163
49
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11254 |
F-1
|
ROS; ALK; ROS Kinase | Angiogenesis; Immunology/Inflammation; Tyrosine Kinase/Adaptors |
F-1 是 ALK 和 ROS1 的双重抑制剂,抑制 ALK 的磷酸化及下游通路,可作用于对 ALKWT (IC50:2.1 nM),ROS1WT (IC50:2.3 nM),ALKL1196M (IC50:1.3 nM) 和 ALKG1202R (IC50:3.9 nM)。 | |||
T19840 |
GSK-F1
PI4KA inhibitor-F1 |
PI4K | PI3K/Akt/mTOR signaling |
GSK-F1 (PI4KA inhibitor-F1) 是一种新型强效 PI4KA 抑制剂。 | |||
T67837 |
(3S)-GSK-F1
PI4KA inhibitor-F1 |
PI4K | PI3K/Akt/mTOR signaling |
(3S)-GSK-F1是一种选择性PI4KIIIα抑制剂,pIC50=8.3。 | |||
T62204 |
NR2F6 modulator-1
|
Others | Others |
NR2F6 modulator-1 是一种核受体亚族 2,F 组第 6 号成员 (NR2F6) 的有效调节剂。NR2F6 modulator-1 能够用于研究免疫调节和肿瘤干细胞活性的调节。 | |||
T30665 |
C.I. Direct Red 1, disodium salt
Japanol Fast Red 1,COLUMBIA FAST RED F,Chrome Fast Red F,Neonyl Red 2B,Enianil Fast Red F |
||
C.I. Direct Red 1, disodium salt is a dye. | |||
T34652 |
SK&F 39728-A
SK&F39728-A,SK&F 1-39728,SK&F-39728-A,Skf 39728-A |
||
SK&F 39728-A is a bioactive chemical. | |||
T72501 |
CYP4A11/CYP4F2-IN-1
|
P450 | Metabolism |
CYP4A11/CYP4F2-IN-1 是一种高效的小分子细胞色素 P450 (CYP) 4A11 和 CYP4F2 抑制剂,对P450 (CYP) 4A11 的 IC50 值为 19 nM,对 CYP4F2 的 IC50 值为 17 nM。CYP4A11/CYP4F2-IN-1 可用于研究肾脏疾病和心脑血管疾病。 | |||
T19688 |
Lodenosine
FddA,3'-dideoxyarabinosyladenine,Fddl,2'-F-dd-ara-A,2'-Fluoro-2',DDG-1 |
||
Lodenosine is an inhibitor of RNA-directed DNA polymerase, and potentially for the treatment of HIV. | |||
T37919 |
Prostaglandin F1α
PGF1α,Prostaglandin F1α |
||
Prostaglandin F1α (PGF1α) is the putative metabolite of dihomo-γ-linolenic acid (DGLA) via the cyclooxygenase (COX) pathway. Both PGF1α and PGF2α have been shown to act as priming pheromones for male Atlantic salmon with a threshold concentration of 10-11 M. [1] PGF1α binds to the ovine corpus luteum FP receptor at only 8% of the relative potency of PGF2α. [2] It is only half as active as PGF2α in inducing human respiratory smooth muscle contractions in vitro. [3] | |||
T19618 |
(R)-(-)-JQ1 Enantiomer
(R)-(-)2-(4-(4-氯苯基)-2,3,9-三甲基-6H-噻吩并[3,2-F][1,2,4]三唑并[4,3-A][1,4]二氮杂环庚烷-6-基)乙酸叔丁酯 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
(R)-(-)-JQ1 Enantiomer 是 (+)-JQ1 的立体异构体。 (+)-JQ1 是一种 BET 溴结构域抑制剂,对BRD4(1/2)的IC50 为 77 和 33 nM。 | |||
TP2476 |
Tnrnflrfamide
Thr-asn-arg-asn-phe-leu-arg-phe-NH2,Peptide F(1), lobster,F1 Peptide, lobster,Lobster peptide F1 |
||
Tnrnflrfamide is a SCP (small cardioactive peptide)-like peptide found in lobster neurons; exhibits FMRFamide-like immunoreactivity. | |||
T79199 |
F-CRI1
|
STING | Immunology/Inflammation |
F-CRI1为高效STING激动剂,Kd值达40.62 nM。该化合物通过18F标记成为放射性探针,适用于肿瘤微环境中STING可视化的研究。 | |||
T126048 |
Coreanoside F1
|
||
Coreanoside F1 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 T126048,CAS号为 132282-69-0。 | |||
T39606 | CE3F4 analog 1 | ||
CE3F4 analog 1 is an analogue of CE3F4. | |||
T125155 | Schidigerasaponin F1 | ||
Schidigerasaponin F1 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 T125155,CAS号为 266998-42-9。 | |||
T36771 |
11-deoxy Prostaglandin F1α
11-deoxy Prostaglandin F1α |
||
