119
26
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6878 |
LJI308
|
S6 Kinase | MAPK; PI3K/Akt/mTOR signaling |
LJI308 是泛RSK 抑制剂,对 RSK1、RSK2 和 RSK3 的IC50分别为 6、4 和 13 nM。它抑制辐照、EGF 处理和表达 KRAS 突变的细胞中 RSK (T359/S363) 和 YB-1 (S102) 的磷酸化。 | |||
T8235 |
L-732138
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
L-732138 是选择性有效和竞争性神经激肽-1受体拮抗剂,IC50为 2.3 nM,可减轻痛觉过敏并具有抗肿瘤作用。它在克隆的人 NK-1受体中的效力比在克隆大鼠 NK-1受体中高 200 倍,比人类 NK-2 和 NK-3 受体高 1000 倍以上。 | |||
T16074 |
Mifobate
SR-202,米福贝特 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Mifobate (SR-202) 是一种有效且特异性的 PPARγ拮抗剂,可选择性抑制噻唑烷二酮 (TZD) 诱导的 PPARγ 转录活性,IC50为140 μM,具有抗肥胖和抗糖尿病作用。 | |||
T8405 |
Vardenafil hydrochloride
伐地那非,盐酸伐地那非 |
PDE | Metabolism |
Vardenafil hydrochloride 是口服具有活性的、高效的、选择性的磷酸二酯酶 5抑制剂。它对 PDE1 (180 nM),PDE6 (11 nM),PDE2,PDE3,PDE4 (>1000 nM) 具有选择性。它能够非竞争性地抑制环磷酸鸟苷水解,提高 cGMP 水平。它可用于勃起功能障碍的研究。 | |||
T0096 |
Vardenafil
伐地那非,Vivanza,Levitra,Vardenafil hydrochloride |
PDE | Metabolism |
Vardenafil (Vivanza) 是选择性、高效的、具有口服活性的磷酸二酯酶5抑制剂,IC50=0.7 nM。它能够非竞争性地抑制环磷酸鸟苷水解,从而提高 cGMP 水平。它对 PDE1 (180 nM),PDE6 (11 nM),PDE2,PDE3,PDE4 (>1000 nM) 具有选择性。它可用于研究勃起功能障碍。 | |||
T4097 |
Vardenafil hydrochloride trihydrate
Vardenafil HCl Trihydrate,BAY38-9456,盐酸瓦地那非三水合物 |
PDE | Metabolism |
Vardenafil hydrochloride trihydrate (BAY38-9456) 是一种新型 PDE 抑制剂,对 PDE5 和 PDE1 的 IC50 分别为 0.7 和 180 nM。 | |||
T4480 |
Vardenafil dihydrochloride
Levitra,Vardenafil Hydrochloride,二盐酸伐地那非 |
PDE | Metabolism |
Vardenafil dihydrochloride (Levitra) 是一种新型 PDE 抑制剂,对 PDE5 和 PDE1 的 IC50 分别为 0.7 和 180 nM。 | |||
TP2365L |
Acetyl tetrapeptide-9 Acetate
Acetyl tetrapeptide-9 Acetate(928006-50-2 Free base) |
Others | Others |
Acetyl tetrapeptide-9 Acetate 在刺激基底膜多糖(lumican)和胶原蛋白 I 的合成中发挥作用。 | |||
T5641 |
RP-54745
|
Interleukin | Immunology/Inflammation |
RP-54745 是一种能抑制噬细胞刺激和的白介素-1 的产生的化合物,对风湿病的治疗具有潜在的研究价值。 | |||
T29087 |
VA-K-14 hydrochloride
VAK14 Hydrochloride,VA K 14 HCl,VA-K-14 HCl,VAK14 HCl |
TSH Receptor | GPCR/G Protein |
VA-K-14 hydrochloride(VAK14 HCl)是一种选择性促甲状腺激素受体 (TSHR) 拮抗剂 (IC50= 12.3 μM),对GD患者血清和单克隆刺激TSHR抗体对TSHR的刺激有抑制作用,可消除 TSHR 信号传导。 | |||
T23536 |
Xamoterol hemifumarate
ICI 118587 hemifumarate,Corwin hemifumarate |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Xamoterol hemifumarate 是一种具有强效性和选择性的β1-肾上腺素受体激动剂。Xamoterol hemifumarate 是研究心律失常和 β1-肾上腺素能刺激与 IKr 之间关系的潜在化合物。 | |||
T9544 |
Compound 1T-0216
|
Others | Others |
Compound 1T-0216 是AKT1-FAK 相互作用的阻滞剂,在不影响基础FAK 磷酸化的情况下,减少对人类SW620结肠癌细胞细胞外压力的FAK 磷酸化的刺激。 | |||
T4068 |
E6446 dihydrochloride
