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Search Results for " f-10 "
Targets Recommended: Others

24

抑制剂 & 化合物

5

天然产物

6

重组蛋白

2

同位素标记化合物

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Cat. No. Product Name Target Signaling Pathways
T29448 50F10

50 F 10,50-F-10

Others Others
50F10 is a stabilizer for the active LPL dimer. It can act by preventing angptl4- and heat-induced inactivation of LPL and reducing postprandial triglyceride levels.
T79883 9-Chloromethyl-10-hydroxy-11-F-Camptothecin

Topoisomerase DNA Damage/DNA Repair
9-Chloromethyl-10-Hydroxy-11-F-Camptothecin是一款喜树碱类衍生化合物,具有DNA拓扑异构酶I (Topo I)抑制活性,应用于癌症治疗的研究领域。
T66988 10-Bromo-5H-dibenzo[b,f]azepine-5-carboxamide

Others Others
10-Bromo-5H-dibenzo[b,f]azepine-5-carboxamide 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66988,CAS号为 59690-97-0。
T32261 Janthitrem F

Janthitrem E monoacetate

Others Others
Janthitrem f, as a 10-0-acetyljanthitrem e or janthitrem e monoacetate, is a type ofnaphthopyran. Janthitrem F is prepared by Penicillium janthinellum. Tremorgenic mycotoxi.
T13907 Sulfo-ara-F-NMN

CZ-48

Others Others
Sulfo-ara-F-NMN 是一种具有细胞渗透性的烟酰胺单核苷酸 (NMN) 的类似物。Sulfo-ara-F-NMN 对激活 SARM1具有选择性,对 CD38具有抑制作用, IC50 约为 10 μM。Sulfo-ara-F-NMN 对具有更高的环化酶活性 CZ-48或 NMN 的激活会引起 SARM1的构象变化,导致 cADPR 的产生、NAD 的消耗和非凋亡细胞死亡。
T64635 8-Phenyl-2,6-diethyl-BODIPY 505/515

Others Others
2,8-Diethyl-5,5-difluoro-1,3,7,9-tetramethyl-10-phenyl-5H-4l4,5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinine 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64635。
T74670 KTX-951

PROTACs PROTAC
KTX-951为一种PROTAC,专门针对IRAK4进行降解(DC50=18 nM)。在大鼠模型中,KTX-951(10 mg/kg)的口服生物利用率达到22%。该化合物展现出显著的抗癌潜力。
T27595 Imarikiren HCl

TAK-272 hydrochloride,TAK-272 HCl. Imarikiren HCl |,TAK272,TAK 272,TAK-272

Others Others
Imarikiren is a potent, selective and orally active direct renin inhibitor. TAK-272 shows potent inhibitory activity against human renin (IC50 = 2.1 nM) in hPRA assay and excellent selectivity against other aspartic proteases, such as cathepsin D (IC50 >
TP2514 BPC 157 acetate

Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val,GEPPPGKPADDAGLV

Others Others
Body Protection Compound 157 (BPC 157) is a pentadecapeptide derived from BPC, identified in gastric juice, exhibiting diverse biological activities. At 2 µg/ml, BPC 157 enhances primary rat tendon fibroblast cell migration and F-actin formation. Furthermore, doses of 0.01 and 10 µg/kg, intraperitoneally (i.p.), mitigate paw swelling, bone erosion, and mononuclear cell infiltration in the joints of rats with rheumatoid arthritis induced by complete Freund's adjuvant (CFA). It also diminishes gas...
T36498 CAY10762

CAY10762

Others Others
CAY10762 is an inhibitor of monoacylglycerol lipase (MAGL; IC50= 34.1 nM).1It reduces hydrogen peroxide-induced lactate dehydrogenase (LDH) release from Neuro2a cells when used at a concentration of 1 μM. CAY10762 (10 mg/kg) increases levels of 2-arachidonoyl glycerol in mouse brain. 1.Castelli, R., Scalvini, L., Vacondio, F., et al.Benzisothiazolinone derivatives as potent allosteric monoacylglycerol lipase inhibitors that functionally mimic sulfenylation of regulatory cysteinesJ. Med. Chem.63(...
T35452 β-Defensin-3 (human) (trifluoroacetate salt)

β-Defensin-3 is a peptide with antimicrobial properties that protects the skin and mucosal membranes of the respiratory, genitourinary, and gastrointestinal tracts. It inhibits the growth of the periodontopathogenic and cariogenic bacteria F. nucleatum, S. mutans, S. sobrinus, S. salivarius, and L. casei (MICs = 12.5-100 mg/l). It also inhibits the growth of S. aureus, S. pyogenes, P. aeruginosa, E. coli, and C. albicans. β-Defensin-3 stimulates gene expression and production of IL-6, IL-10, CXC...
T37939 N-Desethyl Bimatoprost

