87
103
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3587 |
NOD-IN-1
Compound 4 |
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
NOD-IN-1 (Compound 4) 是核苷酸结合寡聚化结构域样受体 NOD1(IC50:5.74 μM)和 NOD2 (IC50:6.45 μM)的抑制剂。 | |||
T4217 |
INF39
|
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
INF39 是无细胞毒性的NLRP3不可逆抑制剂。 | |||
T4164 |
CY-09
CY 09 |
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
CY-09 是NLRP3选择性抑制剂。它能够直接与 NLRP3 NACHT 结构域的 ATP 结合基序结合,对 NLRP3 ATP 酶的活性产生抑制作用,进而抑制 NLRP3 炎症小体的组装和活化。 | |||
T15052 |
Dapansutrile
|
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
Dapansutrile 是一种口服有活性的 NLRP3 炎性小体选择性抑制剂。它具有抗炎特性,可用于研究缓解疼痛。 | |||
T13375 |
YQ128
|
IL Receptor; NOD-like Receptor (NLR); NOD; Interleukin | Immunology/Inflammation; NF-κB |
YQ128 是选择性 NLRP3 炎性体抑制剂(IC50:0.30 µM)。它能显著的、选择性抑制 IL-1β的产生,但不影响 TNF-α 的产生。它能够透过血脑屏障到达中枢神经系统。它具有抗炎作用。 | |||
T9222 |
Emlenoflast
MCC7840 |
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
Emlenoflast (MCC7840) 是一种 NLRP3炎症小体 (NLRP3 inflammasome) 的选择性抑制剂(IC50<100 nM)。它可用于研究炎性疾病。 | |||
T8828 |
CP 424174
|
IL Receptor | Immunology/Inflammation |
CP 424174 是一种具有可逆性的 IL-1β抑制剂(IC50:210 nM),也能够间接性抑制 NLRP3。 | |||
T38361 |
GSK717
|
IL Receptor; NOD | Immunology/Inflammation; NF-κB |
GSK717 是 NOD2(核苷酸结合寡聚结构域 2) 的选择性抑制剂。它抑制壁酰二肽 (MDP) 诱导的 NOD2 介导的信号转导,抑制 MDP 刺激的 HEK293/hNOD2 细胞分泌 IL-8 (IC50为 400 nM)。 | |||
T16159 |
Muramyl dipeptide
MDP |
NOD | Immunology/Inflammation; NF-κB |
Muramyl dipeptide (MDP) 是合成的免疫反应肽,由 N-乙酰壁酸与 L-Ala-D-isoGln 的短氨基酸链相连。它通过MAPK 途径上调 Runx2 基因表达,直接促进成骨细胞分化,通过降低 RANKL/OPG 比值间接抑制破骨细胞分化。它是通过Runx2诱导骨形成的诱导因子,也是NLRP1激动剂。 | |||
T6591 |
Nodinitib-1
ML130,CID-1088438 |
TNF; NOD-like Receptor (NLR); NOD | Apoptosis; Immunology/Inflammation; NF-κB |
Nodinitib-1 (CID-1088438) 是 NOD1抑制剂(IC50:0.56 μM)。 | |||
T3701 |
MCC950
CP-456773 |
NOD | Immunology/Inflammation; NF-κB |
MCC950 (CP-456773) 是NLRP3的选择性抑制剂,能够作用于BMDMs(IC50:7.5 nM) 和 HMDMs(IC50:8.1 nM)。 | |||
T6454 |
CORM-3
CORM3,(OC-6-44)-三羰基氯(甘氨酸基)钌 |
Others; NF-κB; NOD-like Receptor (NLR) | Immunology/Inflammation; NF-κB; Others |
CORM-3 是一种 CO 释放分子,能够减少 NLRP3炎症小体的激活,可以减弱 NF-κB p65的核异位,减少 ROS 的生成,并提高细胞内谷胱甘肽和超氧化物歧化酶的水平。 | |||
T28178 |
NLRP3-IN-9
INF-4E,INF 4E,INF4E |
NOD | Immunology/Inflammation; NF-κB |
NLRP3-IN-9 (INF-4E) 是 NLRP3 ATPase 和 caspase-1 的抑制剂。 NLRP3-IN-9 通过不可逆地捕获硫醇亲核体发挥作用,以时间和浓度依赖性方式防止 ATP 和尼日利亚菌素触发的人 THP-1 细胞焦亡。 | |||
T1404 |
Stavudine
d4T,Sanilvudine,BMY-27857,NSC 163661,司他夫定 |
Apoptosis; Nucleoside Antimetabolite/Analog; HIV Protease; NOD-like Receptor (NLR); Reverse Transcriptase; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Stavudine (BMY-27857) 是一种口服活性核苷逆转录酶抑制剂,还抑制线粒体 DNA 的复制,具有抗HIV-1和HIV-2的活性。它降低 NLRP3 炎症小体激活,调节淀粉样 β 自噬,诱导细胞凋亡。 | |||
