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50

抑制剂 & 化合物

14

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T11281L	FGI-106 tetrahydrochloride	Virus Protease; HCV Protease; Influenza Virus; HIV Protease	Microbiology/Virology; Proteases/Proteasome
	FGI-106 tetrahydrochloride 对多种病毒具有抑制活性，有抗埃博拉病毒，裂谷病毒和登革热病毒的 EC50分别为 100 nM，800 nM 和 400-900 nM，抑制非失血性发热病毒HCV 和HIV-1的EC50分别为 200 nM 和 150 nM 。
T25701	Levosemotiadil SD 3212,SA 3212	LDL; Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Levosemotiadil（SA 3212）是一种新型钙拮抗剂，是一种非常有效的低密度脂蛋白氧化抑制剂。Levosemotiadil 可用于预防致死性心律失常。
T8970	ML162	Ferroptosis; GPX; Glutathione Peroxidase	Apoptosis; Metabolism; oxidation-reduction
	ML162 是一种共价谷胱甘肽过氧化物酶 4 抑制剂。它选择性抑制表达突变 RAS 癌基因的细胞系。
T26240	Surfen dihydrochloride Aminokinuride dihydrochloride,Aminoquinuride dihydrochloride,NSC-12155,Aminokinuride 2HCl,Aminoquinuride 2HCl	FGFR; Antiviral; Antibiotic	Angiogenesis; Immunology/Inflammation; Microbiology/Virology; Tyrosine Kinase/Adaptors
	Surfen dihydrochloride (Aminoquinuride dihydrochloride) 是一种有效的硫酸肝素小分子拮抗剂，具有抗菌和抗病毒活性，抑制炭疽致死因子、凝血因子 X 和致死因子。Surfen dihydrochloride 可抑制普通肝素和低分子量肝素的抗凝活性，抑制肝素的硫酸化和肝素裂解酶的降解。Surfen dihydrochloridn 抑制阻断硫酸乙酰肝素介导的 FGF2 结合和信号转导。Surfen 抑制 SEVI 和精液介导的 HIV 1 型感染增强。
T9575	MRTX9768	Histone Methyltransferase	Chromatin/Epigenetic
	MRTX-9768 是一种有效的、选择性的、具有口服活性的 PRMT5-MTA 复合体抑制剂，可选择性靶向 MTAP/CDKN2A 缺失的肿瘤。
T77520	AOH1996	Apoptosis; DNA/RNA Synthesis	Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	AOH1996 是一种具有口服活性的复制体组分 PCNA (增殖细胞核抗原) 配体，靶向转录-复制冲突 (TRC)。AOH1996 可干扰 PCNA 与其结合蛋白的相互作用，导致 DNA 复制应激，诱导细胞凋亡 (apoptosis)。AOH1996 通过稳定 PCNA 和 RNA 聚合酶 II 的相互作用从而导致蛋白酶体依赖的 rpb1 降解和致命的 DNA 损伤。AOH1996 与 DNA 损伤剂具有协同作用，可抑制肿瘤细胞生长。
T77423	Lirilumab ONO-4483,IPH2102	Virus Protease	Microbiology/Virology
	Lirilumab (IPH2102) 是一种针对杀伤性免疫球蛋白样受体抗体 KIR2D 的抗体，具有抗肿瘤活性，通过 Vav1 依赖性 NF-κB 去抑制增强自然杀伤细胞的抗 HPV+ 宫颈癌活性，可用于研究白血病、头颈部鳞状细胞癌 (SCCHN)。
T33050	Lysine butyrate
	Lysine butyrate protects against lethal effect of encelphalomyocariditis virus in mice.
T37007	Resistoflavine
	Resistoflavine is a metabolite of the marine actinomycete S. chibaensis. It slows the growth of and is cytotoxic to HMO2 and HepG2 cells with mean lethal concentrations (LC50) of 0.013 and 0.016 μg/ml, respectively.
T35756	Avermectin B1a monosaccharide
	Avermectin B1a monosaccharide is a macrolide anthelmintic and monosaccharide form of avermectin B1a . It is lethal to C. elegans with a minimum active concentration (MAC) value of 0.1 μM. Avermectin B1a monosaccharide also stimulates conductance in isolated shore crab muscle.
