231
52
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1216 |
CaM kinase II inhibitor TFA salt
Autocamtide-2-related inhibitory peptide (TFA) |
CaMK | Neuroscience |
CaM kinase II inhibitor TFA salt (Autocamtide-2-related inhibitory peptide(TFA)) 是一种高度特异性和有效的 CaMKII 抑制剂,IC50 为 40 nM。 | |||
T76690 |
Mavrilimumab
CAM 3001 |
Virus Protease; CSF-1R | Microbiology/Virology; Tyrosine Kinase/Adaptors |
Mavrilimumab (CAM 3001) 是一种单克隆抗体,具有抗病毒活性,对粒细胞-巨噬细胞集落刺激因子 (GM-CSF) 受体的 α 亚基有亲和力,并阻止 GM-CSF 下游细胞内信号传导。GM-CSF 可能与呼吸衰竭和死亡相关的过度活跃炎症反应有关,可用于研究类风湿性关节炎。 | |||
T41211 | CAM 833 | ||
CAM 833 是一种有效的正位抑制剂,对 BRCA2 和 RAD51 之间相互作用具有抑制作用,对 ChimRAD51 蛋白的 Kd 为 366 nM。 CAM833 抑制 RAD51 的寡聚,促进 G2/M 阻滞细胞的凋亡 (apoptosis) 进程。 | |||
T70136 |
CAM 4750
|
||
CAM 4750 is a nonpeptide tachykinin NK1 receptor antagonist. | |||
T70137 | CAM 4515 | ||
CAM 4515 is a nonpeptide tachykinin NK1 receptor antagonist. | |||
T70410 | Cam 2445 | ||
Cam 2445 is a nonpeptide, alpha-methyltryptophan derivative; an NK1 neurokinin receptor antagonist that is a potentially useful treatment for arthritis, asthma, migraine, anxiety, psychosis, and emesis. | |||
T28331 |
PD 136450
Cam1189,PD136450,Cam-1189,PD-136450,Cam 1189 |
||
Cholecystokinin type B receptor antagonist PD-136,450 is a partial secretory agonist in the stomach and a full agonist in the pancreas of the rat. Gastrin (cholecystokinin type B (CCK-B)) receptor antagonists may help to elucidate the physiological role o | |||
T70211 |
CAM741
|
||
CAM741 is a novel selective inhibitor of vascular cell adhesion molecule 1 (VCAM1) synthesis in endothelial cells, blocking the process of cotranslational translocation, which is dependent on the signal peptide of VCAM1. | |||
T30442 |
Bialamicol Hydrochloride
Camoform hydrochloride,CAM 807,CAM-807,CI 301 |
||
Bialomicol Hydrochloride is a bio-active chemical. | |||
T41184 |
Clocinnamox mesylate
C-CAM,NIH 10443 |
||
Clocinnamox mesylate is a systemically active, irreversibleμ-opioid receptor antagonist (apparent Kivalues are 0.7, 1.9 and 5.7 nM for mouseμ,δandκreceptors respectively). | |||
T69909 | CAM4066 | ||
CAM4066 is a novel potent and selective CK2alpha inhibitor. | |||
T16366 |
NVR 3-778
|
HBV | Microbiology/Virology |
NVR 3-778 是一种 SBA 类的口服有效HBV CAM 衣壳组装调制剂,具有抗 HBV 活性。 | |||
T69908 |
Pidnarulex HCl
|
||
Pidnarulex HCl is the salt form of CX-5461, a first-in-class non-genotoxic small molecule targeted inhibitor of RNA polymerase I (Pol I) that activates the p53 pathway without causing DNA damage. CX-5461 selectively inhibits rRNA synthesis by Pol I in the nucleolus, but does not inhibit mRNA synthesis by RNA Polymerase II (Pol II) and does not inhibit DNA replication or protein synthesis. Inhibition of Pol I results in nucleolar stress and release of ribosomal proteins (RP) from the nucleolus. T... | |||