|
TLR | Immunology/Inflammation |
E6446 dihydrochloride 是一种新型合成拮抗剂,用于核酸感应 TLR;有效抑制对 HEK:TLR9 细胞的 DNA 刺激,IC50 为 10 nM。 | |||
T5327 |
Amezinium methylsulfate
Amezinium metilsulfate,甲磺美嗪,Amezinium (methylsulfate),Lu-1631 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Amezinium methylsulfate (Lu-1631) 具有多种机制,包括刺激 α 和 β-1 受体以及抑制去甲肾上腺素和酪胺的摄取。 | |||
T9545 |
Compound 1T-0219 (SC)
|
FAK | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Compound 1T-0219 (SC) 是一种 AKT1-FAK 相互作用的阻断剂,可减少对人 SW620 结肠癌细胞中细胞外压力的 FAK 磷酸化的刺激,而不影响基础 FAK 磷酸化。 | |||
T12160 |
N6-Cyclohexyladenosine
CHA,A1受体促进剂 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
N6-Cyclohexyladenosine (CHA) 是一种选择性腺苷 A1 受体激动剂,EC50 为 8.2 nM。 | |||
T13187 |
Topterone
Win 17665 |
Androgen Receptor | Endocrinology/Hormones |
Topterone(Win 17,665) 是一种有效的局部抗雄激素,抑制睾酮和二氢睾酮对阉割未成熟雄性仓鼠腰部器官发育的刺激。 | |||
T16383 |
Olinciguat
IW-1701 |
Guanylate cyclase | GPCR/G Protein |
Olinciguat (IW-1701) 是一种口服鸟苷酸环化酶 (sGC) 刺激剂,在纯化的大鼠和人类酶测定以及全细胞测定中对 sGC 具有浓度依赖性刺激作用。 | |||
T1415 |
Gemfibrozil
吉非罗齐,CI-719,Jezil,Decrelip,Lopid |
P450; Adrenergic Receptor; PPAR | DNA Damage/DNA Repair; GPCR/G Protein; Metabolism; Neuroscience |
Gemfibrozil (CI-719) 是一种PPAR-α激活剂,可作为降脂药。它也是P450非选择性抑制剂,对 CYP2C9、2C19、2C8 和 1A2 的Ki 值分别为 5.8、24、69 和 82 μM。 | |||
TP1896L1 |
Kisspeptin 234 acetate(1145998-81-7 free base)
|
GPR; Kisspeptin | Endocrinology/Hormones; GPCR/G Protein |
Kisspeptin 234 acetate(1145998-81-7 free base) 是Kisspeptin 受体 (KISS1, GPR54) 拮抗剂; 是Kisspeptin-10 类似物。它抑制 Kisspeptin-10 对磷酸肌醇 (IP) (IC50 = 7 nM) 的刺激和促性腺激素释放激素 (GnRH) 的释放。 | |||
T13536 |
Afoxolaner
|
Chloride channel; GABA Receptor; Parasite | Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Afoxolaner 是一种异恶唑啉杀虫剂/杀螨剂,可对抗犬的肩胛硬蜱。 它作用于昆虫的 γ-氨基丁酸(GABA)受体谷氨酸受体,抑制 GABA 和谷氨酸调节的氯离子吸收,导致过度的神经元刺激和节肢动物死亡。 | |||
T4132 |
BPTU
BMS-646786 |
P2Y Receptor | GPCR/G Protein; Neuroscience |
BPTU (BMS-646786) 是一种非核苷酸类P2Y1受体变构拮抗剂,能够阻断位于胃肠道神经肌肉接头的 P2Y1受体,具有抗血栓活性。 | |||
T34532 |
Sari 59-801
Sari-59-801 |
Others | Others |
Sari 59-801 是具有口服活性的降血糖化合物,能够降低几个物种的血糖,且可以提高大鼠和小鼠的血浆中胰岛素水平。 | |||
TP1940L1 |
Ac-RYYRIK-NH2 acetate
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Ac-RYYRIK-NH2 acetate 是 nociceptin/orphanin FQ(noc/OFQ) 受体的激动剂,影响自发运动活动。 它是转染在 CHO 细胞中的 ORL1 的部分激动剂,可拮抗大鼠脑膜和切片中 noc/OFQ 对 [35S]-GTPgammaS 与 G 蛋白结合的刺激。 | |||
T1281 |
Tropicamide
Ro 1-7683,托吡卡胺 |
AChR | Neuroscience |
Tropicamide (Ro 1-7683) 是一种选择性的 M4毒蕈碱乙酰胆碱受体拮抗剂,作为滴眼剂使用时,会产生短效瞳孔扩张和睫状肌麻痹。 | |||
T4042 |
Talabostat mesylate
Val-boroPro,PT100 |
