22
472
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20366 |
beta-Nicotyrine
bata-碱二烯,Nicotyrine,alpha-Nicotyrine |
Others | Others |
beta-Nicotyrine 是一种 Nicotine 的代谢物。它是一种微量的烟草生物碱,提取自普通烟草植物的叶子和香烟烟雾冷凝物。 | |||
T1366 |
3-Pyridylacetic acid hydrochloride
|
DPP-4 | Proteases/Proteasome |
3-Pyridylacetic acid hydrochloride (3-PAA-HCl)尼克酸的高同系物,是尼古丁(和其它烟草生物碱)的分解产物,还可与胺、醇和羧酸等反应,也可在反应中作为酸催化剂。 | |||
T1006 |
Propantheline bromide
Neopepulsan,溴丙胺太林,Pro-Banthine,Neometantyl |
AChR | Neuroscience |
Propantheline bromide (Pro-Banthine) 是一种抗毒蕈碱剂,用于研究多汗症,遗尿,胃肠和膀胱痉挛。 | |||
T11151 |
Ecteinascidin-Analog-1
|
Others | Others |
Ecteinascidins is a family of tetrahydroisoquinoline alkaloids with wide range of antitumor and antimicrobial activities. Ecteinascidin-Analog-1 is a useful intermediate for chemical sythesis of Ecteinascidin analogues. | |||
T74146 |
Ecubectedin
|
||
Ecubectedin (PM14), 作为一种海鞘素衍生物,属于四氢异喹啉类生物碱,展现出广泛的抗肿瘤及抗菌活性。 | |||
T35354 |
BSTFA-TMCS
|
Others | Others |
The combination of BSTFA and TMCS is the preferred reagent for trimethylsilylation of alcohols, alkaloids, amines, biogenic amines, carboxylic acids, phenols, and steroids. TMCS increases the reactivity of BSTFA. BSTFA-TMCS has good solvent properties and can function as a silylation reagent without additional solvents. | |||
T21094 |
Pseudopelletierine free base
NSC 116056,Granatonine,Pseudopelletierine,Granatan-3-one |
||
Pseudopelletierine is the main alkaloid derived from the root-bark of Punica granatum, along with at least three other alkaloids: isopelletierine, methylpelleteirine (C9H17ON) and pelletierine, which yield 1.8, 0.01, 0.20 and 0.52 grams per kilogram of ra | |||
T36973 |
5-Phospho-D-ribose 1-diphosphate (sodium salt hydrate)
|
||
5-Phospho-D-ribose 1-diphosphate (PRPP) is a natural intermediate involved in the pentose phosphate pathway leading to purine, pyrimidine, and histidine metabolism. It is also an intermediate in the synthesis of plant hormones, alkaloids, and other secondary metabolites from glucose. Several phosphoribosyltransferases (PRTases) use PRPP as a substrate to add a 5-phosphoribosyl group to another substrate, as in the production of adenosine monophosphate from adenine and PRPP by adenine PRTase. N/A | |||
T37037 |
Vinflunine ditartrate
|
||
Vinflunine ditartrate, a fluorinated microtubule inhibitor and member of the Vinca alkaloids family, exhibits anti-angiogenic, vascular-disrupting, and anti-metastatic properties. It presents a potential avenue for studying transitional cell carcinoma of the urothelial tract, non-small cell lung cancer, and breast carcinoma[1][2]. | |||