T70210 |
FT-1101 free base
|
||
FT-1101 is an orally bioavailable, potent and selective BET inhibitor. FT-1101 binds to the acetylated lysine recognition motifs in the bromodomain sites of BET proteins, thereby preventing the interaction between the BET proteins and acetylated histones. This disrupts chromatin remodeling and gene expression. Prevention of the expression of certain growth-promoting genes may lead to the inhibition of tumor cell growth. BET proteins, comprised of BRD2, BRD3, BRD4 and BRDT, are transcriptional r... | |||
T23525 |
W-9 hydrochloride
N-(6-aminohexyl)-5-chloronaphthalene-2-sulfonamide hydrochloride |
CaMK | Neuroscience |
W-9 hydrochloride 是一种钙调蛋白拮抗剂。 | |||
T70135 | Nepaprazole sodium dihydrate | ||
Nepaprazole sodium dihydrate is a proton pump inhibitor potentially for treatment of gastric ulcers. | |||
T70409 |
6alpha-Fluorotestosterone
|
||
6alpha-Fluorotestosterone is a synthetic nonaromatizable androgen analog of testosterone. It binds to and activates specific nuclear receptors inhibits and is equipotent to testosterone. | |||
T63717 | CAM833 | ||
CAM833 是有效的抑制 BRCA2 和 RAD51 之间相互作用的正位抑制剂,也能够抑制 RAD51 的寡聚,能够作用于 ChimRAD51 蛋白 (Kd: 366 nM)。 | |||
T20792 |
W-7 hydrochloride
N-(6-氨基己基)-5-氯-1-萘磺胺盐酸盐,W 7 HCl,W7 HCl,W-7 HCl |
CaMK; Apoptosis; Myosin; PDE | Apoptosis; Cytoskeletal Signaling; Metabolism; Neuroscience |
W-7 hydrochloride (W-7 HCl) 是一种选择性的钙调蛋白拮抗剂。它抑制Ca2+-钙调蛋白依赖性磷酸二酯酶和肌球蛋白轻链激酶,IC50值分别为 28 μM 和 51 μM。它可诱导细胞凋亡,具有抗癌活性。 | |||
TP1921L1 |
Autocamtide-2-related inhibitory peptide, myristoylated acetate(201422-04-0 free base)
|
CaMK; Autophagy | Autophagy; Neuroscience |
Autocamtide-2-related inhibitory peptide, myristoylated acetate 是CaM 激酶II 抑制剂;是 Autocamtide-2相关抑制肽的增强细胞渗透性衍生物。 | |||
T1586 |
Tenoxicam
Ro-12-0068,替诺昔康,Tenoxicamum,Mobiflex,Tilcotil |
COX | Immunology/Inflammation; Neuroscience |
Tenoxicam (Tilcotil) 是一种抗炎化合物,具有退热止痛作用。 | |||
T35033L |
(S)-Vamicamide
(S)-Vamicamide (Iso-132373-81-0) |
AChE | Neuroscience |
(S)-Vamicamide 是一种新型抗抗胆碱能化合物。Vamicamide 在 32 mg/kg 或更高 (p.o.) 时增加小鼠的自发运动活动,并在 100 mg/kg 时抑制小鼠强直性惊厥。 | |||
TP2310 |
Autocamtide-2-related inhibitory peptide
|
CaMK; Autophagy | Autophagy; Neuroscience |
Autocamtide-2-related inhibitory peptide 是一种高度特异性和有效的 CaMKII 抑制剂,IC50 为 40 nM。 | |||
TP2057L |
Camstatin acetate
|