17-phenyl trinor Prostaglandin F2α amide

Others Others
N-Desethyl Bimatoprost (17-phenyl trinor PGF2α amide) is an F-series PG analog in which the C-1 carboxyl group has been modified to an unsubstituted amide. PG esters have been shown to have ocular hypotensive activity. PG N-ethyl amides were recently introduced as alternative PG hypotensive prodrugs. Although it has been claimed that PG amides are not converted to the free acids in vivo, studies have shown that bovine and human corneal tissue converts the amides of various PGs to the free acids ...
T69831 RPR-200765A Mesylayte

Others Others
RPR-200765A is a potent and selective inhibitor of p38 MAP kinase (IC50 = 50 nM). It inhibits LPS-stimulated TNFalpha release both in vitro, from human monocytes (EC50 = 110 nM), and in vivo in Balb/c mice (ED50 = 6 mg/kg). At oral doses between 10 and 30 mg/kg/day it reduces the incidence and progression in the rat streptococcal cell wall (SCW) arthritis model when administered in either prophylactic or therapeutic dosing regimens. The compound, which is a mesylate salt and exists as a stable m...
T35451 β-Defensin-2 (human) (trifluoroacetate salt)

β-Defensin-2 is a peptide with antimicrobial properties that protects the skin and mucosal membranes of the respiratory, genitourinary, and gastrointestinal tracts.1It inhibits the growth of periodontopathogenic and cariogenic bacteria, includingP. gingivalisandS. salivarius.2β-Defensin-2 (30 μg/ml) stimulates gene expression and production of IL-6, IL-10, CXCL10, CCL2, MIP-3α, and RANTES by keratinocytes.3It also stimulates calcium mobilization, migration, and proliferation of keratinocytes whe...
T35979 Benastatin C

Others Others
Benastatin C is a polyketide synthase-derived benastatin that has been found inStreptomycesand has diverse biological activities.1,2It inhibits glutathione S-transferase (GST; IC50= 24 μg/ml for the rat liver enzyme).2Benastatin C also inhibits the esterase activity of isolated porcine pancreatic lipase (IC50= 10 μg/ml). It increases LPS- or concanavalin A-induced blastogenesis of isolated mouse spleen lymphocytes in a concentration-dependent manner. 1.Xu, Z., Schenk, A., and Hertweck, C.Molecul...
T38143 Elaidamide

Others Others
Elaidamide is a fatty acid amide that has been found in the cerebrospinal fluid of sleep-deprived cats.1 It inhibits rat microsomal epoxide hydrolase (mEH; Ki = 70 nM).2 Elaidamide also inhibits porcine pancreatic and human synovial phospholipase A2 (PLA2).3 In vivo, elaidamide (10 mg/animal) induces physiological sleep in rats.1References1. Cravatt, B.F., Prospero-Garcia, O., Siuzdak, G., et al. Chemical characterization of a family of brain lipids that induce sleep. Science 268(5216), 1506-150...
T83680 Azurin (50-77) (P. aeruginosa) TFA

Azurin p28,p28

Azurin (50-77)是一种含铜细菌蛋白azurin的肽段,存在于P. aeruginosa中,具有细胞周期停滞、抑制癌细胞增殖和调节血管生成活性。作为VEGFR2的抑制剂(IC20约为10.7 µM),Azurin (50-77)(20 µM)能在MCF-7乳腺癌细胞中诱导G2/M期的细胞周期停滞。在50 µM的浓度下,减少MCF-7和ZR-75-1乳腺癌细胞的增殖。Azurin (50-77)以25 µM的浓度减少VEGF-A诱导的毛细管管腔形成(IC50 = 12 µM),降低人脐静脉内皮细胞(HUVECs)中与细胞膜相关的F-actin、焦点粘附激酶(FAK)和paxillin的水平,并增加胞外的血小板内皮细胞粘附分子-1(PECAM-1)的水平。在体内,Azurin (50-77)(每日10 mg/kg)在MCF-7小鼠异种移植模型中减少肿瘤体积。
TP1816 Urotensin II, mouse

