1163
168
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T24240 |
K-8012
K8012,K 8012 |
Retinoid Receptor; RAR/RXR | Metabolism |
K-8012 是 N 末端截短的 RXRα 的调节剂,并以 RXRα 依赖性方式提高抗癌活性。 | |||
T11742 |
K-7174
|
IL Receptor; TNF | Apoptosis; Immunology/Inflammation |
K-7174 是一种新型细胞粘附抑制剂, 抑制由 IL-1β 或 TNF-α 诱导的血管细胞粘附分子 1 (VCAM-1) 的表达。 | |||
T15639 |
K-756
|
PARP; Wnt/beta-catenin | Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Stem Cells |
K-756 是一种直接的 tankyrase(TNKS) 选择性抑制剂,对 TNKS1和 TNKS2的 ADP-核糖基化活性有抑制作用,IC50分别为 31 和 36 nM。 | |||
T8936 |
Proteinase K
proteinase K for tritirachium album,Protease K,蛋白酶 K |
Others | Others |
Proteinase K (proteinase K for tritirachium album) 是一种非特异性丝氨酸蛋白酶,可用于蛋白消化。它在有 SDS 或尿素存在的情况下,在很大 pH 值 (4-12)、盐浓度和温度单位内均有活性。 | |||
T11733 |
K-604 dihydrochloride
|
Acyltransferase | Metabolism |
K-604 dihydrochloride 是酰基辅酶 A:胆固醇酰基转移酶 1 的选择性抑制剂,IC50为 0.45±0.06 μM。 | |||
T6777 |
Bay K 8644
(±)-BAY-K-8644,SQ 28,873 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Bay K 8644 (SQ 28,873)是一种二氢吡啶化合物,是一种选择性的 L 型 Ca2+ 通道激活剂,IC50 为 17.3 nM。它通过增加通道的开放时间来增加通过肌膜 Ca2+通道的 Ca2+流入。 | |||
TQ0145 |
(R)-(+)-Bay-K-8644
(R)-(+)-Bay K 8644 |
Calcium Channel; PPAR | DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
(R)-(+)-Bay-K-8644 是一种 Ca2+ 通道激动剂,是二氢吡啶激动剂,抑制 Ba2+电流 (IBa),诱导猫的中枢性呼吸抑制,通过竞争性拮抗血栓素 A2-前列腺素 H2 受体抑制血小板活化。 | |||
T9954 |
K-975
|
Others | Others |
K-975是一种高选择性的具有口服活性的TEAD 抑制剂,可有效抑制TEAD 和YAP1/TAZ 之间的蛋白质-蛋白质相互作用。 | |||
T11734 |
K-80003
TX-803 |
Akt; RAR/RXR | Cytoskeletal Signaling; Metabolism; PI3K/Akt/mTOR signaling |
K-80003(TX-803) 是一种有效的类视黄醇 X 受体α调节剂,对 tRXRα 依赖性的 Akt 激活和肿瘤细胞生长有抑制作用。 | |||
TP2009L |
K 41498 aceate
|
CRFR | GPCR/G Protein |
K41498 acetate 是 antisauvagine-30 的类似物,可抑制 suvagine 刺激的 cAMP 在表达 hCRF2α 和 hCRF2β 的细胞中的积累。 K41498 acetate 是一种有效且高度选择性的 CRF2 受体拮抗剂,对人 CRF2α、CRF2β 和 CRF1 受体的 Ki 值分别为 0.66 nM、0.62 nM 和 425 nM。 | |||
TQ0144 |
(S)-(-)-Bay-K-8644
(S)-(-)-Bay K 8644 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
(S)-(-)-Bay-K-8644 ((S)-(-)-Bay K 8644) 是 L 型 Ca2+ 通道的激动剂,可激活 Ba2+ 电流,其EC50 为 32 nM。 | |||
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。 | |||
T5469 |
K-Ras-IN-1
|
Raf; Ras | GPCR/G Protein; MAPK |
K-Ras-IN-1 是K-Ras 抑制剂。K-Ras-IN-1 能与 K-Ras (WT)、K-Ras (G12D)、K-Ras (G12V) 和 H-Ras 结合。它对胰腺癌、结肠癌和肺癌的具潜在的研究价值。 | |||
T11738 |
K-Ras G12C-IN-4
|
Ras | GPCR/G Protein; MAPK |
K-Ras G12C-IN-4 是一种 KRAS G12C 共价抑制剂。 | |||
T4618 |
BGG463
K 0859 |
Bcr-Abl; CDK | Angiogenesis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