Proteasome; DPP-4 | Proteases/Proteasome; Ubiquitination |
Talabostat mesylate (PT100) 是一种具有口服活性和非选择性的二肽基肽酶 IV 抑制剂(IC50< 4 nM;Ki= 0.18 nM)。Talabostat mesylate 是成纤维细胞活化蛋白的第一个临床抑制剂(IC50= 560 nM),抑制 DPP8/9 (IC50= 4/11 nM;Ki= 1.5/0.76 nM),静息细胞脯氨酸二肽酶(IC50= 310 nM)、DPP2 和一些其他 DASH 家族酶。Talabostat mesylate 具有抗肿瘤和造血刺激活性 。 | |||
T28222 |
5-Hydroxy-1-methylhydantoin
HD-003,HD003,5-羟基-1-甲基咪唑啉-2,4-二酮,NZ419,NZ-419,HD 003,NZ 419 |
Bradykinin Receptor | GPCR/G Protein |
5-Hydroxy-1-methylhydantoin (HD-003) 是一种可能用于治疗肾衰竭的抗氧化剂。它是肌酐代谢物,是一种羟基自由基清除剂,此前已显示通过抑制大鼠慢性肾病的进展来提供肾脏保护。 它是一种新型抗氧化药物,可完全抑制 B2-激肽受体(B2KR) 对 VSMC 中高葡萄糖 (25 mM) 刺激的反应,并且还显示可减弱 BK 对 VSMC 重塑的影响。它抑制 BK 诱导的 MAPK 磷酸化增加并减弱 VSMC 中结缔组织生长因子 (CTGF) 蛋白水平的增加。这些研究结果表明,它可能通过其抗氧化特性赋予血管保护免受高葡萄糖浓度和 BK 刺激以改善血管损伤和重塑。 | |||
T21410 |
Triptorelin acetate(57773-63-4 free base)
醋酸曲普瑞林,Wy 42422,Triptorelin Acetate,CL 118532,AY 25650,CL 118,532,Wy 42462,BIM 21003 |
GNRH Receptor | GPCR/G Protein |
Triptorelin acetate(57773-63-4 free base) (CL 118,532) 用作 GnRH 激动剂。它通过引起垂体的持续刺激来减少垂体促性腺激素促黄体激素 (LH) 和促卵泡激素 (FSH) 的分泌。曲普瑞林可用于治疗激素反应性癌症,如乳腺癌或前列腺癌、性早熟、雌激素依赖性疾病和辅助生殖。 | |||
T6602 |
Naratriptan hydrochloride
Naratriptan HCl,Amerge,Naramig,盐酸那拉曲坦,GR-85548A hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Naratriptan hydrochloride (GR-85548A hydrochloride) 是一种5-HT1受体激动剂,有抗偏头疼特性。它还可以通过刺激三叉神经系统感觉神经末梢上的 5-HT1D/1B 受体来发挥其作用,从而减少促炎神经肽的释放。 | |||
T68405 |
KW-2450 free base
|
IGF-1R | Tyrosine Kinase/Adaptors |
KW-2450 free base 是一种 IGF-1R/IR和酪氨酸激酶多重抑制剂 具有抗肿瘤活性。KW-2450 free base 在小鼠 HT-29/GFP 结肠癌异种移植模型中显示出适度的生长抑制活性并抑制 IGF-1 诱导的信号转导。 | |||
TP1219 |
Atrial Natriuretic Peptide (ANP) (1-28), human, porcine Acetate
ANP (1-28), human, porcineANP(1-28) |
||
Atrial Natriuretic Peptide (ANP) (1-28), human, porcine Acetate 是颗粒鸟苷酸环化酶的刺激剂,已被发现通过增加环鸟苷单磷酸的合成来保护分离的心肌细胞免受复氧诱导的高收缩。Atrial Natriuretic Peptide (ANP) (1-28), human, porcine Acetate 也有助于在反复运动期间刺激脂解,并在运动期间控制脂解。 | |||
T25912 |
Oxypyrronium bromide
L.D. 3055,Immetropan,LD 3055,LD3055,LD-3055 |
||
Oxypyrronium bromide 一种含有季铵的抗胆碱能和解痉剂。在动物模型中,它抑制胃运动、迷走神经刺激或乙酰胆碱静脉注射引起的低血压;鼓索神经刺激引起的流涎和节前颈交感神经刺激引起收缩。 | |||
T24603 |
PD-34799-SA
PD 34799-SA,PD34799-SA |
||
PD-34799-SA is an effective inhibitor of vasoconstrictor responses to sympathetic nerve stimulation. | |||
T71863 |
LDDN-0003499
|
||
LDDN-0003499 is a novel Src family tyrosine kinase inhibitor with anti-inflammatory effects in response to Aß stimulation of microglia. | |||
T28431 |
PNU109291
PNU-109291,PNU 109291 |
||