T62683	PRMT5-IN-3
	PRMT5-IN-3 是一种 PRMT5 抑制剂。PRMT5-IN-3 联合 DNA 损伤剂，对肿瘤细胞具有合成致死性。
T62627	Antibacterial agent 69
	Antibacterial agent 69 是一种新型结构抗菌调节剂，并被用来对抗致命的耐多药细菌感染 (MICs: 2.978 μM)。
TP2108	TAPI 2
	ADAM-17 (TACE) and MMP inhibitor (Ki = 120 nM at ADAM-17). Sensitizes cancer stem cells to the lethal effects of 5-FU in vitro. Blocks shedding of TNF-α from cell membranes.
T81948	Latartoxin-1a LtTx-1a
	Latartoxin-1a (LtTx-1a) 是从L. tarabaevi中分离的肽毒素，对昆虫具备麻痹及致死效果，并显示膜结合活性。
T61580	Autophagy inducer 3
	Autophagy Inducer 3 is a chemical compound that exhibits autophagy-induced activity, specifically inducing robust autophagic cell death in various cancer cells while sparing normal cells. This compound induces lethal autophagy through the formation of distinct autophagic vacuoles, LC3 puncta formation, and upregulation of signature autophagy markers such as Beclin and Atg family proteins [1].
T60639	SLEC-11
	SLEC-11 可在E-钙粘蛋白缺陷细胞中作为合成致死(SL)的先导化合物出现，具有治疗胃癌的潜力。
T81926	LiTx3
	LiTx3是一种具有高半胱氨酸含量的致命肽，可自中间乳杆菌粗毒液中分离。该化合物能引起草地贪夜蛾幼虫的弛缓性麻痹。
T37254	Rugulotrosin A
	Rugulotrosin A is an antibiotic originally isolated from Penicillium. It is active against the Gram-positive bacteria E. faecalis, B. cereus, B. subtilis, and S. aureus with 99% lethal dose (LD99) values of 1.6, 3.1, 5.5, and 200 μg/ml, respectively. Rugulotrosin A is inactive against Gram-negative bacteria.
T25365	EGA	Others	Others
	EGA 抑制致命毒素的中毒，并阻止多种其他酸依赖性细菌毒素和病毒进入哺乳动物细胞。EGA 是研究膜运输的有力工具，可用于治疗传染病。
T36630	MRTX9768 hydrochloride
	MRTX9768 hydrochloride is a potent, orally active PRMT5 inhibitor. MRTX9768 hydrochloride is a synthetic lethal-based inhibitor binding the PRMT5-MTA complex[1]. MRTX9768 inhibits SDMA and cell proliferation in HCT116 MTAP-del cells (SDMA IC50 3 nM; prolif. IC50 11 nM) with marked selectivity over HCT116 MTAP-WT cells (SDMA IC50 544 nM; prolif. IC50 861 nM)[1].MRTX9768 selectively targets MTAP/CDKN2A-deleted tumors[2][1]. In xenograft studies, oral administration of MRTX9768 demonstrates dose-de...
T35521	Aflatoxin G2-13C17 Aflatoxin G2-13C17
	Aflatoxin G2-13C17is intended for use as an internal standard for the quantification of aflatoxin G2by GC- or LC-MS. Aflatoxin G2is a mycotoxin that has been found inAspergillus.1It is lethal to ducklings (LD50= 2.83 mg/kg) but is non-toxic to rats when administered at a dose of 200 mg/kg.2 1.Bennett, J.W., and Klich, M.MycotoxinsClin. Microbiol. Rev.16(3)497-516(2003) 2.Wogan, G.N., Edwards, G.S., and Newberne, P.M.Structure-activity relationships in toxicity and carcinogenicity of aflatoxins a...