T36101 |
Psychotridine
|
||
Psychotridine is an alkaloid that has been found inP. forsterianaand has diverse biological activities.1,2,3It inhibits ADP-, collagen-, or thrombin-induced aggregation of washed isolated human platelets with IC50values of 1.4, 1.4, and 3.9 μM, respectively.1Psychotridine (2.5 or 5 μM) is cytotoxic to HTC rat hepatocellular carcinoma cells.2It reduces paw licking induced by capsaicin in mice when administered at doses of 0.5, 2.5, or 5 mg/kg.3 1.Beretz, A., Roth-Georger, A., Corre, G., et al.Pol... | |||
T68249 |
IRC-083927 HCl
|
||
IRC-083927 HCl is novel and potent microtubule inhibitor with potential anticancer activity. IRC-083927 inhibits the tubulin polymerization by a binding to the colchicine site. IRC-083927 inhibits in vitro cell growth of human cancer cell lines in the low nanomolar range. More interesting, it remains highly active against cell lines resistant to microtubule-interacting agents (taxanes, Vinca alkaloids, or epothilones). Chronic oral treatment with IRC-083927 (5 mg/kg) inhibits the growth of two h... | |||
T35484 |
5,7,8-Trimethoxydictamnine
|
||
5,7,8-Trimethoxydictamnine is a quinoline alkaloid that has been found inRutaceaeand has antimalarial activity.1It is active against chloroquine-sensitive and -resistant strains ofP. falciparum(IC50s =19.9 and 5.72 μg/ml, respectively). 1.Basco, L.K.M., S., Skaltsounis, A.-L., Ravvelomanantsoa, N., et al.In vitro activities of furoquinoline and acridone alkaloids against Plasmodium falciparumAntimicrob. Agents Chemother.38(5)1169-1171(1994) | |||
T70070 |
Cisapride tartrate
|
||
Cisapride tartrate is chemically related to metoclopramide, but unlike metoclopramide, it does not cross the blood-brain barrier or have antidopaminergic effects. Cisapride is a serotonin-4 (5-HT4) receptor agonist. Cisapride was indicated for the symptomatic treatment of adult patients with nocturnal heartburn due to gastroesophageal reflux disease. The Food and Drug Administration (FDA) in America stopped the marketing of cisapride as of 14th July 2000. They had received at least 341 reports o... | |||
T7026L |
Kukoamine B mesylate
|
Antioxidant | oxidation-reduction |
Kukoamine B mesylate 是从地骨皮中提取得到的新型阳离子生物碱,具有抗氧化活性,抑制 Kupffer 和 RAW 264。7 细胞中的 LPS 内化,可用于研究急性炎症和糖尿病。 | |||
T77681 |
3-Methoxy-9H-Carbazole
|
Apoptosis | Apoptosis |
3-methoxy-9H-carbazole 是一种光敏剂,是来自克劳塞纳七叶植物和克劳塞纳籼稻的天然化合物。3-methoxy-9H-carbazole具有抗乳腺癌活性,可诱导细胞凋亡。 | |||