NO Synthase | Immunology/Inflammation |
Camstatin acetate 结合钙调蛋白并抑制神经元一氧化氮合酶。它是 PEP-19 的单一钙调蛋白结合 IQ 基序的具有功能活性的 25 个残基片段。 | |||
T9048 |
Ecamsule
|
Others | Others |
Ecamsule 是一种亚苄基樟脑衍生物,其中许多以其出色的光稳定性而闻名。 可添加到防晒霜中以过滤掉 UVA 射线。 | |||
T11237 |
Camizestrant
Estrogen receptor antagonist 2 |
Estrogen Receptor/ERR | Endocrinology/Hormones |
Camizestrant (Estrogen receptor antagonist 2) 是一种雌激素受体拮抗剂,可用于 ER+ HER2 晚期乳腺癌的研究[1]。 | |||
T35033 |
Vamicamide
FK 176,FK-176,FK176 |
AChE | Neuroscience |
Vamicamide (FK 176)是一种新型抗胆碱能化合物。Vamicamide 在 32 mg/kg (p.o.)或更高时增加小鼠的自发运动活动,并在 100 mg/kg 时抑制小鼠强直性惊厥。 | |||
T15050 |
Danicamtiv
MYK-491,SAR 440181 |
Myosin | Cytoskeletal Signaling |
Danicamtiv (MYK-491) 是一种正性肌力药物,也是一种心肌肌球蛋白的选择性变构激活剂,可增加心脏收缩功能并保持机械效率。 | |||
T0818 |
Decamethonium bromide
十烃溴铵,Decacuran,溴化十烃季胺,Syncurine |
AChR; AChE | Neuroscience |
Decamethonium bromide (Syncurine) 是神经肌肉阻滞剂和烟碱型 AChR 部分激动剂。 | |||
T18990 |
Fluorescamine
荧光胺,Ro 20-7234 |
Others | Others |
Fluorescamine (Ro 20-7234) 是一种螺环化合物,其本身无荧光性质,但与初级胺反应后可形成荧光,因此可用于胺和肽的检测。 | |||
T2159 |
CaMKP Inhibitor
|
CaMK | Neuroscience |
CaMKP Inhibitor 可以抑制 CaMKP。 | |||
T67795 |
Camonagrel
|
||
Camonagrel 是一种化合物,对Prostaglandin E2具有抑制作用。 | |||
T9258 |
Aficamten
|
Others | Others |
Aficamten 是一种可研究肥厚型心肌病的新型心肌肌球蛋白抑制剂,IC50为 1.4 μM。 | |||
T16807 |
Rucaparib monocamsylate
瑞卡帕布樟脑磺酸盐,Rucaparib Camsylate |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Rucaparib monocamsylate (Rucaparib Camsylate) 是一种口服有效的 PARP 蛋白抑制剂,对 PARP-1 的Ki 为 1.4 nM。它是六磷酸己糖脱氢酶 (H6PD) 抑制剂,有用于去势抵抗性前列腺癌 (CRPC) 的研究潜力。 | |||
T4111 |
Blarcamesine hydrochloride
Anavex 2-73,AVex-73 hydrochloride,AE-37 hydrochloride |
Sigma receptor | GPCR/G Protein |
Blarcamesine hydrochloride (AVex-73 hydrochloride) 是一个sigma-1受体激动剂,IC50值为 860 nM。 | |||
T38845 |
Dodecamethylpentasiloxane
|
Parasite | Microbiology/Virology |
Dodecamethylpentasiloxane 可用作臭虫杀虫剂。 Dodecamethylpentasiloxane 是硅氧烷的一种成分,可用作硅油。 | |||
T20713 |
Flonicamid
UNII-9500W2Z53J,N-(cyanomethyl)-4-(trifluoromethyl)nicotinamide |
Others | Others |
Flonicamid (N-(cyanomethyl)-4-(trifluoromethyl)nicotinamide) 是一种吡啶甲酰胺杀虫剂,在食用日本萝卜叶的过程中抑制蚜虫(M.persicae)的唾液分泌和汁液摄入。它对棉蚜、红蚜、巴迪蚜、禾谷蚜和大鼠产生毒性。 | |||
T2391 |
Camostat mesylate
FOY-S980,甲磺酸卡莫司他,FOY305,Camostat mesilate |
Serine/threonin kinase; SARS-CoV; Sodium Channel | Cell Cycle/Checkpoint; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
Camostat mesylate (FOY-S980) 是口服活性合成的丝氨酸蛋白酶抑制剂,用于慢性胰腺炎。它是TMPRSS2的抑制剂,对SARS-CoV-2具有抗病毒活性。它抑制前列腺素、胰蛋白酶和苦参多糖的活性。 | |||
T62083 |
Camonsertib
ATR inhibitor 4,RP-3500 |
ATM/ATR | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