BGG463 (K 0859) 是一种具有口服活性的 II 型 CDK2的抑制剂,可抑制 c-ABL-T334I、BCR-ABL 和 BCR-ABL-T315I 变体,IC50分别为 0.25 μM、0.09 μM 和 0.590 μM。 | |||
T1914 |
K02288
K 02288 |
ALK; TGF-beta/Smad | Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors |
K 02288是骨形态发生蛋白 (BMP) I 型受体抑制剂,能够抑制 ALK1 (IC50:1.8nM)、ALK2 (IC50:1.1nM)、ALK6 (IC50:6.4nM)。对 ALK3 和 ALK6 的抑制稍弱,IC50在 5-34 nM 之间。 | |||
T6556 |
K-Ras(G12C) inhibitor 9
|
Raf | MAPK |
K-Ras(G12C) inhibitor 9 是致癌 K-Ras(G12C) 的变构抑制剂。 | |||
T3725 |
K-Ras(G12C) Inhibitor 6
|
Raf | MAPK |
KRas(G12C) inhibitor 6 是一种变构的,选择性的 K-Ras(G12C)抑制剂。 | |||
T6555 |
K-Ras(G12C) inhibitor 12
|
Apoptosis; Raf; Ras | Apoptosis; GPCR/G Protein; MAPK |
K-Ras(G12C) inhibitor 12是一种K-Ras(G12C)抑制剂,作用于H1792细胞,EC50为0.32 μM。 | |||
T24239 |
K201
K-201,JTV 519,JTV-519,K 201 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
K201 (JTV-519) 是一种 Ca2+ 依赖性阻滞剂,通过稳定兰尼碱受体来防止缺血性心脏和骨骼肌 (SkM) 中的肌质网异常 Ca(2+) 泄漏。 | |||
T8659 |
K-Ras-PDEδ-IN-1
|
PDE | Metabolism |
K-Ras-PDEδ-IN-1 是新型的 K-Ras-PDEδ 抑制剂,它能够以低纳摩尔Kd8 nM 与 PDEδ 的法尼基结合袋竞争性结合。 | |||
T27704 |
K00135
K-00135,Imidazol[1,2-b]pyridazine 1,K 00135,IMIDAZOPYRIDAZIN 1 |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
K00135 (IMIDAZOPYRIDAZIN 1) 是 Pim 激酶的选择性抑制剂,可用于胃癌和抗白血病治疗的研究。 | |||
TQ0138 |
K145 hydrochloride
K145盐酸盐 |
Apoptosis; S1P Receptor | Apoptosis; GPCR/G Protein |
K145 hydrochloride 是选择性的,底物竞争性的和口服有效的SphK2抑制剂,IC50为 4.3 µM,Ki 为 6.4 µM。它可诱导细胞凋亡,显示出强大的抗肿瘤活性。 | |||
T15641 |
K777
APC-3316 |
P450; Cysteine Protease; CCR | Immunology/Inflammation; Metabolism; Microbiology/Virology; Proteases/Proteasome |
K777 是有效的,具有口服活性的,不可逆的半胱氨酸蛋白酶 (cysteine protease) 抑制剂。K777是有效的 CYP3A4 抑制剂(IC50= 60 nM)。K777也是选择性的 CCR4 拮抗剂,显示出强的趋化性抑制作用。K777 对 Cruzain(克鲁斯锥虫的主要半胱氨酸蛋白酶)和组织蛋白酶 B 和 L 具有不可逆的抑制作用。K777 通过靶向组织蛋白酶介导的细胞进入,显示出广谱的抗病毒作用。K777 抑制 EBOV 和 SARS-CoV 病毒的进入,IC50 值分别为 0.87 nM 和 0.68 nM。 | |||
T6866 |
AUZ 454
K03861 |
CDK | Cell Cycle/Checkpoint |
AUZ 454 (K03861) 是一种 II 型 CDK2 抑制剂,Kd 值是 8.2 nM。它对 CDK2(WT)、CDK2(C118L)、CDK2(A144C) 和 CDK2(C118L/A144C) 的 Kd 分别为 50 nM、18.6 nM、15.4 nM 和 9.7 nM。 | |||
T3120 |
K858 (Racemic)
K858 Racemic,K858 |
Apoptosis; Kinesin | Apoptosis; Cytoskeletal Signaling |
K858 Racemic (K858) 是一种选择性有丝分裂驱动蛋白 Eg5 抑制剂,以 ATP 非竞争性方式起作用,IC50值为 1.3 μM。 | |||
TP1682L |
Abz-FR-K(Dnp)-P-OH acetate(500799-61-1 free base)
|
Others | Others |
Abz-FR-K(Dnp)-P-OH acetate(500799-61-1 free base) 是一种出色的血管紧张素 I 转换酶 (ACE) 底物,Km 值为 4.0 μM,kcat 值为 210s-1。 | |||
T27710 |
K6PC-5
K6PC5,K6PC 5 |
S1P Receptor | GPCR/G Protein |
