230
28
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23757 |
Ascorbic acid, rutoside drug combination
Rutinoscorbin,Rutascorbin,Ruta C 60,Cerutin |
||
Ascorbic acid, rutoside drug combination is used for treating diabetic retinopathy. | |||
T12829 |
Salmeterol
沙美特罗,GR33343X |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Salmeterol (GR33343X) 是一种选择性的人β2肾上腺素受体激动剂。它能够有效刺激 cAMP 积累,作用于 CHO 细胞,对人β2,β1和β3肾上腺素受体的 pEC50分别为 9.6、6.1 和 5.9。 | |||
T7614 |
Eniluracil
GW776C85,5-Ethynyluracil |
Others | Others |
Eniluracil (GW776C85) 是不可逆的二氢嘧啶脱氢酶(DPD)抑制剂,是一种尿嘧啶类似物,能够使 5-FU 的口服生物利用度提高到 100%,促进均匀吸收和可预测的毒性。 | |||
T3661 |
Citarinostat
ACY241,HDAC-IN-2 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Citarinostat (ACY241) 是一种强效、选择性和口服组蛋白脱乙酰酶 (HDAC) 抑制剂,具有抗肿瘤活性,对 HDAC1、HDAC2、HDAC3、HDAC6 和 HDAC8 的 IC50分别为 35、45、46、2.6 和 137 nM。 | |||
T7744 |
Piperaquine tetraphosphate tetrahydrate
4,4'-(1,3-丙烷双-4,1-哌嗪基)双(7-氯喹啉)磷酸盐水合物,四磷酸哌喹四水合物 |
Parasite | Microbiology/Virology |
Piperaquine tetraphosphate tetrahydrate 是一种双喹啉抗寄生虫剂,可与青蒿素联用研究抗疟。 | |||
T6653 |
Salmeterol Xinafoate
Salmetedur,昔美酸沙美特罗,沙美特罗昔萘酸酯,GR 33343X xinafoate,Arial |
HIV Protease; Adrenergic Receptor | GPCR/G Protein; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Salmeterol Xinafoate (GR 33343X xinafoate) 是选择性人β2肾上腺素受体激动剂。Salmeterol 有效刺激 cAMP 积累,能够作用于 CHO 细胞,对人β2,β1和β3肾上腺素受体的 pEC50分别为 9.6、6.1 和 5.9。 | |||
T7532 |
Piperaquine
|
Parasite | Microbiology/Virology |
Piperaquine 是一种双喹啉化合物,可抑制来自疟疾感染患者的恶性疟原虫分离株的离体生长,IC50 范围为 11.8-217.3 nM。 | |||
T3266 |
Lumefantrine
Benflumetol,dl-Benflumelol,苯芴醇 |
Others; Parasite; Autophagy | Autophagy; Microbiology/Virology; Others |
Lumefantrine (dl-Benflumelol) 是一种抗疟药,用于治疗急性单纯性疟疾。与Artemether 联用,可提高疗效。 | |||
T2554 |
Etofibrate
|
Others | Others |
Etofibrate 是烟酸和氯贝酸的醚二醇-1,2 二酯。它是动物和人类中一种有效的降血脂剂。 | |||
T63166L |
(S, R)-LSN 3318839
(S, R)-LSN 3318839(Isomer-2764704-18-7) |
Glucagon Receptor | GPCR/G Protein |
T7537 |
Norgestimate
炔诺肟酯,诺孕酯 |
Progesterone Receptor | Others |
Norgestimate 是一种具有口服活性、高度选择性的孕激素活性和较小雄激素作用的孕激素,是一种合成的孕激素类似物。它可用作口服的避孕药。 | |||
T1430 |
Betamipron
CS-443,N-Benzoyl-β-alanine,倍他米隆 |
Antibacterial; Antibiotic | Microbiology/Virology |
Betamipron (CS-443) 与Panipenem 联用,可抑制Panipenem 摄取进入肾小管,防止肾毒性。 | |||
T2239L |
Raltegravir
雷特格韦,MK-0518 |
HIV Protease; Integrase | Microbiology/Virology; Proteases/Proteasome |
Raltegravir (MK-0518) 是一种HIV 整合酶抑制剂。 | |||
T27787L |
L-797,591 hydrochloride
L-797,591 hydrochloride(217480-24-5 Free base) |
||
L-797,591 hydrochloride 对生长抑素受体亚型 1 (SSTR1)有活性。L-797,591 hydrochloride 常与 AG1478 联合使用来增强表达 SSTR1的细胞中 p-ERK5的表达。L-797,591 hydrochloride 在共转染的细胞中显著增强了 p38的磷酸化,这一作用在与 AG1478联合处理时被逆转。 | |||