T13303 |
Virginiamycin M1
Pristinamycin IIA,Ostreogrycin A |
Antibacterial | Microbiology/Virology |
Virginiamycin M1 (Pristinamycin IIA)是一种大环内酯肽类抗生素,是链菌素a 类抗生素的成员。 | |||
T35739 |
Evoxanthine
|
||
Evoxanthine is an alkaloid that has been found in O. renieri and has antimalarial and anticancer activities.1,2 It is active against P. falciparum with an IC50 value of 67.6 μg/ml.1 Evoxanthine decreases proliferation of nine sensitive and drug-resistant cancer cell lines (IC50s = 6.11-80.99 μM).2 |1. Khalid, S.A., Farouk, A., Geary, T.G., et al. Potential antimalarial candidates from African plants: And in vitro approach using Plasmodium falciparum. J. Ethnopharmacol. 15(2), 201-209 (1986).|2. ... | |||
T37644 |
Bengamide B
|
||
Potent inhibitor of NF-κB activation (IC50 = 85 nM); decreases IκBα phosphorylation. Attenuates LPS-induced nitric oxide production and expression of TNF-α, IL-6 and MCP. Suppresses proliferation of HeLa and HCT116 cells. Anti-inflammatory and antitumor. Hu et al (2007) Regulation of c-Src nonreceptor tyrosine kinase activity by bengamide A through inhibition of methionine aminopeptidases. Chem.Biol. 14 764 PMID:17656313 |Johnson et al (2012) Myxobacteria versus sponge-derived alkaloids: the be... | |||
T38327 |
Cryogenine
|
||
Cryogenine is an alkaloid originally isolated from H. salicifolia that has anti-inflammatory activity.1 It inhibits prostaglandin synthetase (IC50 = 424 μM). Cryogenine (100 mg/kg per day, p.o.) reduces paw edema and the mean arthritic index in a rat model of adjuvant-induced polyarthritis.2 |1. Lema, W.J., Blankenship, J.W., and Malone, M.H. Prostaglandin synthetase inhibition by alkaloids of Heimia salicifolia. J. Ethnopharmacol. 15(2), 161-167 (1986).|2. Kosersky, D.S., Brown, J.K., and Malon... | |||
T36204 |
Methylatropine (nitrate)
|
||
Methylatropine is an antagonist of muscarinic acetylcholine receptors (IC50= <0.1 nM in a radioligand binding assay using isolated porcine brain membranes) and a derivative of atropine .1,2It reduces acetylcholine-induced decreases in blood pressure in rats when administered intravenously with an ED50value of 5.5 μg/kg.2Methylatropine reduces salivation, induces mydriasis, and increases heart rate in dogs.3 1.Schmeller, T., Sporer, F., Sauerwein, M., et al.Binding of tropane alkaloids to nicotin... | |||
T37843 |
Australine (hydrochloride)
|
||