T63088 |
NOD2 antagonist 1
|
||
NOD2 antagonist 1 (compound 32) 是一种有效的、选择性的 NOD2 拮抗剂 (IC50: 5.23 μM)。NOD2 antagonist 1 在 THP-1 细胞,对 Muramyl dipeptide (MDP) 诱导的 IL-8 分泌表现出抑制作用。NOD2 antagonist 1 在 PBMCs 细胞,可以抑制 MDP 诱导的 IL-6、IL-10 和 TNF-α 的水平升高。 | |||
T6887 |
MCC950 sodium
CRID3 sodium salt,CP-456773,CP-456773 sodium,MCC950 |
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
MCC950 sodium (CP-456773 sodium) 是一种炎症小体 NLRP3 的抑制剂 (IC50=7.5 nM in BMDMs; IC50=8.1 nM in HMDMs),具有高效选择性。MCC950 sodium 对其他炎症小体,如 AIM2、 NLRC4 或 NLRP1 没有作用。 | |||
T68396 |
AC1NOD4Q
|
||
AC1NOD4Q is a novel blocker of hox antisense intergenic rna (hotair) by abrogating the scaffold interaction with ezh2 | |||
T72473 |
NOD1/2 antagonist-1
|
||
NOD1/2 antagonist-1 是一种有效的NOD1/2双拮抗剂,其IC50值分别为 1.13 (NOD1) 和 0.77 μM (NOD2)。NOD1/2 antagonist-1 有可接受的 T1/2(67.6 min)。NOD1/2 antagonist-1 可提高紫杉醇 (PTX) 的抗肿瘤作用。 | |||
T2131 |
Articaine hydrochloride
Ultracaine,盐酸阿替卡因,阿替卡因,Articaine HCl,Hoe-045 |
Sodium Channel | Membrane transporter/Ion channel |
Articaine hydrochloride (Hoe-045) 一种牙科局部麻醉剂。 | |||
T3230 |
NLRP3-IN-2
5-Chloro-N-(p-sulfamoylphenethyl)-o-anisamide,4-[2-(5-氯-2-甲氧基苯甲酰氨基)乙基]苯磺酰胺,NLRP3 Inflammasome Inhibitor I |
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
NLRP3-IN-2 (5-Chloro-N-(p-sulfamoylphenethyl)-o-anisamide) 是一种能够合成格列本脲的中间物,对心肌细胞中NLRP3炎症小体的形成具有抑制作用,在小鼠心肌缺血/再灌注后限制梗死面积,且对代谢无影响。 | |||
T7417 |
Avatrombopag
YM477,AKR-501,1-[3-氯-5-[[[4-(4-氯-2-噻吩基)-5-(4-环己基-1-哌嗪基)-2-噻唑基]氨基]羰基]-2-吡啶基]-4-哌啶羧酸,E5501 |
Thrombin; Thrombopoietin Receptor | Immunology/Inflammation; Proteases/Proteasome |
Avatrombopag (YM477) 是一种新型口服血小板生成素 (TPO) 受体激动剂,可激活 TPO 受体并增加巨核细胞增殖/分化和血小板生成。 | |||
T8489 |
Minodronic acid monohydrate
|
Transferase | Metabolism |
Minodronic acid monohydrate 是一种法尼基二磷酸合成酶抑制剂,可作为骨吸收抑制剂。 | |||
T0996 |
Ethynodiol diacetate
Ethynodiol acetate,双醋炔诺醇,8080 CB |
Estrogen/progestogen Receptor; Progesterone Receptor | Endocrinology/Hormones; Others |
Ethynodiol diacetate (Ethynodiol acetate) 是一种可用作激素避孕药的甾体孕激素,具有相对较少或没有雄激素效果,而具有显著雌激素作用。 | |||
T13507 |
4,4'-Iminodiphenol
4-(4-羟基苯胺)苯酚,Leucoindophenol |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
4,4'-Iminodiphenol (Leucoindophenol) 是基于二苯胺骨架的无活性雌激素受体配体。 | |||
T16335 |
Nonaethylene glycol monododecyl ether
Nonaoxyethylene monododecyl ether,Polidocanol,聚醚醇 |
Others | Others |
Nonaethylene glycol monododecyl ether (Polidocanol) 是一种非离子表面活性剂和聚乙二醇清洁剂,可用于蛋白质分离和纯化,以及用于形成初始聚结的 O/W 乳剂液滴。 | |||
T8436 |
Minodronic acid
Phosphonicacid,(1-hydroxy-2-imidazo(1,2-a)pyridin-3-ylethylidene)bis-,ONO-5920,YM-529 |