T38259	Phenelfamycin E
	Phenelfamycin E is an antibiotic originally isolated from Streptomyces. It is active against β-hemolytic Streptoccus, S. pneumoniae, C. difficile, C. perfringens, and P. magnus128 μg/ml). Phenelfamycin E (4-64 mg/kg) increases survival in a mouse model of lethal S. pyogenes infection in a dose-dependent manner. Dietary administration of phenelfamycin E increases body weight in chickens.
T37680	3-hydroxy Palmitic Acid methyl ester
	3-hydroxy Palmitic acid methyl ester (3-hydroxy PAME) is an esterized long-chain fatty acid involved in quorum sensing in R. solanacearum, a bacteria that causes lethal wilting in plants. 3-hydroxy-PAME (175 nM) increases levels of PhcA-regulated virulence factors, greater than 20-, 30-, and 25-fold for EPS I, EGL, and PME, respectively, in the AW1-83 strain of R. solanacearum.
T61815	AL-GDa62
	AL-GDa62是一种潜在的治疗胃癌的合成致死疗法。该化合物对MCF10A-WT（野生型）和MCF10A-CDH1-/-（突变型）同基因乳腺上皮细胞的EC50分别为3.2 μM和2 μM。
T60419	Cyclic HPMPC
	Cyclic HPMPC 是有效的抗病毒剂，可以增加感染致死性牛痘苗病毒 (IHD 株) 小鼠的动脉氧饱和度水平。用 Cyclic HPMPC 治疗可改善先天性豚鼠巨细胞病毒 (GPCMV) 感染的结果并减少豚鼠模型中的病毒复制。
T78561	M62812 free base
	M62812 (free base) 是一种TLR4信号转导抑制剂，能够抑制内皮细胞和白细胞的活化，有效预防小鼠致死性感染性休克，适用于脓毒症的研究。
T83699	LL-37 (18-37) (human) TFA KR-20,hCAP-18,CAP-18,Cathelicidin,FALL-39
	LL-37 (18-37) 是 LL-37 的一种抗菌肽片段。对S. aureus和C. albicans具有活性，最小致死浓度分别为4 µM 和10 µM。在10到50 µM 的浓度范围内，它还能抑制E. histolytica营养体的生长。
T77973	YD23	PROTACs	PROTAC
	YD23是一种SMARCA2PROTAC，其作用机理为诱导SMARCA2蛋白的降解。鉴于SMARCA2与SMARCA4具有合成致死关系，YD23进一步能减少多个基因（包涵细胞周期以及细胞生长调控基因）增强子的染色质可及性，特别是在缺乏SMARCA4的细胞中。
TMIH-0025	13C-d3-AOH1996
	13C-d3-AOH1996 是 AOH1996 的 13C 和氘代化合物。AOH1996 的 CAS 号为 2089314-64-5。AOH1996 是一种具有口服活性的复制体组分 PCNA (增殖细胞核抗原) 配体，靶向转录-复制冲突 (TRC)。AOH1996 可干扰 PCNA 与其结合蛋白的相互作用，导致 DNA 复制应激，诱导细胞凋亡 (apoptosis)。AOH1996 通过稳定 PCNA 和 RNA 聚合酶 II 的相互作用从而导致蛋白酶体依赖的 rpb1 降解和致命的 DNA 损伤。AOH1996 与 DNA 损伤剂具有协同作用，可抑制肿瘤细胞生长。
T63314	Antifungal agent 31
	Antifungal agent 31 是口服具有活力的、拥有吡咯三嗪酮支架的三唑类抗真菌剂，对念珠菌和丝状真菌表现出一定的抗真菌作用。Antifungal agent 31 能够明显减少两种致死性全身感染小鼠模型的死亡率和肾脏真菌负担。
T80780	w-Conotoxin SVIB
	ω-Conotoxin SVIB为从Conus venoms中分离得到的肽类毒素，具有抑制抽搐反应的能力，IC50值为37 nM。在小鼠体内，ω-Conotoxin SVIB可导致呼吸急迫，并在高浓度下致死。
T63945	Antitubercular agent-19
	Antitubercular agent-19 是一种抗结核剂。Antitubercular agent-19 对 MTB H37Rv 和 MDR-MTB 表现出良好的抗结核效果 (MIC＜0.016 μg/ml)。Antitubercular agent-19 在 BALB/c 小鼠中表现出较低的细胞毒性和相对较高的急性致死毒性。
