48
14
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6231 |
Tebipenem Pivoxil
ME1211,Orapenem,替比培南匹酯 |
Antibacterial; Antibiotic | Microbiology/Virology |
Tebipenem Pivoxil (Orapenem) 是一种碳青霉烯类新型口服抗生素。 | |||
T2691 |
Oritavancin diphosphate
奥利万星二磷酸盐,LY333328 diphosphate |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Oritavancin diphosphate (LY333328 diphosphate) 是一种新型半合成的糖肽抗生素, 可研究革兰氏阳性菌感染。 | |||
T1224 |
Cefuroxime sodium
Anaptivan,头孢呋辛钠,Cefuroxime sodium salt,Biociclin |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefuroxime sodium (Cefuroxime sodium salt) 是一种具有口服活性的头孢菌素抗生素,增加了对 β-内酰胺酶的稳定性。 | |||
T77521 |
HA5
|
Antibacterial | Microbiology/Virology |
HA5 具有抗菌活性,抑制变形链球菌 (Streptococcus mutans) 生物膜形成,IC50 值为 6.42 μM。HA5 抑制变形链球菌葡聚糖的产生和 eDNA 水平,但对链球菌的生长无抑制作用。 | |||
T22279 |
BRD0539
|
CRISPR/Cas9 | DNA Damage/DNA Repair |
BRD0539 是一种具有细胞渗透性的 spCas9 抑制剂,可阻断 spCas9 与 DNA 的结合,抑制化脓性链球菌 Cas9 (SpCas9)。 | |||
T77551 |
6'-hydroxydihydrocinchonidine
|
Antibiotic; Drug Metabolite | Metabolism; Microbiology/Virology |
6'-hydroxydihydrocinchonidine 是奎宁的代谢产物,具有抗菌和抗肿瘤活性,对布氏锥虫和肺炎链球菌有抑制作用。 | |||
T0331L |
Moxifloxacin
Avelox,Moxeza,莫西沙星 |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Moxifloxacin (Avelox) 是一种8-甲氧基喹诺酮类口服有效抗菌药物,用于急性细菌性鼻窦炎,慢性支气管炎的急性细菌性加重和感染性肺炎的研究。 | |||
T4063 |
Delafloxacin
ABT492,WQ-3034,德拉沙星,RX-3341 |
Antibacterial; Antibiotic | Microbiology/Virology |
Delafloxacin (WQ-3034) 是一种广谱氟喹诺酮类抗生素,抑制耐药性的金黄色葡萄球菌,肺炎链球菌和肺炎克雷伯菌。 | |||
T38137 |
3,5-Dimethylbenzaldehyde
|
Endogenous Metabolite; Antifungal | Metabolism; Microbiology/Virology |
3,5-Dimethylbenzaldehyde 具有广谱的抗菌活性,对枯草芽孢杆菌、白假丝酵母菌、大肠杆菌、铜绿假单胞菌、金黄色葡萄杆菌和肺炎链球菌具有抑制作用。 | |||
T14386 |
AZD9567
Mizacorat |
Glucocorticoid Receptor | Endocrinology/Hormones |
AZD9567 是一种强效且具有口服活性和选择性的非类固醇糖皮质激素受体调节剂(SGRM),其 IC50 值为 3.8 nM。它在链球菌细胞壁(SCW)再活化关节炎症模型中显示出卓越的疗效。 | |||
T11265 |
Faropenem daloxate
法罗培南酯,Faropenem medoxil |
Antibacterial; Antibiotic | Microbiology/Virology |
Faropenem daloxate (Faropenem medoxil) 是β-内酰胺类口服抗生素。 | |||
T7872 |
Monolaurin
|
Others | Others |
Monolaurin 是椰子油中的一种表面活性剂和乳化剂。它抑制葡萄球菌、链球菌、加德纳菌、念珠菌和嗜血杆菌的生长,并减少促炎细胞因子的产生。 | |||
T77633 |
G43
G 43,G-43 |
Antibacterial; Transferase | Metabolism; Microbiology/Virology |
G43 是一种有效的选择性 glucosyltransferase 抑制剂,对 GtfB 和 GtfC 具有抑制作用,Kd 值分别为3.7 μM和46.9 nM。G43 在体内外具有抗变形链球菌 (S. mutans)活性,可用于研究龋齿。 | |||
T2331 |
Solithromycin
索利霉素,OP-1068,CEM-101 |
Antibacterial; Antibiotic | Microbiology/Virology |
Solithromycin (OP-1068) 是口服可生物利用的抗菌剂,抑制肺炎链球菌、葡萄球菌、金黄色葡萄球菌和流感嗜血杆菌的细胞活力、蛋白质合成和生长速率, IC50 值分别为 7.5 ng/mL、40 ng/mL 和 125 ng/mL。它可与核糖体的大 50S 亚基结合抑制蛋白质生物合成。 | |||
T0391 |
Linezolid
PNU-100766,雷奈佐利 |
MAO; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology; Neuroscience |
Linezolid (PNU-100766) 是恶唑烷酮类合成抗生素,抑制细菌蛋白质合成的起始阶段,具有抗感染作用。 | |||
T1492 |
Gemifloxacin mesylate
LB-20304a,甲磺酸吉米沙星,SB-265805S,Gemifloxacin mesylate |
DNA gyrase; Topoisomerase; Antibacterial | DNA Damage/DNA Repair; Microbiology/Virology |
Gemifloxacin mesylate (Gemifloxacin mesylate) 是一种喹诺酮类口服广谱抗菌剂,可研究轻中度肺炎和慢性支气管炎的急性细菌性发作。 | |||
T40417 |
Ethylhydrocupreine hydrochloride
