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62

抑制剂 & 化合物

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天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T1312	Nafcillin sodium monohydrate CL 8491,萘夫西林钠,nafcillin sodium	Antibacterial; Antibiotic	Microbiology/Virology
	Nafcillin sodium monohydrate (CL 8491) 是一种抗生素，是可逆的β-lactamase 抑制剂。它用于治疗由耐青霉素的葡萄球菌菌株引起的感染。
T0682	Lamivudine GR109714X,BCH-189,拉米夫定	HIV Protease; Reverse Transcriptase	Microbiology/Virology; Proteases/Proteasome
	Lamivudine (BCH-189) 是一种核苷逆转录酶抑制剂，可抑制HIV 逆转录酶1和2 以及乙型肝炎病毒的逆转录酶。
T0909L	Nalidixic acid sodium salt 萘啶酮酸,萘啶酮酸钠,Baktogram,Sodium nalidixate	Topoisomerase; Antibacterial; Antibiotic	DNA Damage/DNA Repair; Microbiology/Virology
	Nalidixic acid sodium salt (Baktogram) 是一种喹诺酮类抗生素，对革兰氏阳性和革兰氏阴性细菌均有效。它在较低浓度下有抑菌作用，在较高浓度下有杀菌作用。它抑制 DNA 促旋酶和拓扑异构酶IV 的亚基，并可逆地阻止易感细菌中的 DNA 复制。
T6582	Mezlocillin Sodium 美洛西林钠,Baycipen	Antibacterial; Antibiotic	Microbiology/Virology
	Mezlocillin Sodium (Baycipen) 是一种青霉素 β-内酰胺类抗生素，用于治疗由易感染微生物引起的细菌感染。
T19533	Pyraclonil	Others	Others
	Pyraclonil 作为一种除草剂，有效地控制了敏感型(S)和多重抗药性(MHR)E. indica群体。Pyraclonil 作为丙啶类光敏色素原氧化酶(PPO)抑制剂发挥作用。
T38359	Dup-721	Antibacterial	Microbiology/Virology
	DuP-721 是广谱的口服有效的抗菌剂，可以抑制多种临床敏感和耐药细菌，特别是结核杆菌M. tuberculosis。
T1535	Sodium 4-phenylbutyrate 苯丁酸钠,Sodium Phenylbutyrate,Buphenyl,4-苯基丁酸钠盐,TriButyrate	Apoptosis; HDAC; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair
	Sodium 4-phenylbutyrate (TriButyrate) 是一种组蛋白去乙酰化酶和内质网应激抑制剂，可研究癌症和感染等疾病。
T1001	Dicloxacillin Sodium hydrate Dicloxacillin sodium salt monohydrate,双氯西林钠,Dicloxacillin sodium monohydrate	Antibacterial; Antibiotic	Microbiology/Virology
	Dicloxacillin Sodium hydrate 是一种青霉素类窄谱β内酰胺抗生素，可研究革兰氏阳性菌感染。
T0170	Phosphonic acid, [(2R,3S)-3-methyloxiranyl]-, calcium salt (9CI) phosphonomycin calcium,Fosfomycin calcium,磷霉素钙,phosphomycin calcium	Antibiotic	Microbiology/Virology
	Phosphonic acid, [(2R,3S)-3-methyloxiranyl]-, calcium salt (9CI) (phosphonomycin calcium)是一种抗生素，用于治疗敏感菌株引起的尿路感染和肠道感染。
T0400	Nitroxoline 5-Nitro-8-quinolinol,8-Hydroxy-5-nitroquinoline,5-Nitro-8-hydroxyquinoline,5-nitroquinolin-8-ol,硝羟喹啉	Antibacterial; Antibiotic; Autophagy	Autophagy; Microbiology/Virology
	Nitroxoline (5-nitroquinolin-8-ol) 是一种抗生素，防治生物膜感染。它通过从生物膜基质螯合Fe2+和Zn2+离子而发挥作用。
T4683	Alovudine 3'-Deoxy-3'-fluorothymidine,3'-脱氧-3-氟胸苷	Antiviral	Immunology/Inflammation
	Alovudine (3'-Deoxy-3'-fluorothymidine) 是一种 DNA 合成的标志物。与18F-Fluorodeoxyglucose (FDG) 相比，它不易受炎症变化的影响，在胰腺癌中，它是更好的生物标志物。
T40192	dGTP 2′-脱氧鸟苷 5′-(四氢三磷酸酯),2'-Deoxyguanosine-5'-triphosphate	Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	dGTP（2'-Deoxyguanosine-5'-triphosphate）作为脱氧核糖核酸（DNA）合成的基本单元，属于鸟苷核苷酸，对8-O-GDP、8-O-dGTP、8-O-GTP及8-O-dGTP的氧化损伤具有高度敏感性。
T4208	Targocil	Antibacterial	Microbiology/Virology
	Targocil 是一种磷壁酸生物合成的抑菌抑制剂，可抑制甲氧西林敏感金黄色葡萄球菌 (MSSA) 和耐甲氧西林金黄色葡萄球菌 (MRSA) 的生长，对于 MRSA 和 MSSA 的MIC90值都为 2 μg/mL。
T124492	Imipenem N-Formimidoyl thienamycin,MK0787	Antifungal	Microbiology/Virology
	Imipenem (MK0787) 是一种噻吩霉素衍生物，属于抗生素类，具有抗菌活性，对革兰氏阳性和革兰氏阴性菌具有部分的抑制作用。Imipenem 可用于研究碳青霉烯类非易感性感染和铜绿假单胞菌生物膜感染。