T65232 |
HEDTA
N-(2-Hydroxyethyl)ethylenediaminetriacetic acid |
Others | Others |
HEDTA 是一种螯合剂,常与柠檬酸联合用药来研究血液疾病和脑部血液应激。 | |||
T14408 |
Azido-PEG1-CH2CO2H
4-哌啶酮缩乙二醇 |
Others; PROTAC Linker | Others; PROTAC |
Azido-PEG1-CH2CO2H 是属于 alkyl/ether 类的PROTAC linker,可用于合成 PROTAC BRD4 Degrader-1. | |||
T7045 |
Clonidine
Nexiclon,Catapres,Kapvay,可乐定 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Clonidine (Kapvay) 是 alpha2 肾上腺素能激动剂。 | |||
T3139 |
Sultamicillin Tosylate
Bacimex,舒巴西林,舒他西林甲苯磺酸盐,Unacim orale |
Antibacterial; Antibiotic | Microbiology/Virology |
Sultamicillin Tosylate (Unacim orale) 是一种口服活性 β-内酰胺酶抑制剂,具有抗菌活性。 它是舒巴坦与氨苄西林的双酯的甲苯磺酸盐。 | |||
T76877 |
Vofatamab
RG-7444,B-701,MFGR-1877S |
FGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Vofatamab (B-701) 是一种全人源靶向 FGFR3 的单克隆抗体。Vofatamab 具有潜在的抗癌抗肿瘤活性,常与其他化合物联用来治疗癌症。 | |||
T0996 |
Ethynodiol diacetate
Ethynodiol acetate,双醋炔诺醇,8080 CB |
Estrogen/progestogen Receptor; Progesterone Receptor | Endocrinology/Hormones; Others |
Ethynodiol diacetate (Ethynodiol acetate) 是一种可用作激素避孕药的甾体孕激素,具有相对较少或没有雄激素效果,而具有显著雌激素作用。 | |||
T12632L |
(S)-Mirtazapine
(S)-6-Azamianserin,(S)-Org3770 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
(S)-Mirtazapine ((S)-Org3770) 是 Mirtazapine 的 S(+)-对映体。(S)-Mirtazapine 是一种选择性 5-HT2 受体拮抗剂,具有促痛觉作用,常与Mirtazapine 的 R(-)-对映体混合使用来研究抑郁症。 | |||
T67964 |
Terflavoxate
|
Microtubule Associated | Cytoskeletal Signaling |
Terflavoxate 是一种新型的、具有口服活性的半合成的他汀类微管抑制剂,常与卡培他滨一起联合使用。Terflavoxate 用于癌症的研究。 | |||
T4506 |
Gadopentetate dimeglumine
Meglumine gadopentetate,SH-L-451A,Gd-DTPA,Gadopentetic acid dimeglumine,钆喷酸葡胺,Gadopentetic acid dimeglumine salt |
Others | Others |
Gadopentetate dimeglumine (Gd-DTPA) 可用于核磁共振成像 (MRI) 中,使血管、器官和其他非骨组织能够更清晰地被看到。 | |||
T0100 |
Atazanavir sulfate
阿扎那韦硫酸盐,BMS-232632,BMS-232632 sulfate,硫酸阿扎那韦 |
P450; SARS-CoV; HIV Protease; P-gp | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Atazanavir sulfate (BMS-232632 sulfate) 是一种氮杂肽和 HIV 蛋白酶抑制剂,与其他抗 HIV 药物联合用于治疗 HIV 感染和艾滋病。它也是SARS-CoV 3CLpro 抑制剂,IC50为 3.49 μM。 | |||
T40598 |
Norethindrone acetate
19-Norethindroneacetate |
Estrogen Receptor/ERR; Progesterone Receptor | Endocrinology/Hormones; Others |
Norethindrone acetate (19-Norethindroneacetate) 是一种雌性激素,对青少年月经和肝腺瘤有抑制作用,常与孕激素联合使用,可用于研究子宫内膜异位症。 | |||
T19080 |
DOPE
1,2-二油酰-SN-甘油-3-磷酰乙醇胺 |
Others | Others |
DOPE (DOPE) 是一种阳离子脂质体的中性辅助脂质 (helper lipid),能够与阳离子磷脂结合,增强裸 siRNA 的转染效率。 | |||
T2204 |
Diaveridine
二氨藜芦啶,EGIS-5645,敌菌净,CCRIS-3784,AI3-23935 |
DHFR; Antifolate; Antibacterial | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Diaveridine (AI3-23935) 是二氢叶酸还原酶的抑制剂,对于野生型 DHFR 的Ki 值为 11.5 nM。它也是一种抗菌剂。 | |||