Australine is a pyrrolizidine alkaloid originally isolated fromC. australethat has enzyme inhibitory activities.1,2,3It is an inhibitor of glucoamylase (IC50= 5.8 μM) that also inhibits glucosidase I, sucrase, maltase, andA. nigerα-glucosidase (IC50s = 20, 28, 35, and 28 μM, respectively).2,3Australine is selective for these enzymes over glucosidase II, α- and β-mannosidase, and α- and β-galactosidase up to 500 μM, β-glucosidase, with only 5% inhibition at 66 μM, as well as isomaltase and trehal... | |||
T125036 |
Bocconoline
|
||
Bocconoline 是一种在 Bocconia cordata WILLD中发现的生物碱, 具有潜在的抗癌活性,可用于研究帕金森病 (PD) 。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN6792 |
O-Acetylgalanthamine
|
Others | Others |
O-Acetylgalanthamine 是一种天然产物,已在 Narcissus pseudonarcissu 的鳞茎中发现。 | |||
TN6786 |
O-Desmethyl Galanthamine
Sanguinine,O-去甲基加兰他敏 |
AChE | Neuroscience |
O-Desmethyl Galanthamine (Sanguinine) 是一种加兰他敏型生物碱,是一种乙酰胆碱酯酶 (AChE) 抑制剂,其IC50=1.83 μM。 | |||
T7450 |
1-Phenylpropane-1,2-dione
1-Phenyl-1,2-propanedione,Acetyl benzoyl,1-苯基-1,2-丙二酮 |
Others | Others |
1-Phenylpropane-1,2-dione (Acetyl benzoyl) 是麻黄素生物碱的生物合成前体,分离自从嫩麻黄中。 | |||
TN1519 |
(S)-Coclaurine
衡州乌药碱, 乌药碱,Coclaurine |
AChR | Neuroscience |
(S)-Coclaurine (Coclaurine) 是一种从 Sarcopetalum harveyanum 中分离出来的,是一种 nAChR 拮抗剂。 | |||
T8016 |
N-Methylbenzylamine
N-甲基苄胺,N-Benzylmethylamine |
Others | Others |
N-Methylbenzylamine (N-Benzylmethylamine) 是一种存在于胡萝卜中的苯基甲基胺化合物,可用作潜在的生物标记。 | |||
T32570 |
Lappaconine
20-ethyl-1,14,16-trimethoxyaconitane-4,6,8-triol,O(sup 1)-Methyllappaconidine |
Others | Others |
Lappaconine (20-ethyl-1,14,16-trimethoxyaconitane-4,6,8-triol) 衍生自去甲二萜生物碱。 | |||
TN2156 |
Rhombifoline
|
Antioxidant | oxidation-reduction |
Rhombifoline 是一种科从 Anagyrus foetida 叶茎和 Genista tenera 中分离得到的生物碱。 | |||
T5595 |
Tropine
3alpha-Tropanol,托品醇,Pseudotropine |
Others | Others |
Tropine 是一种茄科植物的次生代谢产物,是抗胆碱能试剂。它是一种常见的用于合成各种生物活性生物碱(如 hyoscyamine、scopolamine)的中间体。 | |||
T67922 |
Lepidiline C
|
Others | Others |
Lepidiline C 是一种 从十字花科Lepidium meenii Walpers 根中提取的新型的咪唑类生物碱 ,对HL-60细胞表现出细胞毒活性(IC50为:27.7 μM)。 | |||
TQ0192 |
Senecionine
Aureine,Senecionan-11,16-dione, 12-hydroxy-,千里光宁,Senecionin |
Others | Others |
Senecionine (Senecionin) 是一种吡咯里西啶生物碱,从Senecio vulgaris 中分离得到,它对动物和人类有毒性。 | |||
TN7232 |
Pegamine
|
||
pegamine 是一种在Peganum harmala 和Peganum nigellastrum 中发现的天然产品,是一种新型的生物碱。 | |||
T8770 |
Harmalol
骆驼蓬酚,Harmidol |
AChR | Neuroscience |
Harmalol (Harmidol) 是一种具有生物活性的 β-咔啉,是 harmalal 生物碱的成员 | |||
T7324 |
Chelidonine hydrochloride
|
Others | Others |
Chelidonine hydrochloride 是 Chelidonium majus 的生物碱之一,具有广泛的药理活性。 | |||
T2825 |
Cyclopamine
环巴胺,11-Deoxojervine |
Hedgehog/Smoothened; Endogenous Metabolite; Smo | GPCR/G Protein; Metabolism; Stem Cells |