11-deoxy PGF1α is a synthetic analog of PGF1α. In whole animal studies, a dose of 32 mg/kg inhibited gastric acid secretion by 35%. 11-deoxy PGF1α is also known to cause rat uterine contractions at a dose 0.3 times that of PGF1α. It also exhibits vasopressor and bronchoconstrictor activities at about half the potency of PGF2α in guinea pigs. | |||
T36162 |
8-iso Prostaglandin F1α
8-iso Prostaglandin F1α |
||
8-iso PGF1α is an isoprostane that was first identified in human semen. It is a member of the isoprostane family, which are eicosanoids of non-cyclooxygenase origin. 8-iso PGF1α is present along with its 19-hydroxy congener at 5-10 μg/ml of seminal plasma. | |||
T65682 | 11-(1-Piperazinyl)-dibenzo[b,f][1,4]thiazepine dihydrochloride | ||
11-(1-Piperazinyl)-dibenzo[b,f][1,4]thiazepine dihydrochloride 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 T65682,CAS号为 111974-74-4。 | |||
T83670 |
F1 TFA
Tat-IKIP (46-60),Tat-Inhibitor of NF-κB Kinase-interacting Peptide |
||
F1是一种抗炎肽,由HIV-1 Tat蛋白质转导域与对应于抑制因子NF-κB激酶-相互作用肽(IKIP)46-60残基的15氨基酸肽链接而成。在5 µM浓度下,F1抑制了小鼠腹腔巨噬细胞中LPS诱导的IκB激酶α(IKKα)和IKKβ的磷酸化以及NF-κB(p65)的核内转移。在体内,F1(5 mg/kg)降低了LPS诱导的脓毒症小鼠模型中IL-6、TNF-α和IL-1β的血清水平,并增加了生存率。 | |||
T36163 |
8-iso Prostaglandin F1β
8-iso Prostaglandin F1β |
||
8-iso PGF1β is a potential autoxidation product of DGLA. There are no published reports on its isolation from any biological source or on its biological activity. | |||
T36772 |
11-deoxy Prostaglandin F1β
11-deoxy Prostaglandin F1β |
||
11-deoxy PGF1β is a synthetic analog of PGF1β. In contrast to PGF2α and PGF1α, 11-deoxy PGF1β exhibits vasodepressor and bronchodilator activities in guinea pigs at a dose of 500 μg/kg. | |||
T125598 |
F 11334A1
|
||
T37990 |
15-keto Prostaglandin F1α
15-keto Prostaglandin F1α |
||
15-keto PGF1α is the initial metabolite of PGF1α via 15-hydroxy PGDH. In mammals, oxidation of C-15 markedly attenuates receptor binding and activity. In fish, the 15-keto compounds serve as post-ovulatory pheromones and are more active than the parent prostaglandins. | |||
T72776 |
NR2F1 agonist 1
|
||
NR2F1 agonist 1 是一种核受体 NR2F1激动剂,可特异性激活恶性细胞的休眠程序。NR2F1 agonist 1 上调 NR2F1 和调节休眠的下游靶基因。NR2F1 agonist 1 通过 NR2F1 激活在头颈部鳞状细胞癌 (HNSCC) 中诱导神经嵴样生长抑制。NR2F1 agonist 1 在小鼠原发肿瘤模型中抑制肿瘤生长。 | |||
T69659 |
MC-1-F2
|
||
MC-1-F2 is the first inhibitor of forkhead Box Protein C2 (FOXC2). | |||
T37327 |
Prostaglandin F2α 1,15-lactone
Prostaglandin F2α 1,15-lactone |
||
PGF2α 1,15-lactone is a lipid-soluble internal ester of PGF2α. Hydrolysis of the lactone readily produces free PGF2α in plasma. In rhesus monkeys, a total dose of 15 mg of PGF2α 1,15-lactone terminates early pregnancy, whereas PGF2α is ineffective. | |||
T70074 |
SB1-F-21
|
||
SB1-F-21 is an UCHL1 inhibitor. | |||
T64437 | 5-(11bR)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl-5H-dibenz[b,f]azepine | ||
5-(11bR)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl-5H-dibenz[b,f]azepine 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 T64437。 | |||
T69947 |
SB1-F-78
|
||
SB1-F-78 is an USP30 inhibitor. | |||
T65991 | (S)-4-Phenoxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine | ||