T21432 |
Molindone
(±)-Molindone,Moban,Molindonum,SPN-810M |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Molindone ((±)-Molindone) 是一种治疗性抗精神病药物,通过阻断大脑中多巴胺的作用而用于治疗精神分裂症。Molindone 常与羟色胺联合使用,以剂量依赖性方式增加错误并降低反应率。 | |||
T1119 |
Rasagiline
雷沙吉兰,AGN1135,TVP1012 |
BCL; MAO; Monoamine Oxidase | Apoptosis; Metabolism; Neuroscience |
Rasagiline (AGN1135) 是不可逆的、高效的、选择性的线粒体单胺氧化酶 (MAO) 抑制剂,抑制大鼠脑 MAO B 和 MAO A 的 IC50分别为 4.43 nM 和 412 nM。 | |||
T9585 |
GNE-9815
3-(2-cyanopropan-2-yl)-N-[2-fluoro-4-methyl-5-(7-methyl-8-oxo-7,8-dihydropyrido[2,3-d]pyridazin-3-yl)phenyl]benzamide |
Raf | MAPK |
GNE-9815 (3-(2-cyanopropan-2-yl)-N-[2-fluoro-4-methyl-5-(7-methyl-8-oxo-7,8-dihydropyrido[2,3-d]pyridazin-3-yl)phenyl]benzamide) 是一种高激酶选择性 RAF 抑制剂,可用于通过联合治疗靶向 KRAS 突变癌症。 | |||
T60009 |
YS-370
|
P-gp | Membrane transporter/Ion channel; Neuroscience |
YS-370 是一种具有口服活性的 P-gp 抑制剂,对 CYP3A4 有中度抑制作用。 YS-370 有效逆转对紫杉醇和秋水仙碱的多药耐药性,与紫杉醇联合应用表现出更强的抗肿瘤活性。 | |||
T3335 |
Darunavir Ethanolate
地瑞那韦乙醇盐,UIC 94017,Darunavir Ethanolate,TMC114,达芦那韦乙醇 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Darunavir Ethanolate (UIC 94017) 是一种HIV 蛋白酶抑制剂,可以用于 HIV/AIDS 的相关研究。对野生型 HIV-1 蛋白酶的Ki 值为1 nM。 | |||
T3658 |
Trifluridine/tipiracil hydrochloride mixture
Trifluridine-tipiracil hydrochloride mixture,TAS102,TAS-102,TAS 102 |
Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Trifluridine/tipiracil hydrochloride mixture (TAS-102) 是一种新型口服组合药物,含有摩尔比为 2:1 的曲氟尿苷(TFT) 和盐酸替吡嘧啶 (TTP)。它主要通过抑制胸苷酸合酶 (TS) 和掺入 DNA 来显示抗肿瘤活性。 | |||
T7318 |
Elimusertib
BAY-1895344 |
ATM/ATR | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
Elimusertib (BAY-1895344) 是一种可口服的选择性ATR 抑制剂,IC50值为 7 nM。它具有抗肿瘤活性,可研究实体瘤和淋巴瘤。 | |||
T77440 |
Codrituzumab
RG-7686,RO5137382,GC33 |
||
Codrituzumab (GC3)是一种人源化针对 glypican-3 肝癌蛋白的抗体,可与索拉非尼联合使用来研究不可治愈的晚期肝细胞癌 (HCC) 。 | |||
T8875 |
CD73-IN-3
EX-A4254,LY-3475070 |
CD73 | Immunology/Inflammation |
CD73-IN-3 (LY-3475070) 是一种有效的选择性 CD73 抑制剂,IC50 为 28 nM,具有癌症的研究潜力。 | |||
T8856 |
Ascorbyl Propyl Hyaluronate
|
Others | Others |
Ascorbyl Propyl Hyaluronate 是透明质酸和维生素 C 的完美结合,克服了维生素 C 的不稳定性,是改善皱纹、滋润、镇静肌肤、美白的优质原料。 | |||
T1595 |
Nevirapine
NSC 641530,奈韦拉平,BI-RG 587,奈伟拉平,NVP |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Nevirapine (NVP) 是一种 HIV-1逆转录酶非核苷抑制剂,Ki 值为 270 μM,可用于研究 HIV/AIDS。 | |||
T35394 |
Sintilimab (anti-PD-1)
IBI308,Sintilimab (anti-PD-1) |
PD-1/PD-L1 | Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation |
Sintilimab (IBI308) 是一种人源化的 IgG4 单克隆抗体,具有显著的抗肿瘤活性,通过与 PD-1 结合从而阻断 PD-1 与其配体 (PD-L1 和 PL-L2) 的相互作用,进而恢复内源性抗肿瘤 T 细胞反应。Sintilimab 联合其他化合物来治疗经典霍奇金淋巴瘤、非小细胞肺癌和食管癌。 | |||
T0930 |
Sulfadiazine