Cyclopamine (11-Deoxojervine) 是Hedgehog 通路的拮抗剂,细胞实验中IC50=46 nM。它还是选择性Smo 抑制剂。 | |||
TN7061 |
yuanamide
|
Others | Others |
yuanamide 是一种天然化合物,属于生物碱类。 | |||
TN1078 |
Seneciphylline
千里光菲灵碱,千里光非灵 |
P450; GST | Metabolism; oxidation-reduction |
Seneciphylline 是一种有毒的吡咯烷核生物碱,存在于千里光植物中。它显著增加了环氧水合酶和谷胱甘肽-S-转移酶的特性,但导致细胞色素 P-450 和相关单加氧酶特性的抑制。 | |||
T2797 |
Harmaline
|
Others | Others |
Harmaline 是一种来自harmala 生物碱和β-咔啉的荧光精神活性吲哚生物碱。它是harmine 的还原氢化形式。 | |||
T4953 |
Neotuberostemonine
|
NOS | Immunology/Inflammation |
Neotuberostemonine 是一种结核分枝杆菌根中主要的止咳生物碱,能够阻碍巨噬细胞的募集和活化,从而减轻博来霉素 (Bleomycin) 诱导的肺纤维化。 | |||
T0439 |
L-Tryptophan
(S)-Tryptophan,Tryptophan,L-Tryptophane,Tryptophane,L-色氨酸 |
Amino Acids and Derivatives; Endogenous Metabolite | Metabolism |
L-Tryptophan (Tryptophane) 是一种必需氨基酸,是褪黑素、血清素和维生素B3的前体。 | |||
T6S0659 |
Rhynchophylline
钩藤碱,Rhynchophyllin,Rhyncophylline,Mitrinermine,Mitrinermin |
Calcium Channel; NF-κB | Membrane transporter/Ion channel; Metabolism; NF-κB |
Rhynchophylline (Mitrinermine) 是一种生物碱类化合物,从钩藤中分离得到,具有很高的生物活性,被广泛用于抗炎、神经保护等方面的研究。 | |||
T8769 |
Harmaline hydrochloride
Harmidine hydrochloride |
Others | Others |
Harmaline hydrochloride (Harmidine hydrochloride) 是一种荧光吲哚生物碱,来自 harmala 生物碱和 β-咔啉。它是 harmine 的部分氢化形式。 Harmaline 通过诱导下橄榄神经元的节律性放电在正常大鼠中产生全身性震颤。 | |||
T5S2361 |
Epiberberine
|
ERK; Beta-Secretase; MEK; BACE; AMPK; AChR; AChE | Chromatin/Epigenetic; MAPK; Neuroscience; PI3K/Akt/mTOR signaling |
Epiberberine 是一种从黄连中得到的生物碱,是AChE 和BChE 抑制剂,和非竞争性BACE1抑制剂。在 3T3-L1 细胞分化早期,它能够下调 Raf/MEK1/2/ERK1/2 和 AMPKα/Akt 信号通路。它具有抗氧化作用,能够清除 ONOO-,可用于阿尔滋海默症和糖尿病的研究。 | |||
TN4889 |
(R)-Reticuline
|
NADPH-oxidase | Immunology/Inflammation |
(R)-Reticuline is the biosynthetic precursor of the morphinan alkaloids. | |||
T19128 | 3-Pyridineacetic acid | Others | Others |
3-Pyridineacetic acid is a homolog of nicotinic acid, a breakdown product of nicotine and other tobacco alkaloids. | |||
TN4784 |
Picraline
|
SGLT | GPCR/G Protein |
A series of a hydroxy substituted derivatives 21-28 at C-17 of the Picraline-type alkaloids have been derived as having potent SGLT inhibitory activity. | |||
TN4346 |
Jaconine
|
Others | Others |
Jaconine, jacoline,jacobine, and jacozine, the hepatotoxic alkaloids, are potentially carcinogenic, mutagenic, and teratogenic and may pose health hazards to the human consumer. | |||
T34599 |
Secologanin
NSC 640525 |
||
Secologanin is a monoterpene that has been found in V. rosea and is an intermediate in the synthesis of monoterpene indole alkaloids from geraniol. | |||