T73652	Eritoran
	Eritoran是一种Toll样受体4 (TLR4) 拮抗剂，能够保护小鼠免受包括埃博拉病毒(EBOV)、马尔堡病毒(MARV)在内的致命流感病毒感染。该化合物通过降低粒细胞增多水平，可能有助于减轻“细胞因子风暴”的严重程度，抑制丝状病毒感染的发病机制。
T35513	13C15-Nivalenol 13C15-Nivalenol
	13C15-Nivalenol is intended for use as an internal standard for the quantification of nivalenol by GC- or LC-MS. Nivalenol is a trichothecene mycotoxin that has been found inFusarium.1It is lethal to mice (LD50= 6.9 mg/kg).2Nivalenol (5, 10, and 15 mg/kg) also induces thymic, splenic, and Peyer's patch cell apoptosis in mice.3 1.Yang, Z., Concannon, J., Ng, K.S., et al.Tetrandrine identified in a small molecule screen to activate mesenchymal stem cells for enhanced immunomodulationSci. Rep.63026...
TMIH-0091	AOH-d3
	AOH-d3 是 AOH 的氘代化合物。AOH 的 CAS 号为 2089314-64-5。AOH1996 是一种具有口服活性的复制体组分 PCNA (增殖细胞核抗原) 配体，靶向转录-复制冲突 (TRC)。AOH1996 可干扰 PCNA 与其结合蛋白的相互作用，导致 DNA 复制应激，诱导细胞凋亡 (apoptosis)。AOH1996 通过稳定 PCNA 和 RNA 聚合酶 II 的相互作用从而导致蛋白酶体依赖的 rpb1 降解和致命的 DNA 损伤。AOH1996 与 DNA 损伤剂具有协同作用，可抑制肿瘤细胞生长。
T80279	Urumin	Influenza Virus	Microbiology/Virology
	Urumin 对人类甲型流感病毒显示出抗病毒活性，通过靶向 H1 血凝素的保守茎部位，能有效中和耐药 H1 流感病毒。它在抑制 PR8 流感病毒的生长中的半抑制浓度（IC50）为 3.8 μM，并能保护幼鼠免遭致命流感病毒感染。
T62907	TAS-117 hydrochloride
	TAS-117 hydrochloride 是一种选择性的、有效的、口服具有活力的别构 Akt 抑制剂，作用于 Akt1 (IC50: 4.8 nM) 、Akt2 (IC50: 1.6 nM) 和 Akt3 (IC50: 44 nM)。TAS-117 hydrochloride 能够激发抗骨髓瘤活性，增强蛋白酶体抑制诱导的致命内质网应激，可以诱导细胞凋亡和自噬。
T78938	H3B-968	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	H3B-968为一种高效Werner综合征蛋白(WRN)抑制剂，IC50约为10 nM，可抑制具有解旋酶、ATP酶和外切酶活性的WRN。WRN在癌症研究中具有显著的合成致死潜力。H3B-968通过与ATP竞争抑制WRN解旋酶活性。
T73183	SMYD3-IN-2
	SMYD3-IN-2为一种针对SMYD3的抑制剂，具备通过诱导程序性自噬来抑制胃癌的能力。其对SMYD3及BGC823细胞展现出显著的抑制效果，IC50值分别达到0.81 μM与0.75 μM。因此，SMYD3-IN-2主要适用于癌症相关研究领域。
T64640	Melanin probe-2
	Melanoma is a lethal skin cancer. The early detection of melanoma using positron emission tomography (PET) probes is critical for improving the survival of melanoma patients. Melanin probe-2 is a non-radioactive bromo-picolinamide precursor that has been used for the synthesis of18F-picolinamides based PET probe (melanin probe-1). The tumor-targeting efficacy and imaging property of three melanin probes were evaluated in B16F10 tumor-bearing mice.18F-1 and18F-3 had much lower tumor uptake compar...
T27647	J-104132 L753037,L 753037,J104132,J 104132,L-753037
	J-104132 is a potetn and selective endothelin A/B receptor antagonist (Ki: cloned human ETA = 0.034 nM; cloned human ETB = 0.104 nM) . In vitro, J-104132 is a potent antagonist of ET-1-induced accumulation of [3H]inositol phosphates in Chinese hamster ova
