98
46
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T36968 |
ARN-21934
|
Topoisomerase | DNA Damage/DNA Repair |
ARN-21934 是高选择性的人拓扑异构酶 II α 抑制剂,具有血脑屏障通透性。依托泊苷抑制 DNA 松弛的IC50为120 μM,ARN-21934 抑制 DNA 松弛的IC50为 2 μM。ARN-21934具有良好的体内药代动力学特性。 | |||
T5993 |
ARN-3236
|
AMPK; SIK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
ARN-3236 是一种口服有活性的、具有选择性的盐诱导激酶2 (SIK2)抑制剂,它能够抑制SIK1 (IC50:21.63 nM)、SIK2(IC50<1 nM)和 SIK3(IC50:6.63 nM)。它具有抗肿瘤作用。 | |||
T5357 |
ARN272
ARN 272 |
FAAH | Metabolism; Neuroscience |
ARN272 是大麻素转运抑制剂的一种。 | |||
T2339 |
Apalutamide
ARN-509 |
Androgen Receptor; GABA Receptor | Endocrinology/Hormones; Membrane transporter/Ion channel; Neuroscience |
Apalutamide (ARN-509) 是一种有效、竞争性的雄激素受体 (AR) 拮抗剂(IC50:16 nM)。 | |||
T25109 |
ARN-6039
ARN 6039,ARN6039 |
||
ARN-6039 is an orally available inverse agonist of RORγ for Autoimmune Neuroinflammatory Demyelinating Disease. The activity of ARN-6039 against RORγ was demonstrated in a RORγ-activated IL-17A Prom/LUCPorter assay in HEK 293 cells (360 nM) and in IL-17 r | |||
T9528 |
ARN19702
|
Others | Others |
ARN19702 是一种选择性,具有口服活性的,可逆的,可透过血脑屏障的 N-乙酰乙醇胺酸酰胺酶 (NAAA) 抑制剂,对人 NAAA 的 IC50为 230 nM。ARN19702 具有广泛的镇痛作用。 | |||
T21658 |
ARN14974
|
Others | Others |
ARN14974 是一种有效的全身活性的胞内酸性神经酰胺酶抑制剂 (IC50=79 nM),是一种苯并恶唑酮甲酰胺化合物。 | |||
T5118 |
Brilanestrant
GDC0810,GDC 0810,GDC-0810,ARN-810,RG 6046 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Brilanestrant (GDC-0810) 是一种雌激素选择性降能器 (selective estrogen receptor degrader)(IC50:0.7 nM),口服具有活性。 | |||
T7490 |
ARN2966
|
Beta Amyloid | Neuroscience |
ARN2966 是高效的,针对 APP 表达的转录后调节剂,能够抑制 APP 的表达从而使 Aβ的量降低。 | |||
T71554 | ARN 14494 | ||
ARN 14494 is a potent serine palmitoyltransferase inhibitor (SPT; IC50 = 27.3 nM). ARN 14494 inhibits synthesis of long chain ceramides and dihydroceramides in an in vitro model of Alzheimer's diease. The compound prevents the synthesis of proinflammatory cytokines and the oxidative stress-related enzymes iNOS and COX-2 in mouse primary cortical astrocytes. ARN 14494 is neuroprotective against β-amyloid 1-42 induced neurotoxicity in primary cortical neurons co-cultured with astrocytes. | |||
T10370 |
ARN 077
URB913 |
Others | Others |
ARN 077 is a selective N-acylethanolamine acid amidase (NAAA) inhibitor (IC50: 7 nM for human NAAA). ARN 077 significantly increases palmitoyl ethanolamine (PEA) levels within the CNS. | |||
T83950 |
ARN 11391
|
||