K6PC-5 is a ceramide derivative that acts as an activator of sphingosine kinase 1 (SPHK1), inducing a swift and temporary rise in intracellular calcium levels. With its potential applications in skin diseases associated with abnormal keratinocyte function, as well as in studies on neurodegeneration and virus infection, K6PC-5 presents a promising compound for research purposes. | |||
T33581 |
Nafetolol
K 5407,K-5407 |
Others | Others |
Nafetolol (K 5407) 是一种生化试剂,可用于合成其他化合物。 | |||
T125462 |
Gnetifolin K
GnetifolinK |
||
Gnetifolin K (GnetifolinK) 是一种来自 Gnetum parvifolium 的新型二苯乙烯二葡萄糖苷,具有潜在的神经保护活性,可用于研究DNA损伤。 | |||
TQ0107 |
Pemafibrate
(R)-K-13675 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Pemafibrate ((R)-K-13675) 是一种高度特异性的 PPARα 激动剂 (EC50: 1 nM)。 | |||
T36100 | K-TMZ | ||
K-TMZ is a DNA alkylating agent. It increases the concentration of O6-methylated deoxyguanosine in U87 glioblastoma multiforme (GBM) cells in a concentration-dependent manner. K-TMZ reduces cell viability of GBM cell lines lacking (IC50s = 18-44 μM) or expressing O6-methylguanine DNA methyltransferase (MGMT; IC50s = 115-240 μM). K-TMZ can cross the blood-brain barrier and increases survival in a Br23c mouse xenograft model of GBM when administered at a dose of 14.9 mg/kg. | |||
T70949 | K-8986 | ||
K-8986 is a novel h1-receptor antagonist | |||
T27832 |
Lifibrol
U 83860,K-12148,K-12.148,U-83860,K12148 |
Lipid | Metabolism |
Lifibrol (U-83860) 是一种胆固醇合成抑制剂。Lifibrol 具有抗胆固醇和降血脂的作用,可促进高胆固醇血症和混合型高脂血症患者体内低密度脂蛋白载脂蛋白 B-100 的转化。 | |||
T9418 | NEUROPEPTIDE K | ||
NEUROPEPTIDE K 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 T9418,CAS号为 106441-70-7。 | |||
T40537 | Ibuprofen Impurity K | ||
Ibuprofen Impurity K is a compound that serves as an impurity in Ibuprofen. Ibuprofen itself is an anti-inflammatory inhibitor specifically designed to target COX-1 and COX-2. It exhibits inhibitory activity with IC50 values of 13 μM and 370 μM for COX-1 and COX-2, respectively. | |||
T25682 |
Leucinostatin K
Leucinostatin-K |
||
Leucinostatin K is a new peptide antibiotic from Paecilomyces lilacinus. | |||
T32354 |
K 8409
K8409,K-8409 |
||
K 8409 is a bioactive chemical. | |||
T69760 |
TT-10
TAZ-K |
YAP | Stem Cells |
TT-10 (TAZ-K) 作为YES相关蛋白(YAP)-转录增强因子结构域(TEAD)活性的激活剂,适用于心肌细胞丢失伴随心脏病研究。 | |||
T32349 |
K 2604
K-2604,K2604 |
||
K 2604 is a bioactive chemical. | |||
T22886 |
K 579
|
Others | Others |
K 579 is a dipeptidyl peptidase IV inhibitor. | |||
T32352 |
K 486
K486,K-486,K 486, CARBANILIC ACID |
||
K 486 is a bioactive chemical. | |||
T8882 |
Vodobatinib
K-0706 |