Camonsertib (RP-3500) 是一种选择性的、口服具有活力的 ATR 激酶抑制剂 (ATRi),在生化试验中的 IC50: 1.00 nM,表现出有效的抗肿瘤作用。RP-3500 对 ATR 的选择性是 mTOR 的 30 倍 (IC50: 120 nM),是 ATM、DNA-PK 和 PI3Kα 激酶的 2,000 倍以上。 | |||
T13147 |
ICAM-1-IN-1
|
Integrin | Cytoskeletal Signaling |
ICAM-1-IN-1 是选择性的 ICAM-1和 E-selectin 抑制剂,IC50值分别为5和7 nM。 | |||
T7465 |
4-Methylbenzylidene camphor
Enzacamene,4-甲基苄亚基樟脑,3-(4-甲基苯亚甲基)樟脑,4-MBC |
AChE | Neuroscience |
4-Methylbenzylidene camphor 是有机的樟脑衍生物,应用于化妆品行业,具有保护皮肤抵抗紫外线(特别是紫外线B 辐射)的能力。 | |||
T37535 |
Camrelizumab
SHR-1210 |
||
Camrelizumab (SHR-1210) 是一种具有高亲和力且针对 PD-1的人源 IgG4-κ单克隆抗体。Camrelizumab 与 PD-1 的结合亲和力高达 3 nM,对 PD-1/PD-L1具有抑制作用, IC50 为 0.70 nM。Camrelizumab 具有抗肿瘤活性和耐受性,可用于研究包括 NSC-LC、ESCC、霍奇金淋巴瘤和晚期 HCC 等的癌症。 | |||
TP1217L |
Autocamtide 2 TFA(129198-88-5 free base)
|
CaMK | Neuroscience |
Autocamtide 2 TFA(129198-88-5 free base) 是钙/钙调蛋白依赖性蛋白激酶 II (CaMKII) 的高选择性肽底物。 Autocamtide 2 TFA 可用于 CaMKII 活性测定。 | |||
T2006 |
Omecamtiv mecarbil
CK-1827452 |
ATPase; Myosin | Cytoskeletal Signaling; Membrane transporter/Ion channel |
Omecamtiv mecarbil (CK-1827452) 是一种心脏特异性的肌球蛋白激活剂,用于研究心脏相关疾病。 | |||
T20856 |
Dicamba
Dianat,麦草畏,Mediben,Banlen,Banvel |
Others | Others |
Dicamba (Banvel) 是一种氯化有机除草剂。 Dicamba 可用于防治阔叶杂草。 | |||
T1673 |
Acamprosate calcium
calcium acetylhomotaurinate,N-Acetylhomotaurine Calcium,Alcomed,阿坎酸钙,Sobriol,Campral EC,Calcium N-acetylhomotaurinate |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Acamprosate calcium (Campral EC) 是 GABA 受体激动剂和谷氨酸能系统调节剂,用于治疗酒精依赖。 | |||
T11508L |
Camicinal hydrochloride
GSK962040 hydrochloride |
Others; Motilin Receptor | GPCR/G Protein; Others |
Camicinal hydrochloride (GSK962040 hydrochloride) 是胃动素受体的特异性激动剂 (pEC50 = 7.9)。 | |||
T27209 |
Droxicam
Droxicamum,屈昔康 |
Others | Others |
Droxicam (Droxicamum) 是一种非甾体抗炎化合物,可用于缓解肌肉骨骼疾病的炎症和疼痛的研究。 | |||
T7780 |
Blarcamesine
AE-37,AVex-73 |
AChR | Neuroscience |
Blarcamesine (AVex-73) 是一种毒蕈碱 M1 激动剂,具有抗惊厥、抗失忆、神经保护和抗抑郁的特性,可能用于治疗阿尔茨海默病。 | |||
T73718 |
N-methyl-N-dithiocarboxyglucamine sodium
|
||
N-methyl-N-dithiocarboxyglucamine (MDCG) sodium 在小鼠模型中动员并促进金属硫蛋白结合109Cd的排泄,显著降低肝脏和肾脏中的镉含量。肝脏和肾脏为镉诱导毒性影响的主要易感器官。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1008 |
Psoralenoside
|
CaMK; Calcium Channel; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Psoralenoside 是源于补骨脂中的苯并呋喃苷,具有抗肿瘤、抗菌、促进成骨细胞增殖和雌激素样活性。它对组胺 H1、钙调素和电压门控 l 型钙通道具有较高的亲和力。 | |||
T8846 |
beta-Escin
B-escin,AESCINE,beta-七叶素 |
Immunology/Inflammation related | Immunology/Inflammation |
beta-Escin 是七叶树种子的主要活性成分。它可抑制碱性成纤维细胞生长因子所诱导的增殖、迁移、管形成以及体内 CAM 血管生成。它具有研究抗血管生成作用的分子机制的潜力。 | |||