ARN 11391是ITPR1 (Inositol 1,4,5-trisphosphate (IP3) receptor type 1)的增效剂,它直接作用于ITPR1,从而增强细胞内钙离子信号。ARN 11391还能增强表达突变型ITPR1细胞中的钙信号,这与SCA29型脊髓小脑共济失调有关。 | |||
T36969 | ARN24139 | ||
ARN24139 is a topoisomerase II poison (IC50= 7.3 μM in a topoisomerase II decatenation assay).1It inhibits proliferation of DU145, HeLa, and A549 cells (IC50s = 4.7, 3.8, and 3.1 μM, respectively). 1.Arencibia, J.M., Brindani, N., Franco-Ulloa, S., et al.Design, synthesis, dynamic docking, biochemical characterization, and in vivo pharmacokinetics studies of novel topoisomerase II poisons with promising antiproliferative activityJ. Med. Chem.63(7)3508-3521(2020) | |||
T39859 | ARN19689 | ||
ARN19689 is an effective inhibitor of human NAAA, demonstrating high potency in the low nanomolar range (IC 50 = 0.042 μM). The compound acts through a non-covalent mechanism, highlighting its ability to interact with the enzyme for inhibition. | |||
T36468 |
ARN14988
|
||
ARN14988 is a potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme). It inhibits acid ceramidase activity and increases levels of C16 dihydro ceramide and C16 ceramide in A375, G361, M14, MeWo, MNT-1, and SK-MEL-28 melanoma cells. ARN14988 also reduces growth of A375 and G361 melanoma cells (EC50s = 41.8 and 67.7 μM, respectively). | |||
T69606 |
ARN23746
|
||
ARN23746 is a NKCC1 Inhibitor for the Treatment of Core Symptoms in Down Syndrome. | |||
T71553 |
Ainsliadimer A
|
||
Ainsliadimer A 是一种来自 Ainsliaea macrocephala 的倍半萜内酯二聚体,具有抗肿瘤活性,可诱导各种癌细胞的细胞死亡。 | |||
T61360 |
ARN25068
|
GSK-3; DYRK; Microtubule Associated; Src | Angiogenesis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Stem Cells; Tyrosine Kinase/Adaptors |
ARN25068是三种蛋白激酶(GSK-3β、FYN和DYRK1A)的亚微摩尔抑制剂,可用于治疗tau相关神经系统疾病。 | |||
T14321 |
ARN19874
|
Others | Others |
ARN19874 is a selective, reversible uncompetitive N-acylphosphatidylethanolamine phospholipase D (NAPE-PLD) activity inhibitor. With an IC50 of ~34 μM[1]. | |||
T30137 |
ARN14686
|
||
ARN14686 is an activity-based affinity probe for the detection of N-acylethanolamine acid amidase (NAAA) using click chemistry. | |||
T60456 |
ARN726
|
||
ARN726 是 N-酰基乙醇胺酸酰胺酶的有效抑制剂 (IC50 = 0.073 μM),它以剂量依赖性方式降低饮酒动机。 | |||
T61883 |
ARN5187
|
||
ARN5187 是一种亲溶酶体化合物,是 REV-ERBβ的配体。ARN5187抑制 REV-ERB 介导的转录调控和细胞自噬。ARN5187 显示出溶酶体效力和细胞毒性,可诱导细胞凋亡 (apoptosis)。 | |||
T61256 |
ARN1468
|
||
ARN1468 (compound 5) is a highly effective orally active inhibitor of serpins. Inhibition of serpins activity by ARN1468 enables release of proteases, thereby reducing prion accumulation. ARN1468 demonstrates pronounced anti-prion effects in ScGT1 RML, ScGT1 22L, ScN2a RML, and ScN2a 22L cell lines, with EC 50 values of 8.64, 19.3, 11.2, and 6.27 μM [1]. | |||