Apoptosis; P2X Receptor | Apoptosis; Membrane transporter/Ion channel; Neuroscience |
Minodronic acid(YM-529) 是一种 P2X2/3 受体拮抗剂, 具有抗癌活性,可直接或间接的抑制癌细胞增殖,诱导细胞凋亡。Minodronic-acid 对各种类型的癌细胞的转移具有抑制作用。Minodronic-acid 可用于研究骨质疏松。 | |||
T3601 |
Benodanil
麦锈灵,Calirus |
Antifungal | Microbiology/Virology |
Benodanil (Calirus) 是一种杀菌剂。 | |||
T9516 |
Binodenoson
WRC 0470,MRE-0470,比诺地松,2-(cyclohexylmethylidenehydrazino)adenos |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Binodenoson (WRC 0470) 是一种选择性A2A 腺苷受体激动剂,KD 为270 nM。它是一种短效冠状动脉血管扩张剂,作为放射性示踪剂的辅助剂,用于心肌应激成像。 | |||
T1364 |
7-Aminodeacetoxycephalosporanic acid
7-ADCA,Cephalexin Impurity B,Cefalexine EP IMpurity B,Deacetoxycephalosporanic Acid,头孢氨苄杂质B,7-Aminodesacetoxycephalosporanic acid |
Antibiotic | Microbiology/Virology |
7-Aminodeacetoxycephalosporanic acid (Cefalexine EP IMpurity B) 是一种头孢菌素合成中的关键中间体。 | |||
T0628 |
Iminodibenzyl
|
Others | Others |
Iminodibenzyl 用作抗癫痫药carbamazepine 的中间体。 | |||
T15719 |
Latanoprostene bunod
LBN,NCX116 |
Others | Others |
Latanoprostene bunod (LBN) 是一氧化氮 (NO) 供体前列腺素 F2a 类似物,有用于开角型青光眼或高眼压 (OHT) 患者降低眼压 (IOP) 的局部眼科的研究潜力。 | |||
T30465 |
Bis(2-methylpropyl)phosphinodithioic acid
J663.879A,Diisobutyl dithiophosphinate,Diisobutyldithiophosphinic acid |
||
Bis(2-methylpropyl)phosphinodithioic acid is a bioactive chemical. | |||
T23662 |
Aganodine
Aganodin |
||
Aganodine is a guanidine that activates presynaptic imidazoline receptors. Aganodine inhibits the presynaptic release of norepinephrine through its agonism at imidazoline receptors. | |||
T72467 |
5-Iminodaunorubicin
5-亚氨基柔红霉素 |
||
5-Iminodaunorubicin 是一种醌改性蒽环类药物,具有抗肿瘤活性。5-Iminodaunorubicin 在癌细胞中可诱导 DNA 链断裂。 | |||
T76216 |
Lonodelestat TFA
|
||
Lonodelestat TFA (POL6014 TFA) 是一种有效的、口服活性的、选择性的肽类hNE抑制剂,展现了治疗囊性纤维化(CF)的潜力。 | |||
T0171 |
Norethynodrel
Lynestrol,异炔诺酮 |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Norethynodrel (Lynestrol) 是一种合成的孕激素,其作用和用途类似于孕酮。它已被用于治疗功能性子宫出血和子宫内膜异位症。它作为避孕药,通常与 MESTRANOL 联合使用。 | |||
TF0042 |
Sucrose Monododecanoate
|
||
Sucrose Monododecanoate 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 TF0042,CAS号为 25339-99-5。 | |||
T33595 |
Naproxcinod
AZD3582,Nitronaproxen,AZD-3582,Naproxen-N-butyl nitrate,HCT3012,AZD 3582 |
||
Naproxcinod, a nitric oxide-releasing NSAID derivative, significantly improved skeletal muscle strength and fatigue resistance in sedentary and exercise mice, reducing inflammatory infiltration and fibrotic deposition in the myocardium and diaphragm. In a | |||
T126126 |
Ganoderitriol M
|
||
Ganoderitriol M 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T126126,CAS号为 1265906-35-1。 | |||
T34269 |
Razinodil
Razinodilum |
||
Razinodil is a vasodilator. | |||