T6322	Copanlisib BAY 80-6946,可泮利塞,库潘尼西	Apoptosis; PI3K	Apoptosis; PI3K/Akt/mTOR signaling
	Copanlisib (BAY 80-6946) 是一种选择性的和 ATP 竞争性的泛 I 类PI3K 抑制剂，具有抗肿瘤活性，对PI3Kα，PI3Kδ，PI3Kβ和PI3Kγ的IC50分别为 0.5 nM、0.7 nM、3.7 nM 和 6.4 nM。
T1435	Praziquantel 吡喹酮,Pyquiton,Droncit,Biltricide	Calcium Channel; Antibiotic; Parasite	Membrane transporter/Ion channel; Metabolism; Microbiology/Virology
	Praziquantel (Droncit) 是一种外消旋混合物，由 (R)-Praziquantel 和 (S)-Praziquantel 组成。它可研究血吸虫病。
T3211	Midostaurin 米哚妥林,N-Benzoylstaurosporine,PKC412,CGP41231,CGP 41251,苯甲酰基十字孢碱	Others; PKC	Chromatin/Epigenetic; Cytoskeletal Signaling; Others
	Midostaurin (PKC412) 是一种多靶点蛋白激酶抑制剂，有抗肿瘤活性，对 PKCα/β/γ、Syk、Flk-1、Akt、PKA、c-Kit、c-Fgr、c-Src、FLT3、PDFRβ和VEGFR1/2的IC50值范围为 22 到500 nM 之间。
T3705	GDC0084 GDC-0084,RG7666,GDC 0084	PI3K; mTOR	PI3K/Akt/mTOR signaling
	GDC0084 (RG7666) 是一种具有潜在抗肿瘤活性的 PI3K 抑制剂。 GDC0084 (RG7666) 特异性抑制 PI3K/AKT 激酶（或蛋白激酶 B）信号通路中的 PI3K，从而抑制 PI3K 信号通路的激活。这可能导致易感肿瘤细胞群中的细胞生长和存活受到抑制。
T1631	Sulbactam CP45899,舒巴坦,舒巴坦酸	Antibacterial; Antibiotic	Microbiology/Virology
	Sulbactam (CP45899) 是一种竞争性、不可逆的 β-内酰胺酶抑制剂，抑制耐多药不动杆菌-鲍曼不动杆菌复合物。它具有抗菌活性。
T3712	Mivebresib ABBV-075,米维布塞	Apoptosis; Epigenetic Reader Domain	Apoptosis; Chromatin/Epigenetic
	Mivebresib (ABBV-075) 是一种有效的，口服活性的溴结构域和末端结构域 (BET) 抑制剂，结合BRD4的Ki 值是 1.5 nM。
T68104	Mofarotene Ro-40-8757,Ro 40-8757	Retinoid Receptor	Metabolism
	Mofarotene (Ro-40-8757) 是一种小分子化合物，在许多癌细胞系中显示出相当大的抗肿瘤活性，可用于治疗肿瘤和呼吸系统疾病。Mofarotene 是一种维甲酸类似物，可结合并激活维甲酸受体(RARs)，从而改变某些基因的表达，导致易感细胞的细胞分化和细胞增殖降低。
T26368	Tosufloxacin tosylate Tosufloxacin,T-3262,T3262,T 3262
	Tosufloxacin is a fluoroquinolone antibiotic used to treat susceptible infections.
T0395L	Pyrantel Strongid,Pyrantelum,Pyrequan,Pin-X,Pirantele
	Pyrantel is a nicotinic receptor agonist and a depolarizing neuromuscular-blocking agent, that causes persistent nicotinic activation resulting in spastic paralysis of susceptible nematodes.
T33359	Meticillin Staphcillin,Methicillin,Dimethoxyphenyl Penicillin,Metin
	Methicillin is a narrow-spectrum beta-lactam antibiotic of the penicillin-like family, used to treat infections caused by susceptible gram-positive bacteria, in particular penicillase-producing organisms such as Staphylococcus aureus.
T32020	Gusperimus Deoxyspergualin,15-Deoxyspergualin
	Gusperimus was synthesized by chemical modification of spergualin and in combination with cyclosporine A to prevent diabetes in susceptible NOD mice.
T11006	Desmethyl ferroquine SSR97213	Others	Others
	Desmethyl ferroquine is the active and major metabolite of Ferroquine.Desmethyl ferroquine shows significant activity against Chloroquine-susceptible and resistant P. falciparum strains. Ferroquine is an antimalarial.
T70758	Copanlisib HCl hydrate
	Copanlisib Dihydrochloride is a novel phosphoinositide 3-kinase (pi3k) inhibitor, inhibiting the activation of the pi3k signaling pathway, resulting in inhibition of tumor cell growth and survival in susceptible tumor cell populations
T40564	Neoabietic acid
	Neoabietic acid is an abietic-type acid isolated from the oleoresin and rosin of Pinus palustris . Neoabietic acid is highly susceptible to mineral acid. Neoabietic acid has antibacterial activity in vitro.