T2318 |
Sacubitril/Valsartan
Sacubitril mixture with Valsartan,沙库必曲/缬沙坦,Valsartan,Sacubitril,LCZ696 |
Apoptosis; RAAS; Neprilysin | Apoptosis; Endocrinology/Hormones; Metabolism |
Sacubitril/Valsartan (LCZ696),以1:1摩尔比由Valsartan(一种ARB)和Sacubitril(AHU377)组成,为创新口服血管紧张素受体-脑啡肽酶(ARN)双重抑制剂,旨在治疗高血压与心力衰竭。其作用机制包括抑制炎症、氧化应激及细胞凋亡,有助于改善糖尿病心肌病。 | |||
T63476 |
ARN5187 trihydrochloride
|
||
ARN5187 trihydrochloride 是一种亲溶酶体 REV-ERBβ 配体,对 REV-ERB 介导的转录调控和细胞自噬具有抑制作用。ARN5187 trihydrochloride 具有溶酶体效力和细胞毒性,能够诱导细胞凋亡 (apoptosis)。 | |||
T0220 |
Foscarnet sodium
Phosphonoformate,膦甲酸钠 |
Virus Protease; Reverse Transcriptase; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Foscarnet sodium (Phosphonoformate) 是一种病毒 DNA 聚合酶活性抑制剂,可逆地抑制病毒复制。它是一种用于治疗巨细胞病毒性视网膜炎的抗病毒剂。 | |||
T21841 |
(±)-Hexanoylcarnitine chloride
DL-Hexanoylcarnitine chloride |
Others | Others |
(±)-Hexanoylcarnitine chloride 是一种脂肪酸代谢产物,能将脂肪酸分解成能够被身体利用的小分子化合物。(±)-Hexanoylcarnitine chloride 可通过大鼠骨骼肌毒性特异性从而作为一种生物标志物。 | |||
T6302 |
Lonafarnib
Sarasar,氯那法尼,Sch66336 |
Raf; Transferase; Autophagy; Ras | Autophagy; GPCR/G Protein; MAPK; Metabolism |
Lonafarnib (Sch66336) 是一种可口服的 FPTase 抑制剂,作用于 H-ras、K-ras 和 N-ras,IC50分别为 1.9 nM、5.2 nM 和 2.8 nM。它具有抗肝炎三角洲病毒的活性。 | |||
T5856 |
Barnidipine hydrochloride
盐酸巴尼地平,YM-09730-5 hydrochloride,Mepirodipine (hydrochloride) |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Barnidipine hydrochloride (YM-09730-5 hydrochloride) 是一种二氢吡啶类钙通道阻滞剂,对 CaA 受体具有选择性作用。它是一种抗高血压药物,通过减少其血管扩张作用继发的外周血管阻力起作用。 | |||
T1182 |
Levocarnitine propionate hydrochloride
Propionyl-L-carnitine hydrochloride,L-Propionylcarnitine chloride,丙酰左旋肉碱盐酸盐,ST-261,丙酰肉碱盐酸盐 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Levocarnitine propionate hydrochloride (ST-261) 可用于肾功能恶化,充血性心脏衰竭,间歇性跛行等疾病的研究。 | |||
T7099 |
Gefarnate
|
Others | Others |
Gefarnate 是一种胃炎和胃溃疡的研究药物,目前也用于研究干眼症。 | |||
T6271 |
Tipifarnib
替吡法尼,R115777,Zarnestra,IND 58359 |
Transferase | Metabolism |
Tipifarnib (IND 58359) 能够抑制法尼基转移酶 (FTase),IC50=0.86 nM,具有潜在抗肿瘤特性。 | |||
T68079 |
Gedocarnil
ZK 113315,SH 530 |
Others | Others |
Gedocarnil(ZK 113315) 可用于研究中枢神经系统疾病。 | |||
T20535 |
Carnidazole
ME 108,NSC293873,NSC 293873,ME-108,NSC-293873,ME108 |
Antibiotic; Parasite | Microbiology/Virology |
Carnidazole (ME-108) 具有抗原生动物活性,可用于治疗滴虫感染的研究。 | |||
T22484 |
(±)-Propionylcarnitine chloride