TMS2262 |
(-)-CAMPHOR
L-Camphor,左旋樟脑 |
Others | Others |
(-)-CAMPHOR (L-Camphor) 是樟脑的手性中间体,在食品中用作风味添加剂和甜味剂。 | |||
T5S1952 |
9-Methoxycamptothecin
|
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
9-Methoxycamptothecin 是从臭味假柴龙树中分离得到的一种天然产物,通过抑制拓扑异构酶起到抗肿瘤作用,具有强效的诱导 G2/M 期细胞和癌细胞凋亡的作用。 | |||
T2764 |
(S)-10-Hydroxycamptothecin
10-羟喜树碱,10-羟基喜树碱,10-Hydroxycamptothecin,10-HCPT |
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
(S)-10-Hydroxycamptothecin (10-HCPT) 是一种从喜树中分离的 DNA 拓扑异构酶 I 抑制剂。它显著诱导细胞凋亡,可研究肝癌、胃癌、结肠癌和白血病。 | |||
T4S2157 |
Campesterol
菜油甾醇,(24R)-5-Ergosten-3β-ol |
Endogenous Metabolite | Metabolism |
Campesterol ((24R)-5-Ergosten-3β-ol) 是一种植物甾醇,具有降胆固醇和抗癌的活性。 | |||
T1123 |
Camptothecin
NSC-100880,Campathecin,喜树碱,(S)-(+)-Camptothecin,CPT |
Apoptosis; Influenza Virus; Topoisomerase; Antibiotic; Antifungal | Apoptosis; DNA Damage/DNA Repair; Microbiology/Virology |
Camptothecin (CPT) 属于生物碱类天然产物,是一种 DNA 拓扑异构酶 I (Topo I) 的抑制剂 (IC50=679 nM),具有特异性。Camptothecin 具有抗肿瘤活性,可以诱导细胞凋亡。 | |||
T5037 |
Midecamycin
Antibiotic SF-837,Turimycin P3,Medecamycin A1,Rubimycin,麦迪霉素,Platenomycin B1,Espinomycin A |
Antibacterial; Antibiotic | Microbiology/Virology |
Midecamycin (Medecamycin A1) 是乙酰氧基取代的大环内酯类抗生素,对革兰氏阳性和阴性菌有效。 | |||
T3S1955 |
7-Ethylcamptothecin
|
Others | Others |
7-Ethylcamptothecin 是一种喜树碱类似物。其中喜树碱是一种细胞毒性生物碱,从喜树中分离出得到,对 L1210 白血病和 Walker 256 癌肉瘤模型具有很强的抗肿瘤活性。 | |||
T4S1951 |
10-Methoxycamptothecin
|
Others | Others |
10-Methoxycamptothecin 是分离自喜树的喜树碱衍生物,具有高抗癌特性。通过对 2774 细胞系的抗肿瘤活性测定,发现它比 10-羟基喜树碱的细胞毒性更高。 | |||
T17143 |
Toyocamycin
丰加霉素,Vengicide |
Apoptosis; Others; IRE1; Antibiotic; Antifungal | Apoptosis; Cell Cycle/Checkpoint; Microbiology/Virology; Others |
Toyocamycin (Vengicide) 是放线菌类产生的腺苷类似物,为 X 盒结合蛋白 1 (XBP1) 抑制剂,抑制 IRE1α 诱导的 ATP 依赖性 XBP1 mRNA 的断裂,IC50值为 80 nM。它还诱导凋亡。 | |||
T14329 |
Ascamycin
|
Nucleoside Antimetabolite/Analog; Others; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Ascamycin 是一种由链霉菌属产生的 5'-O-磺酰胺核糖核苷抗生素,对黄单胞菌类显示出选择性的抗菌活性,对柠檬黄单胞菌、口蹄疫黄单胞菌和噬菌体具有抑制作用,MIC 值分别为0.4μg/mL、12.5μg/mL 和12.5μg/mL。 | |||
T3853 |
Camelliaside B
山茶苷 B,山茶甙B |
Others | Others |
Camelliaside B 是一种类黄酮,来自于油茶种子残渣的甲醇提取物。 | |||
T1468 |
Lornoxicam
Ro 13-9297,Chlortenoxicam,TS110,氯诺昔康 |
COX; Endogenous Metabolite | Immunology/Inflammation; Metabolism; Neuroscience |
Lornoxicam (Chlortenoxicam) 是一种新型非甾体抗炎药,是高活性 COX-1 和 COX-2 抑制剂,IC50 分别为 5 和 8 nM。 | |||
T20191 |
(-)-Camphoric acid
(-)-樟脑酸,L-Camphoric acid,Camphoric acid, (-)- |
GluR | Neuroscience |
(-)-Camphoric acid (L-Camphoric acid) 是一种活性较低的樟脑酸对映异构体,樟脑酸可诱导 GluR 表达。 | |||