Sulphadiazine,磺胺嘧啶 |
Antibacterial; Antibiotic; Parasite; Autophagy | Autophagy; Microbiology/Virology |
Sulfadiazine (Sulphadiazine) 是一种磺胺类抗生素具有抗疟活性,可研究弓形虫病。 | |||
T77466 |
Tremelimumab
Ticilimumab,CP-675206 |
Others | Others |
Tremelimumab 是一种细胞毒性T淋巴细胞相关抗原-4(CTLA-4)阻断抗体.Tremelimumab 常与 Durvalumab 联合使用来治疗肝癌、肺癌等实体癌。 | |||
T9718 | Ethoxylated hydrogenated castor oil | Others | Others |
Ethoxylated hydrogenated castor oil 是一种聚乙二醇与天然蓖麻油的混合物,可用于水包油 (o/w) 乳浊液的乳化和增溶,是动物实验的良好助溶剂。 | |||
T9277 |
ALC-0315
|
||
ALC-0315是一种可电离的氨基脂质,已与其他脂质组合用于形成脂质纳米颗粒。脂质纳米颗粒已经用于 mRNA (COVID-19) 疫苗的研究。 | |||
T2324 |
Darunavir
地瑞那韦,达芦那韦,TMC114 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Darunavir (TMC114) 是一种 HIV 蛋白酶抑制剂,用于治疗艾滋病和 HIV 感染。 由于单独使用时会出现抗病毒药物耐药性,因此与其他抗 HIV 药物联合使用。 | |||
T9498 |
BAY-8400
|
DNA-PK | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
BAY-8400是一种具有口服活性、有效和选择性 DNA 依赖蛋白激酶 (DNA-PK) 抑制剂(IC50=81 nM),与靶向α疗法联合使用显示协同疗效。BAY-8400 可用于癌症研究。 | |||
T76788 |
Demcizumab
OMP 21M18 |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
Demcizumab (OMP 21M18) 是一种抗 DLL4 单克隆抗体。Demcizumab 是一种有效的 Notch 通路抑制剂。Demcizumab 在多种癌症模型中无论使单独还联合化疗试剂使用都是有效的。 | |||
T1784 |
Everolimus
依维莫司,RAD001,SDZ-RAD |
Apoptosis; Others; mTOR; Autophagy | Apoptosis; Autophagy; Others; PI3K/Akt/mTOR signaling |
Everolimus (SDZ-RAD) 是 Rapamycin 的衍生物,也是一种口服活性的mTOR1选择性抑制剂。它与FKBP-12结合可产生免疫抑制复合物,还抑制肿瘤细胞增殖并诱导细胞凋亡和自噬,有免疫抑制和抗癌活性。 | |||
T4100 |
AS8351
NSC51355,AS-8351,AS 8351 |
Histone Demethylase | Chromatin/Epigenetic |
AS8351 (NSC51355) 是一种组蛋白去甲基化酶抑制剂,可以诱导人胎儿肺成纤维细胞重编程为功能性心肌细胞。 | |||
T6246 |
Cobicistat
Tybost,GS-9350,考西司他 |
P450; HIV Protease | Metabolism; Microbiology/Virology; Proteases/Proteasome |
Cobicistat (GS-9350) 是一种细胞色素酶P450 3A 的选择性抑制剂,IC50值为30-285 nM。它是一种药代动力学增强剂,可增强抗 HIV 药物的吸收。 | |||
T1649 |
Tenofovir
替诺福韦,泰诺福韦,PMPA,TDF,GS 1278 |
HBV; HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Tenofovir (GS 1278) 是一种核苷酸逆转录酶抑制剂,可研究 HIV 和慢性乙型肝炎。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN2943 |
3-Hydroxy-6-methoxyflavone
|
Others | Others |
3-Hydroxy-6-methoxyflavone 可与抗生素联合用药来治疗 ESKAPE 病原体感染。 | |||
TJS0339 |
Coumarin-3-carboxylic acid
香豆素-3-羧酸,3-Carboxycoumarin |
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Coumarin-3-carboxylic acid (3-Carboxycoumarin) 是一种合成香豆素的重要起始化合物。其中香豆素是具有多种生物活性的天然产物。它的镧系复合物对 K-562 细胞具有抗增殖活性。 | |||
T24403 |
Folinic acid
HSDB 6544,Leucovorin |
Endogenous Metabolite; Antifolate | Cell Cycle/Checkpoint; Metabolism |
Folinic acid (Leucovorin) 是一种可用于治疗甲氨蝶呤的生物叶酸,通常与 Methotrexate (MTX) 联用来降低 MTX 诱导的毒性,可用于辅助治疗结肠癌。 | |||
T0004 |
Salicylamide
水杨酰胺,Salamide,2-Hydroxybenzamide |
COX | Immunology/Inflammation; Neuroscience |