T39172	SMAP-29
	SMAP-29 is a broad spectrum antibacterial and antifungal α-helical cathelicidin-derived peptide with strong potential as an antiinfective agent. It effectively permeabilizes bacterial membranes and induces significant alterations in the surface morphology of susceptible microorganisms.
T36540	Nodusmicin
	Nodusmicin is a macrolide antibiotic. It has activity against antibiotic-susceptible and -resistant S. aureus with MIC values of 125, 250, and 250 μg/ml for UC-76, UC-6685, and UC-6690 strains, respectively.
T73911	Antibacterial agent 12
	Antibacterial agent 12 是一种联芳基恶唑烷酮类似物，是一种针对抗生素敏感和耐药革兰氏阳性菌的抗菌剂。
T26990	CGI-17341 CGI17341
	CGI-17341 is an orally active representative of the 5-nitroimidazole series of antimicrobial agents. CGI 17341 inhibits the drug-susceptible and multi-drug-resistant strains of Mycobacterium tuberculosis at concentrations ranging from 0.1 to 0.3 microgram
T37881	Oritavancin(LY-333328)
	Oritavancin is a novel semisynthetic glycopeptide antibiotics. On August 6, 2014, the FDA approved oritavancin for treatment of skin infections. Oritavancin possesses potent and rapid bactericidal activity in vitro against a broad spectrum of both resistant and susceptible Gram-positive bacteria, including Staphylococcus aureus, MRSA, enterococci, and streptococci.
T82051	IRBP derived peptide, R16
	R16，一种IRBP衍生肽，具有生物活性。该肽可在易感动物品系中诱导实验性自身免疫性葡萄膜炎（EAU）。
T36653	Anti-SARS-80R mAb
	Anti-SARS-80R mAb (SARS-80R) is a human IgG1 monoclonal antibody that is derived from CHO cells. Its main function is to selectively bind to the Spike (S1) protein, effectively preventing the infection of susceptible cells by the SARS virus[1].
T38502	IGF-1R inhibitor-2
	IGF-1R inhibitor-2 (example 121) is a compound that inhibits the insulin-like growth factor-1 receptor (IGF-1R). By downregulating the IGF-1R, it has the potential to reverse the transformed phenotype of tumor cells and make them more susceptible to apoptosis.
T37290	Resolvin D3 methyl ester
	Resolvin D3 methyl ester is a methyl ester version of the free acid that may act as a lipophilic prodrug form that will alter its distribution and pharmacokinetic properties. The methyl ester moiety is susceptible to cleavage by intracellular esterases, leaving the free acid.
T76618	VPLSLYSG
	VPLSLYSG 是一种可被基质金属蛋白酶-9 (MMP-9)、MMP-1和MMP-2降解的八肽。VPLSLYSG 在MMP 底物中有潜在应用。
T73095	PNU-101603
	PNU-101603 是Sutezolid 的亚砜代谢物。PNU-101603 单独使用或与SQ109 联用均展现了出色的抗分枝杆菌 (MTB) 活性，以及抗药敏和耐多药结核病活性。
T82240	Haloxyfop-P-methyl
	Haloxyfop-P-methyl为一种芳氯氧苯氧丙酸类(herbicide)，通过根部或叶片被目标植物吸收，其作用机制为抑制脂肪酸的合成并促进氧化应激。
T82050	IRBP derived peptide, R16 acetate
	R16 acetate，作为IRBP（光感受器间视黄酸结合蛋白）源的生物活性肽段，能在敏感的动物模型中诱导实验性自身免疫性葡萄膜炎（EAU）。
T61170	Antibacterial agent 96
	Antibacterial agent 96 (compound 4k) 是一种有效的抗菌剂。Antibacterial agent 96 对药物敏感和耐多药的结核分枝杆菌 (M.tuberculosis)显示出抗结核活性。Antibacterial agent 96 对 HepG2 和 Vero 细胞有毒性。
T37169	Resolvin D2 methyl ester