T36349	CGP 74514 dihydrochloride
	Potent cdk1 inhibitor (IC50 = 25 nM). Reduces Akt phosphorylation and increases mitochondrial damage in leukemia cells in vitro in combination with LY 294002. Yu et al (2013) The lethal effects of pharmacological cyclin-dependent kinase inhibitors in human leukemia cells proceed through a phosphatidylinositol 3-kinase/Akt-dependent process. Cancer Res. 63 1822 PMID:12702569 \|Furet et al (2000) Structure-based design of potent CDK1 inhibitors derived from olomoucine. J.Comput.Aided Mol.Des. 14 40...
T36049	Linearmycin B
	Linearmycin B is a polyene antibiotic that has been found inStreptomyces.1It induces lysis and degradation ofB. subtilisas a component ofStreptomycesMg1 extract.2 1.Sakuda, S., Guce-Bigol, U., Itoh, M., et al.Novel linear polyene antibiotics: LinearmycinsJ. Chem. Soc., Perkin Trans. 1182315-2319(1996) 2.Stubbendieck, R.M., and Straight, P.D.Escape from lethal bacterial competition through coupled activation of antibiotic resistance and a mobilized subpopulationPLoS Genet.11(12)e1005722(2015)
T71252	PC-046
	PC-046 is a potent tubulin-binding agent, which was originally identified for development based on selective activity in deleted in pancreas cancer locus 4 (DPC4/SMAD4) deficient tumors. PC-046 has growth inhibitory activity in a variety of tumor types in vitro, and efficacy in SCID mice was shown in human tumor xenografts of MV-4-11 acute myeloid leukemia, MM.1S multiple myeloma, and DU-145 prostate cancer. Pharmacokinetic studies demonstrated relatively high oral bioavailability (71 %) with di...
T71055	Albendazole-d7
	Albendazole-d7 is intended for use as an internal standard for the quantification of albendazole by GC- or LC-MS. Albendazole is an orally bioavailable benzimidazole anthelmintic that is active against a variety of helminths, including liver flukes, tapeworms, and roundworms. It eliminates Trichostrongylus in the fourth stomach of cattle and sheep when orally administered at doses ranging from 2.5 to 10 mg/kg as well as other species in the fourth stomach and the small and large intestine. Alben...
T71966	PD-128763
