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Search Results for " p11 "

20

Compounds

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.
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.
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...
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...
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