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Search Results for " cam "

20

Compounds

Cat No. Product Name Synonyms Targets
TP1216 CaM kinase II inhibitor TFA salt Autocamtide-2-related inhibitory peptide (TFA) CaMK
CaM kinase II inhibitor TFA salt (Autocamtide-2-related inhibitory peptide (TFA)) is a highly specific and potent inhibitor of CaMKII with an IC50 of 40 nM.
T76690 Mavrilimumab CAM 3001 Virus Protease , CSF-1R
Mavrilimumab (CAM 3001) is a monoclonal antibody with antiviral activity that has an affinity for the α subunit of the granulocytic-macrophage colony-stimulating factor (GM-CSF) receptor and blocks downstream intracellul...
T70136 CAM 4750
CAM 4750 is a nonpeptide tachykinin NK1 receptor antagonist.
T41211 CAM 833
CAM 833 is an effective positivity inhibitor, which can inhibit the interaction between BRCA2 and RAD51. The Kd of ChimRAD51 protein is 366 nM. CAM 833 inhibited the oligocoagulation of RAD51 and promoted the process of ...
T70410 Cam 2445
Cam 2445 is a nonpeptide, alpha-methyltryptophan derivative; an NK1 neurokinin receptor antagonist that is a potentially useful treatment for arthritis, asthma, migraine, anxiety, psychosis, and emesis.
T70137 CAM 4515
CAM 4515 is a nonpeptide tachykinin NK1 receptor antagonist.
T28331 PD 136450 Cam1189,PD136450,Cam-1189,PD-136450,Cam 1189
Cholecystokinin type B receptor antagonist PD-136,450 is a partial secretory agonist in the stomach and a full agonist in the pancreas of the rat. Gastrin (cholecystokinin type B (CCK-B)) receptor antagonists may help to...
T30442 Bialamicol Hydrochloride Camoform hydrochloride,CAM 807,CAM-807,CI 301
Bialomicol Hydrochloride is a bio-active chemical.
T41184 Clocinnamox mesylate C-CAM,NIH 10443
Clocinnamox mesylate is a systemically active, irreversibleμ-opioid receptor antagonist (apparent Kivalues are 0.7, 1.9 and 5.7 nM for mouseμ,δandκreceptors respectively).
T16366 NVR 3-778 HBV
NVR 3-778 is a first-in-Class and oral bioavailable HBV CAM belonging to the SBA class It has anti-HBV activity.
T70211 CAM741
CAM741 is a novel selective inhibitor of vascular cell adhesion molecule 1 (VCAM1) synthesis in endothelial cells, blocking the process of cotranslational translocation, which is dependent on the signal peptide of VCAM1.
T69908 Pidnarulex HCl
Pidnarulex HCl is the salt form of CX-5461, a first-in-class non-genotoxic small molecule targeted inhibitor of RNA polymerase I (Pol I) that activates the p53 pathway without causing DNA damage. CX-5461 selectively inhi...
T69909 CAM4066
CAM4066 is a novel potent and selective CK2alpha inhibitor.
TN1008 Psoralenoside CaMK , Calcium Channel , Histamine Receptor
Psoralenoside is a natural product isolated from the fruits of Psoralea corylifolia, shows estrogen-like activity, osteoblastic proliferation accelerating activity, antitumor effects and antibacterial activity.
T70210 FT-1101 free base
FT-1101 is an orally bioavailable, potent and selective BET inhibitor. FT-1101 binds to the acetylated lysine recognition motifs in the bromodomain sites of BET proteins, thereby preventing the interaction between the B...
T8846 Beta-Escin B-escin,AESCINE Immunology/Inflammation related
beta-Escin is a natural mixture of triterpenoid saponins isolated from horse chestnut (Aesculus hippocastanum) seeds, can be used as a vasoprotective anti-inflammatory, anti-edematous and anti-nociceptive agent.
T70135 Nepaprazole sodium dihydrate
Nepaprazole sodium dihydrate is a proton pump inhibitor potentially for treatment of gastric ulcers.
T70409 6alpha-Fluorotestosterone
6alpha-Fluorotestosterone is a synthetic nonaromatizable androgen analog of testosterone. It binds to and activates specific nuclear receptors inhibits and is equipotent to testosterone.
T23525 W-9 hydrochloride N-(6-aminohexyl)-5-chloronaphthalene-2-sulfonamide hydrochloride CaMK
W-9 hydrochloride is a calmodulin antagonist.
T20792 W-7 hydrochloride W 7 HCl,W7 HCl,W-7 HCl CaMK , Apoptosis , Myosin , PDE
W-7 hydrochloride (W-7 HCl), a calmodulin antagonist, inhibits Ca2+-calmodulin-dependent myosin light chain kinase and phosphodiesterase, W-7 hydrochloride induces apoptosis and has antitumor activity.
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