T67867 |
Mycaminosyltylonolide
|
Antibacterial | Microbiology/Virology |
Mycaminosyltylonolide 是一种大环内酯类抗生素,它是 tyololide 在位置5上具有β - d -mycaminosyl 残基。Mycaminosyltylonolide 是一种有效的抗生素,具有抗菌活性和抑制荧光素酶的合成。 | |||
T7959 |
(+)-ISOPINOCAMPHEOL
|
Others | Others |
(+)-ISOPINOCAMPHEOL 是一种天然产物。 | |||
T10668 |
Camalexin
|
Reactive Oxygen Species; ROS; Antibacterial; Antifungal | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Camalexin 是从Camelina sativa 和Arabidopsis 中分离出来的一种植物抗毒素,可诱导活性氧的产生,具有抗菌、抗真菌、抗增殖和抗癌活性。 | |||
T13229 |
Tunicamycin
|
Influenza Virus; Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Tunicamycin 是一种抗生素的混合物,通过阻断 GlcNAc 磷酸转移酶 (GPT),抑制 N-连接糖基化。Tunicamycin 具有抗肿瘤活性,还具有抗细菌、抗真菌和抗病毒活性。 | |||
T40179 |
Sodium Camptothecin
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Sodium Camptothecin 是一种植物生物碱,具有抗肿瘤活性。它是可逆 RNA 合成抑制剂,可以抑制腺病毒的复制。它能抑制 DNA 合成,并引起细胞内预形成的病毒 DNA 断裂。 | |||
T0882 |
(+)-Camphor
D-(+)-Camphor,D-Camphor,(+)-樟脑,(1R)-(+)-Camphor |
Antibacterial; TRP/TRPV Channel | Membrane transporter/Ion channel; Microbiology/Virology |
(+)-Camphor (D-Camphor) 是一种食品添加剂,在医学上可用作防腐剂。 | |||
T3854 |
Camelliaside A
山茶苷 A,山茶甙A |
Others | Others |
Camelliaside A 是一种的类黄酮化合物,来源于油茶种子残渣的甲醇提取物中。 | |||
T2952 |
Camphor
樟脑,(±)-Camphor,Bornan-2-one,2-Camphanone,2-Bornanone,Formosa |
Influenza Virus; TRP/TRPV Channel | Membrane transporter/Ion channel; Microbiology/Virology |
Camphor (2-Camphanone) 是一种双环单萜酮,广泛存在于植物中,尤其是樟脑。 它是一种激动剂,局部用作皮肤止痒剂和抗感染剂,具有抗病毒,镇咳和抗癌活性。 | |||
T2S0271 |
Voacamine
老刺木胺,Voacanginine |
Cannabinoid Receptor; P-gp | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Voacamine (Voacanginine) 是非洲马铃果中的一种吲哚生物碱,可抑制多药耐药肿瘤细胞中的 P-糖蛋白作用,具有强效的大麻素 CB1受体拮抗活性。 | |||
T1286 |
Vincamine
Angiopac,Oxybral,Devincan,Novicet,Equipur,长春胺,Perval |
GPR; Others | Endocrinology/Hormones; GPCR/G Protein; Others |
Vincamine (Perval) 是从长春花中提取的单萜类吲哚生物碱,可作为外周血管扩张剂,对脑微血管循环有选择性的血管调节作用。它可改善体内葡萄糖稳态,对 2 型糖尿病具有研究潜力。它是GPR40激动剂,通过改善 β 细胞功能障碍和促进葡萄糖刺激型胰岛素分泌发挥 β 细胞保护作用。 | |||
T82786 | Campneoside II | ||
Campneoside II, 分离自毛泡桐,展现出显著的抗补体活性。 | |||
TN4025 | Eucamalduside A | Others | Others |
Eucamalduside A is a natural product from Eucalyptus camaldulensis var. obtusa. | |||
T4952 |
9-Hydroxycamptothecin
9-HCPT,9-羟基喜树碱,10-Hydroxycampothecin |
Topoisomerase | DNA Damage/DNA Repair |
9-Hydroxycampothecin 是具有抗癌活性的喜树碱衍生物。 | |||
T82002 |
Juniper camphor
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Juniper camphor为倍半萜烯类化合物,可通过分馏樟脑蓝油的高沸点馏分进行分离。 | |||
TN3573 |
Camaric acid
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Antifection | Microbiology/Virology |