Propionyl-DL-carnitine chloride |
Endogenous Metabolite | Metabolism |
(±)-Propionylcarnitine chloride (Propionyl-DL-carnitine chloride) 是一种短链酰基肉碱的混合物,可用作膳食补充剂,可用于研究慢性糖尿病。 | |||
T17102 |
Tipifarnib (S enantiomer)
Tipifarnib S enantiomer,(S)-(-)-R-115777,(S)-Tipifarnib,IND-58359 S enantiomer |
Transferase | Metabolism |
Tipifarnib S enantiomer ((S)-(-)-R-115777) 是Tipifarnib 的 S 型对映体,它比 Tipifarnib 特性低。其中 Tipifarnib 是farnesyltransferase 高效特异性抑制剂,IC50=0.6 nM。 | |||
T37735 |
Stearoyl-L-carnitine chloride
C18 Carnitine,Stearoylcarnitine chloride |
||
Stearoyl-L-carnitine chloride(Acylcarnitine C18:0) 是一种存在于小脑中的长链酰基肉碱,抑制 GlyT2 ,是研究脂代谢的重要组成部分。 | |||
T37359 |
Myristoyl-L-carnitine chloride
L-Myristoylcarnitine chloride |
Endogenous Metabolite | Metabolism |
Myristoyl-L-carnitine chloride (L-Myristoylcarnitine chloride) 是人体的代谢物之一,与遗传代谢疾病有关。Tetradecanoylcarnitine 是研究糖尿病和自身免疫性肝炎的潜在标记物。 | |||
T7550 |
Barnidipine
YM-09730-5(Free base),(4S)-2,6-二甲基-4-(间硝基苯基)-1,4-二氢吡啶-3,5-二羧酸 (3S)-1-苄基-3-吡咯烷基-甲基酯,Mepirodipine |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Barnidipine (YM-09730-5(Free base)) 是一种二氢吡啶类钙通道阻滞剂,对 CaA 受体具有选择性作用。它是一种抗高血压药物,通过减少其血管扩张作用继发的外周血管阻力起作用。 | |||
T38253 |
Lauroyl-L-carnitine (chloride)
Lauroyl-L-carnitine Hydrochloride |
||
Lauroyl-L-carnitine (chloride) (Lauroyl-L-carnitine Hydrochloride)是一种酰基肉碱和表面活性剂,已被用于渗透猪肠细胞,以输送极性荧光探针荧光黄。 | |||
T26551 |
Acetyl-L-carnitine
RO 447190,L-Acetylcarnitine,LAC,L-O-Acetylcarnitine,ALCAR,Acetyl L carnitine |
Endogenous Metabolite | Metabolism |
Acetyl-L-carnitine(RO 447190) 是一种可透过血脑屏障的氨基酸左旋肉碱,常作为膳食补充剂,对神经炎症有益。Acetyl-L-carnitine 具有神经保护作用,可用以研究像阿尔茨海默病类的神经疾病。 | |||
TP1088 |
N-Acetylcarnosine
N-Acetyl-L-carnosine,N-乙酰肌肽 |
Others | Others |
N-Acetylcarnosine (N-Acetyl-L-carnosine) 是一种含有组氨酸的天然二肽,是药理学上主要的 L-carnosine 的来源。它是一种眼科药物,对人类白内障具有潜在的应用价值。 | |||
T12356 |
Palmitoylcarnitine
Palmitoyl DL-carnitine |
Endogenous Metabolite | Metabolism |
Palmitoylcarnitine (Palmitoyl DL-carnitine) 是一种线粒体脂肪酸氧化中间体,可作为表面活性剂。 | |||
T13810 |
Palmitoylcarnitine chloride
Palmitoyl DL-carnitine chloride |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Palmitoylcarnitine chloride (Palmitoyl DL-carnitine chloride) 是一种线粒体脂肪酸氧化中间体,可介导脂质内心脏保护。Palmitoylcarnitine chloride 通过消耗谷胱甘肽来消除结直肠癌细胞的存活,诱导癌细胞死亡,调节蛋白激酶 C βII 与其受体 RACK1 之间的相互作用。 | |||
T32098L |
Homocarnosine acetate
|
GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Homocarnosine acetate 是大脑特有的二肽,由 γ-氨基丁酸 (GABA) 和组氨酸组成。它具有抗氧化和抗炎作用、预防 DNA 损伤和抑制晚期糖基化终产物形成 | |||