	Resolvin D2 (RvD2) is a lipid mediator biosynthesized by the sequential oxygenation of docosahexaenoic acid by 15- and 5-lipoxygenase. It evokes diverse anti-inflammatory effects which may mediate the resolution of inflammation. RvD2 methyl ester is a methyl ester version of the free acid which may act as a lipophilic prodrug form that will alter its distribution and pharmacokinetic properties. The methyl ester moiety is susceptible to cleavage by intracellular esterases, leaving the free acid.
T68227	BMS-214662 HCl
	BMS-214662 is a Farnesyltransferase inhibitor , is also a nonsedating benzodiazepine derivative with potential antineoplastic activity. BMS-214662 inhibits the enzyme farnesyltransferase and the post-translational farnesylation of number of proteins involved in signal transduction, which may result in the inhibition of Ras function and apoptosis in susceptible tumor cells. This agent may reverse the malignant phenotype of H-Ras-transformed cells and has been shown to be active against tumor cell...
T36693	FD-211
	FD-211 is a δ lactone originally isolated from M. lutea with anticancer activity.1 It is cytotoxic to adriamycin-susceptible P388, T-24, HeLa, A549, and HL-60 cancer cells (IC50s = 4, 0.5, 1, 1, and 0.2 μg/ml, respectively), as well as adriamycin-resistant HL-60/ADR cells (IC50 = 0.1 μg/ml). FD-211 also inhibits DNA, RNA, and protein synthesis in HeLa cells (IC50 = 1.25 μg/ml for all). \|1. Nozawa, O., Okazaki, T., Sakai, N., et al. A novel bioactive δ lactone FD-211. Taxonomy, isolation and char...
T37168	Resolvin D1 methyl ester Resolvin D1 methyl ester
	Resolvin D1 is produced physiologically from the sequential oxygenation of docosahexaenoic acid by 15- and 5-lipoxygenase . It reduces human polymorphonuclear leukocyte transendothelial migration, the earliest event in acute inflammation, with an EC50 value of ~30 nM. RvD1 methyl ester is a methyl ester version of the free acid that may act as a lipophilic prodrug form that will alter its distribution and pharmacokinetic properties. The methyl ester moiety is susceptible to cleavage by intracell...
T79379	Antitubercular agent-39
	Antitubercular agent-39 (Compound P1)为高效抗结核药物，活跃于耐药及药敏感临床分离菌株。其对Mtb菌株H37Rv的MIC值低于1 μM。
T69995	Chlorhexidine-d8 HCl
	Chlorhexidine-d8 is intended for use as an internal standard for the quantification of chlorhexidine by GC- or LC-MS. Chlorhexidine is a bis(biguanide) antimicrobial disinfectant and antiseptic agent. It inhibits growth of clinical methicillin-resistant S. aureus (MRSA) isolates (MIC90 = 4 μg/ml). It is also active against canine isolates of MRSA, methicillin-susceptible S. aureus (MSSA), methicillin-resistant S. pseudintermedius (MRSP), and methicillin-susceptible S. pseudintermedius (MSSP; MIC...
T26574	AG-7404 AG 7404
	AG-7404 is a potent protease inhibitor with anti-poliovirus activity. AG-7404 was active against all virus with EC50 values ranging from 0.080 to 0.674 μM. AG-7404 was fully active against V-073-resistant variants with EC50 values ranging from 0.218 to 0.
T74803	Levonadifloxacin
	Levonadifloxacin ((S)-(-)-Nadifloxacin; WCK 771)，作为一种宽谱抗葡萄球菌药物，对甲氧西林敏感金黄色葡萄球菌(MSSA)及对甲氧西林耐药金黄色葡萄球菌(MRSA)显示出显著的抗菌活性，并能有效减少THP-1单核细胞对MRSA和MSSA菌株的吞噬。