T126539 | Ganoderic acid M | ||
Ganoderic acid M 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T126539。 | |||
T36908 |
Bimatoprost grenod
15-(6-nitroxyhexanoyl)-17-phenyl trinor Prostaglandin F2α |
||
Bimatoprost grenod(15-(6-nitroxyhexanoyl)-17-phenyl trinor PGF2α) is a nitric oxide-donating derivative of 17-phenyl trinor PGF2α.1It increases cGMP levels in rabbit aqueous humor and iris ciliary body when topically administered at a concentration of 0.042%. Topical administration of 15-(6-nitroxylhexanoyl)-17-phenyl trinor PGF2α(0.14%) reduces intraocular hypertension (IOP) in a rabbit model of hypertonic saline-induced transient ocular pressure. It also reduces IOP in a cynomolgus monkey mode... | |||
T124467 | Vernodalol | ||
Vernodalol 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T124467,CAS号为 65388-17-2。 | |||
T68327 | Dexnafenodone Free Base | ||
Dexnafenodone Free Base is a potent inhibitor of noradrenaline, and to a lesser degree of serotonin reuptake, induced changes in the pattern of sleep which are comparable to those of non‐sedating tricyclic antidepressants. | |||
T14967 |
Cimlanod
BMS-986231,CXL-1427 |
Others | Others |
Cimlanod is a second-generation Nitroxyl (HNO) donor for heart failure with positive lusitropic and inotropic as well as vasodilatory effects. Cimlanod delivers HNO via pH-dependent chemical breakdown when exposed to the neutral pH environment of the bloo | |||
T34605 |
Selenodiglutathione
Seleno-di-glutathione,Bis(glutathione) selenide |
||
Selenodiglutathione is a primary Se metabolite conjugated with two glutathione (GSH) moieties. | |||
T18488 |
NH2-MPAA-NODA
|
Others | Others |
NH2-MPAA-NODA, a nitroveratryl-based photocleavable linker featuring a NODA motif and a methyl phenyl acetic acid (MPAA) backbone, serves as a radiolabel when labeled with 18F-fluoride. | |||
TF0071 |
Hexaethylene Glycol Monododecyl Ether (C12E6)
|
||
Hexaethylene Glycol Monododecyl Ether (C12E6) 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 TF0071,CAS号为 3055-96-7。 | |||
T71919 |
Boc-10-Aminodecanoic acid
|
||
Boc-10-Aminodecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Boc-10-Aminodecanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | |||
T69147 | Cinodine (free base) | ||
Cinodine (free base) is a glycocinnamoylspermidine antibiotic; gyrase inhibitor found in Nocardia. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S1256 |
Ruscogenin
|
NOS; NF-κB; NOD-like Receptor (NLR) | Immunology/Inflammation; NF-κB |
Ruscogenin 是一种重要甾体皂苷元,提取自麦冬。它能够抑制 TXNIP/NLRP3炎症体激活和 MAPK 途径,改善脑缺血诱导的血脑屏障功能障碍,具有显著抗血栓、抗炎作用。 | |||
T0772 |
Troxerutin
曲克芦丁,Trihydroxyethylrutin,维脑路通 |
