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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
TP1879L1 | P11 acetate | Integrin | |
P11 acetate is an integrin αvβ3-vitronectin interaction antagonist(IC50 = 2.74 nM). | |||
TP2326L | Oligopeptide P11-4 acetate(593266-60-5 free base) | Others | |
Oligopeptide P11-4 acetate is a peptide | |||
T34081 | Piromelatine | NEU-P-11,NEU-P 11,NEU-P11 | P2X Receptor , 5-HT Receptor , MT Receptor , Sodium Channel , TRP/TRPV Channel |
Piromelatine is an agonist of melatonin MT1/MT2 receptors, 5-HT1A and 5-HT1D, and an antagonist of 5-HT2B.Piromelatine has antinociceptive activity with inhibitory effects on P2X3, TRPV1, and Nav1.7 channels, and can be ... | |||
TP1879 | HSDVHK-NH2 | P11 | |
Potent antagonist of the integrin αvβ3-vitronectin interaction (IC50 = 25.72 nM). Blocks proliferation and induces apoptosis in HUVECs; antiangiogenic. | |||
T24586 | PAFAH1b2 | PAFAH-1-b-2,3-IN-P11,3INP11,3 IN P11,PAFAH 1 b 2 | |
PAFAH1b2 is a selective platelet-activating factor acetylhydrolases 1b2 and 1b3 inhibitor that acts by impairing cancer cell survival. | |||
T10922 | CYP11B2-IN-1 | P450 | |
CYP11B2-IN-1 is an effective and selective inhibitor of CYP11B2 with IC50s of 2.3 nM and 142 nM for CYP11B2 and CYP11B1. | |||
TP1947L | P110 TFA | Others | |
P110 TFA is a dynamin-related protein 1 (Drp1) inhibitor, inhibits Drp1 GTPase activity. | |||
T16422 | P110δ-IN-1 | PWT-143 | PI3K |
P110δ-IN-1 (PWT-143) is an effective and selective inhibitor of P110δ (IC50: 8.4 nM). | |||
T3969 | I-CBP112 | Epigenetic Reader Domain , Histone Acetyltransferase | |
I-CBP112 is a specific and potent acetyl-lysine competitive protein-protein interaction inhibitor targeting the CBP/p300 bromodomains. | |||
T7334 | NP118809 | 39-1B4 | Calcium Channel |
NP118809 (39-1B4) is a potent N-type calcium channel blocker(IC50 : 0.11 μM). | |||
T9596 | AP1189 acetate | Melanocortin Receptor | |
AP1189 acetate is a biased agonist at melanocortin 1 and melanocortin 3 receptors. | |||
T4247 | I-CBP112 hydrochloride | Epigenetic Reader Domain | |
I-CBP112 is a selective inhibitor of the bromodomain-containing transcription factors. I-CBP112 (1 mM) has little activity against other bromodomains. I-CBP112 targets the CBP/p300 bromodomains. I-CBP112 significantly re... | |||
T4472 | NMS-P118 | PARP | |
NMS-P118 is a potent, selective and orally available Inhibitor of PARP-1 for cancer therapy. | |||
T24437 | MCP110 | MCP-110,MCP 110 | Raf , Ras |
MCP110 is an inhibitor of the interaction of Ras with Raf-1 and can be used in studies about the treatment of human tumors. | |||
T64249 | CYP11B1-IN-2 | ||
CYP11B1-IN-2 (compound 7aa) is a selective, orally active inhibitor of CYP11B1 that acts on human CYP11B1 (IC50: 9 nM) and rat CYP11B1 (IC50: 25 nM). CYP11B1-IN-2 can be used to study diseases caused by cortisol overload... | |||
T72397 | PARP11 inhibitor ITK7 | ITK7 | |
PARP11 Inhibitor ITK7 (ITK7) is a potent, selective inhibitor of PARP11, demonstrating significant efficacy with an IC50 value of 14 nM. It is primarily utilized in research focused on cellular localization. | |||
T78033 | SDP116 | ||
SDP116, a synthetic peptide derivative of the GPR116 Stachel sequence, exhibits ADGRF5 agonistic activity [1]. | |||
T68254 | WP1193 | ||
WP1193 is an inhibitor of the JAK2/STAT3 pathway. | |||
T38005 | P11149 | ||
P11149, a derivative of Galanthamine, acts as a competitive, orally active, and selective AChE inhibitor with the ability to weakly penetrate the blood-brain barrier (BBB). It demonstrates selective inhibition, exhibitin... | |||
T78204 | CYP11A1-IN-1 | ||
CYP11A1-IN-1 (compound 30) is a selective inhibitor of the enzyme CYP11A1, displaying an IC50 ranging from 201-2000 nM. It is applicable in the study of steroid receptor-mediated diseases, specifically targeting the andr... | |||
