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Search Results for " p 32 "

Targets Recommended: Others

20

抑制剂 & 化合物

2

天然产物

2

重组蛋白

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Cat. No.	Product Name	Target	Signaling Pathways
T38771	P32/98 P32/98	Others	Others
	P32/98 is a potent inhibitor of dipeptidyl peptidase IV . P32/98 improves glucose tolerance, insulin sensitivity and β-cell responsiveness in preclinical studies using the fatty Zucker rat, an animal model for IGT (impaired glucose tolerance).
T16423	p32 Inhibitor M36 M36	Others	Others
	p32 inhibitor M36 is an inhibitor of p32 mitochondrial protein. It binds directly to p32 and inhibits the p32 association with LyP-1.
T30260	AZD-5672 AZD 5672,AZD5672,UNII-61XQN688TW	HER; P-gp; CCR	Angiogenesis; Immunology/Inflammation; JAK/STAT signaling; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Tyrosine Kinase/Adaptors
	AZD-5672 是 CCR5 的拮抗剂，IC50 为 0.32 nM。 AZD-5672 抑制 hERG 心脏离子通道结合和 P-gp 介导的地高辛转运，IC50 为 7.3 μM 和 32 μM。 AZD-5672 可用于类风湿性关节炎的研究。
T39958	(32-Carbonyl)-RMC-5552	Others	Others
	(32-Carbonyl)-RMC-5552 is a highly effective mTOR inhibitor, exhibiting inhibitory effects on both mTORC1 and mTORC2 substrate phosphorylation. Specifically, it significantly suppresses the phosphorylation of p-P70S6K-(T389), p-4E-BP1-(T37/36), and p-AKT1/2/3-(S473) with pIC50 values > 9, >9 and 8~9, respectively.
T80275	Lynronne-2
	Lynronne-2是抗菌肽，对革兰氏阳性细菌，包含MDR菌株具有活性（耐甲氧西林MRSA菌株MIC: 32-256 μg/mL）。该化合物亦对P. aeruginosa感染展现效用。
T80091	Ranalexin
	Ranalexin为一抗菌肽，对金黄色葡萄球菌、大肠杆菌及铜绿假单胞菌的最小抑菌浓度(MIC)分别为4、32、128 μg/mL。
T75001	Antibacterial agent 128	Others	Others
	Antibacterial agent 128 是一种带有可裂解接头的铁载体类似物-环丙沙星 (Ciprofloxacin (Ciprofloxacin )) 偶联物。Antibacterial agent 128 显示出针对铜绿假单胞菌 (MIC 值为 0.25-64 μg/mL) 和类鼻疽伯克氏菌 (MIC 值为 1-32 μg/mL) 的抗生素活性。
T60465	Anti-infective agent 2	Others	Others
	Anti-infective agent 2 (化合物 3k) 是一种抗原生动物和抗分枝杆菌剂。Anti-infective agent 2对P. falciparum 和T. brucei rhodesiense 显示出抗寄生虫活性，IC50值分别为 0.07 和 2.20 μM。Anti-infective agent 2 对耻垢分枝杆菌显示出抗分支杆菌活性，其MIC 为 32 μg/mL。
T80274	Lynronne-1
	Lynronne-1 是一种具备抗革兰氏阳性细菌能力的抗菌肽，尤其对包括多重耐药(MDR)菌株有效（MRSA菌株的MIC为8-32 μg/mL）。在MRSA感染的伤口小鼠模型中，Lynronne-1能显著降低细菌负荷。此外，Lynronne-1对P. aeruginosa感染也显示出活性。
T80276	Lynronne-3
	Lynronne-3 是一种具有抗革兰氏阳性细菌活性的抗菌肽，涵盖 MDR 菌株（对MRSA菌株的 MIC 为 32-128 μg/mL）。此外，Lynronne-3 亦对 P. aeruginosa 感染显示出效力。
T36746	Leoidin	Others	Others
	Leoidin is a depsidone originally isolated from L. gangaleoides that has antibacterial and enzyme inhibitory activities.1,2,3 It is active against the bacteria E. faecalis, H. influenzae, M. catarrhalis, S. aureus, and S. pneumoniae (MICs = 8, 32, 1, 128, and 64 μg/ml, respectively).2 Leoidin inhibits phenylalanyl-tRNA synthetase (PheRS) isolated from P. aeruginosa (IC50 = 42 μM). It also inhibits organic anion-transporting polypeptide 1B1 (OATP1B1) and OATP1B3 with Ki values of 0.08 and 1.84 μM...
T68667	Oxanosine	Others	Others
	Oxanosine is an analog of guanosine that has been found in S. capreolus and has diverse biological activities, including antibacterial, antiviral, and anticancer properties. It is active against a variety of bacteria, including S. flexneri, P. mirabilis, and E. coli (MICs = 6.25, 12.5, 25 µg/ml, respectively, on peptone, but not nutrient, agar). Oxanosine inhibits replication of the HIV-1 strain IIIb in infected CEM and U937, but not H9, cells (EC50s = 7, 27, and >500 µg/ml, respectively). It al...
T64160	MraY-IN-3	Others	Others
	MraY-IN-3 (12a) 是一种细菌转位酶 MraY 的有效抑制剂 (IC50: 140 μM)。MraY-IN-3 能够作用于 E. coli K12 (MIC: 7 μg/ml)、B. subtilis W23 (MIC: 32 μg/ml)、P. fluorescens Pf-5 (MIC: 46 μg/ml)。
T35757	Beauvericin A	Others	Others