PNU109291, a potent and selective agonist of the 5-HT1D receptor, effectively mitigates dural plasma extravasation induced by trigeminal ganglion stimulation. | |||
T33696 |
NK-1145
NK-1145 hydrocholdoride,NK 1145,NK1145 |
||
Nk-1145 is a parasympathetic drug of the autonomic nervous system, which can cause behavioral stimulation and excitement. | |||
T68782 |
Ono 11006
|
||
Ono 11006 is a thromboxane agonist that dose dependently reduced the positive inotropic effect induced by field stimulation. | |||
T19762 |
Clobenpropit 2HBr
VUF-9153,VUF 9153,Clobenpropit Dihydrobromide,VUF9153 |
||
Clobenpropit 2HBr is a histamine H3 receptor antagonist. It has neuroprotective effects via stimulation of GABA release in the brain. | |||
T71803 | Mabuterol hydrochloride | ||
Mabuterol hydrochloride is a selective β2 adrenoreceptor agonist. Mabuterol has a specific effect on beta 2-adrenoceptors with no beta 1-stimulation. | |||
TP1896 |
Kisspeptin 234
|
||
Kisspeptin 234 is a kisspeptin receptor (KISS1, GPR54) antagonist; kisspeptin-10 analog. Inhibits kisspeptin-10 stimulation of inositol phosphate (IP) (IC50 = 7 nM) and release of gonadotrophin-releasing hormone (GnRH). | |||
TP2365 |
Acetyl tetrapeptide-9
LS9745,N-Acetyl-gln-asp-val-his,Dermican,LS-9745,LS 9745 |
||
Acetyl tetrapeptide-9 is important for the stimulation of basement membrane polysaccharide (lumican) and the synthesis of collagen I. | |||
T71051 | OSU-53 | ||
OSU-53 is an AMPK activator, inhibiting mTOR signaling and autophagy stimulation. OSU-53 also activates mutations in RAS or BRAF. | |||
T26959 | Cazpaullone | ||
Cazpaullone is an inhibitor of glycogen synthase kinase-3 (GSK-3). It also shows transient stimulation of the mRNA expression of the beta cell transcription factor Pax4. | |||
T40898 |
DMHCA
|
||
DMHCA, a potent, selective LXR agonist, specifically activates the LXR pathway's cholesterol efflux arm, avoiding triglyceride synthesis stimulation. This compound exhibits anti-inflammatory properties and is utilized in researching cholesterol homeostasis and diabetes. | |||
T29213 |
Zelandopam free base
YM-435,YM435,MYD-37,MYD37,Zelandopam |
||
Zelandopam is a dopamine D1 agonist. Zelandopam is a potent stimulant of pancreatic exocrine secretion by acting on DA D1 receptors of the pancreas in dogs. Intravenous administration of Zelandopam produces renal vasodilating and diuretic/natriuretic effe | |||
T19511 |
PGlu-3-methyl-His-Pro-NH2 TFA
A-42872 TFA |
Others | Others |