Salicylamide(2-Hydroxybenzamide) 是一种止痛剂和抗热解药剂,是一种微粒体 UDP-葡糖醛酸基转移酶抑制剂。 | |||
TN1877 |
Lonicerin
忍冬苦苷,金银花 |
Apoptosis; Antibacterial | Apoptosis; Microbiology/Virology |
Lonicerin 是一种抗藻酸盐分泌蛋白的黄酮类化合物,对铜绿假单胞菌有抑制作用。它可预防脂多糖诱导的急性肺损伤的炎症和细胞凋亡。 | |||
T4S0094 |
Hydroxygenkwanin
羟基芫花素,Luteolin 7-methylether,7-O-Methylluteolin |
Antioxidant | oxidation-reduction |
Hydroxygenkwanin (Luteolin 7-methylether) 是一种丁香达芙妮的主要成分,是一种天然的类黄酮化合物。它具有抗氧化,抗神经胶质瘤能力和抗癌作用。 | |||
T1589 |
D-Cycloserine
RO-1-9213,D-环丝氨酸 |
Others; Antibacterial; Antibiotic; iGluR | Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Others |
D-Cycloserine (RO-1-9213) 是一种抗生素,靶向细菌细胞壁肽聚糖生物合成酶。它是一种NMDA 部分激动剂,可以改善认知功能,可研究耐多药结核病。 | |||
T4915 |
β-Glycerophosphate disodium salt hydrate
|
Phosphatase; Endogenous Metabolite | Metabolism |
β-Glycerophosphate disodium salt hydrate 是一种磷酸酶抑制剂,是内源性代谢产物的一种。 | |||
T6S1683 |
Demethoxycurcumin
Curcumin II,去甲氧基姜黄素,Desmethoxycurcumin,脱甲氧姜黄,Monodemethoxycurcumin |
Apoptosis; Antioxidant; Antibacterial; Autophagy | Apoptosis; Autophagy; Microbiology/Virology; oxidation-reduction |
Demethoxycurcumin (Desmethoxycurcumin) 是姜黄素的主要活性成分,有抗炎和抗癌作用。 | |||
T3S0364 |
L-Arginine
L-精氨酸,L-Arg,(S)-(+)-Arginine |
IL Receptor; Endogenous Metabolite; NO Synthase | Immunology/Inflammation; Metabolism |
L-Arginine (L-Arg) 是内皮型一氧化氮合酶(eNOS) 的底物。L-Arginine 通过阳离子氨基酸转运体家族转运到血管平滑肌细胞,并被代谢成一氧化氮、多胺或 L-脯氨酸。 | |||
TN1362 |
Afzelin
阿福豆苷,Kaempferol-3-O-rhamnoside |
PTEN; p38 MAPK; TNF; Mitochondrial Metabolism; Antibacterial; Prostaglandin Receptor; Autophagy | Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation; MAPK; Metabolism; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Afzelin (Kaempferol-3-O-rhamnoside) 具有多种细胞活性,例如 DNA 保护、抗菌、抗氧化和抗炎以及 UV 吸收活性,并且可以通过 UV 吸收和细胞活性的组合保护人体皮肤免受 UVB 引起的损伤。 Afzelin 减轻线粒体损伤,增强线粒体生物合成并降低线粒体自噬相关蛋白、parkin 和 putative kinase 1 的水平。 | |||
T5074 |
Cholesteryl palmitate
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Others; Endogenous Metabolite | Metabolism; Others |
Cholesteryl palmitate 是一种慢性间质性肺炎的有用预后生物标志物。 | |||
T5S0053 |
Coptisine
黄连碱,Coptisin |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Coptisine (Coptisin) 是一种从黄连中分离到的生物碱,是非竞争性的IDO 抑制剂,Ki=为 5.8 μM,IC50=6.3 μM。 | |||
T2S1865 |
Octyl gallate
Gallic acid octyl ester,n-Octylgallate,Octyl 3,4,5-trihydroxybenzoate,Progallin O,Stabilizer GA-8,没食子酸辛酯 |
Antioxidant; Influenza Virus; Reactive Oxygen Species; Antibacterial; Antifungal; HSV | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; oxidation-reduction |
Octyl gallate (Octyl 3,4,5-trihydroxybenzoate) 具有抗菌、抗氧化作用,有选择性和敏感性的荧光特性,广泛用作食品添加剂。它对 HSV-1,水泡性口炎病毒和脊髓灰质炎病毒有显著的抗病毒作用。 | |||
