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Results for "

μ-opr

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    2251
    TargetMol | All_Pathways
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    TargetMol | Compound_Libraries
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    TargetMol | Recombinant_Protein
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    TargetMol | Antibody_Products
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    TargetMol | All_Pathways
OPR-003
T9901A-1654
OPR-003 is a human monoclonal antibody that targets IL-6. [OPR-003] is applicable in research related to hematologic malignancies and rheumatoid arthritis.
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DAMGO
RX-783006, Dagol, DAGO
T435178123-71-4
DAMGO (DAGO) is an opioid receptor agonist with the ability to affect the locomotive activity in rodents. Possible analgesic agent due to μ-opiod receptor interaction.
  • $43
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TargetMol | Citations Cited
Rosiglitazone
BRL49653
T0334122320-73-4
Rosiglitazone (BRL49653) is a PPARγ agonist, TRPC5 activator, and TRPM3 inhibitor with oral activity. Rosiglitazone is also a hypoglycemic agent and a thiazolidinedione insulin sensitizer.
  • $33
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Edaravone
MCI-186
T040789-25-8
Edaravone (MCI-186) is a potent new free radical scavenger used for the therapy of patients with acute brain infarction.
  • $30
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Rutin
Rutoside, Quercetin 3-O-rutinoside
T0795153-18-4
Rutin (Quercetin 3-O-rutinoside), a flavonoid, has a variety of biological activities including antiallergic, anti-inflammatory, antiproliferative, and anticarcinogenic properties.
  • $36
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Fludarabine
NSC 118218, Fludarabinum, F-ara-A
T103821679-14-1
Fludarabine (Fludarabinum) is a fluorinated purine analog, an inhibitor of nucleic acid synthesis and an inhibitor of STAT1 activation. Fludarabine has antitumor activity and can be used for the treatment of leukemia and lymphoma.
  • $50
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
DCPLA-ME
Methyl 8-[2-[(2-pentylcyclopropyl)methyl]cyclopropyl]octanoate, Methyl 8-(2-((2-pentylcyclopropyl)methyl)cyclopropyl)octanoate, DCPLA methyl ester, 2-[(2-Pentylcyclopropyl)methyl]cyclopropaneoctanoic acid methyl ester
T1098056687-67-3In house
DCPLA-ME (2-[(2-Pentylcyclopropyl)methyl]cyclopropaneoctanoic acid methyl ester) is the methyl ester form of DCPLA. DCPLA-ME is a highly selective PKCε activator with antioxidant and anti-inflammatory activities. DCPLA-ME can be used in research on neurodegenerative diseases.
  • $59
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TargetMol | Inhibitor Hot
Tunicamycin
T1322911089-65-9
Tunicamycin is a mixture of antibiotics that inhibit N-linked glycosylation by blocking GlcNAc phosphotransferase (GPT). Tunicamycin has antitumor activity, as well as anti-bacterial, anti-fungal, and anti-viral activity.
  • $113
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Ac4ManNAz
T14093361154-30-5In house
Ac4ManNAz is an azide-containing metabolic glycoprotein labeling reagent that can selectively modify proteins and can be used for cell labeling, tracking, and proteomic analysis.
  • $32
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TargetMol | Inhibitor Hot
Doxycycline
Vibramycin, Doxytetracycline, Doxycyclinum, Doxiciclina
T1687564-25-0
Doxycycline is an orally active tetracycline antibiotic with broad-spectrum inhibitory effects on matrix metalloproteinases (MMPs), possessing both antibacterial and antitumor activities, and is commonly used in inducible gene expression ON-OFF systems.
  • $30
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Doxycycline (hyclate)
WC2031, Doxycycline hydrochloride hemiethanolate hemihydrate, Doxycycline hyclate
T1687L24390-14-5
Doxycycline (hyclate) is an orally active tetracycline antibiotic with broad-spectrum inhibitory activity against matrix metalloproteinases (MMPs), possessing both antibacterial and antitumor properties, and is commonly used in inducible gene expression ON-OFF systems.
  • $41
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Valspodar
PSC 833
T17216121584-18-7
Valspodar (PSC 833) is a small-molecule inhibitor and a P-glycoprotein (P-gp) inhibitor with high selectivity and chemosensitizing properties. This compound can effectively reverse P-gp-mediated multidrug resistance (MDR) and is used in experimental research on drug-resistant tumors such as advanced epithelial ovarian cancer.