Optochin hydrochloride,乙氢去甲奎宁盐酸盐;奥普托欣盐酸盐 |
Antibacterial; Parasite | Microbiology/Virology |
Ethylhydrocupreine hydrochloride (Optochin hydrochloride) 是奎宁的一种衍生物,具有抗菌作用,可抑制肺炎链球菌的活性。Ethylhydrocupreine hydrochloride 具有抗疟活性,对 Plasmodium falciparum 的IC50为 25.75 nM。Ethylhydrocupreine hydrochloride 是Gallus gallus2 受体 (ggTas2r1,ggTas2r2和ggTas2r7) 激动剂。 | |||
T28209 | NSC65847 | ||
NSC65847 is a novel dual inhibitor of viral and Streptococcus pneumoniae neuraminidase. | |||
T34318 |
Rhizopterin
Formylpteroic acid |
||
Rhizopterin is a growth factor for Streptococcus lactis R. | |||
T32990 |
LY 164846
LY164846,LY-164846,7-Bgmcc |
||
LY 164846 is a novel oral cephalosporin that is effective against Staphylococcus, Streptococcus, Haemophilus influenzae, Catabella and Neisseria. | |||
T70835 |
(4R,9S)-AG 205
|
||
AG-205 is a potent inhibitor of FabK, the enoyl-ACP reductase in Streptococcus pneumoniae. | |||
T38559 |
Competence-Stimulating Peptide-2 (CSP-2)
|
||
Competence-Stimulating Peptide-2 (CSP-2) is a quorum sensing signal peptide synthesized by Streptococcus pneumoniae. ComD2, a compatible receptor of CSP-2, exhibits an EC 50 value of 50.7 nM. | |||
T13406L |
Zabofloxacin hydrochloride
DW-224a |
Raf | MAPK |
Zabofloxacin hydrochloride is a potent and seletive bacterial type II and IV topoisomerases inhibitor, has excellent activity against gram-positive pathogens including Steptococcus aureus, Streptococcus pyogenes and S.pneumonia. | |||
T25767 |
Lysobactin
Katanosin A, 7-L-isoleucine-,Katanosin B |
||
Lysobactin, also known as katanosin B, is an effective antibiotic with in vivo efficacy against Staphylococcus aureus and Streptococcus pneumoniae. It was previously shown to inhibit peptidoglycan (PG) biosynthesis. | |||
T5189L |
Omadacycline mesylate
PTK 0796,PTK-0796,PTK0796 |
||
Omadacycline is an aminomethylcycline antibiotic. Omadacycline demonstrated net cidal activity in relation to the initial burden against four strains of Streptococcus pneumoniae. | |||
T24990 |
8-Deazafolic acid
NSC-173522,NSC173522,NSC 173522 |
||
8-Deazafolic acid is a potent folate-dependent bacteria inhibitor, Streptococcus faecium (ATCC 8043) and Lactobacillus casei (ATCC 7469), and to have activity against lymphoid leukemia L1210 in mice. | |||
T13406 |
Zabofloxacin
DW-224a Free base |
Others | Others |
Zabofloxacin is a potent and seletive bacterial type II and IV topoisomerases inhibitor, and has excellent activity against gram-positive pathogens including Steptococcus aureus, Streptococcus pyogenes and S.pneumonia. | |||
T70878 | P516-0475 | ||
P516-0475 is a novel chemical inducer of Streptococcus quorum sensing acts by inhibiting the pheromone-degrading endopeptidase PepO. This compound induces quorum sensing by stabilizing SHP pheromones in culture. | |||
T76467 |
Acetyl-Adhesin (1025-1044) amide
|
||
Acetyl-Adhesin (1025-1044) amide,为变形链球菌细胞表面粘连蛋白20肽段,充当抗菌肽,特异性阻止粘连素同唾液受体结合,避免变形链球菌再定植。 | |||
T80317 |
Combi-2
|
||
Combi-2为针对S.aureus、S.sanguis及E.coli具有抗菌活性的肽类化合物。 | |||
TP1358 |
Peptide M
|
||
Peptide M is a synthetic Peptide, 50 aa, derived from streptococcus M protein, containing an additional c-terminal cysteine residue. | |||