	PD-128763 is a selective inhibitor of poly(ADP-ribose) polymerase. PD-128763 has an IC50 value against the purified enzyme approximately 50X lower than 3-aminobenzamide (3-AB), a widely used specific inhibitor of the enzyme. Exposure of exponentially growing cells to a noncytotoxic concentration (0.5 mM) of PD 128763 for 2 h immediately following X irradiation increased their radiation sensitivity, modifying both the shoulder and the slope of the survival curve. When recovery from sublethal dama...
T35453	β-Defensin-4 (human) (trifluoroacetate salt)
	β-Defensin-4 is a peptide with antimicrobial properties that protects the skin and mucosal membranes of the respiratory, genitourinary, and gastrointestinal tracts. It induces migration of monocytes in vitro when used at a concentration of 10 nM but does not affect migration of neutrophils and eosinophils. β-Defensin-4 (30 μg/ml) stimulates gene expression and production of IL-6, IL-10, CXCL10, CCL2, MIP-3α, and RANTES by keratinocytes. It also stimulates calcium mobilization, migration, and pro...
T36048	Linearmycin A
	Linearmycin A is a polyene antibiotic that has been found inStreptomyces.1It is active against the bacteriaS. aureusandE. coli(MICs = 3.1 and 1.6 μg/disc, respectively), the fungiS. cerevisiaeandC. albicans(MICs = 0.1 and 1.6 μg/disc, respectively), and the plant pathogenic fungusA. nigerin disc assays (MIC = 0.2 μg/disc). Linearmycin A induces lysis and degradation ofB. subtilisas a component ofStreptomycesMg1 extract.2 1.Sakuda, S., Guce-Bigol, U., Itoh, M., et al.Novel linear polyene antibiot...
T35520	Aflatoxin G1-13C17 Aflatoxin G1-13C17
	Aflatoxin G1-13C17is intended for use as an internal standard for the quantification of aflatoxin G1by GC- or LC-MS. Aflatoxin G1is a mycotoxin that has been found inA. terricola.1In vivo, aflatoxin G1is lethal to ducklings (LD50= 1.18 mg/kg).2It induces hepatocellular carcinoma tumor formation and lethality in rats when administered at doses of 1.4 and 3 mg/animal, respectively. Aflatoxin G1also inhibits liver and kidney succinate dehydrogenase and fumarase, as well as kidney cytochrome oxidase...
T36055	Nitisinone-13C6 Nitisinone-13C6
	Nitisinone-13C6is intended for use as an internal standard for the quantification of nitisinone by GC- or LC-MS. Nitisinone is an inhibitor of 4-hydroxyphenylpyruvate dioxygenase (HPPD), which converts 4-hydroxyphenylpyruvate (HPPA) to homogentisate in the tyrosine catabolic pathway.1Nitisinone increases urinary levels of HPPA and 4-hydroxyphenyllactate (HPLA) in rats when administered at a dose of 10 mg/kg. Nitisinone (3 mg/kg) prevents the neonatal lethality of fumarylacetoacetate hydrolase (F...