化合物

Nafcillin sodium monohydrate

Cat.No: T1312

Synonym: CL 8491,萘夫西林钠,nafcillin sodium

Target: Antibacterial, Antibiotic

Cat.No: T0682

Synonym: GR109714X,BCH-189,拉米夫定

Target: HIV Protease, Reverse Transcriptase

Nalidixic acid sodium salt

Cat.No: T0909L

Synonym: 萘啶酮酸,萘啶酮酸钠,Baktogram,Sodium nalidixate

Target: Topoisomerase, Antibacterial, Antibiotic

Mezlocillin Sodium

Cat.No: T6582

Synonym: 美洛西林钠,Baycipen

Target: Antibacterial, Antibiotic

Cat.No: T19533

Target: Others

Cat.No: T38359

Target: Antibacterial

Sodium 4-phenylbutyrate

Cat.No: T1535

Synonym: 苯丁酸钠,Sodium Phenylbutyrate,Buphenyl,4-苯基丁酸钠盐,TriButyrate

Target: Apoptosis, HDAC, Autophagy

Dicloxacillin Sodium hydrate

Cat.No: T1001

Synonym: Dicloxacillin sodium salt monohydrate,双氯西林钠,Dicloxacillin sodium monohydrate

Target: Antibacterial, Antibiotic

Phosphonic acid, [(2R,3S)-3-methyloxiranyl]-, calcium salt (9CI)

Cat.No: T0170

Synonym: phosphonomycin calcium,Fosfomycin calcium,磷霉素钙,phosphomycin calcium

Target: Antibiotic

Cat.No: T0400

Synonym: 5-Nitro-8-quinolinol,8-Hydroxy-5-nitroquinoline,5-Nitro-8-hydroxyquinoline,5-nitroquinolin-8-ol,硝羟喹啉