T38586 |
Grepafloxacin
dl-Grepafloxacin,OPC-17116 |
||
Grepafloxacin (OPC-17116) is a fluoroquinolone antibiotic that is administered orally. It possesses strong efficacy against community-acquired respiratory pathogens, notably Streptococcus pneumonia. Grepafloxacin exhibits excellent tissue penetration and demonstrates a promising pharmacodynamic profile. | |||
T30481 |
BK 218
BK218,BK-218 |
||
BK 218 is a novel cephalosporin, which is active against streptococcus pneumoniae, Haemophilus influenza, and Moraxella catarrase, but has a higher MIC against penicillin-resistant strains. Bk-218 has dual administration routes and the activity spectrum m | |||
T38608 |
Brilacidin tetrahydrochloride
PMX 30063 tetrahydrochloride |
||
Brilacidin tetrahydrochloride (PMX 30063 tetrahydrochloride) is a defensin mimetic antibiotic compound, exhibiting potent anti-infective antimicrobial activity against a range of bacteria. It demonstrates MIC90 values of 1 μg/mL and 8 μg/mL against the Gram-positive bacteria Streptococcus pneumoniae and Streptococcus viridans, respectively. Additionally, it has a MIC90 value of 8 μg/mL for the Gram-negative bacteria Haemophilus influenzae and a MIC90 value of 4 μg/mL for Pseudomonas aeruginosa. | |||
T28311 |
PD 116152
PD116,152,PD 116,152,PD116152,PD-116,152,PD-116152 |
||
PD 116152 is a highly substituted phenazine with antitumor activity isolated from the culture broth of a Streptomyces sp. The antitumor activity versus murine P388 leukemia is T/C 149. PD 116152 is selectively active versus the bacterium Streptococcus pne | |||
T80280 |
TLN-58
|
||
TLN-58是一种抗菌肽,对S. aureus、S. epidermidis和group A Streptococcus显示出抗菌活性。此外,TLN-58能够在正常人角质形成细胞及NCL-SG3细胞中诱导炎症细胞因子mRNA的上调。 | |||
T30311 |
Bederocin
REP 8839,REP-8839,REP8839 |
Antibacterial | Microbiology/Virology |
Bederocin (REP8839) 是一种新型的甲硫酰基tRNA 合成酶(METS)抑制剂,对临床分离的金黄色葡萄球菌、化脓性链球菌和其他临床重要的革兰氏阳性细菌具有有效的抗菌活性。 | |||
T81071 |
Suicin 65
|
||
Suicin 65, 一种B型抗生素,源自链球菌,对所有猪链球菌展现出活性。 | |||
T81737 |
MurF-IN-1
|
||
MurF-IN-1 (Compound 7),一种MurF抑制剂,展现了针对S. pneumoniae MurF的显著抑制活性,其pIC50值为5.19。 | |||
T80252 |
BMAP-18
|
||
BMAP-18为一抗菌肽,是Cathelicidin肽家族中的成员,为BMAP-27的截短版,具备针对Staphylococcus aureus、Streptococcus uberis和Escherichia coli的快速杀菌作用。相比其亲本BMAP-27,BMAP-18展现出优越的细胞选择性,降低了对人红细胞和中性粒细胞的溶血作用,同时保留其抗菌能力。 | |||
T37433 |
Erythromycin lactobionate
|
||
Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 50S ribosomal subunit, blocking the progression of nascent polypeptide chains.[1] It is effective against a host of bacterial genera, including Streptococcus, Staphylococcus, and Haemophilus (MIC90s range from 0.015-2.0 mg/l).[2] Erythromycin is known to potently inhibit the cytochrome P450 isoform CYP3A4, which can affect the metabolism of numerous clinically relevant medications.[3],[4] Erythromyc... | |||
T28314 |
PD 117588
PD117588,PD-117588 |
||
PD 117588 is a quinolone against bacterial isolates from cancer patients. PD 117558 has a broad antimicrobial spectrum with excellent activity against all Gram-positive isolates (including methicillin-resistant Staphylococcus aureus, coagulase-negative st | |||