PGlu-3-methyl-His-Pro-NH2 TFA, enhances binding to pituitary TRH receptors and increases stimulation of thyroid-stimulating hormone (TSH) release from the pituitary. | |||
T25918 |
Palmitoyl-L-aspartic acid
L-N-Palmitoylaspartic acid |
||
Palmitoyl-L-aspartic acid is a natural N-acylaspartate that suppresses Hedgehog signaling after stimulation with Smoothened agonist or non-sterol-modified Sonic Hedgehog. It does not alter the activity of cannabinoid receptors or fatty acid amide hydrolas | |||
T69270 |
Amezinium
|
||
Amezinium is a sympathomimetic drug used for the treatment of low blood pressure. It has multiple mechanisms, including stimulation of alpha and beta-1 receptors and inhibition of noradrenaline and tyramine uptake. | |||
T34430 |
RU 24411
RU24411,RU-24411 |
||
RU 24411是一种合成的19-nor 类固醇化合物。在没有葡萄糖的情况下,RU 24411 与醛固酮一样能够刺激钠的转运。 | |||
T76646 |
Acetyl-ACTH (7-24) (human, bovine, rat)
|
||
Acetyl-ACTH (7-24) (human, bovine, rat) 可导致 ACTH 诱发的皮质酮和醛固酮释放显著减少。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2198 |
Arecoline hydrobromide
Arecoline HBr,氢溴酸槟榔碱,Arecoline bromide |
AChR | Neuroscience |
Arecoline hydrobromide (Arecoline HBr) 是从槟榔中得到的一种生物碱,具有刺激、警觉、抗焦虑和抗寄生虫作用。它是烟碱和毒蕈碱乙酰胆碱受体的部分激动剂,可诱导氧化应激。 | |||
TQ0273 |
Neopterin
D-(+)-Neopterin,2-Amino-6-((1S,2R)-1,2,3-trihydroxypropyl)pteridin-4(3H)-one,新蝶呤 |
Endogenous Metabolite | Metabolism |
Neopterin (D-(+)-Neopterin) 是三磷酸腺苷的一种分解产物,是细胞免疫系统激活的标志物。 | |||
T6S1010 |
Allomatrine
槐定碱,别苦参碱 |
Others | Others |
Allomatrine 是一种来源槐花树皮的生物碱。它能够激活 κ-阿片受体,进而产生缓解疼痛的作用。 | |||
T6S0627 |
Mesaconitine
新乌碱,新乌头碱;中乌头碱 |
TNF | Apoptosis |
Mesaconitine 是乌头属植物的一种主要活性成分,通过循环 AMP 和刺激中枢 β-肾上腺素能系统具有镇痛活性,还有抗炎活性。 | |||
TN1100 |
Nepodin
|
transporter; COX; AMPK; Parasite | Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling |
Nepodin 是从Rumex crispus 中分离的一种醌氧化还原酶抑制剂,具有抗糖尿病和抗疟疾的作用。。它通过激活 AMPK 刺激 GLUT4 向质膜的转运。 | |||
T0131 |
Cepharanthine
NSC-623442,千金藤碱,千金藤素 |
Apoptosis; TNF; HIV Protease; Autophagy | Apoptosis; Autophagy; Microbiology/Virology; Proteases/Proteasome |
Cepharanthine (NSC-623442) 是从Stephania cepharanthaHayata 中提取的一种生物碱,具有抗炎、抗氧化作用。它可抑制肿瘤坏死因子 (TNF)-α 介导的 NFκB 刺激、质膜脂质过氧化和血小板聚集,并抑制细胞因子的产生。 | |||
T5814 |
Aurantiamide
TMC-58B,橙黄胡椒酰胺 |
p38 MAPK; NF-κB | MAPK; NF-κB |
Aurantiamide 是马齿苋的活性成分,具有多种生物活性(如抗氧化、抗血小板、抗炎、抗肿瘤活性等),具有口服活性。 | |||
T5S1989 |
Apiin
Apioside,芹菜苷 |
Others | Others |
Apiin (Apioside) 是Apium graveolens 叶片的一种主要成分,具有抗炎作用。它在体外抑制亚硝酸盐产生的IC50值为0.08 mg/mL,在 LPS 激活的 J774.A1 细胞中抑制 iNOS 的表达的IC50值为0.049 mg/ mL。 | |||
T5120 |
Rhamnose
6-Deoxyhexopyranose,L-鼠李糖,6-Deoxy-L-mannose,alpha-L-Rhamnose |