化合物

FGI-106 tetrahydrochloride

Cat.No: T11281L

Target: Virus Protease, HCV Protease, Influenza Virus, HIV Protease

Cat.No: T25701

Synonym: SD 3212,SA 3212

Target: LDL, Calcium Channel

Cat.No: T8970

Target: Ferroptosis, GPX, Glutathione Peroxidase

Surfen dihydrochloride

Cat.No: T26240

Synonym: Aminokinuride dihydrochloride,Aminoquinuride dihydrochloride,NSC-12155,Aminokinuride 2HCl,Aminoquinuride 2HCl

Target: FGFR, Antiviral, Antibiotic

Cat.No: T9575

Target: Histone Methyltransferase

Cat.No: T77520

Target: Apoptosis, DNA/RNA Synthesis

Cat.No: T77423

Synonym: ONO-4483,IPH2102

Target: Virus Protease

Lysine butyrate

Cat.No: T33050

Cat.No: T37007

Avermectin B1a monosaccharide

Cat.No: T35756

Cat.No: T62683

Antibacterial agent 69

Cat.No: T62627

Cat.No: TP2108

Cat.No: T81948

Synonym: LtTx-1a

Autophagy inducer 3

Cat.No: T61580

Cat.No: T60639

Cat.No: T81926

Cat.No: T37254

Cat.No: T25365

Target: Others

MRTX9768 hydrochloride

Cat.No: T36630

Aflatoxin G2-13C17

Cat.No: T35521

Synonym: Aflatoxin G2-13C17

Phenelfamycin E

Cat.No: T38259

3-hydroxy Palmitic Acid methyl ester

Cat.No: T37680

Cat.No: T61815

Cat.No: T60419

M62812 free base

Cat.No: T78561

LL-37 (18-37) (human) TFA

Cat.No: T83699

Synonym: KR-20,hCAP-18,CAP-18,Cathelicidin,FALL-39

Cat.No: T77973

Target: PROTACs

Cat.No: TMIH-0025

Antifungal agent 31

Cat.No: T63314

w-Conotoxin SVIB

Cat.No: T80780

Antitubercular agent-19

Cat.No: T63945

Cat.No: T73652

13C15-Nivalenol

Cat.No: T35513

Synonym: 13C15-Nivalenol

Cat.No: TMIH-0091

Cat.No: T80279

Target: Influenza Virus

TAS-117 hydrochloride

Cat.No: T62907

Cat.No: T78938

Target: DNA/RNA Synthesis

Cat.No: T73183

Melanin probe-2

Cat.No: T64640

Cat.No: T27647

Synonym: L753037,L 753037,J104132,J 104132,L-753037

CGP 74514 dihydrochloride

Cat.No: T36349

Cat.No: T36049

Cat.No: T71252

Cat.No: T71055

Cat.No: T71966

β-Defensin-4 (human) (trifluoroacetate salt)