T7882 |
Indomethacin farnesil
吲哚美辛法呢酯,Infree |
Others; COX; Autophagy | Autophagy; Immunology/Inflammation; Neuroscience; Others |
Indomethacin farnesil (Infree) 是具有口服活性的 Indomethacin 前药,可通过干扰溶酶体的正常功能来破坏自噬流,有抗炎和抗风湿作用。它是一种可透过血脑屏障的,非选择性的 COX1和 COX2抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的IC50值分别为 18 nM 和 26 nM。 | |||
T73766 | Isobutyryl-L-carnitine chloride | ||
Isobutyryl-L-carnitine chloride 是酰基辅酶 A 脱氢酶的产物。 | |||
T10684L |
Carnostatine hydrochloride
SAN9812 hydrochloride |
Others | Others |
Carnostatine hydrochloride (SAN9812 hydrochloride) 是一种有效的选择性肌肽酶 1 (CN1) 抑制剂,对人重组 CN1 的Ki 值为 11 nM。Carnostatine hydrochloride 可用于治疗糖尿病性肾病 (DN) 。 | |||
T73752 | Glutarylcarnitine lithium | ||
Glutarylcarnitine lithium 丙二酸尿症和 I 型戊二酸尿症的重要诊断代谢物。 | |||
T78081 |
Farnesyl Pyrophosphate ammonium
Farnesyl diphosphate ammonium |
||
Farnesyl pyrophosphate ammonium salt为15碳类异戊二烯代谢中间体,源自MVA途径,兼具TRPM2激动剂功能,能够触发TRPM2通道开放并促进离子流入细胞。它亦是胆固醇合成、泛醌合成、蛋白质法尼基化修饰以及GGPP合成的关键底物。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN7168 |
Farnesylacetone
(5E,9E)-6,10,14-Trimethylpentadeca-5,9,13-trien-2-one,法尼基丙酮,Farnesyl acetone,E,E-farnesylacetone |
Others | Others |
Farnesylacetone ((5E,9E)-6,10,14-Trimethylpentadeca-5,9,13-trien-2-one) 是一种海洋来源的天然产物,存在于Sargassum micracanthum。 | |||
T9352 |
hydrocotarnine
|
Others | Others |
hydrocotarnine 是 Cbl 的抑制剂。 | |||
T0743 |
DL-Carnitine
Carnitina,Carnitine,卡尼丁 |
Others | Others |
DL-Carnitine (Carnitina) 是肝脏和横纹肌的成分。在治疗上它用于刺激胰腺和胃的分泌并治疗高脂蛋白血症。 | |||
T19564 |
Stearoylcarnitine
Stearoyl-L-carnitine |
Endogenous Metabolite | Metabolism |
Stearoylcarnitine (Stearoyl-L-carnitine) 是一种脂肪酯脂质分子,是一种人内源代谢产物,可作为早发型子痫前期和晚发性子痫前期的生物标志物。 | |||
TN6835 |
(E)-β-Farnesene
(6E)-7,11-dimethyl-3-methylidenedodeca-1,6,10-triene,trans-β-Farnesene |
Antifungal | Microbiology/Virology |
(E)-β-Farnesene (trans-β-Farnesene) 是一种存在于 Phlomis aurea Decne中的倍半萜烃,是许多蚜虫报警信息素的主要成分,可中断蚜虫摄食。(E)-β-Farnesene 通过破坏昆虫激素平衡来损害 Chilo suppressalis 幼虫的发育和存活。 | |||
T8249 |
Hexahydrofarnesyl acetone
植酮,Phytone |
Others; Antibacterial | Microbiology/Virology; Others |
Hexahydrofarnesyl acetone (Phytone) 是从Launaea mucronata 中分离得到的倍半萜,具有抗菌和抗炎活性,可研究缓解疼痛。 | |||
T2203 |
D-Carnitine hydrochloride
(S)-Carnitine Hydrochloride,L-Carnitine hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
D-Carnitine hydrochloride ((S)-Carnitine Hydrochloride) 已被用于研究麦角硫因素转运蛋白 SLC22A4 和肉毒碱转运蛋白 SLC22A5,也被用于使棕榈酸进入线粒体。 | |||
T19340 |
Glutarylcarnitine
O-glutaroyl-L-carnitine |
Endogenous Metabolite | Metabolism |