Jump to search UTS2 Identifiers Aliases UTS2, PRO1068, U-II, UCN2, UII, urotensin 2 External IDs OMIM: 604097 MGI: 1346329 HomoloGene: 4939 GeneCards: UTS2 hide Gene location (Human) Chr. Chromosome 1 (human)[1] Band 1p36.23 Start 7,843,083 bp[1] En
T35799 MBX-8025 (sodium salt)

Others Others
MBX-8025 is an agonist of peroxisome proliferator-activated receptor δ (PPARδ).1 It is greater than 750- and 2,500-fold selective for PPARδ over PPARα and PPARγ. MBX-8025 (10 mg/kg per day for eight weeks) reduces increases in fasting blood glucose and serum insulin levels, and decreases insulin resistance in Alms1 mutant (foz/foz) mice fed an atherogenic diet as a model of diet-induced obesity, type 2 diabetes, and non-alcoholic steatohepatitis (NASH).2 It also decreases serum alanine transamin...
T35893 rac-1,2-bis-Palmitoyl-3-chloropropanediol

Others Others
rac-1,2-bis-Palmitoyl-3-chloropropanediol is a 3-monochloropropane-1,2-diol (3-MCPD) ester.1It has been found as a contaminant in edible olive oils, with the lowest and highest concentrations in extra virgin and olive pomace oils, respectively.rac-1,2-bis-Palmitoyl-3-chloropropanediol has also been found in cottonseed and palm oils, as well as in shortening.2It induces renal tubular necrosis and a decrease in spermatids, but no gross pathological changes, in mice.3 1.Hung, W.-C., Peng, G.-J., Ts...
T35975 6,9-Dichloro-1,2,3,4-tetrahydroacridine

Others Others
6,9-Dichloro-1,2,3,4-tetrahydroacridine is a synthetic intermediate in the synthesis of tacrine-based acetylcholinesterase (AChE) inhibitors.1It is also an intermediate in the synthesis of multifunctional tacrine hybrids that possess radical scavenging, amyloid-β aggregation inhibitory, and/or β-secretase 1 (BACE1) inhibitory activities in addition to their activity as AChE inhibitors.2,3 1.Recanatini, M., Cavalli, A., Belluti, F., et al.SAR of 9-amino-1,2,3,4-tetrahydroacridine-based acetylchol...
T36629 Givinostat

Others Others
Givinostat (ITF-2357) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively. Givinostat (ITF2357) suppresses total LPS-induced IL-1β production robustly compared with the reduction by ITF3056. At 25, 50, and 100 nM, Givinostat reduced IL-1β secretion more than 70%. Givinostat (ITF-2357) suppresses the production of IL-6 in PBMCs stimulated with TLR agonists as well as the combination of IL-12 plus IL-18. IL-6 secretion decreases to 50% at 50 nM Givinostat, but at 1...
T37347 6'-Sialyllactose Sodium Salt

6'-Sialyllactose Sodium Salt,6'-N-Acetylneuraminyl-D-lactose

Others Others
6'-Sialyllactose consists of the monosaccharide N-acetylneuraminic acid linked to the galactosyl subunit of lactose at the 6 position. This connection is at the 3 position in the related compound, 3’-sialyllactose. Both are major milk oligosaccharides that avidly bind several viral strains, including strains of influenza, HIV-1, reovirus, and polyomavirus.[1],[2],[3],[4],[5],[6] These compounds can be used to differentiate and characterize the binding domains of viruses that recognize N-acetylne...
T38174 Mpro inhibitor N3 hemihydrate

Others Others
Mpro inhibitor N3 hemihydrate is a potent inhibitor of SARS-CoV-2 Mpro with an EC50 of 16.77 μM for SARS-CoV-2. Mpro inhibitor N3 hemihydrate specifically inhibits Mpro from multiple coronaviruses, including SARS-CoV and MERS-CoV. Mpro inhibitor N3 hemihydrate displays inhibition against HCoV-229E, FIPV, and MHV-A59 with individual IC50 of 4.0 μM, 8.8 μM, and 2.7 μM, respectively[1][2]. Mpro inhibitor N3 hemihydrate (0-0.64 μM) is able to penetrate cells to inhibit the replication of IBV viruses...