Cat.No: T35453

Cat.No: T36048

Aflatoxin G1-13C17

Cat.No: T35520

Synonym: Aflatoxin G1-13C17

Nitisinone-13C6

Cat.No: T36055

Synonym: Nitisinone-13C6

Cat. No.	Product Name	Target	Signaling Pathways
T2S2169	Naringenin trimethyl ether 柚皮素三甲醚,5,7,4'-Trimethoxyflavanone	Others	Others
	Naringenin trimethyl ether (5,7,4'-Trimethoxyflavanone) 是四季米仔兰枝、叶的成分。它具有明显的杀螺作用，对 P. canaliculata 作用的 LC50值为 3.9 μg/ mL。
T13669	(E)-Cinnamamide trans-Cinnamamide,肉桂酰胺	Others	Others
	(E)-Cinnamamide (trans-Cinnamamide) 是 Cinnamamide 的活性较低的异构体，Cinnamamide 是一种有效的非致命化学驱虫剂，适用于减少鸟类害虫的损害。
TN1343	8-Geranyloxypsoralen 8-香叶草氧基补骨脂素	Anti-infection; P450; BACE	Metabolism; Microbiology/Virology; Neuroscience
	8-Geranyloxypsoralen 是一种呋喃香豆素，分离自葡萄柚，是 P450 3A4 的有效抑制剂(IC50:3.93 μM)。
T0729	Benzyl benzoate Ascabiol,Novoscabin,Scabitox,苯甲酸苄酯,Benzoic acid benzyl ester	Parasite	Microbiology/Virology
	Benzyl benzoate (Benzoic acid benzyl ester) 是化妆品中的香料成分，可研究疥疮和蠕形螨相关的炎症性皮肤病。
T35908	Paraherquamide E
	Paraherquamide E is a fungal metabolite originally isolated from P. charlesii with anthelmintic and insecticidal activities. It is lethal to C. elegans (LD50 = 6 μg/ml). Paraherquamide E is also lethal to O. fasciatus (LD50 = 0.089 μg/nymph). Oral administration of paraherquamide E (0.5-4 mg/kg) reduces T. colubriformis fecal egg count in gerbils.
TN3719	Cristacarpin	p38 MAPK; ROS; CDK; Antifection; p53	Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation; MAPK; Microbiology/Virology
	Cristacarpin exhibits moderate but selective activity towards DNA repair-deficient yeast mutants. It promotes endoplasmic reticulum (ER) stress, leading to sub-lethal reactive oxygen species (ROS) generation and which eventually terminates by triggering s
T80357	Bombinin H7
	Bombinin H7 是一种抗菌肽，提取自铃蟾Bombina的皮肤分泌物。该化合物对Bacillus megateriumBm11显示出高效活性，其致死浓度达到25.2 μM。
T80355	Bombinin H1
	Bombinin H1是Bombina variegata蛾皮肤中提取的抗菌肽。该肽对大肠杆菌D21的致死浓度为3.8μM，而对金黄色葡萄球菌Cowan 1的致死浓度为2.1μM。
T80358	Bombinin H3
	Bombinin H3为源自蛾Bombina variegata皮肤的抗菌肽。其对大肠杆菌D21的致死浓度为3.7 μM，而针对金黄色葡萄球菌Cowan 1的致死浓度为2.4 μM。
TN5243	Vitexilactone	NADPH-oxidase; HIV Protease; Antifection	Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	Vitexilactone is a HIV-1 reverse transcriptase inhibitor in virtual screening against Indonesian Herbal Database using AutoDock4 performed on HIV-1 reverse transcriptase. It has trypanocidal activity, the minimum lethal concentration against epimastigotes
T80360	Bombinin H4
	Bombinin H4，蛾Bombina variegata皮肤中的抗菌肽，其对大肠杆菌D21和金黄色葡萄球菌Cowan 1的致死浓度分别为4.8 μM和3.3 μM。
T80403	Nv-CATH
	Nv-CATH是一种具有广谱抗菌活性的蛙源抗菌肽，有效针对革兰氏阳性菌和革兰氏阴性菌。它能显著提供保护，防止小鼠遭受金黄色葡萄球菌致命感染，并且通过免疫调节和抗微生物机制双重作用抵御细菌感染。
TN4084	Fumitremorgin B	Antifection	Microbiology/Virology
	Fumitremorgen B is a mycotoxin, it exhibits a certain degree of genotoxicity, it can cause DNA damage in human lymphocytes; it shows an inhibitory activity on the cell cycle progression of mouse tsFT210 cells in the M phase, with the MIC value of 26.1 mic
T35751	Violacein
	Violacein is a bacterial metabolite originally isolated from C. violaceum that has antibacterial and antiprotozoal activities.[1] [2] It is produced by C. violaceum as a purple pigment in response to N-hexanoyl homoserine lactone , a property that has been modified to create a strain of C. violaceum used in detecting quorum-sensing molecules.[3] Violacein is active against Gram-positive bacteria, including B. subtilis and S. aureus (MICs = 0.8 and 1.6 &#181M, respectively). It is also active aga...

天然产物

Naringenin trimethyl ether

Cat.No: T2S2169

Synonym: 柚皮素三甲醚,5,7,4'-Trimethoxyflavanone

Target: Others

(E)-Cinnamamide

Cat.No: T13669

Synonym: trans-Cinnamamide,肉桂酰胺

Target: Others

8-Geranyloxypsoralen

Cat.No: TN1343

Synonym: 8-香叶草氧基补骨脂素

Target: Anti-infection, P450, BACE

Benzyl benzoate

Cat.No: T0729

Synonym: Ascabiol,Novoscabin,Scabitox,苯甲酸苄酯,Benzoic acid benzyl ester

Target: Parasite

Paraherquamide E

Cat.No: T35908

Cat.No: TN3719

Target: p38 MAPK, ROS, CDK, Antifection, p53

Cat.No: T80357

Cat.No: T80355

Cat.No: T80358

Cat.No: TN5243

Target: NADPH-oxidase, HIV Protease, Antifection

Cat.No: T80360

Cat.No: T80403

Fumitremorgin B

Cat.No: TN4084

Target: Antifection

Cat.No: T35751

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