NOD-like Receptor (NLR) | Immunology/Inflammation |
Troxerutin (Trihydroxyethylrutin) 是一种天然生物类黄酮芦丁的三羟乙基化衍生物,也被称为维生素 P4,可抑制活性氧的产生并抑制 ER 应激介导的NOD 活化。 | |||
TQ0165 |
Arglabin
阿格拉宾,(+)-Arglabin |
NOD-like Receptor (NLR); Transferase; NOD; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Arglabin ((+)-Arglabin) 是从青蒿中分离出的一种天然产物,是一种 NLRP3 炎性体抑制剂,具有抗动脉粥样硬化和抗癌作用。 | |||
T4S0350 |
Licochalcone B
甘草查尔酮 B,甘草查尔酮B |
Beta Amyloid; Others | Neuroscience; Others |
Licochalcone B 是从Glycyrrhiza inflate 根中提取的。它能够抑制淀粉样蛋白 β 自聚集作用 (IC50=2.16 μM) ,分解预先形成的 Aβ42原纤维,并通过螯合金属离子抑制金属诱导的 Aβ42聚集。 | |||
T3092 |
Nigericin sodium salt
尼日利亚菌素,尼日利亚菌素钠盐 |
Potassium Channel; NOD-like Receptor (NLR); Antibacterial; Antibiotic; NOD | Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; NF-κB |
Nigericin sodium salt 属于抗生素,是一种 NLRP3 激活剂,也是一种阳离子离子载体。Nigericin sodium 可以触发 NALP3 炎性体的激活,可抑制高尔基体功能并抑制革兰氏阳性菌的生长。 | |||
T2893 |
Muscone
3-Methylcyclopentadecanone,Methylexaltone,麝香酮 |
MMP; TNF; NF-κB; NOD-like Receptor (NLR); P-gp; Interleukin | Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; NF-κB; Proteases/Proteasome |
Muscone (3-Methylcyclopentadecanone) 是中药麝香的一种主要活性单体。它抑制NF-κB 和NLRP3炎性小体的活化,显著降低炎性细胞因子水平,并最终改善心脏功能和存活率。 | |||
T5247 |
Trimethylamine N-oxide dihydrate
二水氧化三甲胺,TMANO Dihydrate |
Others; Endogenous Metabolite | Metabolism; Others |
Trimethylamine N-oxide dihydrate (TMANO Dihydrate) 是内源性代谢产物的一种。 | |||
T5S1131 |
Ganoderic acid C6
灵芝酸C6 |
Others | Others |
Ganoderic acid C6 是醛糖还原酶活性的抑制剂。 | |||
TN4661 |
Nodosin
|
IL Receptor; Autophagy | Autophagy; Immunology/Inflammation |
Nodosin 是一种二萜化合物,从Isodon trichocarpusKudo 和I. JaponicusHARA 中提取得到。 | |||
TN2215 |
Taurochenodeoxycholic acid sodium
牛磺鹅去氧胆酸钠盐,Sodium taurochenodeoxycholate,牛磺鹅去氧胆酸钠 |
Apoptosis; Endogenous Metabolite | Apoptosis; Metabolism |
Taurochenodeoxycholic acid sodium (Sodium taurochenodeoxycholate) 是动物胆汁酸的主要生物活性物质之一。它可诱导细胞凋亡,具有抗炎和免疫调节作用。 | |||
TN1553 |
Deacetyl ganoderic acid F
|
Others | Others |
Deacetyl ganoderic acid F (DeGA F) 是从灵芝 Ganoderma lucidum 中提取的三萜类化合物,在体外和体内对脂多糖(LPS)诱导的炎症有抑制作用。 | |||
TN1651 |
Furanodiene
|
Apoptosis; PARP; Reactive Oxygen Species; Caspase; CDK; P-gp | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB; Proteases/Proteasome |
Furanodiene 是从姜黄中提取的一种萜类天然产物,可抑制外排转运蛋白Pgp 功能并降低 Pgp 蛋白水平。它通过抗血管生成和诱导ROS 产生,DNA 链断裂和细胞凋亡发挥抗癌作用。 | |||
TN1059 |
Ganoderic acid B
|
IL Receptor; HIV Protease; JAK; STAT | Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Proteases/Proteasome; Stem Cells |
Ganoderic acid B 是从灵芝中分离的一种三萜类天然产物。它是端粒酶抑制剂,抑制 Epstein-Barr 病毒抗原的活化。它是 HIV-1 蛋白酶抑制剂。 | |||
TN1661 |
Ganoderic acid C2
灵芝酸 C2 |