Calcium Channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism |
alpha-L-Rhamnose (6-Deoxy-L-mannose) 是存在植物和细菌中的一种单糖。Rhamnose- 免疫原连接物能被用于免疫疗法。Rhamnose 能通过胞外途径穿过上皮细胞,能够作为肠吸收的标志。 | |||
TL0007 |
Bisdemethoxycurcumin
双去甲氧基姜黄素,Curcumin III,Didemethoxycurcumin |
Epigenetic Reader Domain; Wnt/beta-catenin | Chromatin/Epigenetic; Cytoskeletal Signaling; Stem Cells |
Bisdemethoxycurcumin (Curcumin III) 是一种具有抗炎及抗氧化作用的姜黄素。 | |||
T3874 |
Diosgenin glucoside
延龄草苷,地索苷,Disogluside,Trillin |
Apoptosis; Others; Autophagy | Apoptosis; Autophagy; Others |
Diosgenin glucoside (Trillin) 是一种来自蒺藜的皂苷元类天然产物,可通过调节自噬和减轻细胞凋亡来保护脊髓免受损伤。它通过调节小胶质细胞 M1 极化提供神经保护,和其他具有类似活性的合成糖苷可用于治疗高胆固醇血症和动脉粥样硬化。 | |||
T20879 |
Tacrolimus monohydrate
FK-506,FR 900506,Prograf,FR900506,Tacrolimus hydrate,LCP-Tacro,他克莫司一水合物,FK 506 |
Phosphatase; Others; Antibacterial; Antibiotic; Autophagy | Autophagy; Metabolism; Microbiology/Virology; Others |
Tacrolimus monohydrate (LCP-Tacro) 是大环内酯类化合物,它与 FK506 结合蛋白 (FKBP) 结合形成复合物并抑制钙调神经磷酸酶,从而抑制 T 淋巴细胞信号转导和 IL-2 转录。具有强免疫抑制特性。 | |||
T5S1177 |
Aloin B
Isobarbaloin,芦荟苷B,芦荟素B |
Others | Others |
Aloin B (Isobarbaloin) 是一种芦荟素的异构体。其中芦荟素是芦荟中的具生理活性蒽醌化合物。 | |||
T4S0867 |
Pogostone
DHELWANGIN,广藿香酮 |
Apoptosis; Antibacterial; Autophagy | Apoptosis; Autophagy; Microbiology/Virology |
Pogostone (DHELWANGIN) 是从薄荷中分离出,对革兰氏阴性菌、革兰氏阳性菌、大肠埃希菌等具有强效抗菌、抗真菌活性。它诱导细胞凋亡和自噬。 | |||
T6S2140 |
β-Anhydroicaritin
Anhydroicaritin,Beta-Anhydroicaritin,脱水淫羊藿素 |
MMP; Others; TNF; Interleukin | Apoptosis; Immunology/Inflammation; Others; Proteases/Proteasome |
β-Anhydroicaritin 是从乳香提取的一种天然产物,具有重要的生物学和药理学作用,如抗骨质疏松症,雌激素调节和抗肿瘤特性。它改善牙周组织的降解,抑制糖尿病大鼠 TNF-α 和 MMP-3 的合成和分泌。它抑制细胞内 Ca2+的升高,并显著降低 iNOS 蛋白的表达。 | |||
T3S1612 |
kuwanon G
桑黄酮G,Moracenin B,桑黄酮 G,Kuwanone G |
Phosphatase; Antibacterial; Bombesin Receptor; AChR; AChE; Glucosidase | GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Kuwanon G (Moracenin B) 是一种从桑树中得到的黄酮类蛙皮素受体拮抗剂,具有杀菌作用。 | |||
T3S0860 |
Gitogenin
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UGT | Metabolism |
Gitogenin 是一种从Tribulus longipetalus 整株中分离出来的天然类固醇,是一种 UDP-葡萄糖醛酸转移酶 1A4 (UGT1A4) 和 α-葡萄糖苷酶的选择性抑制剂,其IC50分别为 0.69 µM (使用三氟拉嗪为底物) 和 37.2 μM,对人类主要细胞色素 P450 亚型的活性无抑制作用。 | |||
TN6442 |
Esculentoside C
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Esculentoside C exerts proinflammatory effects synergistically, it can induce inflammatory stimulation. | |||
TN4986 |
Selinidin
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IκB/IKK; p38 MAPK; TNF | Apoptosis; MAPK; NF-κB |