Glutarylcarnitine (O-glutaroyl-L-carnitine) 是大多数串联质谱新生儿筛查计划中监测的丙二酸尿症和谷草酸尿症 I 型的诊断代谢物。 | |||
T12295 |
Oleoylcarnitine
Oleoyl-L-carnitine |
Endogenous Metabolite | Metabolism |
Oleoylcarnitine (Oleoyl-L-carnitine) 抑制腺嘌呤核苷酸转位酶 (AdNT) 活性,ic50为14 μM。Oleoylcarnitine 是检测神经分裂的重要指标。 | |||
T13280 |
Valerylcarnitine
VALERYL-L-CARNITINE |
Endogenous Metabolite | Metabolism |
Valerylcarnitine (VALERYL-L-CARNITINE) 是一种短链脂肪酸,可用于研究 2 型糖尿病。 | |||
T2563 |
Acetyl-L-carnitine hydrochloride
Acetyl L-carnitine hydrochloride,O-Acetylcarnitine,乙酰-L-肉(毒)碱盐酸盐,O-acetyl-L-carnitine,O-Acetyl-L-carnitine hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Acetyl-L-carnitine hydrochloride (Acetyl L-carnitine hydrochloride) 是一种由内源性左旋肉碱的乙酰化形式的盐酸盐组成的营养补充剂,具有潜在的神经保护、认知增强、抗抑郁和免疫调节活性。还可缓解化疗、糖尿病或其他疾病引起的周围神经病变。此外,乙酰左旋肉碱可能通过增加T淋巴细胞成熟来调节免疫反应,并可能下调促炎细胞因子对病毒(如SARS-CoV-2)的反应。它还可能破坏ACE2信号通路并抑制活性氧(ROS)的产生。 | |||
T6475 |
(±)-Carnitine chloride
Monocamin,DL-Carnitine HCl,Bicarnesine,混旋肉碱盐酸盐,DL-Carnitine chloride |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
(±)-Carnitine chloride (Monocamin) 有D 和L 两种异构体。其中 L-carnitine 在脂肪酸的 β-氧化中起重要作用,也具有抗氧化作用和抗炎活性。 | |||
T4957 |
Carnosic acid
|
Apoptosis; ROS; Antibacterial | Apoptosis; Immunology/Inflammation; Microbiology/Virology |
Carnosic acid 抑制细胞增殖,有抗菌、抗炎和抗氧化应激作用。 | |||
T19581 |
Tiglyl carnitine
|
Endogenous Metabolite | Metabolism |
Tiglyl carnitine 与肺癌和肉碱和甘氨酸对3-酮硫解酶缺乏症有关 。 | |||
T19384 |
Isovalerylcarnitine
|
Apoptosis; Cysteine Protease | Apoptosis; Proteases/Proteasome |
Isovalerylcarnitine (3-methylbutyrylcarnitine) 是 L-亮氨酸分解代谢和异戊酸的积累产生的小分子化合物,也是一种具有选择性和有效性的钙蛋白酶 (calpain) 激活剂,可促使细胞凋亡,与异戊酸血症有关,可作为异戊酸血症的标志。 | |||
T12014 |
Methyl carnosate
|
Others | Others |
Methyl camosate, a diterpene sourced from Salvia officinalis or Rosmarinus officinalis, exhibits pronounced antioxidant and antibacterial properties. | |||
TN1405 |
Arnicolide D
山金车内酯 D,山金车内酯D |
Akt; Caspase; PI3K; STAT; mTOR | Apoptosis; Cytoskeletal Signaling; JAK/STAT signaling; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
Arnicolide D 是从石胡荽中分离出的一种倍半萜内酯,以浓度和时间依赖性方式抑制鼻咽癌细胞活力。它调节细胞周期,激活 caspase 信号通路并抑制 PI3K/AKT/mTOR 和 STAT3 信号通路。 | |||
T19398 |
L-Octanoylcarnitine
|
Endogenous Metabolite | Metabolism |
L-Octanoylcarnitine 是存在于血浆中的活性辛酰肉碱,是一种乳腺癌的潜在生物标志物。 | |||
TN1111 |
Arnidiol
|
Immunology/Inflammation related | Immunology/Inflammation |
Arnidiol 是一种五环三萜烯,从Barleria Longiflora LinnF. 中提取得到。 | |||
T0846 |
L-Carnitine
L(-)-Carnitine,Levocarnitine,左旋肉碱 |