(S)-4-Phenoxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 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 T65991。 | |||
T65992 | (R)-4-Phenoxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine | ||
(R)-4-Phenoxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 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 T65992。 | |||
T36148 |
13,14-dihydro-15-keto Prostaglandin F1α
13,14-dihydro-15-keto Prostaglandin F1α |
||
13,14-dihydro-15-keto Prostaglandin F1α (13,14-dihydro-15-keto PGF1α) is a metabolite of PGF1α that has been reported in the rat stomach. The measurement of 13,14-dihydro-15-keto PGF1α can be used as a marker of the in vivo production of PGF1α. | |||
T36724 |
6,15-diketo-13,14-dihydro Prostaglandin F1α
6,15-diketo-13,14-dihydro Prostaglandin F1α |
||
6,15-diketo-13,14-dihydro PGF1α is a metabolite of PGI2. It was shown to enhance intracellular cAMP and cholesterol catabolism in bovine arterial smooth muscle cells. | |||
T83662 |
2,3-dinor-8-iso Prostaglandin F1α
2,3-dinor-8-iso PGF1α,2,3-dinor-iPF1α-III,2,3-dinor-5,6-dihydro-15-F2t-Isoprostane,2,3-dinor-5,6-dihydro-15-F2t-IsoP |
||
2,3-dinor-8-iso Prostaglandin F1α(2,3-dinor-8-iso PGF1α)是一种异前列腺素和花生四烯酸的活性代谢物,也是血小板聚集抑制剂8-iso PGF2α的产物。它通过花生四烯酸的非酶促自由基过氧化作用形成。2,3-dinor-8-iso PGF1α在孤立的猪视网膜和大脑微血管中引起血管收缩(EC50s分别为12.8和18.5 nM),但在31 µM的浓度下使用时不会引起孤立的大鼠主动脉环的收缩。在1 µM的浓度下使用时,它能增加孤立的猪大脑切片中的血栓素B2(TXB2)水平,这一效应可以通过血栓素A合成酶抑制剂CGS 12970、电压门控钙通道抑制剂SKF 96365或烟碱型乙酰胆碱受体(nAChR)拮抗剂α-conotoxin来逆转。 | |||
T67397 | (11aS)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine | ||
(11aS)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine 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 T67397。 | |||
T67396 |
(11aR)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine
|
||
(11aR)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine 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 T67396。 | |||
T78341 |
Human IgG1 (F405L) kappa, Isotype Control
|
||
HumanIgG1(F405L) kappa, Isotype Control为人-鼠嵌合型单克隆抗体,作为HumanIgG1(F405L)κ抗体的同型对照使用。 | |||
T65432 |
10,11-Dihydro-11-oxodibenzo[b,f][1,4]thiazepine
|
||
10,11-Dihydro-11-oxodibenzo[b,f][1,4]thiazepine 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 T65432,CAS号为 3159-07-7。 | |||
T65416 |
Pyrrolo[2,1-f][1,2,4]triazin-4-amine
|
||
Pyrrolo[2,1-f][1,2,4]triazin-4-amine 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 T65416,CAS号为 159326-68-8。 | |||
T78270 |
Anti-Mouse PD-L1 Antibody (10F.9G2)
|
PD-1/PD-L1 | Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation |
Anti-MousePD-L1Antibody为针对小鼠PD-L1的IgG2b类免疫抗体,起源宿主为大鼠(Rat)。 | |||
T64639 | (11AS)-5-(4,5,6,7-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-yl)-5H-dibenzo[b,f]azepine | ||
(11AS)-5-(4,5,6,7-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-yl)-5H-dibenzo[b,f]azepine 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 T64639。 | |||
T64496 | 7-Iodopyrrolo[2,1-f][1,2,4]triazin-4-amine | ||
7-Iodopyrrolo[2,1-f][1,2,4]triazin-4-amine 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 T64496,CAS号为 1770840-43-1。 | |||
T66114 |