Reductase; Histamine Receptor; Immunology/Inflammation related | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Ganoderic acid C2 是分离自灵芝的一种三萜化合物, 具有潜在的抗肿瘤生物活性,以及抗组胺、抗衰老和细胞毒性作用。它对rat lens aldose reductase 具有很高的抑制活性,IC50为 3.8 µM。 | |||
TN1658 | Ganoderenic acid D | Apoptosis; Others | Apoptosis; Others |
Ganoderenic acid D 是从灵芝提取物 (GLE) 的有效化合物中分离出来的天然产物。 Ganoderenic acid D 诱导细胞周期停滞和细胞凋亡并抑制癌细胞的增殖。 | |||
T5259 |
Glycochenodeoxycholic acid sodium salt
GCDCA,甘氨鹅脱氧胆酸钠,Sodium glycochenodeoxycholate |
Apoptosis; Others; Endogenous Metabolite | Apoptosis; Metabolism; Others |
Glycochenodeoxycholic acid sodium salt (GCDCA) 是一种从脱氧鹅胆酸和甘氨酸在肝脏中形成的胆汁盐,可诱导肝细胞凋亡。它起到洗涤剂的作用,可溶解脂肪吸收,并本身被吸收。 | |||
TN1656 |
Ganoderenic acid A
灵芝烯酸A,灵芝烯酸 A |
Others | Others |
Ganoderenic acid A 是三萜类化合物。它对 CCl4 诱导的肝损伤具有保护作用。它是β-葡萄糖醛酸酶抑制剂。 | |||
T3875 |
CLINODISIDE A
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Others | Others |
Clinodiside A 是来自中草药Clinopodium chinensis 中。 | |||
T4588 |
Glycochenodeoxycholic Acid
甘氨鹅脱氧胆酸,Glycine chenodeoxycholate,Chenodeoxycholylglycine,GCDCA,Glycochenodeoxycholate,Lithocholylglycine |
Apoptosis; Endogenous Metabolite | Apoptosis; Metabolism |
Glycochenodeoxycholic Acid (Lithocholylglycine) 是一种从脱氧鹅胆酸和甘氨酸在肝脏中形成的胆汁盐,可诱导肝细胞凋亡。它有洗涤剂的作用,可溶解脂肪吸收,并本身被吸收。 | |||
T2A2481 |
Taurochenodeoxycholic Acid
Chenodeoxycholyltaurine,TCDCA,Chenyltaurine,Taurochenodeoxycholate,12-Deoxycholyltaurine,牛磺鹅去氧胆酸 |
Apoptosis; TNF; Caspase; Endogenous Metabolite | Apoptosis; Metabolism; Proteases/Proteasome |
Taurochenodeoxycholic Acid (12-Deoxycholyltaurine) 是动物胆汁酸的主要生物活性物质之一,可诱导细胞凋亡,具有明显的抗炎和免疫调节作用。 | |||
T4S0544 |
Furanodienone
呋喃二烯酮,莪术呋喃二烯酮 |
Apoptosis; HER | Angiogenesis; Apoptosis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Furanodienone 是来源于姜黄根茎的一种主要生物活性成分,可诱导细胞凋亡。 | |||
T3872 |
Nodakenin
紫花前胡苷,(+)-Marmesinin |
AChE | Neuroscience |
Nodakenin ((+)-Marmesinin) 是一种Peucedanum decursivum Maxim 根中的主要香豆素苷。它能够抑制乙酰胆碱酯酶活性,IC50=84.7 μM。 | |||
T11363 |
Ganoderic acid F
|
Others | Others |
Ganoderic acid F 是一种灵芝酸。它具有抗肿瘤和抗转移的活性,与抑制血管生成和涉及细胞增殖和细胞死亡,致癌作用,氧化应激,钙信号传导和内质网应激的蛋白质改变等机制相关。 | |||
TN1664 |
Ganoderic acid H
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NF-κB; DNA/RNA Synthesis; CDK | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; NF-κB |
Ganoderic acid H 是一种羊毛脂烷型三萜,提取自灵芝中。它能够抑制转录因子AP-1 和 NF-kappaB 信号,并抑制乳腺癌细胞细胞的生长和入侵。 | |||
T5S1413 |
Nodakenetin
闹达柯裂亭,Prangeferol,(-)-Prangeferol,Nodakenitin |
Others | Others |
Nodakenetin ((-)-Prangeferol) 是分离自Angelica decursiva 中,具有抗氧化、抗炎作用、抗关节炎及神经强化的作用。 | |||
T6S1141 |
Ganoderic acid A
灵芝酸 A,灵芝酸A |
Apoptosis; NF-κB; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Metabolism; NF-κB |