Bcr-Abl | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Vodobatinib (K-0706) 是第三代具有口服活性的Bcr-Abl1酪氨酸激酶抑制剂,IC50=7 nM,对大多数 BCR-ABL1 点突变体具有活性,但对 BCR-ABL1T315I 无活性。它可用于研究慢性粒细胞白血病 (CML)。 | |||
T24215 |
JS-K
JSK,JS K |
||
JS-K is a Nitric oxide donor. It has antiproliferative activity. | |||
T21950 |
K 00546
|
||
K00546 是一种有效的细胞周期蛋白依赖性激酶CDK1和CDK2抑制剂,对CDK1/cyclin B 和CDK2/cyclin A 的IC50分别为 0.6 nM 和 0.5 nM。K00546 也是一种有效的 CDC2 样激酶 1 (CLK1) 和CLK3抑制剂,IC50分别为 8.9 nM 和 29.2 nM。 | |||
T25564 |
K-13
K-13 (Ace inhib) |
||
K-13 is used as an ACE inhibitor produced by Micromonospora halophytics subsp. exilisia K-13. | |||
T32350 |
K 308
K-308,K308 |
||
K 308 is a bioactive chemical. | |||
TP2304 |
pGlu-K(-NBD)-Q-R-L-G-N-Q-W-A-V-G-H-L-M-N
|
Others | Others |
pGlu-K(-NBD)-Q-R-L-G-N-Q-W-A-V-G-H-L-M-N 是一种肽。 | |||
T12966 | Sofosbuvir impurity K | HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Sofosbuvir impurity K is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity. | |||
T71419 | Diclazuril K | ||
Diclazuril K is a coccidiostat and GAPDH inhibitor used to prevent parasitic contamination of livestock and poultry feed. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5S2309 |
Hosenkoside K
凤仙萜四醇苷K,(+)-Hosenkoside K |
Others | Others |
Hosenkoside K ((+)-Hosenkoside K) 是一种糖苷,分离自凤仙花种子。 | |||
T8200 |
Ginkgolide K
银杏内酯 K,银杏内酯K |
AMPK; Autophagy | Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Ginkgolide K 是从银杏中分离得到的一种二萜类天然产物,有神经保护活性,可通过 AMPK/mTOR/ULK1信号通路诱导保护性自噬。 | |||
T19603 |
Vitamin K
Kephton,维生素K,Vitamin K1(20) |
Endogenous Metabolite | Metabolism |
Vitamin K (Kephton) 具有凝血作用,对凝血因子、基质-Gla 蛋白和骨钙素很重要。 | |||
T3811 |
Ginsenoside C-K
20(S)-人参皂苷 C-K,Ginsenoside compound K,Ginsenoside K,人参皂苷 C-K |
P450; cell cycle arrest; COX; NO Synthase | Cell Cycle/Checkpoint; Immunology/Inflammation; Metabolism; Neuroscience |
Ginsenoside C-K (Ginsenoside K) 是 Ginsenoside Rb1 的细菌代谢物,可通过抑制诱生型一氧化氮合酶和COX-2来发挥抗炎作用。它在人肝微粒体中抑制CYP2C9和CYP2A6活性,IC50分别为 32.0±3.6 和 63.6±4.2 μM。 | |||
T0449 |
Menadione
维生素K3,Vitamin K3,甲萘醌 |
Thrombin; Endogenous Metabolite | Metabolism; Proteases/Proteasome |
Menadione (Vitamin K3) 是合成的萘醌,能够在体内转化成活性维生素 K2。 | |||
T2570 |
Vitamin K4
维生素K4,维生素 K4,Kapilin,Menadiol Diacetate,acetomenaphthone |
Apoptosis; Endogenous Metabolite | Apoptosis; Metabolism |
Vitamin K4 (Menadiol Diacetate) 是一种维生素药物,用于治疗因缺乏 VK4 引起的凝血障碍。 | |||
TN5268 |
Yadanzioside K
|
Others | Others |
Yadanzioside K is a natural product from Brucea javanica. | |||
TN2266 |
Terrestrosin K
|
Others | Others |
Terrestrosin K is a natural product | |||