	Beauvericin A is a cyclodepsipeptide and derivative of beauvericin originally isolated fromB. bassianathat has diverse biological activities.1,2,3It is active againstM. tuberculosis(MIC = 25 μg/ml) andP. falciparum(IC50= 12 μg/ml).2Beauvericin A is toxic to brine shrimp (LD100= 32 μg/ml).3 1.Gupta, S., Montillor, C., and Hwang, Y.-S.Isolation of Novel Beauvericin Analogues from the Fungus Beauveria bassianaJ. Nat. Prod.58(5)733-738(1995) 2.Nilanonta, C., Isaka, M., Kittakoop, P., et al.Antimycob...
T35902	Milbemycin A4 oxime	Others	Others
	Milbemycin A4 oxime is a derivative of milbemycin A4 and a component of milbemycin oxime , compounds that both have insecticidal and nematocidal activity. Milbemycin A4 oxime (0.05 mg/kg) reduces the number of microfilariae of the heartworm D. immitis in naturally infested dogs. It inhibits the growth of clinical isolates of C. glabrata with MIC80 values ranging from 16 to greater than 32 μg/ml. Milbemycin A4 oxime (2.5 μg/ml) blocks efflux of fluconazole from a clinical isolate of C. glabrata, ...
T37455	C18 D-threo Ceramide (d18:1/18:0) C18 D-threo Ceramide (d18:1/18:0)	Others	Others
	C18 D-threoCeramide (d18:1/18:0) is a synthetic ceramide and stereoisomer of C18 ceramide .1It inhibits rat brain mitochondrial ceramidase (mt-CDase) with an IC50value of 16.6 μM.2[Matreya, LLC. Catalog No. 1855] 1.Koolath, S., Murai, Y., Suga, Y., et al.Chiral combinatorial preparation and biological evaluation of unique ceramides for inhibition of sphingomyelin synthaseChirality32(3)308-313(2019) 2.Usta, J., El Bawab, S., Roddy, P., et al.Structural requirements of ceramide and sphingosine bas...
T37006	Previridicatumtoxin	Others	Others
	Previridicatumtoxin is a fungal metabolite that has been found inP. aethiopicumand has diverse biological activities.1,2It is an intermediate in the biosynthesis of the mycotoxin viridicatumtoxin . Previridicatumtoxin is active against methicillin-resistantS. aureus(MRSA) and vancomycin-resistantE. faecalis(IC50s = 4.4 and 4.8 μM, respectively), as well asC. albicansandS. cerevisiae(MIC = 32 μg/ml for both).2,1It is cytotoxic to NCI H460, KB-3-1, and SW620 cancer cells (IC50s = 5.3, 4.1, and 6 μ...
T37692	Piericidin B	Others	Others
	Piericidin B is a bacterial metabolite that has been found inS. mobaraensisand has insecticidal and antimicrobial activities.1,2,3It inhibits NADH oxidase activity in isolated bovine heart mitochondria and inhibits respiration in isolated rat liver mitochondria and isolated cockroach (P. americana) muscle mitochondria.2,3Topical application of piericidin B (4 μg/insect) induces mortality in 87.5% of houseflies (M. domestica).1It induces 93.3, 100, and 100% mortality in rice stem borer (C. simple...
T36401	DCVC	Others	Others
	DCVC inhibits pathogen-stimulated TNF-α in human extra placental membranes in vitro.Target: TNF-αin vitro: DCVC inhibits pathogen stimulated cytokine release from tissue punch cultures. DCVC (5-50 μM) significantly inhibits LTA-, LPS-, and GBS-stimulated cytokine release from tissue cultures as early as 4 h (P ≤ 0.05). In contrast, TCA (up to 500 μM) does not inhibit LTA-stimulated cytokine release from tissue punches. DCVC effects on LTA-stimulated and LPS-stimulated TNF-α release from tissue p...
T38269	Purfalcamine	Others	Others
	Purfalcamine is an orally active, selective Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1) inhibitor with an IC50 of 17 nM and an EC50 of 230 nM. Purfalcamine has antimalarial activity and causes malaria parasites developmental arrest at the schizont stage[1][2]. Purfalcamine has low activity against Toxoplasma gondii calcium-dependent protein kinase 3 (TgCDPK3)[1]. Purfalcamine (225, 450 nM) has no effect on the parasitemia in the first 32 hours. After about 40 hours, paras...