化合物

50F10
Cat.No: T29448
Synonym: 50 F 10,50-F-10
Target: Others
9-Chloromethyl-10-hydroxy-11-F-Camptothecin
Cat.No: T79883
Synonym:
Target: Topoisomerase
10-Bromo-5H-dibenzo[b,f]azepine-5-carboxamide
Cat.No: T66988
Synonym:
Target: Others
Janthitrem F
Cat.No: T32261
Synonym: Janthitrem E monoacetate
Target: Others
Sulfo-ara-F-NMN
Cat.No: T13907
Synonym: CZ-48
Target: Others
8-Phenyl-2,6-diethyl-BODIPY 505/515
Cat.No: T64635
Synonym:
Target: Others
KTX-951
Cat.No: T74670
Synonym:
Target: PROTACs
Imarikiren HCl
Cat.No: T27595
Synonym: TAK-272 hydrochloride,TAK-272 HCl. Imarikiren HCl |,TAK272,TAK 272,TAK-272
Target: Others
BPC 157 acetate
Cat.No: TP2514
Synonym: Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val,GEPPPGKPADDAGLV
Target: Others
CAY10762
Cat.No: T36498
Synonym: CAY10762
Target: Others
β-Defensin-3 (human) (trifluoroacetate salt)
Cat.No: T35452
Synonym:
Target:
N-Desethyl Bimatoprost
Cat.No: T37939
Synonym: 17-phenyl trinor Prostaglandin F2α amide
Target: Others
RPR-200765A Mesylayte
Cat.No: T69831
Synonym:
Target: Others
β-Defensin-2 (human) (trifluoroacetate salt)
Cat.No: T35451
Synonym:
Target:
Benastatin C
Cat.No: T35979
Synonym:
Target: Others
Elaidamide
Cat.No: T38143
Synonym:
Target: Others
Azurin (50-77) (P. aeruginosa) TFA
Cat.No: T83680
Synonym: Azurin p28,p28
Target:
Urotensin II, mouse
Cat.No: TP1816
Synonym:
Target:
MBX-8025 (sodium salt)
Cat.No: T35799
Synonym:
Target: Others
rac-1,2-bis-Palmitoyl-3-chloropropanediol
Cat.No: T35893
Synonym:
Target: Others
6,9-Dichloro-1,2,3,4-tetrahydroacridine
Cat.No: T35975
Synonym:
Target: Others
Givinostat
Cat.No: T36629
Synonym:
Target: Others
6'-Sialyllactose Sodium Salt
Cat.No: T37347
Synonym: 6'-Sialyllactose Sodium Salt,6'-N-Acetylneuraminyl-D-lactose
Target: Others
Mpro inhibitor N3 hemihydrate
Cat.No: T38174
Synonym:
Target: Others
Cat. No. Product Name Target Signaling Pathways
TN6864 Prosaikogenin F

前柴胡皂苷F

Others Others
Prosaikogenin F ((2R,3R,4S,5R,6R)-2-{[(1S,2R,4S,5R,8R,9S,10R,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-en-10-yl]oxy}-6-methyloxane-3,4,5-triol) 是一种单糖苷,具有溶血和抗癌特性。
TMA0958 Forsythoside F

连翘酯苷F,Arenarioside,三糖苯丙素苷

Xanthine Oxidase Metabolism
Forsythoside F (Arenarioside) 是一种黄嘌呤氧化酶 (xanthine oxidase) 抑制剂,具有抗高尿酸活性。
TN5750 Petiolin F

Petiolin F 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5750,CAS号为 1204251-10-4。
TN5988 16,25-Di-O-acetylcucurbitacin F

16,25-O-Diacetyl-cucurbitane F,Cucurbitacin F 16,25-diacetate

16,25-Di-O-acetylcucurbitacin F 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5988,CAS号为 2062685-10-1。
TN5599 12-Demethylneocaesalpin F

12-Demethylneocaesalpin F 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5599,CAS号为 1228964-10-0。

天然产物

Prosaikogenin F
Cat.No: TN6864
Synonym: 前柴胡皂苷F
Target: Others
Forsythoside F
Cat.No: TMA0958
Synonym: 连翘酯苷F,Arenarioside,三糖苯丙素苷
Target: Xanthine Oxidase
Petiolin F
Cat.No: TN5750
Synonym:
Target:
16,25-Di-O-acetylcucurbitacin F
Cat.No: TN5988
Synonym: 16,25-O-Diacetyl-cucurbitane F,Cucurbitacin F 16,25-diacetate
Target:
12-Demethylneocaesalpin F
Cat.No: TN5599
Synonym:
Target:
Cat. No. Product Name Species Expression System
TMPJ-00707 Coagulation factor X/F10 Protein, Mouse, Recombinant (His)

Stuart factor,Coagulation factor X,F

Mouse HEK293 Cells
Mouse coagulation factor X / F10 a member of the peptidase S1 family. The mature F10 is composed mostly of two EGF-like domains, one Gla gamma-carboxy-glutamate domain and one peptidase S1 domain. Factor Xa is a vitamin K-dependent plasma protease that converts prothrombin to thrombin in the presence of factor Va, calcium and phospholipid during blood clotting. The two chains of F10 are formed from a single-chain precursor by the excision of two Arg residues. A single-chain precursor is initiall...
TMPH-01329 FBXW7 Protein, Human, Recombinant (His)

F-box protein FBX30,hCdc4,F-box a...