T75675 |
Nepasaikosaponin K
|
Antiviral | Immunology/Inflammation |
Nepasaikosaponin K 是一种从柴胡根中分离出来小分子化合物,具有抗流感和抗病毒活性,可用于研究病毒感染。 | |||
TN1843 |
Kushenol K
|
PDE; HSV | Metabolism; Microbiology/Virology |
Kushenol K is a potent and Selective Inhibitor of cGMP Phosphodiesterase 5, it also has inhibitory effects on diacylglycerol acyltransferase (DGAT). Kushenol K shows weak antiviral activity against Herpes simplex virus types I and II. | |||
TN1388 |
Angelol K
|
Others | Others |
Angelol K shows significant activity on human platelet aggregation. | |||
TN1945 |
Momordicoside K
|
Others | Others |
Momordicoside K has antidiabetic activity. | |||
TN4971 | Sculponeatin K | Others | Others |
Sculponeatin K是一种天然产物,属于唇形科香茶菜属,其产品编号为 TN4971,CAS号为 477529-70-7。Sculponeatin K可用作对照参考。 | |||
TN5664 |
Epimedonin K
|
||
Epimedonin K 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 TN5664,CAS号为 2222285-85-8。 | |||
TN4942 |
Sanggenone K
|
Others | Others |
Sanggenone K 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 TN4942,CAS号为 86450-77-3。 | |||
TN4481 |
Macrocarpal K
|
Others | Others |
Macrocarpal K 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 TN4481,CAS号为 218290-59-6。 | |||
TN6589 | Grossamide K | ||
Grossamide K exerts a particularly strong anti-melanogenic activity on the cells without high cell toxicity. | |||
TN5465 |
Derrisisoflavone K
|
||
Derrisisoflavone K 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 TN5465,CAS号为 2172624-68-7。 | |||
TN3646 |
Chlorovaltrate K
|
Others | Others |
Chlorovaltrate K shows moderate cytotoxicity against lung adenocarcinoma (A 549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8) and hepatoma (Bel 7402) cell lines with IC50 values of 0.89-9.76 uM. | |||
T15638 |
K-252c
|
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
K-252c is a staurosporine analog isolated from Nocardiopsis sp. and is a cell-permeable PKC inhibitor (IC50: 2.45 μM). K-252c also inhibits β-lactamase, chymotrypsin, and malate dehydrogenase. K-252c causes apoptosis in human chronic myelogenous leukemia cancer cells. | |||
TN4362 | k-Strophanthoside | Others | Others |
k-Strophanthoside 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 TN4362,CAS号为 33279-57-1。 | |||
TN4589 |
Mulberrofuran K
|
Others | Others |
Mulberrofuran K shows potent anti-oxidation activities. | |||
TN3971 |
Epimedin K
|
Others | Others |
Epimedin K is a natural product from Epimedium koreanum NAKAI (Berberidaceae). | |||
TN5846 |
Mumeose K
|
||