Target: Antibacterial, Antibiotic, Autophagy

Cat.No: T4683

Synonym: 3'-Deoxy-3'-fluorothymidine,3'-脱氧-3-氟胸苷

Target: Antiviral

Cat.No: T40192

Synonym: 2′-脱氧鸟苷 5′-(四氢三磷酸酯),2'-Deoxyguanosine-5'-triphosphate

Target: Nucleoside Antimetabolite/Analog, DNA/RNA Synthesis

Cat.No: T4208

Target: Antibacterial

Cat.No: T124492

Synonym: N-Formimidoyl thienamycin,MK0787

Target: Antifungal

Cat.No: T6322

Synonym: BAY 80-6946,可泮利塞,库潘尼西

Target: Apoptosis, PI3K

Cat.No: T1435

Synonym: 吡喹酮,Pyquiton,Droncit,Biltricide

Target: Calcium Channel, Antibiotic, Parasite

Cat.No: T3211

Synonym: 米哚妥林,N-Benzoylstaurosporine,PKC412,CGP41231,CGP 41251,苯甲酰基十字孢碱

Target: Others, PKC

Cat.No: T3705

Synonym: GDC-0084,RG7666,GDC 0084

Target: PI3K, mTOR

Cat.No: T1631

Synonym: CP45899,舒巴坦,舒巴坦酸

Target: Antibacterial, Antibiotic

Cat.No: T3712

Synonym: ABBV-075,米维布塞

Target: Apoptosis, Epigenetic Reader Domain

Cat.No: T68104

Synonym: Ro-40-8757,Ro 40-8757

Target: Retinoid Receptor

Tosufloxacin tosylate

Cat.No: T26368

Synonym: Tosufloxacin,T-3262,T3262,T 3262

Cat.No: T0395L

Synonym: Strongid,Pyrantelum,Pyrequan,Pin-X,Pirantele

Cat.No: T33359

Synonym: Staphcillin,Methicillin,Dimethoxyphenyl Penicillin,Metin

Cat.No: T32020

Synonym: Deoxyspergualin,15-Deoxyspergualin

Desmethyl ferroquine

Cat.No: T11006

Synonym: SSR97213

Target: Others

Copanlisib HCl hydrate

Cat.No: T70758

Neoabietic acid

Cat.No: T40564

Cat.No: T39172

Cat.No: T36540

Antibacterial agent 12

Cat.No: T73911

Cat.No: T26990

Synonym: CGI17341

Oritavancin(LY-333328)