Human E. coli
FBXW7 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 83.7 kDa and the accession number is Q969H0.
TMPY-01751 DR3/TNFRSF25 Protein, Human, Recombinant (hFc)

TRAMP,TR3,WSL-1,TNFRSF12,DR3,WSL-LR,tumor ...

Human HEK293 Cells
DR3/TNFRSF25 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 45.9 kDa and the accession number is Q93038-10.
TMPY-02300 BIN1 Protein, Human, Recombinant (His)

AMPHL,bridging integrator 1,AMPH2,SH3P9

Human E. coli
Amphiphysin 2, also named bridging integrator-1 (BIN1) or SH3P9, Amphiphysin2/BIN1 is a crescent-shaped N-BAR protein playing a key role in forming deeply invaginated tubes in muscle T-tubules, has been recently implicated in rare and common diseases affecting different tissues and physiological functions. BIN1 downregulation is linked to cancer progression and also correlates with ventricular cardiomyopathy and arrhythmia preceding heart failure. Increased BIN1 expression is linked to increased...
TMPY-05760 DR3/TNFRSF25 Protein, Human, Recombinant (hFc), Biotinylated

TRAMP,tumor necrosis factor receptor superf

Human HEK293 Cells
DR3/TNFRSF25 Protein, Human, Recombinant (hFc), Biotinylated is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 45.9 kDa and the accession number is Q93038-10.
TMPY-00961 ADAM15 Protein, Human, Recombinant (His)

MDC15,ADAM metallopeptidase domain 15

Human HEK293 Cells
ADAM15 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 54 kDa and the accession number is Q13444-10.

重组蛋白

Coagulation factor X/F10 Protein, Mouse, Recombinant (His)
Cat.No: TMPJ-00707
Species: Mouse
Expression System: HEK293 Cells
FBXW7 Protein, Human, Recombinant (His)
Cat.No: TMPH-01329
Species: Human
Expression System: E. coli
DR3/TNFRSF25 Protein, Human, Recombinant (hFc)
Cat.No: TMPY-01751
Species: Human
Expression System: HEK293 Cells
BIN1 Protein, Human, Recombinant (His)
Cat.No: TMPY-02300
Species: Human
Expression System: E. coli
DR3/TNFRSF25 Protein, Human, Recombinant (hFc), Biotinylated
Cat.No: TMPY-05760
Species: Human
Expression System: HEK293 Cells
ADAM15 Protein, Human, Recombinant (His)
Cat.No: TMPY-00961
Species: Human
Expression System: HEK293 Cells
Cat. No. Product Name Target Signaling Pathways
T35698 Octanoic Acid-13C

Octanoic acid-13C is intended for use as an internal standard for the quantification of octanoic acid by GC- or LC-MS. Octanoic acid is a medium-chain saturated fatty acid. It has been found in Teleme cheeses made from goat, ovine, or bovine milk.1 Octanoic acid is active against the bacteria S. mutans, S. gordonii, F. nucleatum, and P. gingivalis (IC80s = <125, <125, 1,403, and 2,294 μM, respectively).2 Levels of octanoic acid are increased in the plasma of patients with medium-chain acyl-CoA d...
T35775 HT-2 Toxin-13C22

HT-2 Toxin-13C22

HT-2 toxin-13C22is intended for use as an internal standard for the quantification of HT-2 toxin by GC- or LC-MS. HT-2 toxin is a type A trichothecene mycotoxin and an active, deacetylated metabolite of the trichothecene mycotoxin T-2 toxin .1,2Like T-2 toxin, HT-2 toxin inhibits protein synthesis and cell proliferation in plants.2HT-2 toxin also reduces viability of HepG2, A549, HEp-2, Caco-2, A-204, U937, Jurkat, and RPMI-8226 cancer cells with IC50values ranging from 3.1 to 23 ng/ml and human...

同位素标记化合物

Octanoic Acid-13C
Cat.No: T35698
Synonym:
Target:
HT-2 Toxin-13C22
Cat.No: T35775
Synonym: HT-2 Toxin-13C22
Target:
TargetMol Loading
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