Mumeose K 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 TN5846,CAS号为 2132384-01-9。 | |||
T25563 |
K 41
K-41,K41,Antibiotic K-41A,37454 RP,Antibiotic A 32887 |
||
K 41 is a polycyclic polyether antibiotic from Streptomyces hygroscopicus. | |||
T15637 |
K-252b
|
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
K-252b is an indolocarbazole isolated from the actinomycete Nocardiopsis and is a PKC inhibitor. K-252b can be used to inhibit extracellular kinases of cells in culture because it can’t pass through the cell membrane freely. | |||
TN4805 |
Platycoside K
|
Others | Others |
Platycoside K 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 TN4805,CAS号为 899447-64-4。 | |||
TN3105 |
5-Dehydroxyparatocarpin K
|
Others | Others |
5-Dehydroxyparatocarpin K是一种天然产物,属于豆科补骨脂属,其产品编号为 TN3105,CAS号为 124858-37-3。5-Dehydroxyparatocarpin K可用作对照参考。 | |||
T15636 |
K-252a
Antibiotic K 252a,Antibiotic SF 2370,SF2370 |
Others | Others |
K-252a is a staurosporine analog isolated from Nocardiopsis sp. soil fungi. K-252a inhibits protein kinase (IC50: 470 nM, 140 nM, 270 nM, and 1.7 nM for PKC, PKA, Ca2+/calmodulin-dependent kinase type II, and phosphorylase kinase, respectively). | |||
TN4103 |
Ganoderic acid K
|
||
Ganoderic acid K is an angiotensin-converting enzyme inhibitor. It has anti-tumor, and anti-inflammatory activities. | |||
TN1631 |
Eupalinolide K
[3AR-[3AR*,4R*(E),6E,9S*,10E,11AR*]]-4-羟基-2-甲基-2-丁烯酸 2,3,3A,4,5,8,9,11A-八氢-9-羟基-6,10-二甲基-3-亚甲基-2-氧代环癸五烯并[B]呋喃-4-基酯,野马追内酯 K,野马追内酯K |
STAT | JAK/STAT signaling; Stem Cells |
Eupalinolide K 是来自野马追的一种倍半萜内酯,是 STAT3抑制剂,可作为迈克尔反应受体。 | |||
TN1763 |
Ilexsaponin B3
冬青苷K,Ilexoside K |
Others | Others |
Ilexoside K is a natural product from Ilex pubescens. | |||
T2336 |
Vitamin K2
Menatetrenone,四烯甲萘醌 |
Endogenous Metabolite | Metabolism |
Vitamin K2 (Menatetrenone) 是内源性代谢产物的一种。 | |||
T20754 |
Deltamethrin
Butoss,RU-22974,Esbecythrin,溴氰菊酯,K-Othrin,Decamethrin,RU 22974 |
Others | Others |
Deltamethrin (RU 22974) 是一种具有神经毒性的拟除虫菊酯杀虫剂,在大鼠中能够产生一系列可逆的运动症状(如包括后肢僵硬、舞蹈性关节炎)。 | |||
T1719 |
Bufalin
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ATPase | Membrane transporter/Ion channel |
Bufalin 是蟾酥中的一种成分,是Na+/K+-ATPase 抑制剂,具有抗肿瘤活性,可与其基 α1、α2 和 α3 结合,Kd 值分别为 42.5、45 和 40 nM。 | |||
T2913 |
Schisantherin A
五味子酯甲,Schisanwilsonin H,Gomisin-C,Wuweizi ester-A,Schizantherin-A,Arisanschinin K |
NF-κB | NF-κB |
Schisantherin A (Wuweizi ester-A) 是一种利用 IκBα 降解,抑制p65-NF-κB 易位进入细胞核的木脂素。 | |||
T41124 |
Kizuta saponin K11
