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Search Results for " a-118 "

20

Compounds

Cat No. Product Name Synonyms Targets
T28883 Sultroponium A118,A-118,A 118
Sultroponium may be used as an anticholinergic agent or antispasmodic.
T6735 XL413 hydrochloride BMS-863233 Hydrochloride,XL413,BMS-863233 cholecystokinin , Casein Kinase , Pim , CDK
XL413 hydrochloride (BMS-863233 Hydrochloride) is a potent, selective and ATP competitive inhibitor of Cdc7, with an IC 50 of 3.4 nM. XL413 hydrochloride also exhibits potent effect with IC 50 s of 215, 42 nM on CK2, PIM...
T3355 Naloxegol oxalate NKTR-118,NKTR-118 oxalate,AZ 13337019,AZ-13337019 oxalate P450
Naloxegol oxalate (NKTR-118) is a peripherally-selective opioid antagonist for the treatment of opioid-induced constipation.
T6100 Torin 2 Apoptosis , ATM/ATR , DNA-PK , mTOR , Autophagy
Torin 2(IC50=0.25 nM), a specific and effective mTOR inhibitor, is the 800-fold greater specific activity for mTOR than PI3K and improves pharmacokinetic properties. The EC50 of Torin 2 for ATM/ATR/DNA-PK inhibition is 2...
T36374 Naloxegol (NKTR-118)
Naloxegol (NKTR-118; AZ-13337019) is an opioid-receptor antagonist[1]. [1]. Yoon SC, et al. Naloxegol in opioid-induced constipation: a new paradigm in the treatment of a common problem. Patient Prefer Adherence. 2017 Ju...
TP1077 Nucleoprotein (118-126) Nucleoprotein 118-126,NP(118-126)
Nucleoprotein (118-126),a fragment of Nucleoprotein, is a 9-aa peptide .
T38050 CP-609754 Transferase
CP-609754 (LNK-754) is a potent and reversible farnesyltransferase inhibitor with potential anticancer activity.The IC50 for inhibiting farnesylation of recombinant human H-Ras is 0.57 ng/mL and recombinant K-Ras is 46 n...
T75887 [Ala113]MBP(104-118) TFA
[Ala113]MBP(104-118) TFA is a peptide inhibitor operating noncompetitively against protein kinase C (PKC), exhibiting inhibitory concentrations (IC50) in the range of 28-62 μM [1].
T65704 2-(Hydroxymethyl)isoindoline-1,3-dione
2-(Hydroxymethyl)isoindoline-1,3-dione is a useful organic compound for research related to life sciences. The catalog number is T65704 and the CAS number is 118-29-6.
T68461 HA-118
HA-118 is a dopamine receptor agonist.
T79202 Anticancer agent 118
Anticancer Agent 118, an N‑acylated ciprofloxacin derivative, exhibits antibacterial efficacy against Gram-positive strains and antiproliferative effects on prostate PC3 cells, making it a potential candidate for antitum...
T82890 BFGF (119-126)
bFGF (119-126) is a biologically active peptide corresponding to the residues of human, bovine (119-126), mouse, rat (118-125), and Heparin-Binding Growth Factor 2 (118-125) within bFGF. It functions to inhibit the dimer...
T69647 UCM-05194
UCM-05194 is a potent Agonist of the Type 1 Lysophosphatidic Acid Receptor (LPA1). UCM-05194 Shows Efficacy in Neuropathic Pain Amelioration. UCM-05194 stands out as the most potent and selective LPA1 receptor agonist de...
T75886 [Ala107]MBP(104-118) TFA
[Ala107]MBP(104-118) TFA is a noncompetitive peptide inhibitor of protein kinase C (PKC), exhibiting IC50 values between 46-145 μM.
T79178 WRN inhibitor 2 DNA/RNA Synthesis
WRN Inhibitor 2 (example 118), a potent inhibitor of the WRN (Werner Syndrome ATP-dependent helicase enzyme), exhibits a pIC50 value of 7.0 or greater [1].
T61665 Antibacterial agent 118
Antibacterial agent 118 (also known as compound 20) is a potent antimycobacterial compound with activity against various mycobacterial strains, including Mtb H37Ra, M. aurum, M. smegmatis, Mtb H37Rv, and M. avium. The mi...
T81605 Ontorpacept TTI-621
Ontorpacept (TTI-621) is a soluble fusion protein comprising the N-terminal (1-118) of human SIRPα fused to the Fc region of human IgG1. This N-terminal (1-118) segment serves as the binding domain for CD47, an inhibitor...
T76523 HCV Core Protein (107-114)
HCV Core Protein (107-114), identified as the binding site within the region 101-118, is a minimally immunogenic fragment of the primary linear HCV core regions. This segment, comprising two residues that vary between ge...
T70844 CM-118
CM-118 is a potent and selective dual inhibitor of c-Met and ALK which potently abrogates hepatocyte growth factor (HGF)-induced c-Met phosphorylation and cell migration, as well as phosphorylation of ALK, EML4-ALK, and ...
T9669 EST73502 hydrochloride
EST73502 hydrochloride is a selective, orally active and blood-brain barrier (BBB) penetrant dual μ-opioid receptor (MOR) agonist and σ1 receptor (σ1R) antagonist, with K i s of 64 nM and 118 nM for MOR and σ1R, respecti...
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