T40850 | [D-Trp11]-Neurotensin | [D-Trp11]-Neurotensin | |
[D-Trp11]-Neurotensin is a compound that functions as a selective antagonist of Neurotensin (NT) in perfused rat hearts, while exhibiting full agonist properties in guinea pig atria and rat stomach strips. Additionally, ... | |||
T80291 | PP113 | ||
PP113 is an antimicrobial peptide with activity against both Gram-negative and Gram-positive bacteria, exhibiting minimum inhibitory concentrations (MICs) of 73.3 µM for E. coli, 23.3 µM for B. subtilis, 13 µM for S. aur... | |||
T14940 | CGP11952 | Others | |
CGP11952 is same the benzodiazepines in its pharmacological action and it also is an experimental benzodiazepine derivative. | |||
T15783 | LP117 | Others | |
LP117 is a novel and effective inhibitor of 5-Lipoxygenase (5-LO) product synthesis (IC50: 1.1 μM). | |||
T61329 | HP1142 | ||
HP1142 is a highly effective and specific inhibitor targeting the FLT3 receptor tyrosine kinase, with a particular affinity for its mutant variant FLT3/ITD. It exhibits a benzoimidazole scaffold-based structure, making i... | |||
T10387 | ASP1126 | Others | |
ASP1126 is a selective and orally active sphingosine-1-phosphate (S1P) agonist (EC50s: 7.12 nM, 517 nM for hS1P1 and hS1P3). | |||
T23491 | UBP1112 | Others | |
group III mGlu receptor antagonist | |||
TP1947 | P110 | ||
Dynamin-related protein 1 (Drp1) inhibitor, inhibits Drp1 GTPase activity. Displays no effect on dynamin 1 or other mitochondrial dynamics-related proteins. Inhibits mitochondrial fission, dysfunction and reactive oxygen... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T19328 | Fructo-oligosaccharide DP11/GF10 | Others | |
Fructo-oligosaccharide DP11/GF10 is a fructooligosaccharide (FOS) compound with a degree of polymerization (DP) equal to 11. FOS consists of 10 fructose units connected by (2→1)-β-glycosidic bonds, with a single D-glucos... |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-01926 | S100A10 Protein, Human, Recombinant (His) | Human | E. coli |
S100 protein is a family of low molecular weight protein found in vertebrates characterized by two EF-hand calcium-binding motifs. There are at least 21 different S100 proteins, and the name is derived from the fact that... | |||
TMPH-01879 | PARP11 Protein, Human, Recombinant (His) | Human | E. coli |
Mono-ADP-ribosyltransferase that mediates mono-ADP-ribosylation of target proteins. Plays a role in nuclear envelope stability and nuclear remodeling during spermiogenesis. PARP11 Protein, Human, Recombinant (His) is exp... | |||
TMPH-01181 | CYP11B2 Protein, Human, Recombinant (His & SUMO) | Human | E. coli |
CYP11B2 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli. | |||
TMPH-01084 | CYP11A1 Protein, Human, Recombinant (His & SUMO) | Human | E. coli |
CYP11A1 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 72.1 kDa and the accession number is P05108. | |||
TMPY-00510 | FKBP11 Protein, Human, Recombinant (mFc) | Human | HEK293 Cells |
FKBP11 serve as biomarker and/or therapeutic target for Acute aortic dissection (AAD). FKBP11 during the development of HCC and FKBP11 has the potential to be an early marker for HCC. | |||
TMPH-02775 | Mup11 Protein, Mouse, Recombinant (His) | Mouse | E. coli |
Mup11 Protein, Mouse, Recombinant (His) is expressed in E. coli. | |||
TMPY-03455 | FGFR1OP Protein, Human, Recombinant (His & GST) | Human | Baculovirus Insect Cells |
FOP( fibroblast growth factor receptor 1 oncogene partner) is a largely hydrophilic protein postulated to be a leucine-rich protein family member. FOP contains 1 LisH domain. A t(6;8)(q27;p11) chromosomal translocati... |