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Kizuta saponin K11 is a saponin derived from Kalopanax pictum var. maximowiczii leaves, which is a widely used Korean medicinal plant. | |||
T20198 |
Potassium gluconate
Kalium-beta,Kalium Gluconate,Kaon elixir,Kaon,Potassium D-gluconate,HSDB 3165,K-Iao |
Endogenous Metabolite; Antifungal | Metabolism; Microbiology/Virology |
Potassium gluconate (Potassium D-gluconate) 是一种具有口服活性和螯合性质的氧化型羧酸,具有杀菌活性。 | |||
T1075 |
Vitamin K1
Phylloquinone,维生素K1,叶绿醌,Phytomenadione,Phytonadione,Phyllohydroquinone |
Others; Endogenous Metabolite | Metabolism; Others |
Vitamin K1 (Phylloquinone)是天然存在的维生素。Vitamin K1是血液凝固,骨和血管代谢所必须的。 | |||
T4898 |
Potassium 1-carboxyvinyl hydrogenphosphate
PEP-K,磷酸烯醇丙酮酸单钾盐,Phospho(enol)pyruvic acid monopotassium |
Others; Endogenous Metabolite | Metabolism; Others |
Potassium 1-carboxyvinyl hydrogenphosphate (PEP-K) 是内源性代谢产物的一种。 | |||
T7106 |
Menaquinone-4
四烯甲萘醌,Vitamin K2,Menaquinone K4 |
Others; Endogenous Metabolite | Metabolism; Others |
Menaquinone-4 (Vitamin K2) 是维生素 K 的一种,用作止血剂,有潜力用于骨质疏松的研究。 | |||
TJP2872 |
Acevaltrate
Acevaltratum,乙酰缬草三酯,Acetoxyvaltrate |
ATPase; Others | Membrane transporter/Ion channel; Others |
Acevaltrate (Acevaltratum) 对人小细胞肺癌细胞系 GLC(4) 和人结肠直肠癌细胞系 COLO 320 具有高细胞毒性,IC50 值为 1-6 uM。它抑制大鼠肾和脑半球中 Na+/K+-ATP 酶活性,IC50分别为 22.8 和 42.3 μM。 | |||
T7050 |
alpha-Tocopherolquinone
托可醌,Metarene |
Antioxidant | oxidation-reduction |
alpha-Tocopherolquinone (Metarene) 会下调线粒体的呼吸活动。在还原为生育酚氢醌后,它还显示出抗氧化活性。在大鼠缺氧期间,已发现它的水平升高。 | |||
T83110 |
Angulatin K
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Angulatin K为Celastrus angulatus根皮中发现的天然倍半萜多元醇酯。 | |||
T75480 | Guignardone K | ||
Guignardone K,一种二萜化合物,从内生真菌(Guignardia sp.)的固体培养物中分离出来,具有抗真菌活性。 | |||
T79936 |
Forrestiacids K
|
ATP Citrate Lyase | Metabolism |
Forrestiacids K, 萜类化合物,源自Pseudotsuga forrestii,作为ATP-citrate lyase (ACL) 的抑制剂。 | |||
T81972 |
Kuwanon K
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Kuwanon K为从Morus Lhou分离得到的天然化合物。 | |||
T81302 |
Regaloside K
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Regaloside K (Compd 1) 是从Easter Lily (Lilium longiflorum Thunb.) 提取的天然化合物。 | |||
T82629 |
Cytochalasin K
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Cytochalasin K (化合物7) 是一种IC50为22.58 μM的细胞松弛素,能抑制小麦根系伸长。 | |||
T37709 |
2,2,2-Trichloroethanol
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Potassium Channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism |
2,2,2-Trichloroethanol 是非经典的 K2P 通道 TREK-1和 TRAAK 的激动剂。 | |||
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