Ganoderic acid A 能够抑制 JAK-STAT3信号通路,也能抑制细胞增殖,存活率和 ROS。 它对人骨肉瘤 HOS 和MG-63细胞具有增殖抑制、凋亡和侵袭抑制作用。 | |||
T3S1149 |
Ganoderic acid G
|
Others | Others |
Ganoderic acid G 分离自灵芝菌管层表面。 | |||
TN1219 |
20-Hydroxyganoderic acid G
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20-Hydroxyganoderic acid G 是从灵芝 (Ganoderma curtisii) 子实体乙醇提取物中获得的羊毛甾烷三萜类化合物。20-Hydroxyganoderic Acid G 对由 LPS 激活的 BV-2 小胶质细胞有抑制作用,IC50 值为 21.33 μM。20-Hydroxyganoderic Acid G 用于研究由LPS 激活的小胶质细胞相关的神经炎症疾病。 | |||
T2S1120 |
Ganoderenic acid B
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P-gp | Membrane transporter/Ion channel; Neuroscience |
Ganoderenic acid B 是一种从Ganoderma lucidum 中提取的天然产物,可以通过抑制ABCB1的转运功能,增强化疗药物对ABCB1介导的耐多药癌细胞的细胞毒性来发挥作用。 | |||
T0847 |
Chenodeoxycholic acid
CDCA,鹅去氧胆酸,Chenodiol |
Potassium Channel; FXR; Endogenous Metabolite; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Chenodeoxycholic acid (CDCA) 是一种胆汁酸,通常与甘氨酸或牛磺酸结合。它作为清洁剂溶解脂肪以供肠道吸收,并被小肠重新吸收。它被用作利胆剂、利胆泻药,以及预防或溶解胆结石。 | |||
T5S1133 |
Ganoderic acid D
灵芝酸D,灵芝酸 D |
Apoptosis; Sirtuin | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Ganoderic acid D 是高度氧化的四环三萜,是灵芝的主要活性成分,可诱导 HeLa 人宫颈癌细胞凋亡。它上调 SIRT3的蛋白质表达并通过 SIRT3 诱导脱乙酰化的亲环蛋白 D 。它抑制结肠癌细胞的能量重编程,包括结肠癌细胞中的葡萄糖摄取,乳酸、丙酮酸和乙酰辅酶的产生。 | |||
TN1061 | Ganoderol B | Androgen Receptor | Endocrinology/Hormones |
Ganoderol B is a potent β ±-glucosidase and angiotensin-converting enzyme inhibitor, with an IC(50) of β ±-glucosidase is 119.8 uM. It may be useful in prostate cancer and benign prostatic hyperplasia (BPH) therapy through suppressing the function of andr | |||
T25445 | Ganoderiol B | ||
Ganoderiol B is a moderately active HIV-1 PR inhibitor (IC50: 0.17-0.23 mM). | |||
T75562 | Ganoderic acid GS-1 | ||
Ganoderic acid GS-1 是一种高度氧化的羊毛甾烷型三萜类化合物,具有抗 HIV-1蛋白酶活性,IC50为 58 μM。 | |||
T75626 | Ganoderenic acid K | ||
Ganoderenic acid K,一种从灵芝子实体分离得到的天然产物,对HMG-CoA还原酶(HMGCR)显示出强抑制作用,IC50值为16.5 μM。 | |||
TN6246 |
Actinodaphnine
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Actinodaphnine 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6246,CAS号为 517-69-1。 | |||
TN1655 |
Ganoderal A
|
Others | Others |
The oxygenated sterols( 26-oxygenosterols ganoderol A, ganoderol B, ganoderal A, and ganoderic acid Y) from G. lucidum can inhibit cholesterol biosynthesis via conversion of acetate or mevalonate as a precursor of cholesterol. | |||
TN4107 | Ganoderic acid X | ERK; Mdm2; MAPK; Caspase; Topoisomerase; JNK; p53 | Apoptosis; DNA Damage/DNA Repair; MAPK; Proteases/Proteasome |
Ganoderic acid X is a potential Mdm2 inhibitor(K(i) = 16nM). It is a potential anticancer drug, inhibits topoisomerases and induces apoptosis of cancer cells. | |||