Endogenous Metabolite; Fatty Acid Synthase | Metabolism |
L-Carnitine (L(-)-Carnitine) 是一种人内源性分子,在人体内以蛋氨酸和赖氨酸为底物进行生物合成,并参与脂肪酸代谢。L-Carnitine 将长链脂肪酰辅酶A 转运到线粒体。L-Carnitine 能够改善许多先天性代谢错误的代谢失衡。 | |||
T8028 |
Farnesyl acetate
Farnesyl Acetate (mixture of isomers),3,7,11-三甲基-2,6,10-十二烷三烯-1-醇乙酸酯,乙酸法呢醇酯 |
Others | Others |
Farnesyl acetate (Farnesyl Acetate(mixture of isomers)) 是一种倍半萜,分离自 Amomum gagnepainii 中。它对红棕榈象虫幼虫有显著的毒性(LD50:7867 ppm)。 | |||
T4732 |
L-Carnosine
Karnozin,L-肌肽,beta-Alanyl-L-histidine |
Antioxidant; Endogenous Metabolite | Metabolism; oxidation-reduction |
L-Carnosine (Karnozin) 是 由beta-丙氨酸和组氨酸组成的二肽,具有抑制衰老的作用。 | |||
T15157 |
Dodecanoylcarnitine
Lauroylcarnitine |
Endogenous Metabolite | Metabolism |
Dodecanoylcarnitine((-)-Lauroylcarnitine) 和脂肪酸氧化紊乱有关,使用 Dodecanoylcarnitine 可使鲑鱼降钙素的通透性增加。 | |||
T14840 |
Butyrylcarnitine
|
Endogenous Metabolite | Metabolism |
Butyrylcarnitine 是血浆中的代谢物,是疾病引起异常代谢的指标,可用于诊断心力衰竭和胰腺囊肿。 | |||
TN7254 |
(E,E)-Farnesol
(2E,6E)-Farnesol |
Others | Others |
(E,E)-Farnesol ((2E,6E)-Farnesol) 是一种由细菌、原生动物、真菌、植物和动物产生的倍半萜无环醇。(E,E)-Farnesol 可促进血管扩张。 | |||
T17048 |
Tetradecanoylcarnitine
L-Myristoylcarnitine,Myristoyl-L-(-)-carnitine |
Endogenous Metabolite | Metabolism |
Tetradecanoylcarnitine (L-Myristoylcarnitine) 是一种酰基肉碱,参与长链脂肪酸的β-氧化,是极长链酰辅酶A脱氢酶缺乏症的一种潜在标记物。 | |||
T6S1302 |
Carnosol
|
Nrf2; Endogenous Metabolite; S6 Kinase | Immunology/Inflammation; MAPK; Metabolism; PI3K/Akt/mTOR signaling |
Carnosol 是 Nrf2激活剂,增加 Nrf2 的水平以及能促进血红素氧合酶 1(HMOX1) 表达。它是核糖体 S6激酶(RSK2)抑制剂,可用于胃癌相关研究,IC50值约为 5.5 μM。 | |||
TN2601 |
12-O-Methylcarnosic acid
|
Reductase | Endocrinology/Hormones; Metabolism |
12-O-Methylcarnosic acid 是分离自小叶丹参的丙酮提取物的一种二萜肉桂酸,可抑制 5α-还原酶 (5α-reductase) 活性,IC50为 61.7 μM。它抑制 LNCaP 细胞的增殖。它具有抗微生物活性、抗氧化和抗癌活性。 | |||
T4586 |
(Rac)-Arnebin 1
β,β-二甲基丙烯酰阿卡宁,beta, beta-dimethylacrylshikonin |
Others | Others |
(Rac)-Arnebin 1 (beta, beta-dimethylacrylshikonin) 具有抗肿瘤作用,是β,β-Dimethylacrylalkannin 和 β,β-Dimethylacrylshikonin 的消旋体。β,β-Dimethylacrylalkannin 和 β,β-Dimethylacrylshikonin 是分离自紫草属植物中的萘醌类化合物。 | |||
T7868 |
Farnesol
法呢醇,里哪醇 |
Endogenous Metabolite; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology |
Farnesol 是一种半萜醇,能够调节细胞间的通讯,有抑菌活性。 | |||
TN5828 |
(2Z,6Z,10E,14E,18E)-Farnesylfarnesol
|
||
(2Z,6Z,10E,14E,18E)-Farnesylfarnesol 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 TN5828,CAS号为 90695-03-7。 | |||
TN2798 |
20-Deoxocarnosol
|
ROS; Antifection | Immunology/Inflammation; Microbiology/Virology |