T71266 | Omadacycline HCl | ||
Omadacycline, also known as PTK 0796 and Amadacyclin, is a novel first-in-class aminomethylcycline with potent activity against important skin and pneumonia pathogens, including community-acquired methicillin-resistant Staphylococcus aureus (MRSA), β-hemolytic streptococci, penicillin-resistant Streptococcus pneumoniae, Haemophilus influenzae, and Legionella. Omadacycline is active against strains expressing the two main forms of tetracycline resistance (efflux and ribosomal protection). The pri... | |||
T37432 |
Erythromycin A N-oxide
|
||
Erythromycin A N-oxide is a potential impurity found in commercial preparations of erythromycin. Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 50S ribosomal subunit, blocking the progression of nascent polypeptide chains. It is effective against a host of bacterial genera, including Streptococcus, Staphylococcus, and Haemophilus (MIC90s = 0.015-2.0 mg/l). Erythromycin is known to potently inhibit the cytochrome P450 isoform CYP3A4, which can af... | |||
T35731 |
Deethylindanomycin
|
||
Deethylindanomycin is a polyether antibiotic that has been found in S. setonii. It is active against a variety of Gram-positive bacteria, including various strains of S. aureus and Streptococcus, as well as one strain of S. pneumoniae (MICs = 4, 4, and 2 μg/ml, respectively). It is also active against coccidia in vitro, inhibiting E. tenella development, but is inactive against E. tenella infection in chicks when administered at a dose of 200 μg/g in the diet. Deethylindanomycin acts as an ionop... | |||
T74591 |
Ceftaroline fosamil (hydrate)(acetate)
|
||
Ceftaroline fosamil hydrate acetate 是一种高效的头孢菌素类抗生素(antibiotic),对多种病原体有广谱活性,特别是针对革兰氏阳性病原体,如耐甲氧西林金黄色葡萄球菌(MRSA)和耐多药肺炎链球菌,以及常见的革兰氏阴性微生物。此外,Ceftaroline fosamil hydrate acetate 在治疗复杂皮肤及皮肤结构感染(cSSSIs)和社区获得性肺炎(CABP)方面表现出显著的抗感染活性。 | |||
T61489 | VEGFR-2/DHFR-IN-1 | ||
VEGFR-2/DHFR-IN-1 (compound 8b) 是 VEGFR-2和DHFR 的抑制剂,其IC50值分别为 0.384 和 7.881 μM。VEGFR-2/DHFR-IN-1 对大肠埃希菌,粪链球菌,肠沙门氏菌,金黄色酿脓葡萄球菌,MSSA 和MRSA 显示了良好的抗菌活性,MIC 值分别为 16,16,16,8 和 16 μg/mL。VEGFR-2/DHFR-IN-1 对 C26,HepG2 和 CF7 癌细胞系具有良好的细胞毒性,IC50值为 2.97-7.12 μM。VEGFR-2/DHFR-IN-1 可用于癌症的研究。 | |||
T36409 |
Roccellic Acid
|
||
Roccellic acid is a lichen secondary metabolite that has been found in R. montagnei and has antibacterial and anticancer activities.1,2 It is active against the bacteria S. gordonii and P. gingivalis (MIC = 46.9 μg/ml for both).1 Roccellic acid (100 μg/ml) inhibits proliferation of MDA-MB-231, MCF-7, and DLD-1 cancer cells by 65.3, 75.8, and 87.9%, respectively.2 |1. Sweidan, A., Chollet-Krugler, M., Sauvager, A., et al. Antibacterial activities of natural lichen compounds against Streptococcus ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1774 |
Isobavachromene
|
Others; Antibacterial | Microbiology/Virology; Others |
Isobavachromene 是一种抗菌剂。 | |||
T3866 |
Macelignan
安五脂素,Anwuligan,(+)-Anwulignan |
Others; COX | Immunology/Inflammation; Neuroscience; Others |
Macelignan (Anwuligan) 是一种从肉豆蔻中分离得到的木脂素,具有抗炎、抗癌、抗糖尿病和神经保护活性。 | |||