7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine
|
||
7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine 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 T66114,CAS号为 937046-98-5。 | |||
T64513 |
(11aR)-5-(4,5,6,7-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-yl)-5H-dibenzo[b,f]azepine
|
||
(11aR)-5-(4,5,6,7-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-yl)-5H-dibenzo[b,f]azepine 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 T64513。 | |||
T64587 | p44/42 MAPK (Erk1/2) (137F5) Rabbit mAb #4695R | ||
p44/42 MAPK (Erk1/2) (137F5) Rabbit mAb #4695R 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 T64587。 | |||
T65901 |
3-Chloro-6,11-dihydro-6-methyl-5,5,11-trioxodibenzo[c,f][1,2]thiazepine
|
||
3-Chloro-6,11-dihydro-6-methyl-5,5,11-trioxodibenzo[c,f][1,2]thiazepine 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 T65901,CAS号为 26638-53-9。 | |||
T66942 |
Ethyl 8-hydroxy-5-methyl-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-3-carboxylate
|
||
Ethyl 8-hydroxy-5-methyl-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-3-carboxylate 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 T66942,CAS号为 131666-45-0。 | |||
T64635 | 8-Phenyl-2,6-diethyl-BODIPY 505/515 | ||
2,8-Diethyl-5,5-difluoro-1,3,7,9-tetramethyl-10-phenyl-5H-4l4,5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinine 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 T64635。 | |||
T67388 | N-(1-((6aR,8R,9aR)-9-Cyano-9-hydroxy-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide | ||
N-(1-((6aR,8R,9aR)-9-Cyano-9-hydroxy-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide 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 T67388。 | |||
T67601 |
(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxohexadecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid
|
||
(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxohexadecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid 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 T67601,CAS号为 103335-55-3。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3401 |
Ginsenoside F1
人参皂苷 F1,20(S)-Ginsenoside F1 |
P450; Endogenous Metabolite | Metabolism |
Ginsenoside F1 (20(S)-Ginsenoside F1) 是一种 Ginsenoside Rg1 的酶促修饰衍生物,它竞争性抑制CYP3A4,对 CYP2D6 具有较弱的抑制作用。 | |||
T5S2139 |
Epimedin A1
朝藿定A1,Hexandraside F |
Others | Others |
Epimedin A1 (Hexandraside F) 是一种黄酮类化合物,从常用中药淫羊藿中提取得到。 | |||
T8716 |
physalin F
酸浆苦味素F,酸浆苦素 F |
Apoptosis | Apoptosis |
Physalin F 是一种分泌型甾体,诱导人外周血单个核细胞凋亡,降低人 T 淋巴细胞 1 型病毒感染后的自发增殖和细胞因子的产生,具有强烈抗炎和免疫调节作用。 | |||
TN4161 |
Goshonoside F1
|
||
Goshonoside F1是半糯米品种水稻的脂质代谢产物,可被当作培育优良水稻的一个指标。 | |||
TN1942 |
Momordicoside F1
苦瓜皂苷 F1 |
Others | Others |
Momordicoside F1 may have antiproliferative activities against MCF-7, WiDr, HEp-2, and Doay human tumor cell lines. | |||
T3920 |
Pseudoginsenoside F11
Ginsenoside A1,拟人参皂苷 F11,拟人参皂苷F11 |
Others; Endogenous Metabolite | Metabolism; Others |
Pseudoginsenoside F11 (Ginsenoside A1) 从人参根和叶中分离得到。PF11在一系列心血管和中枢神经系统疾病中具有广泛的保护作用。 | |||
TN1989 |
Niga-ichigoside F1
苦莓苷F1 |
Others; Nrf2 | Immunology/Inflammation; Others |
