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Cat. No. | Product Name | Target | Signaling Pathways |
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T60020 |
5'-Fluoro-5'-deoxyadenosine
5'-Fluoro-5'-deoxy-adenosine |
Others | Others |
5'-Fluoro-5'-deoxyadenosine (5'-Fluoro-5'-deoxy-adenosine) 常用作研究放线菌卡特链霉菌的工具。 | |||
T34643 |
Simaomicin alpha
L D42067alpha,LL D42067alpha,LL-D42067alpha |
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Simaomicin alpha is an actinomycete metabolite isolated from an actinomycete strain. | |||
T33705 |
N-Methylstreptothricin F
A37812,A 37812,A-37812 |
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N-Methylstreptothricin F is a streptothrycin isolated from actinomycete. | |||
T25732 |
Lincomycin-B
U21699,U-21699,U 21699,Antibiotic U 21699 |
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Lincomycin-B is a lincosamide antibiotic isolated from the actinomycete Streptomyces lincolnensis. | |||
T25994 | Propioxatin B | ||
Propioxatin B is an enkephalinase B inhibitor isolated from actinomycete. | |||
T25993 |
Propioxatin A
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Propioxatin A is an enkephalinase B inhibitor isolated from actinomycete. | |||
T34493 |
Salinosporamide B
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Salinosporamide B is a deschloro analog isolated from the marine Actinomycete Salinispora tropica. | |||
T26455 |
A 83016F
A-83016F,A83016F |
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A 83016F, an antibiotic from an actinomycete designated A83016, exhibits weak antimicrobial activity. | |||
T34494 |
Salinosporamide C
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Salinosporamide C is a decarboxylated pyrrole analogue isolated from the marine Actinomycete Salinispora tropica. | |||
T32949 |
Luminamicin
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Luminamicin is active against anaerobic bacteria, especially Clostridium sp.; isolated from actinomycete strain OMR-59. | |||
T35735 |
Drimentine A
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Drimentine A is a terpenylated diketopiperazine antibiotic originally isolated from Actinomycete bacteria. It is active against Gram-positive and Gram-negative bacteria, fungi, and yeast and has anthelmintic properties. | |||
T38386 |
Drimentine C
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Drimentine C is a terpenylated diketopiperazine antibiotic originally isolated from Actinomycete bacteria. It inhibits proliferation of NS-1 murine β lymphocyte myeloma cells by 63 and 98% in vitro when used at concentrations of 12.5 and 100 μg/ml, respectively. | |||
T37007 |
Resistoflavine
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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. | |||
T37509 |
Saccharocarcin B
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Saccharocarcin B 是从放线菌 Saccharothrix aerocolongenes subsp.antibiotica SCC1886 的发酵液中分离出来的。 | |||
T76282 |
Friulimicin D
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Friulimicin D 是一种脂肽类抗生素,同 Friulimicin B 一样,都是从放线菌Actinoplanes friuliensis 中分离得到。 | |||
T76281 |
Friulimicin A
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Friulimicin A 是一种脂肽类抗生素,同 Friulimicin B 一样,都是从放线菌Actinoplanes friuliensis 中分离得到。 | |||
T37546 |
TPU-0037C
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TPU-0037C is a metabolite of the marine actinomycete S. platensis that is structurally similar to lydicamycin . It is active against Gram-positive bacteria (MICs = 0.39-3.13 μg/ml), including methicillin-resistant S. aureus strains (MIC = 3.13 μg/ml), but is ineffective against Gram-negative bacteria (MICs = >50 μg/ml). | |||
T40676 |
Erythromycin A dihydrate
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Erythromycin dihyrate dihydrate is a macrolide antibiotic produced by actinomycete Streptomyces erythreus with a broad spectrum of antimicrobial activity. Erythromycin dihyrate acts by binding to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid. | |||
T68207 |
Elsamitrucin
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Elsamitrucin is a heterocyclic antineoplastic antibiotic isolated from the bacterium Actinomycete strain J907-21. Elsamitrucin intercalates into DNA at guanine-cytosine (G-C)-rich sequences and inhibits topoisomerase I and II, resulting in single-strand breaks and inhibition of DNA replication. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus). | |||
