

Synonym: PIK-III analogue

Target: PI3K

Cat.No: T40542

Synonym: ACT-519276,Sinbaglustat,OGT2378

Target: Transferase

Cat.No: T3436

Synonym: lys05 (free base)

Target: Autophagy

D-Mannose-6-Phosphate sodium salt hydrate

Cat.No: T37986

Target: Others

Cat.No: T38344

Synonym: ZINC795230

Target: Antibacterial

Cat.No: T27730

Synonym: KGP-94,KGP 94

Target: Cysteine Protease

Cat.No: T20626

Target: Proton pump, Cysteine Protease

Cat.No: T6583

Synonym: ALLN,Ac-LLnL-CHO,Calpain inhibitor I,Calpain inhibitor-1,MG101,钙蛋白酶抑制剂I

Target: Cysteine Protease, Proteasome

Cat.No: T11191

Target: Proton pump, Autophagy

Cat.No: T21992

Target: PI3K, Autophagy

Cat.No: T15635

Target: Lipase, MAGL

Cat.No: T5538

Target: Apoptosis, Autophagy

Cat.No: T60122

Synonym: Compound IA-47 (Br- base 2246625-81-8)

Target: Others, AMPK

Cat.No: T6056

Synonym: TMG

Target: Others, Autophagy

2-benzylsulfanyl-6-methoxy-4-methylquinazoline

Cat.No: T72072

Target: ROS

Gly-Phe β-naphthylamide acetate

Cat.No: T41308L

Synonym: Gly-Phe β-naphthylamide acetate(21438-66-4 Free base)

Target: Others

Cat.No: T3437

Synonym: Lys01 trihydrochloride

Target: lysosomal autophagy, Autophagy

Cat.No: T39518

Target: Others

Cat.No: T72073

L-Leucyl-L-Leucine methyl ester hydrochloride

Cat.No: T7739

Synonym: Leu-Leu-ome hydrochloride

Target: Others, Endogenous Metabolite

Cat.No: T6040

Synonym: E64d,Loxistatin,阿洛司他丁,E64c ethyl ester

Target: SARS-CoV, Cysteine Protease

Cat.No: T4473

Synonym: Venglustat,SAR402671,GZ402671

Target: Transferase

1-Dodecylimidazole

Cat.No: T37885

Target: Antifungal

Cat.No: T60202

Synonym: 7-[(2,3-dichlorophenyl)-(pyridin-2-ylamino)methyl]quinolin-8-ol

Target: Ferroptosis

Cat.No: T23978

Synonym: Deoxysappanone-B-7,4 dimethyl ether,Deox-B-7,4,Deoxysappanone B 7,4 dimethyl ether,DeoxB7,4

LCL521 dihydrochloride

Cat.No: T11835L

Synonym: 1,3DMG-B13 dihydrochloride

Target: Others

Cat.No: T61883

ARN5187 trihydrochloride

Cat.No: T63476

Cat.No: T11835

Target: Others, Phospholipase

Cat.No: T36805

Synonym: TPC2-A1-N

Cat.No: T40046

Synonym: UGT8-IN-1

Cat.No: T36960

Synonym: LysoFP-NH2

NAMPT degrader-1

Cat.No: T74615

Baicalein monohydrate

Cat.No: T69385

N-CBZ-Phe-Arg-AMC TFA

Cat.No: T76010

SP-Chymostatin B

Cat.No: T26202

Synonym: alpha-Mapi

Cat.No: T70336

Beta-glucuronidase (bovine liver)

Cat.No: T80055

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-Mannopyranose

Cat.No: T37045

C16 Lactosylceramide (d18:1/16:0)

Cat.No: T35804

KRAS degrader-1

Cat.No: T79147

Ganglioside GM2

Cat.No: T82340

Glucocerebrosidase

Cat.No: T78573

Synonym: GCase,Glucosylceramidase

Target: Endogenous Metabolite

Cat.No: T22036

N-4′-(p-Trifluoromethylphenyl)butyl-DAB

Cat.No: T81713

C20 Sphingomyelin (d18:1/20:0)