Niga-ichigoside F1(NI) has anti-inflammatory, gastroprotective ,antinociceptive, and cytotoxic effects. | |||
TN2341 |
Cucurbitacin Q1
葫芦素F-25-乙酸酯,葫芦素Q1 |
Others | Others |
Cucurbitacin Q1 是一种天然的四环三萜,来源于Cucumis prophetarum。 | |||
TN6864 |
Prosaikogenin F
(2R,3R,4S,5R,6R)-2-{[(1S,2R,4S,5R,8R,9S,10R,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-en-10-yl]oxy}-6-methyloxane-3,4,5-triol,前柴胡皂苷F |
Others | Others |
Prosaikogenin F ((2R,3R,4S,5R,6R)-2-{[(1S,2R,4S,5R,8R,9S,10R,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-en-10-yl]oxy}-6-methyloxane-3,4,5-triol) 是一种单糖苷,具有溶血和抗癌特性。 | |||
TN2119 |
Pulsatilla saponin H
白头翁属皂苷H,白头翁皂苷 H,3-O-Β-D-葡萄糖( 1→4)-[ A -L-鼠李糖(1→2)]- A-L-阿拉伯糖 常春藤配基- 28-O-鼠李糖(1→4)葡萄糖(1→6)葡萄糖苷 |
Others | Others |
Pulsatilla saponin H 是一种从 Pulsatilla koreana 的根中分离出来的天然产物。 | |||
TN1080 |
Kaji-ichigoside F1
蔷薇苷 |
||
Kaji-ichigoside F1 shows antiinflammatory/antinociceptive action in acetic acid-induced writhing and hot plate testing and in a carrageenan-induced paw edema model in mice and rats. Kaji-ichigoside F1 exhibits in vivo hepatoprotective effects, it inhibite | |||
TN6859 |
Saikogenin F
(1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-ene-2,10-diol |
Others | Others |
Saikogenin F ((1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-ene-2,10-diol) 是一种具有抗癌活性的天然产物。 | |||
T81853 |
Marstenacisside F1
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Marstenacisside F1(化合物1)为从通关藤(Marsdenia tenacissima)分离的抗炎聚氧孕烷苷,能抑制脂多糖激活的RAW 264.7细胞产生一氧化氮(NO),属Tenacigenin B衍生物。 | |||
TMA2270 |
Alisol F 24-acetate
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P-gp | Membrane transporter/Ion channel; Neuroscience |
Alisol F 24-acetate 是一种从 Alisma plantago-aquatica Linn [1] 中分离出来的天然产物。 Alisol F 24 Acetate 通过抑制 P-糖蛋白介导的药物流出来增强 MCF-7/DOX 细胞的化学敏感性和凋亡。 | |||
T2S0491 |
Isoeugenol acetate
乙酸异丁香酚酯,Isoeugenyl acetate,Acetisoeugenol,Acetylisoeugenol,乙酸异丁香酚酯,乙酰基异丁香酚;2-甲氧基-4-丙烯基苯基乙酸酯 |
AChE; Antifungal | Microbiology/Virology; Neuroscience |
Isoeugenol acetate (Acetylisoeugenol) 是肉豆蔻,丁香和肉桂的精油成分,对某些代谢酶如乙酰胆碱酯酶,能够抑制α-糖苷酶和 α-淀粉酶。它用于医疗和化妆品工业,具有抗氧化,抗癌,抗菌和抗炎作用。 | |||
T5S1054 |
Wilforgine
雷公藤晋碱,雷公藤精碱 |
Others | Others |
Wilforgine 是一种具有生物活性的倍半萜烯生物碱,存在于Tripterygium wilfordiiHook. F 中。它能诱导分离出丝状体幼虫肌肉的微结构和超微结构变化,其作用部位被认为是肌肉系统中的钙受体或通道。 | |||
T4S0498 |
Glaucocalyxin A
蓝萼甲素,Wangzaozin B,Leukamenin F |
Apoptosis; Akt; Caspase; PI3K | Apoptosis; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Glaucocalyxin A (Leukamenin F) 是来自日本黑纹病菌的一种对映型月桂基二萜,具有抗肿瘤作用。它通过调节PI3K/Akt 信号通路抑制 GLI1 的核易位,诱导骨肉瘤凋亡。 | |||
T36914 |
2-Hydroxyanthraquinone
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Others | Others |
2-Hydroxyanthraquinone 是一种天然产物,显示出抗肿瘤和免疫抑制活性。 | |||
T3S0027 |
Picropodophyllotoxin
AXL 1717,Picropodophyllin,苦鬼臼毒素 |
IGF-1R | Tyrosine Kinase/Adaptors |
Picropodophyllotoxin (AXL 1717) 是一种环木脂素生物碱,存在于五月树(Podophyllum peltatum) 中,是一种具有潜在抗肿瘤活性的胰岛素样生长因子 1 受体 (IGF1R) 的小分子抑制剂。它特异性抑制 IGF1R 的活性并下调细胞表达,而不干扰其他生长因子受体的活性,例如胰岛素受体、表皮生长因子、血小板衍生生长因子、成纤维细胞生长因子和肥大/干细胞生长因子 (KIT) )。该药剂在抑制肿瘤细胞增殖和诱导肿瘤细胞凋亡方面显示出有效的活性。 IGF1R 是一种在多种人类癌症中过度表达的受体酪氨酸激酶,在多种癌细胞的生长和存活中起关键作用。 | |||