Camaric acid shows antibacterial activity against Staphylococcus aureus and methicillin resistant S. aureus with IC50 values 8.74 and 8.09 uM, respectively, it also shows moderate antileishmanial activity and highly potent antitrypanosomal activity. Camar | |||
T1521 |
(±)-10-Hydroxycamptothecin
Hydroxy Camptothecine,10-羟基喜树碱,10-Hydroxycamptothecin |
Topoisomerase | DNA Damage/DNA Repair |
(±)-10-Hydroxycamptothecin (Hydroxy Camptothecine) 是一种从喜树茎木中分离出来的生物碱,抑制拓扑异构酶 I 活性,具有广谱抗肿瘤活性。 | |||
TN2620 | 14,15-Didehydrovincamenine | Others | Others |
14,15-Didehydrovincamenine 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 TN2620,CAS号为 112219-48-4。 | |||
T21098 |
Decamethylcyclopentasiloxane
Dekamethylcyklopentasiloxan,Cyclopentasiloxane, decamethyl- |
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Decamethylcyclopentasiloxane is a cyclic methylsiloxane with volatile properties. | |||
TN5954 | Camaldulenic acid | ||
Camaldulenic acid是一种天然产物,属于唇形科鼠尾草属,其产品编号为 TN5954,CAS号为 71850-15-2。Camaldulenic acid可用作对照参考。 | |||
TN5830 |
Campsiketalin
Rengyoxide dimethyl ketal |
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Campsiketalin 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 TN5830,CAS号为 93675-96-8。 | |||
TN4471 |
Lysicamine
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IL Receptor; Antifection | Immunology/Inflammation; Microbiology/Virology |
Lysicamine shows significant antioxidant capacity in the ORAC(FL) assay and it is active against S. epidermidis and C. dubliniensis, with MIC values in the range 12.5-100 microg mL(-1). Lysicamine has antimicrobial and anti-inflammation activity, the mini | |||
T21047 |
Apovincamine
cis-Apovincamine |
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Apovincamine is a vinca alkaloid and a chemical precursor of Vinpocetine, which is a derivative of Vincamine with vasodilating activity. | |||
TN1464 |
Camellianin A
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RAAS | Endocrinology/Hormones |
Camellianin A has anticancer activity, it can inhibit the proliferation of the human hepatocellular liver carcinoma Hep G2 and human breast adenocarcinoma MCF-7 cell lines in a dose-dependent manner and induce the significant increase of the G0/G1 cell po | |||
TN1176 |
10-Nitro-camptothecin
9-硝基喜树碱 |
Others | Others |
10-Nitro-camptothecin is a natural product | |||
T38481 | Camellianin B | ||
Camellianin B, a flavonoid compound and metabolite of Camellianin A, exhibits antioxidant properties and acts as an angiotensin converting enzyme (ACE) inhibitor. | |||
TN2681 |