T35736 |
Drimentine B
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Drimentine B is a terpenylated diketopiperazine antibiotic originally isolated from Actinomycete bacteria. It is active against Gram-positive and Gram-negative bacteria, fungi, and yeast, and has anthelmintic properties. Drimentine B inhibits proliferation of NS-1 murine β lymphocyte myeloma cells by 41 and 59% in vitro when used at concentrations of 50 and 100 μg/ml, respectively. | |||
T36402 |
Kibdelone C
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Kibdelone C is a member of a family of natural heterocyclic polyketides first isolated from a soil actinomycete, Kibdelosporangium. Kibdelones have been described as having potent and selective cytotoxicity against a panel of human tumor cell lines, and kibdelone C has low nanomolar effectiveness in these assays. Kibdelone C disrupts the actin cytoskeleton without directly binding actin or affecting its polymerization in vitro. | |||
T78124 |
SF2312 ammonium
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Antibiotic | Microbiology/Virology |
SF2312铵是SF2312的铵盐形式,后者为一种膦酸盐类抗生素兼烯醇酶抑制剂。该化合物可从放线菌小单孢菌分离而得,在缺氧环境中活性显著。SF2312对ENO1基因缺失的神经胶质瘤细胞显示出选择性毒杀作用。 | |||
T35742 | IKD-8344 | ||
IKD-8344 is a macrocyclic dilactone originally isolated from an actinomycete species and has diverse biological activities, including anticancer, antimicrobial, and anthelmintic properties.1,2,3 It is cytotoxic to L5178Y murine leukemia cells (IC50 = 0.54 ng/ml).1 IKD-8344 inhibits growth of the mycelial form of C. albicans (MIC = 6.25 μg/ml) and potentiates the activity of polymyxin B against the multidrug-resistant pathogenic bacterium B. cenocepacia.2,3 It is active against T. spiralis in vit... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T1032 |
Erythromycin
红霉素,E-Mycin |
ribosome; Antibacterial; Antibiotic | Microbiology/Virology |
Erythromycin (E-Mycin) 是由放线菌产生的大环内酯类抗生素。它结合细菌的 50S 核糖体亚基,通过阻断转肽和易位反应来抑制 RNA 依赖性蛋白的合成。 | |||
T15277 |
Fervenulin
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Parasite | Microbiology/Virology |
Fervenulin 具有杀灭线虫活性,抑制线虫M. incognita 卵孵化和 J2 的校正死亡率,MIC 分别为 30 μg/mL 和 120 μg/mL。 | |||
T0895 |
Oxytetracycline
土霉素,Terramycin |
ribosome; Endogenous Metabolite; Antibacterial; Antibiotic; HSV | Metabolism; Microbiology/Virology |
Oxytetracycline (Terramycin) 是一种四环素类抗生素。它强力抑制革兰氏阴性和革兰氏阳性细菌。它是一种蛋白质合成抑制剂,可阻止 aminoacil-tRNA 与复杂的核糖体 RNA 结合,具有抗 HSV-1的活性。 | |||
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。 | |||
T28764 |
SF2312
SF-2312,SF 2312 |
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SF2312 is an enolase inhibitor produced by the actinomycete Micromonospora, which is active under anaerobic conditions. | |||
T81660 |
Nocarimidazole A
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Nocarimidazole A,一种来源于海洋放线菌Nocardiopsis的白色无定形固体生物碱,具紫外线活性。 | |||
T1235L |
Lincomycin
U 10149,U10149,U-10149 |
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Lincomycin is a lincosamide antibiotic that comes from the actinomycete Streptomyces lincolnensis. Although similar in structure, antibacterial spectrum, and mechanism of action to macrolides, lincomycin is also effective against other organisms including | |||
T15637 |
K-252b
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PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
K-252b is an indolocarbazole isolated from the actinomycete Nocardiopsis and is a PKC inhibitor. K-252b can be used to inhibit extracellular kinases of cells in culture because it can’t pass through the cell membrane freely. | |||
T73915 | Luisol A | ||
Luisol A 是一种芳香族四醇,是链霉菌属的河口海洋放线菌的主要代谢产物。Luisol A 是一种蒽醌抗生素类似物,是 ADC 细胞毒素 (ADC Cytotoxin)。 | |||
T11233 | Erythromycin thiocyanate | Antibacterial | Microbiology/Virology |
Erythromycin thiocyanate acts by binding to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid .Erythromycin thiocyanate | |||
T75522 | Wychimicin C | ||
Wychimicin C为源自罕见放线菌Actinocrispum wychmicini菌株MI503-AF4的螺旋藻酸聚酮类化合物。此化合物展现出卓越的抗菌效果,尤其对耐甲氧西林的Staphylococcus. aureus(IC50=0.125-0.5 μg/mL)和Enterococcus. Faecalis/faecium(IC50=0.125-0.25 μg/mL)展现显著的抑制活性。 | |||
T75523 | Wychimicin A | ||
Wychimicin A 是一种螺旋藻酸聚酮,可从罕见的放线菌 Actinocrispum wychmicini 菌株 MI503-AF4 中分离得到。Wychimicin A 具有强抗菌活性,显著抑制耐甲氧西林的金黄色葡萄球菌Staphylococcus. aureus(IC50=0.125-0.5 μg/mL) 和 肠球菌Enterococcus. Faecalis/faecium(IC50=0.25 μg/mL)。 |