T4S1551 |
Cinnamaldehyde
Cinnamic Aldehyde,肉桂醛 |
HIF | Angiogenesis; Chromatin/Epigenetic |
Cinnamaldehyde (Cinnamic Aldehyde) 具有解热作用。 它是镇静剂。它抑制MDA-MB-435S 细胞的侵袭能力与下调miR-27a 的表达有关。它诱导活性氧的产生,发挥血管扩张和抗癌作用。 它似乎是一种有希望的候选药物,可作为与 5-氟尿嘧啶 (5-FU) 和奥沙利铂 (OXA) 这两种用于 CRC 治疗的化疗药物联合治疗的辅助剂。其作用的可能机制可能涉及药物代谢基因的调节。 它在抑制黑色素瘤的发生和发展方面具有一定的作用,其作用机制可能表现为抑制VEGF 和HIF-α的表达,从而使血管模拟和黑色素瘤细胞新生血管的形成,促进肿瘤的生长。 | |||
T11895 |
Luteolin-7-rutinoside
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Others | Others |
Luteolin-7-rutinoside has both antifungal activities and anti-arthritic, can result in a combination therapy for the treatment of fungal arthritis due to C. albicans infection. | |||
TN2524 |
1-Acetyl-β-carboline
1-Acetyl-beta-carboline |
Antifection | Microbiology/Virology |
Combination of 1-acetyl-beta-carboline with ampicillin exhibits synergistic antibacterial activity against MRSA. | |||
TN5466 |
Boeravinone B
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Boeravinone B, a novel efflux pump inhibitor, apart from inhibiting the MdeA mediated efflux, also significantly inhibit the biofilm formation of S. aureus, boeravinone B may be used in combination with mupirocin for further development. Boeravinone B exh | |||
TN1349 | 9-Hydroxycalabaxanthone | Antifection | Microbiology/Virology |
9-Hydroxycalabaxanthone exhibits cytotoxicity against the HT-29 cell line with ED50 values of 9.1 microM. The combination of 9-hydroxycalabaxanthone with α±-mangostin shows the synergistic antimalarial interaction in both clones. | |||
T40859 |
5-Hydroxy-8-methoxypsoralen
5-Hydroxyxanthotoxin,5-Hydroxy-8-methoxypsoralen |
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5-Hydroxy-8-methoxypsoralen (5-Hydroxyxanthotoxin) is a metabolite derived from Xanthotoxin, which acts as a potent tricyclic furocoumarin suicide inhibitor of CYP (cytochrome P-450). It is employed as an agent for the treatment of psoriasis, eczema, vitiligo, and certain cutaneous Lymphomas, in combination with phototherapy involving exposure to sunlight. | |||
TMA1008 |
Ganoderic acid S
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Others | Others |
A novel combination of triterpenoids includes at least ganoderic acid S (GAS), ganoderic acid T (GAT), ganoderic acid Me (GAMe), ganoderic acid R (GAR), and ganodermic acid S (GMAS), the composition is suitable for the treatment or prophylaxis of colon ca | |||
TN1498 |
Cimigenol
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Others | Others |
Cimigenol is a potential antitumor compound, combination of it with an autophagy inhibitor may be a valuable strategy for the chemoprevention or treatment of colon cancer. It exerted potent cytotoxic activity against SMMC-7721 (7.87μM) and A-549 (12.16 μM | |||