T75654 | F-14329 | ||
F-14329 是一种四元酸真菌代谢物。 | |||
T80864 | Virgaureagenin F | ||
Virgaureagenin F, 一种从Rhizoma bolbostemmae中提取的皂苷。 | |||
T83216 |
Abiesadine F
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Abiesadine F为从Abies georgei Orr分离出的一种二萜化合物。 | |||
T83107 |
Anhuienside F
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Anhuienside F,一种从Anemone vitifolia Buch.-Ham根部提取的天然化合物。 | |||
T82399 |
Fipsomin
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Fipsomin为从F. nipponica果实中提取的天然化合物。 | |||
TN4411 |
Lappaol F
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CDK; P-gp; JNK | Cell Cycle/Checkpoint; MAPK; Membrane transporter/Ion channel; Neuroscience |
1. Lappaol F has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. <br/> 2. Lappaol F has potential chemosensitizing activity, it may be candidates for developing novel adju | |||
T79992 |
Sarglaroids F
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Caspase | Apoptosis; Proteases/Proteasome |
Sarglaroids F(化合物6)为从草珊瑚根部提取的抗炎剂,影响K+外排并降低Caspase-1(P20)水平以抑制LPS/ATP诱导的IL-1β释放,对RAW264.7细胞无细胞毒性。 | |||
T81093 | Sterebin F | ||
Sterebin F, 一种甾类化合物,来源于Stevia rebaudiana叶的分离提取,表现出降血糖的活性。 | |||
T82738 |
Chisocheton compound F
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Chisocheton compound F,一种从Melia toosendan茎皮中分离的天然产物。 | |||
TMA0593 | Broussoflavonol F | Tyrosinase | Proteases/Proteasome |
Broussoflavonol F has antiplatelet effect, is partially due to an inhibitory effect on cyclooxygenase, can inhibit arachidonic acid (AA)-induced platelet aggregation. Broussoflavonol F shows inhibitory activities on mushroom tyrosinase. Broussoflavonol F | |||
T83565 | (2E)-Leocarpinolide F | ||
(2E)-Leocarpinolide F(化合物20),为从Sigesbeckia orientalis中提取的香叶鹤型倍半萜。 | |||
TN6249 | (+)-Isoampelopsin F | ||
(+)-Isoampelopsin 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 TN6249,CAS号为 354553-38-1。 | |||
TN5988 |
16,25-Di-O-acetylcucurbitacin F
16,25-O-Diacetyl-cucurbitane F,Cucurbitacin F 16,25-diacetate |
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16,25-Di-O-acetylcucurbitacin 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 TN5988,CAS号为 2062685-10-1。 | |||
T83108 |
Anhuienoside B
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Anhuienoside B为从C. anhuiensis K. F. Wu鲜叶中提取的天然产物,能应对CuCl2诱导的非生物胁迫。 | |||
T80941 | Triptonoterpene Me ether | ||
Triptonoterpene Me ether(compound 5)为一种从中药雷公藤(Tripterygium wilfordii Hook. f.)分离出的松香烷型二萜类化合物。 | |||
T81941 | Leocarpinolide F | ||
Leocarpinolide F,一天然提取自Siegesbeckia orientalis的类倍半萜烯。 | |||
T82338 |
Ganoapplanoid F
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Ganoapplanoid F,一种三萜类化合物,源自Ganoderma applanatum,具有抑制脂肪细胞脂质积累的功能,适用于肥胖研究领域。 | |||
TN4977 | Scutebata F | Others | Others |
Scutebata 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 TN4977,CAS号为 1207181-62-1。 | |||
T79937 |
Mortatarin F
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Glucosidase | Metabolism |
Mortatarin F (Compound 1) 是一种具有戊烯基化类黄酮结构的葡萄糖苷酶抑制剂,其IC50值为8.7 μΜ。该化合物可从桑叶中提取,并应用于研究降低血糖效果。 | |||
T82067 |
Inonotusol F