20-Deoxocarnosol has antioxidant activity of measuring the decay of the radical cation diphenyl-picrylhydrazyl (DPPH).It also exhibits non-specific antiprotozoal activity due to high cytotoxicity. | |||
T19391 |
L-Hexanoylcarnitine
|
Others | Others |
L-Hexanoylcarnitine is found to be associated with celiac disease, is an acylcarnitine. | |||
TMA0716 | Mearnsitrin | Others | Others |
Mearnsitrin是一种天然产物,属于芸香科黄皮属,其产品编号为 TMA0716,CAS号为 30484-88-9。Mearnsitrin可用作对照参考。 | |||
T20123 |
L-Carnitine hydrochloride
L-Carnitine chloride,LC 80,Levocarnitine chloride,(R)-Carnitine hydrochloride,LC-80,LC80 |
||
Carnitine is a quaternary amine that occurs naturally in most mammalian tissue. Carnitine is present in relatively high concentrations in skeletal muscle and heart where it is involved in regulating energy metabolism. It has also been used to allow the en | |||
T19381 |
Isobutyryl-L-carnitine
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Isobutyryl-L-carnitine is a member of the class of compounds known as acylcarnitines. Isobutyryl-L-carnitine is a product of the acyl-CoA dehydrogenases. | |||
T73764 | L-Palmitoylcarnitine TFA | ||
L-Palmitoylcarnitine TFA 是一种长链酰基肉碱和脂肪酸代谢产物,在缺血期间积聚于肌膜并扰乱膜脂环境。L-Palmitoylcarnitine TFA 通过与Kir6.2的相互作用抑制KATP 通道活性,而不影响单通道电导。 | |||
T75458 | (-)-10,11-Dihydroxyfarnesol | ||
(-)-10,11-Dihydroxyfarnesol 是一种从 Cryptomarasmius aucubae 内生真菌中分离出来的化合物,该化合物显着抑制一氧化氮(NO)的产生。 | |||
T3837 |
Mearnsetin
|
Antioxidant | oxidation-reduction |
Mearnsetin 具有抗氧化活性。 | |||
T40582 |
α-Farnesene
|
||
α-Farnesene, a sesquiterpene, is a herbivore-induced plant volatile (HIPV) that plays a significant role in insect resistance across various plant species. | |||
TN1404 |
ArnicolideC
山金车内酯C,山金车内酯 C,Arnicolide C |
Others | Others |
Arnicolide C exhibits significant antiallergy activity. | |||
T27304 |
Farnesiferol C
Farnesiferol-C |
||
Farnesiferol C induces apoptosis via regulation of L11 and c-Myc. | |||
T82966 | Arnocoumarin | ||
Arnocoumarin为自X. arnottianum MAXIM分离出的天然化合物。 | |||
T75441 | (8′α,9′β-Dihydroxy)-3-farnesylindole | ||
(8'α,9'β-Dihydroxy)-3-farnesylindole 对枯草芽孢杆菌具有较强的抑制活性(EC509.8μM)。 | |||
TN4237 |
Hydrocotarnine hydrobromide
|
Others | Others |
Hydrocotarnine hydrobromide 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 TN4237,CAS号为 5985-00-2。 | |||
TN7122 |
Micromarin F
E-Methylarnottinin,5'-hydroxylosthole |
Others | Others |
Micromarin F (E-Methylarnottinin) 是从 Micromelum minutum Wight et Arn 的茎中提取的香豆素衍生物。 |