T37751 |
Streptazolin
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Streptazolin is a fungal metabolite originally isolated from S. viridochromogenes. It increases NF-κB activity when used at concentrations ranging from 60 to 130 μg/ml, at least in part, via PI3K signaling. Streptazolin enhances TNF-α secretion induced by LPS and enhances IL-8 secretion when used alone or in combination with LPS in THP-1 Blue cells. | |||
T14047 |
5-Aminolevulinic acid
5-Amino-4-oxopentanoic acid |
Others | Others |
5-Aminolevulinic acid 是血红素合成的中间体,是卟啉合成途径中的一个化合物。它是一种光敏剂、抗肿瘤剂和前药。它也可以(以盐酸盐的形式)与蓝光照明结合使用,用于治疗面部或头皮的轻度至中度厚的光化性角化病。 | |||
T36886 |
Pestalotin
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Pestalotin is a fungal metabolite originally isolated from P. cryptomeriaecola with diverse biological activities. It induces reducing sugar release in embryoless rice endosperms when used at concentrations ranging from 3 to 100 mg/L and enhances growth of rice seedlings (O. sativa) when used in combination with gibberellin A3 at concentrations ranging from 30 to 500 mg/L. Pestalotin has antifungal activity, reducing the growth of C. albicans, C. neoformans, T. rubrum, and A. fumigatus (MICs = 1... | |||
T36417 |
Nargenicin
Antibiotic 47444 |
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Nargenicin is a macrolide antibiotic that selectively inhibits the growth of S. aureus, methicilin resistant S. aureus (MRSA), and M. luteus (MICs = 0.6, 0.3, and 2.5 μg/ml, respectively) over a panel of 11 Gram-positive and Gram-negative bacteria (MICs = >80 μg/ml). [1] It dose-dependently inhibits S. aureus DnaE in the presence of DNase I-activated DNA and E. coli DnaE when used at concentrations of 0.00001-0.1 and 0.01-100 μg/mL, respectively. [2] In murine BV-2 microglial cells, nargenicin (... | |||
TN3708 | Coronarin D | BCL; c-Myc; TNF; NF-κB; Caspase; COX; Antifection | Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome |
Coronarin D shows promising antifungal activity against C. albicans in vitro, the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration (MFC) were 2 and 4 mg/mL, respectively; it is active against tested Gram-positive bacteria, i | |||
TN4291 | Isofuranodiene | IL Receptor; NOS | Immunology/Inflammation |
Isofuranodiene protects GalN/LPS-induced liver injury in SD rats, it may be a potential functional food ingredient for the prevention and treatment of liver diseases. Isofuranodiene has anticancer activity, by inhibiting the proliferation and inducing apo |