TN3237 |
7-Isopentenyloxy-gamma-fagarine
|
Others | Others |
7-Isopentenyloxy-gamma-fagarine has highly cytotoxicity against the MCF-7and Jurkat cell line. It has been used as a precursor for the chemical asymmetric synthesis of the enantiopure alkaloids: evoxine, anhydroevoxine and evodine. | |||
TN6686 |
Cyclo(Pro-Pro)
|
||
Cyclo(Pro-Pro) tasted bitter.Verpacamides A-D, a sequence of C11N5 diketopiperazines relating cyclo(Pro-Pro) to cyclo(Pro-Arg), from the marine sponge Axinella vaceleti is possible biogenetic precursors of pyrrole-2-aminoimidazole alkaloids. | |||
T3S1873 |
Talatisamine
塔拉乌头胺,塔拉萨敏 |
Potassium Channel | Membrane transporter/Ion channel |
Talatisamine 是一种乌头生物碱,对K+通道有特异性阻滞作用。它能减弱 beta- 淀粉样低聚物对培养的皮层神经元的毒性。 | |||
T7853 |
(+)-Sparteine
鹰爪豆碱,(+)-鹰爪豆碱,Pachycarpine |
AChR | Neuroscience |
(+)-Sparteine (Pachycarpine) 是从苏格兰扫帚中提取的一种生物碱,是钠通道阻滞剂和 1a 类抗心律失常剂。它在神经细胞中竞争性地抑制烟碱型乙酰胆碱受体活性,是神经节阻滞剂。 | |||
T8185 |
(+)-Viroallosecurinine
别一叶萩碱,Viroallosecurinine |
Antibacterial | Microbiology/Virology |
(+)-Viroallosecurinine (Viroallosecurinine) 是一种具有抗菌活性的天然生物碱,抑制Ps. Aeruginosa 和Staph. aureus,MIC 为 0.48 μg/mL。 | |||
TN7066 |
Coryneine
2-(3,4-dihydroxyphenyl)ethyl-trimethylazanium,Quaternary dopamine,Trimethyl(3,4-dihydroxyphenethyl)aminium,棍掌碱,Dopamine methiodide |
Others | Others |
Coryneine (Trimethyl(3,4-dihydroxyphenethyl)aminium) 是从附子根中提取的多巴胺的季铵衍生物。 | |||
TN6783 |
Corysamine chloride
紫堇沙明碱,CORYSAMINE CHLORIDE(RG) |
AChE | Neuroscience |
Corysamine chloride (CORYSAMINE CHLORIDE(RG)) 被确定可抑制 ACHE 的活性。 | |||
TN7032 |
4'-O-Methylpyridoxine
4-methoxymethylpyridoxine,Ginkgotoxin |
Antioxidant | oxidation-reduction |
4'-O-Methylpyridoxine(MPN)是从银杏叶中发现的维生素类化合物,具有抗氧化活性和细胞毒性。 | |||
T0086 |
Galanthamine hydrobromide
Galantamine hydrobromide,Galanthamine HBr,氢溴酸加兰他敏 |
AChR; AChE | Neuroscience |
Galanthamine hydrobromide (Galantamine hydrobromide) 是一种长效的中枢活性 AChE 抑制剂,IC50为 410 nM。它是神经元烟碱型 ACh 受体的变构增强剂,IC50值为 0.35 µM,可用于阿尔茨海默症的研究。 | |||
TN4171 |
Grossamide
|
NO Synthase | Immunology/Inflammation |
Grossamide (GSE) 是一种来自虎杖的木脂酰胺。Grossamide 具有抗炎症活性,可通过上调精氨酸酶和下调诱导型一氧化氮合酶来抑制精氨酸产生一氧化氮(NO),抑制NO对OXPHOS的抑制作用。 | |||
T0970 |
Racanisodamine
山莨菪碱,Anisodamine,7β-Hydroxyhyoscyamine,Raceanisodamine,消旋山莨菪碱 |
Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Racanisodamine (7β-Hydroxyhyoscyamine) 是 anisodamine 的消旋体,是非选择性的毒蕈碱拮抗剂,是近视控制滴眼液的有效成分。 | |||
T3S0057 |
Dihydrochelerythrine
12,13-Dihydrochelerythrine,二氢白屈菜红碱 |
Antifungal | Microbiology/Virology |