Cat.No: T35809

Cat.No: T73544

Cat. No.	Product Name	Target	Signaling Pathways
T5689	20-DEOXYINGENOL	Others; Autophagy	Autophagy; Others
	20-Deoxyingenol 是从甘遂的根中分离出的一种二萜类天然产物。它可通过促进体外转录因子 EB 的核易位来促进自噬和溶酶体生物发生，可研究骨关节炎。
T8678	Naphthazarin 萘茜,5,8-Dihydroxy-1,4-naphthoquinone,DHNQ	Apoptosis	Apoptosis
	Naphthazarin (5,8-Dihydroxy-1,4-naphthoquinone) 是来自毛紫草的一种天然产物，通过氧化应激、线粒体凋亡诱导因子的激活、微管的解聚、干扰溶酶体功能和 p53 依赖性 p21 激活，可触发细胞凋亡并具有抗肿瘤作用。
TN1711	Gossypetin	Antioxidant; p38 MAPK; MAPK; Antibacterial	MAPK; Microbiology/Virology; oxidation-reduction
	Gossypetin 是一种可从Rhodiola rosea Linn.中提取的六羟基化的类黄酮，是一种有效的 MKK3 和 MKK6 抑制剂，可强烈减弱 MKK3/6-p38 信号传导途径。Gossypetin 具有抗突变、抗动脉粥样硬化、抗氧化以及细胞保护和抗菌作用，它通过下调溶酶体酪蛋白酶 K 的活性和诱导肌动蛋白环破骨细胞中的自噬相关蛋白来抑制骨吸收。
T15702	Lactacystin	Proteasome	Proteases/Proteasome; Ubiquitination
	Lactacystin is an antibiotic Streptomyces spp. the metabolite and is an effective and selective proteasome inhibitor (IC50: 4.8 μM for 20S proteasome). Lactacystin inhibits cell growth and induces neurite outgrowth and also inhibits the lysosomal enzyme cathepsin A.
T82428	Euphorblin R EOF2
	Euphorblin R (EOF2)为鼠李叶烷二萜类化合物，从龙骨木 (Euphorbia resinifera) 中分离。该化合物或促进溶酶体生物合成，具研究溶酶体相关疾病潜力。
T37291	Lyso-Globotriaosylceramide (d18:1) Lyso-Globotriaosylceramide (d18:1)
	Lyso-globotriaosylceramide is a form of globotriaosylceramide that is lacking the fatty acyl group. It binds to Shiga toxin 1 (Stx1) in the presence of cholesterol and phosphatidylcholine but does not bind Stx2. It also reduces viability and aggregation of human neutrophils induced by phorbol 12-myristate 13-acetate when used at concentrations of 50 and 1 μM, respectively. Lyso-globotriaosylceramide accumulates in the brain, heart, kidney, liver, lung, and spleen in a mouse model of Fabry diseas...
TN2344	Swainsonine Tridolgosir	Apoptosis; Others; Antibiotic	Apoptosis; Microbiology/Virology; Others
	Swainsonine (Tridolgosir) 是一种从黄芪中分离出来的一种生物碱，是一种强效和可逆的α-甘露糖苷酶抑制剂。Swainsonine 具有抗肿瘤活性，可诱导细胞凋亡和细胞周期停滞在 G2/M 期。

天然产物

20-DEOXYINGENOL

Cat.No: T5689

Target: Others, Autophagy

Cat.No: T8678

Synonym: 萘茜,5,8-Dihydroxy-1,4-naphthoquinone,DHNQ

Target: Apoptosis

Cat.No: TN1711

Target: Antioxidant, p38 MAPK, MAPK, Antibacterial

Cat.No: T15702

Target: Proteasome

Cat.No: T82428

Synonym: EOF2

Lyso-Globotriaosylceramide (d18:1)

Cat.No: T37291

Synonym: Lyso-Globotriaosylceramide (d18:1)

Cat.No: TN2344

Synonym: Tridolgosir

Target: Apoptosis, Others, Antibiotic

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