Cat.No: T37881

IRBP derived peptide, R16

Cat.No: T82051

Anti-SARS-80R mAb

Cat.No: T36653

IGF-1R inhibitor-2

Cat.No: T38502

Resolvin D3 methyl ester

Cat.No: T37290

Cat.No: T76618

Cat.No: T73095

Haloxyfop-P-methyl

Cat.No: T82240

IRBP derived peptide, R16 acetate

Cat.No: T82050

Antibacterial agent 96

Cat.No: T61170

Resolvin D2 methyl ester

Cat.No: T37169

Cat.No: T68227

Cat.No: T36693

Resolvin D1 methyl ester

Cat.No: T37168

Synonym: Resolvin D1 methyl ester

Antitubercular agent-39

Cat.No: T79379

Chlorhexidine-d8 HCl

Cat.No: T69995

Cat.No: T26574

Synonym: AG 7404

Levonadifloxacin

Cat.No: T74803

Cat. No.	Product Name	Target	Signaling Pathways
T0909	Nalidixic acid 萘啶酸,NSC-82174	Topoisomerase; Antibacterial; Antibiotic	DNA Damage/DNA Repair; Microbiology/Virology
	Nalidixic acid (NSC-82174) 是一种喹诺酮类抗生素，对革兰氏阳性和革兰氏阴性细菌有效。它在较低浓度下有抑菌作用，而在较高浓度下有杀菌作用。它抑制 DNA 促旋酶和拓扑异构酶 IV 的亚基，并可逆地阻止易感细菌中的 DNA 复制。
T8046	Tosufloxacin tosylate hydrate Tosufloxacin p-Toluenesulfonate Hydrate,A-61827 tosylate hydrate,对甲苯磺酸妥舒沙星水合物,T-3262 Tosylate Hydrate	Others; Antibacterial; Antibiotic	Microbiology/Virology; Others
	Tosufloxacin tosylate hydrate (A-61827 tosylate hydrate) 是一个氟喹诺酮类抗菌剂。
T1126	Penicillin V Potassium 青霉素V钾,Penicillin V potassium salt,Phenoxymethylpenicillin potassium salt	Antibacterial; Antibiotic	Microbiology/Virology
	Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) 是一种有口服活性的抗生素。它可抑制链球菌，艰难梭菌和金黄色葡萄球菌的生长，可研究中耳炎，鼻窦炎，咽炎和扁桃体炎。
TN1524	Continentalic acid	NOS; COX; Antibacterial; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience
	Continentalic acid 是来自 Aralia continentalis 的，对金黄色葡萄球菌的 MIC 约为 8-16 µg/mL，包括对甲氧西林敏感的金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌标准菌株。
T6491	(-)-(S)-Equol (−)-Equol,Equol,4',7-Dihydroxyisoflavan,4',7-Isoflavandiol,雌马酚	Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite	Endocrinology/Hormones; Metabolism
	(-)-(S)-Equol (4',7-Dihydroxyisoflavan) 是雌激素受体β的高亲和力配体。
T35400	β-Muricholic Acid β-MCA,5β-Cholanic Acid-3α,6β,7β-triol,β-Muricholic Acid
	β-Muricholic acid (β-MCA) is a murine-specific primary bile acid.[1],[2] Dietary administration of β-MCA reduces HMG-CoA reductase activity in liver microsomes from mice fed a high cholesterol and cholic acid diet.[3] Dietary administration of β-MCA also dissolves 100% of gallstones in a gallstone-susceptible mouse model of diet-induced cholesterol gallstones.[4]
TN4691	Octadecyl caffeate	Others	Others
	z-Octadecyl caffeate may have pain-relieving activity. Octadecyl caffeate and coptisonine can stimulate glucose uptake at 25 and 50 ug/mL. Octadecyl caffeate and octadecyl coumarate applied to the surface of susceptible varieties in laboratory bioassays r
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...
T38330	Collinin
	Collinin is a coumarin that has been found in Z. schinifolium and has diverse biological activities.1,2,3,4 It is active against drug-susceptible and -resistant strains of M. tuberculosis (MIC50s = 3.13-6.25 μg/ml).1 Collinin inhibits LPS-induced nitric oxide (NO) production (IC50 = 5.9 μM) and reduces COX-2 protein levels in RAW 264.7 cells.2 It completely inhibits aggregation of isolated rabbit platelets induced by arachidonic acid , collagen, or platelet activating factor (PAF) when used at a...

天然产物

Cat.No: T0909

Synonym: 萘啶酸,NSC-82174

Target: Topoisomerase, Antibacterial, Antibiotic

Tosufloxacin tosylate hydrate

Cat.No: T8046

Synonym: Tosufloxacin p-Toluenesulfonate Hydrate,A-61827 tosylate hydrate,对甲苯磺酸妥舒沙星水合物,T-3262 Tosylate Hydrate

Target: Others, Antibacterial, Antibiotic

Penicillin V Potassium

Cat.No: T1126

Synonym: 青霉素V钾,Penicillin V potassium salt,Phenoxymethylpenicillin potassium salt

Target: Antibacterial, Antibiotic

Continentalic acid

Cat.No: TN1524

Target: NOS, COX, Antibacterial, Prostaglandin Receptor

Cat.No: T6491

Synonym: (−)-Equol,Equol,4',7-Dihydroxyisoflavan,4',7-Isoflavandiol,雌马酚

Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor, Endogenous Metabolite

β-Muricholic Acid

Cat.No: T35400

Synonym: β-MCA,5β-Cholanic Acid-3α,6β,7β-triol,β-Muricholic Acid

Octadecyl caffeate

Cat.No: TN4691

Target: Others

Cat.No: T35751

Cat.No: T38330

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