Dihydrochelerythrine (12,13-Dihydrochelerythrine) 是一种从榕树叶片分离出的天然化合物,具有抗真菌活性,有潜力治疗多丝蚴引起的严重感染。 | |||
T1334 |
Hydroquinidine
奎宁树,氢化奎宁定,Hydroconchinine,Dihydroquinidine,Hydroconquinine,(+)-Hydroquinidine,Dihydroquinine |
Potassium Channel; Sodium Channel | Membrane transporter/Ion channel |
Hydroquinidine ((+)-Hydroquinidine) 是 Quinidine(一种抗心律不齐药) 的衍生物。它能够延长 QT 间隔,表现出抗心律不齐活性。 | |||
T2850 |
Bicuculline
荷包牡丹碱,(+)-Bicuculline,d-Bicuculline |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Bicuculline ((+)-Bicuculline) 是从东北延胡索中提取的一种生物碱,能阻断 Ca2+激活钾 (SK) 通道。它是一种竞争性的神经递质 GABAA 受体拮抗剂,IC50为 2 μM。 | |||
T4S1876 |
3-Deoxyaconitine
|
Sodium Channel | Membrane transporter/Ion channel |
3-Deoxyaconitine 是一种二萜类生物碱,对钠离子通道有激活作用。 | |||
T5746 |
Dictamine
Dictamnine,Dectamine,白鲜碱 |
Apoptosis; Anti-infection; Antibacterial; Antifungal | Apoptosis; Microbiology/Virology |
Dictamine (Dectamine) 显示抗胆碱酯酶、抗炎、致突变、抗菌和抗真菌活性。 它具有在人子宫颈、结肠和口腔癌细胞中发挥细胞毒性的能力。 | |||
T5799 |
Arecaidine hydrochloride
|
Others | Others |
Arecaidine hydrochloride 是一种具有高效 GABA 吸收抑制功能的吡啶生物碱。它是 H+偶联的氨基酸转运蛋白 1 (PAT1,SLC36A1) 的底物,能够竞争性抑制 L-脯氨酸的摄取。 | |||
TN6779 |
Clausine E
|
Others | Others |
Clausine E 是脂肪量和肥胖相关蛋白 (FTO) 脱甲基酶活性的抑制剂。 Clausine E 与 FTO 的结合是由正熵和负焓变化驱动的。 | |||
TN7042 |
N-methyltyramine
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
N-methyltyramine 是一种从豆科植物大叶相思中分离出的生物碱,是一种 α2-肾上腺素受体拮抗剂,通过酶促肾上腺素合成调节肾上腺素能受体,可用于研究肠道疾病。 | |||
T38373 |
2-heptyl-3-hydroxy-4(1H)-Quinolone
2-heptyl-3-hydroxy-4(1H)-Quinolone,PQS,Pseudomonas Quinolone Signal |
Others | Others |
2-heptyl-3-hydroxy-4(1H)-Quinolone (Pseudomonas Quinolone Signal) 是一种铜绿假单胞菌为应对细胞密度增加而产生的一种法定人数感应信号分子。 它增加了铜绿假单胞菌中lasB 基因的表达,增加代谢物焦蓝蛋白和凝集素PA-IL 的分泌,以及增加铜绿假单胞菌种群的生物膜生产。当使用浓度为40 μM 时,它还会降低铜绿假单胞菌生长介质中的铁含量,并在硫酸铁溶液中充当一种铁螯合剂。 | |||
T3786 |
Tomatine
lycopersicin,番茄素,番茄碱 |
Apoptosis; Proteasome | Apoptosis; Proteases/Proteasome; Ubiquitination |
Tomatine (lycopersicin) 是从番茄植物中发现的一种糖苷生物碱。它促进神经母细胞瘤细胞中核凋亡诱导因子的上调,还抑制20S 蛋白酶体活性。它以 RIP1 激酶和 caspase 非依赖性的方式引发神经毒性。 | |||
T2972 |
Rutaecarpine
Rutacarpine,吴茱萸次碱,Rhetine,Rutecarpine |
COX | Immunology/Inflammation; Neuroscience |
Rutaecarpine (Rhetine) 是从槐木中提取的一种生物碱,是 COX-2的抑制剂,IC50值为0.28 μM。 | |||
TN6775 |
Acetylcytisine
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one,3-acetyl-1,2,3,4,5,6-hexahydro-, (1R)-,11-Acetyl-6-oxo-7,11-diazatricyclo[7.3.1.0<2,7>]trideca-2,4-diene |
Others | Others |
Acetylcytisine (11-Acetyl-6-oxo-7,11-diazatricyclo[7.3.1.0<2,7>]trideca-2,4-diene) 是 Genista tinctoria L. 草药的天然产物。 | |||
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