Selinidin decreases phosphorylation of phospholipase C-gamma1, p38 mitogen-activated protein kinase, and IkappaB-alpha upon FcepsilonRI stimulation. | |||
TN1533 |
Cucurbitacin A
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ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Cucurbitacin I, cytotoxic triterpenoid sterols isolated from plants, elicits the formation of actin/phospho-myosin II co-aggregates by stimulation of the RhoA/ROCK pathway and inhibition of LIM-Kinase. | |||
TN2001 |
Oblongine
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Others | Others |
Oblongine chloride may have potential haemodynamic effects, it can cause a dose-dependent reduction of systolic and diastolic blood pressure, and that these effects are not mediated by α²-adrenergic receptor stimulation. | |||
TN3744 |
Cyclomorusin
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NOS; AChR | Immunology/Inflammation; Neuroscience |
Cyclomorusin exhibits competitive inhibition toward monophenolase activity of mushroom tyrosinase, the IC50 value of 0.092 microM. It evokes the stimulation of superoxide anion generation in fMLP-stimulated rat neutrophils. Cyclomorusin , neocyclomorusin | |||
TN4624 | Nantenine | Others | Others |
Nantenine is an acetylcholinesterase inhibitor, it functions as an effective antagonist against a wide range of MDMA-induced effects in mice. Nantenine has anticonvulsant effect, which seems attributable to its stimulation and the resultant decrease of Ca | |||
TN4489 | Manassantin A | ERK; cAMP; TNF; NF-κB; MAPK; COX; HIF; Prostaglandin Receptor; JNK; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; MAPK; Neuroscience; NF-κB; Stem Cells |
Manassantin A is a high potent HIF-1 inhibitor, it protects the gastric mucosa from ethanol-induced acute gastric injury, and suggest that these protective effects might be associated with COX/PGE2 stimulation, inhibition of iNOS production and NF-κB act | |||
T83319 |
4-epi-Withaferin A
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4-epi-Withaferin A(化合物28)是Withaferin A的一个类似物,它增强了细胞毒性及细胞保护性热休克诱导活性(HSA)。此外,4-epi-Withaferin A还展现了通过激活细胞防御机制来研究蛋白质聚集相关疾病的潜力。 | |||
TN4291 | Isofuranodiene | IL Receptor; NOS | Immunology/Inflammation |
Isofuranodiene protects GalN/LPS-induced liver injury in SD rats, it may be a potential functional food ingredient for the prevention and treatment of liver diseases. Isofuranodiene has anticancer activity, by inhibiting the proliferation and inducing apo |