化合物

Cat.No: T38771

Synonym: P32/98

Target: Others

p32 Inhibitor M36

Cat.No: T16423

Synonym: M36

Target: Others

Cat.No: T30260

Synonym: AZD 5672,AZD5672,UNII-61XQN688TW

Target: HER, P-gp, CCR

(32-Carbonyl)-RMC-5552

Cat.No: T39958

Target: Others

Cat.No: T80275

Cat.No: T80091

Antibacterial agent 128

Cat.No: T75001

Target: Others

Anti-infective agent 2

Cat.No: T60465

Target: Others

Cat.No: T80274

Cat.No: T80276

Cat.No: T36746

Target: Others

Cat.No: T68667

Target: Others

Cat.No: T64160

Target: Others

Cat.No: T35757

Target: Others

Milbemycin A4 oxime

Cat.No: T35902

Target: Others

C18 D-threo Ceramide (d18:1/18:0)

Cat.No: T37455

Synonym: C18 D-threo Ceramide (d18:1/18:0)

Target: Others

Previridicatumtoxin

Cat.No: T37006

Target: Others

Cat.No: T37692

Target: Others

Cat.No: T36401

Target: Others

Cat.No: T38269

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
TN5629	Averantin
	Averantin exhibits antifungal activity against Fusariumsolani, pathogenic fungus of P. notoginseng, with minimum inhibitory concentrations (MICs) of 16-32 ug/mL, and shows antibacterial activity against Bacillussubtilis with MICs of 16-32 ug/mL.
T36000	3-Hydroxyterphenyllin	Others	Others
	3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi...

天然产物

Cat.No: TN5629

3-Hydroxyterphenyllin

Cat.No: T36000

Target: Others

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPY-01998	C1QBP Protein, Mouse, Recombinant (His) AA986492,gC1qBP,AA407365,HABP1,P<...	Mouse	E. coli
	C1QBP Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 24.7 kDa and the accession number is Q8R5L1.
TMPK-01278	CD69 Protein, Cynomolgus, Recombinant (His) CLEC2C,AIM,EA1,MLR-3,GP32,BL-AC,BL-AC/...	Cynomolgus	HEK293 Cells
	CLEC2C (CD69) is a membrane-bound, type II C-lectin receptor and acts as a costimulatory molecule for T cell activation and proliferation. It is involved in lymphocyte proliferation and functions as a signal transmitting receptor in lymphocytes, natural killer (NK) cells, and platelets. CLEC2C is a disulfide-linked homodimer protein with two differentially glycosylated subunits.

重组蛋白

C1QBP Protein, Mouse, Recombinant (His)

Cat.No: TMPY-01998

Species: Mouse

Expression System: E. coli

CD69 Protein, Cynomolgus, Recombinant (His)

Cat.No: TMPK-01278

Species: Cynomolgus

Expression System: HEK293 Cells

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