  • $212
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TargetMol | Inhibitor Hot
Tiomolibdate diammonium
NSC 286644, Coprexa, ATTM, Ammonium tetrathiomolybdate, Ammonium molybdenum sulfide
T1966815060-55-6
Tiomolibdate diammonium (NSC-286644) is an inhibitor of superoxide dismutase 1 (SOD1) exerting antiangiogenic and antitumor activities. Tiomolibdate diammonium inhibits the activities of cuproenzymes, including SOD1 and COX.
  • $35
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Fedratinib
TG-101348, SAR 302503
T1995936091-26-8
Fedratinib (TG-101348) (TG101348) is an ATP-competitive inhibitor of JAK2 (IC50: 3 nM) with significantly less potent activity against JAK3.
  • $45
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Elacridar
GW120918, GW0918, GG918, GF120918
T2657143664-11-3
Elacridar (GG918) is a potent inhibitor of P-glycoprotein and BCRP.
  • $33
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TargetMol | Inhibitor Hot
Ilomastat
GM6001, Galardin
T2743142880-36-2
Ilomastat (GM6001) (GM6001, Galardin) is a broad spectrum matrix metalloprotease (MMP) inhibitor.
  • $41
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Astragaloside IV
AST-IV, AS-IV
T297384687-43-4
Astragaloside IV (AS-IV), an active component isolated from Astragalus membranaceus, suppresses the activation of ERK1/2 and JNK, and downregulates matrix metalloproteases (MMP)-2, (MMP)-9 in MDA-MB-231 breast cancer cells. Astragaloside IV is a bioactive saponin first isolated from the dried plant roots of the genus Astragalus, which is used in traditional Chinese medicine.1 It dose-dependently inhibits human adenovirus type 3 (HAdV-3) in A549 cells (IC50 = 23 μM; LC50 = 865 μM).It inhibits replication of HAdV-3 and decreases HAdV-3-induced apoptosis. It has diverse protective effects for the cardiovascular, immune, digestive, and nervous systems. In particular, it reduces myocardial infarct size in dogs when administered prior to coronary ligation and reduces reperfusion arrhythmias in isolated rat hearts.
  • $32
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Amifostine
WR2721, Gammaphos, Ethyol
T328920537-88-6
Amifostine (Ethyol) anhydrous is a cytoprotective agent, acts as a free radical scavenging activity.
  • $30
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Ginkgetin
T4S2126481-46-9
1. Ginkgetin has anti-influenza virus and anti-fungal activities. 2. Ginkgetin has anti-inflammatory activity, can down-regulates COX-2 induction in vivo against skin inflammatory responses. 3. Ginkgetin is a good STAT3 inhibitor and may be a useful lead
  • $40
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Prostaglandin E2
Prostaglandin E2 (PGE2), PGE2, Dinoprostone
T5014363-24-6
Prostaglandin E2 (PGE2) is a natural hormone-like substance involved in various physiological functions, including the contraction and relaxation of smooth muscles, dilation and constriction of blood vessels, regulation of blood pressure, and modulation of inflammation. It can be used to induce neuropathic pain models.
  • $30
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
SRI-011381 hydrochloride
SRI-011381 hydrochloride [1629138-41-5(free base)]
T51292070014-88-7
SRI-011381 hydrochloride, a new-type agonist of the TGF-beta signaling pathway, is utilized in the treatment of Alzheimer's disease.
  • $30
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited
thermospermine
N'-[3-(3-aminopropylamino)propyl]butane-1,4-diamine, 1,12-Diamino-4,8-diazadodecane
T6006670862-11-2
Thermospermine is a structural isomer of spermine that plays a role in inhibiting xylem differentiation and can enhance the translation of SAC51 and SACL1 in Arabidopsis thaliana. Thermospermine is also used in studies as a plant growth regulator and for controlling wood biomass production.
  • $146
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TargetMol | Inhibitor Hot
Marimastat
TA2516, KB-R8898, BB2516
T6885154039-60-8
Marimastat (BB2516) (BB-2516) is a potent, broad spectrum matrix metalloprotease (MMP) inhibitor. MMP-9 (IC50=3 nM), MMP-1 (IC50=5 nM), MMP-2 (IC50=6 nM), MMP-14 (IC50=9 nM)and MMP-7 (IC50=13 nM).
  • $54
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TargetMol | Inhibitor Hot
Salvianolic acid A
Dan Phenolic Acid A
T6S044496574-01-5
Salvianolic acid A (Dan Phenolic Acid A) is a natural product and an inhibitor of matrix metalloproteinase 9 (MMP-9). Salvianolic acid A has antioxidant and anti-inflammatory activity and protects the blood-brain barrier.
  • $45
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TargetMol | Inhibitor Hot
TargetMol | Citations Cited