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Inonotusol F, 一种三萜化合物,可在Inonotus obliquus中分离出。该化合物对D-半乳糖胺诱导的WB-F344细胞损伤显示出保肝效应。 | |||
T80002 |
Wulfenioidin F
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Virus Protease | Microbiology/Virology |
Wulfenioidin F是从Orthosiphon wulfenioides全草分离的二萜类化合物。该化合物对抗寨卡病毒(ZIKV)活性显著,其半数有效浓度(EC50)为8.07 μM。Wulfenioidin F的抗病毒机制通过抑制ZIKV包膜(E)蛋白的表达,从而干扰病毒复制。 | |||
T82459 |
Epicornuin F
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Epicornuin F,一种源自Epimedium brevicornu叶片的异戊二烯黄酮化合物,展现了对HepG2细胞线的显著细胞毒性,IC50为33.4 μM,适用于癌症研究领域。 | |||
T82986 |
Apigenin triacetate
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Apigenin triacetate, 作为禾谷镰刀菌的代谢产物,其含量可通过壳聚糖处理以实现下调。该化合物系由芹菜素派生。 | |||
T83479 |
1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-3,11-dioxanaphth[2,1-e]azulene-10,12-dione
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1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-3,11-dioxanaphth[2,1-e]azulene-10,12-dione 是一种从丹参酮 (Salvia miltiorrhiza f. alba) 中提取的化学物质,具有二氢异丹参酮结构,显示出细胞毒性和抗肿瘤的活性。 | |||
TMA1012 |
Ganoderiol F
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Androgen Receptor; HIV Protease; Autophagy | Autophagy; Endocrinology/Hormones; Microbiology/Virology; Proteases/Proteasome |
Ganoderiol F has anti-inflammatory, cytotoxic and anti-HIV activity, it inhibits activity of topoisomerases in vitro, and it inhibits human immunodeficiency virus-1 protease with IC(50) values of 20-40 microM. It induced HO-1 expression, activation of the mitogen-activated protein kinase EKR and up-regulation of cyclin-dependent kinase inhibitor p16 and suppressed lipopolysaccharide (LPS)-induced nitric oxide (NO) production. | |||
T81676 |
NG-012
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NG-012为一种神经生长因子(NGF)增强剂,来源于Penicillium verruculosum F-4542的培养液。该化合物能在大鼠嗜铬细胞瘤细胞系(PC12)中提升NGF引导的神经突生长效应。 | |||
T81531 |
Pedunculosumoside F
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Pedunculosumoside F,一种从Ophioglossum pedunculosum分离得到的同型黄酮苷,对HepG2 2.2.15细胞表现出细胞毒性,其CC50值为56.7 μM,但缺乏抗HBV活性。然而,其类似物能够抑制HBV感染的HepG2 2.2.15细胞中HBsAg的分泌。 | |||
T75540 |
Ipomoeassin F
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Ipomoeassin F 是一种高效且具有选择性的内质网(ER)蛋白转位抑制剂,它通过作用于ER膜上的Sec61复合物(Sec61α)的成孔亚基来实现其功能。此化合物能特异性抑制SARS-CoV-2蛋白在ER膜上的转位,同时阻碍分泌蛋白和I型跨膜蛋白(TMP)的ER转运,但对III型TMP的转运不产生影响。 | |||
T36000 |
3-Hydroxyterphenyllin
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3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi... | |||
T36954 |
Nemorosone
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Nemorosone is a polycyclic polyprenylated acylphloroglucinol (PPAP) originally isolated from C. rosea that has antiproliferative properties.1 Nemorosone inhibits growth of NB69, Kelly, SK-N-AS, and LAN-1 neuroblastoma cells (IC50s = 3.1-6.3 μM), including several drug-resistant clones, but not MRC-5 human embryonic fibroblasts (IC50 = >40 μM).2 It increases DNA fragmentation in LAN-1 cells in a dose-dependent manner, and decreases N-Myc protein levels and phosphorylation of ERK1/2 by MEK1/2. Nem... |