T7999 |
7-Hydroxyflavanone
|
Anti-infection | Microbiology/Virology |
7-Hydroxyflavanone 对肺炎链球菌临床分离株显示出抗菌活性。 | |||
T10933 |
D-Cysteine
|
Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology |
D-Cysteine 是一种大肠杆菌生长的有力抑制剂,是半胱氨酸的 D 型异构体。它由 D-氨基酸氧化酶介导产生 H2S,是一种对抗小脑共济失调的神经保护剂。 D-半胱氨酸可以抑制由变形链球菌和链球菌血红蛋白形成的两种生物膜的生长和致龋性。 | |||
T12830 |
Sapienic acid sodium
|
Antibacterial | Microbiology/Virology |
Sapienic acid sodium,主要存在于皮肤和粘膜中的脂肪酸,对皮肤和口腔内的革兰氏阳性及阴性细菌展现出不同程度的抗菌效果。其对血链球菌、微生物链球菌与核纤梭菌的抗菌活性表现,MBC值分别为31.3 μg/mL、375.0 μg/mL与93.8 μg/mL。 | |||
T12830L |
Sapienic acid
|
Others | Others |
Sapienic acid is a fatty acid commonly found on the skin and in the mucosa. Sapienic acid is active against Streptococcus sanguinis, Streptococcus mitis, and Fusobacterium nucleatum with MBC values of 31.3 μg/mL, 375.0 μg/mL and 93.8 μg/mL, respectively. | |||
TN3995 |
Erythrabyssin II
|
Antifection | Microbiology/Virology |
Erythrabyssin II actives against several strains of Staphylococcus and Streptococcus with an MIC range of 0.78-1.56 microg/ml. It inhibits bacterial neuraminidase in a dose-dependent manner with significant inhibition (IC(50)=0.09-3.25 μM). | |||
TN4097 | Gancaonin G | Antifection | Microbiology/Virology |
Gancaonin G shows antibacterial effects on the MRSA strains with MIC values of 16 microg/ml, it also shows more moderate antibacterial activity against Streptococcus mutans. | |||
TN1409 |
Asimilobine
|
AChR; Antifection | Microbiology/Virology; Neuroscience |
(-)-Asimilobine shows antioxidative, anti-acetylcholinesterase (AChE), anti-α±-glucosidase, anti-leishmanial and anti-fungal activities; it displays weak inhibition against Streptococcus mutans (ATCC 25175), with a minimum inhibition concentration (MIC) o | |||
TN4840 |
Psoromic acid
|
Others | Others |
Psoromic acid is a selective and covalent rab-prenylation inhibitor targeting autoinhibited RabGGTase, it shows antibacterial activities against Streptococcus gordonii and Porphyromonas gingivalis, and it is an effective and safe natural drug plausible fo | |||
T38706 |
Erlose
|
||
Erlose, a trisaccharide present in soybean aphid honeydew and composed of sucrose, acts as a sweetener substitute to inhibit dental caries formation by oral microorganisms, primarily Streptococcus mutans. Erlose can serve as a reference compound in high-performance liquid chromatography (HPLC) methods employed for the analysis of sugar content in various food samples. | |||
TN4399 | Kushenol C | SGLT; NF-κB; ROS; BACE; Antifection | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience; NF-κB |
Kushenol C is a good 1,1-diphenyl-2-picrylhydrazyl (DPPH) scavenger, and it exhibits inhibitory activity against Sodium-dependent glucose cotransporter 2(SGLT2). Kushenol C shows antimicrobial activity against Staphylococcus aureus and Streptococcus mutan | |||
T79993 |
Oleanolic aldehyde
|
||
Oleanolic aldehyde 是一种具有抗菌性质的化合物,能够抑制口腔内细菌生长。该化合物对变形链球菌和牙龈卟啉单胞菌——与龋齿和牙周病有关的细菌——显示出显著的抑制效果,其最低抑菌浓度(MICs)分别为488 μg/mL和250 μg/mL。 | |||
TN4471 |
Lysicamine
|
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 |