Elasticamide
2-(2'-Hydroxytetracosanoylamino)-octadecane-1,3,4-triol |
Others | Others |
(2S,3S,4R,2'R)-2-(2'-hydroxytetracosanoylamino)octadecane-1,3,4-triol shows selectively inhibitory activity against phospholipase A 2 (PLA 2) secreted from Crotalus adamenteus venom at concentration of 100 ug/mL. | |||
TN4667 |
Norcamphor
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Others | Others |
Norcamphor 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 TN4667,CAS号为 497-38-1。 | |||
T16726 |
Rebeccamycin
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Topoisomerase | DNA Damage/DNA Repair |
Rebeccamycin is an antitumor antibiotic+ inhibits DNA topoisomerase I. Rebeccamycin appears to exert its primary antineoplastic effect by poisoning topoisomerase I. It also has a negligible effect on protein kinase C and topoisomerase II. | |||
T31651 |
Epicoccamide
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Epicoccamide is a marine fungal metabolite originally isolated from E. purpurascens. | |||
TN2642 |
16,17-Dihydroapovincamine
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Others | Others |
16,17-Dihydroapovincamine 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 TN2642,CAS号为 57130-30-0。 | |||
TN4026 |
Eucamalol
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Others | Others |
Eucamolol exhibits significant repellent activity against Aedes albopictus, and inhibits its feeding as well as DEET, is effective repellent (75%) up to 3 h after exposure to mosquito. | |||
T83520 |
(S)-Campesterol
5-Ergosten-3β-ol |
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(S)-Campesterol (5-Ergosten-3β-ol),一种植物甾醇,存在于多种食物和植物源中,对人体健康具有潜在益处。 | |||
TN2460 |
12-Ethyl-9-hydroxycamptothecin
7-乙基-10-羟基喜树碱,7-Ethyl-10-Hydroxy-Camptothecin |
Others | Others |
12-Ethyl-9-hydroxycamptothecin 是一种 Camptothecin 的衍生物。其中Camptothecin (CPT) 是一种生物碱,也是 DNA 拓扑异构酶I 抑制剂(IC50:679 nM)。 | |||
T38299 |
Tunicamycin V
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Tunicamycin 15:1 is a mixture of tunicamycin structural isomers that contains a 15-carbon N-acyl chain with variable branching patterns.References Tunicamycin 15:1 is a mixture of tunicamycin structural isomers that contains a 15-carbon N-acyl chain with variable branching patterns. References | |||
T74198 |
Beauverolide Ja
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Beauverolide Ja 是一种环四缩酚肽,是一种有效的钙调蛋白 (CaM) 抑制剂,对 Ca2+-CaM 的Kd 为 0.078 μM,Ki 为 0.39 μM。Beauverolide Ja 是Isaria fumosorosea 的次级代谢产物。 | |||
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