TMA0993 |
Ganoderic acid E
灵芝酸F,Ganoderic acid F |
Antiviral | Immunology/Inflammation |
Ganoderic acid F has anti-hepatitis B, anti-inflammatory, and anti-tumor-promoting activities. | |||
TN3696 | Conodurine | AChR | Neuroscience |
Conodurine shows leishmanicidal and antibacterial activities, it shows inhibition activity for acetyl (AChE) and butyrylcholinesterase (BuChE). | |||
T72737 | Ganoderic acid R | ||
Ganoderic acid R为一种高效的抗癌化合物,通过促进肿瘤细胞系的凋亡(apoptosis)机制来抑制其生长。它对多药耐药(MDR)肿瘤细胞系(KB-A-1/Dox)及敏感肿瘤细胞系(KB-A-1)展现出显著的细胞毒性效应。 | |||
T75630 | Ganoderic acid Mf | ||
Ganoderic acid Mf为具有抗肿瘤活性的三萜类化合物,能导致细胞周期在G1期停滞,并在正常细胞与癌细胞中显示高度选择性,通过线粒体介导途径促进细胞凋亡(apoptosis)。 | |||
TN1663 |
Ganoderic acid DM
灵芝酸DM,灵芝酸 DM |
PARP; Androgen Receptor; CDK | Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; Endocrinology/Hormones |
Ganoderic acid DM is an antiandrogenic osteoclastogenesis inhibitor, it especially suppresses the expression of c-Fos and nuclear factor of activated T cells c1 (NFATc1), this suppression leads to the inhibition of dendritic cell-specific transmembrane pr | |||
TMA0986 |
Ganoderenic acid F
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Others | Others |
Ganoderenic acid F 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TMA0986,CAS号为 120462-47-7。 | |||
T25788 |
Melianodiol
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Melianodiol is potential used as a biopesticide against Aedes aegypti. | |||
T69213 |
Cynodontin
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Cynodontin was tested in vitro for fungitoxicity and was found to be a potent inhibitor of the growth of Sclerotinia minor, Sclerotinia sclerotiorum, and Botrytis cinerea and, to a lesser extent, of Verticillium dahliae. | |||
T72798 |
Ganodermaones B
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Ganodermaones B 是一种肾纤维化抑制剂,抑制 TGF-β1诱导的 collagen I 和 fibronectin 的表达。 | |||
TN3973 |
Epinodosin
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Others | Others |
Epinodosin induces significant DNA damage to HepG2 cells in a time- and dose-dependent manner.Epinodosin has a biphasic, dose-dependent effect on root growth and a strong inhibitory effect on root hair development in Lactuca sativa L. seedlings. | |||
TN1671 |
Ganoderone A
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Integrase; HSV | Microbiology/Virology |
Ganoderone A exhibits potent inhibitory activity against herpes simplex virus. | |||
T82335 |
Ganodermacetal
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Ganodermacetal是从G. amboinense中分离的高度氧化羊毛甾烷三萜类化合物,对丰年虾幼虫表现出显著毒性。 | |||
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