Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty
Filter
Applied FilterClear all
TargetMol | Tags By Target
  • Endogenous Metabolite
    (178)
  • Apoptosis
    (146)
  • Antibacterial
    (81)
  • Autophagy
    (65)
  • NF-κB
    (65)
  • Antioxidant
    (59)
  • COX
    (53)
  • Antifection
    (52)
  • Antifungal
    (43)
  • Others
    (1622)
Filter
Search Result
Results for "

3,4-dcpg

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    3226
    TargetMol | Inhibitors_Agonists
  • Compound Libraries
    4
    TargetMol | Compound_Libraries
  • Peptide Products
    116
    TargetMol | Peptide_Products
  • Inhibitory Antibodies
    6
    TargetMol | Inhibitory_Antibodies
  • Dye Reagents
    46
    TargetMol | Dye_Reagents
  • PROTAC Products
    43
    TargetMol | PROTAC
  • Natural Products
    1720
    TargetMol | Natural_Products
  • Reagent Kits
    6
    TargetMol | Reagent_Kits
  • Recombinant Protein
    230
    TargetMol | Recombinant_Protein
  • Isotope Products
    44
    TargetMol | Isotope_Products
  • Antibody Products
    223
    TargetMol | Antibody_Products
  • Disease Modeling
    11
    TargetMol | Disease_Modeling_Products
  • Cell Research
    77
    TargetMol | Inhibitors_Agonists
(R)-3,4-DCPG HCl
(R)-3,4-DCPG HCl(201730-10-1 Free base)
T23215L In house
(R)-3,4-DCPG HCl is a potent and selective mGlu8a receptor agonist that activates metabotropic glutamate receptors on primary afferent terminals in the neonatal rat spinal cord.
  • $195
In Stock
Size
QTY
(S)-3,4-DCPG HCl
(S)-3,4-Dicarboxyphenylglycine HCl, (S)-3,4-DCPG HCl(201730-11-2 Free base)
T23288L In house
(S)-3,4-DCPG HCl ((S)-3,4-Dicarboxyphenylglycine HCl) is a selective metabotropic glutamate receptor 8a (mGluR8a) agonist that has an effect on human mGluR8-expressing AV12-664 cells with an EC50 of 31 nM.
  • $193
In Stock
Size
QTY
NPEC-caged-(S)-3,4-DCPG
T230841257323-85-5
mGlu8a agonist
  • $2,270
10-14 weeks
Size
QTY
(R)-3,4-DCPG
T23215201730-10-1
AMPA receptor antagonist with weak activity at NMDA receptors and little activity at kainate receptors
  • $1,520
Inquiry
Size
QTY
(RS)-3,4-DCPG
T23257176796-64-8
antagonist of AMPA receptors and agonist of mGluR8
  • $1,520
6-8 weeks
Size
QTY
(S)-3,4-DCPG
(S)-3,4-Dicarboxyphenylglycine
T23288201730-11-2
(S)-3,4-DCPG ((S)-3,4-Dicarboxyphenylglycine) is a selective agonist of human metabotropic glutamate receptor 8a (mGluR8a).
  • TBD
35 days
Size
QTY
Staurosporine
CGP 41251, Antibiotic AM-2282, AM-2282
T668062996-74-1
Staurosporine (AM-2282) is a protein kinase inhibitor with ATP-competitive and non-selective inhibitory activity (IC50=6 15 2 3 3000 nM) against PKC, PKA, c-Fgr, phosphorylase kinase and TAOK2. Staurosporine also induces apoptosis.
  • $56
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Lenvatinib
E7080
T0520417716-92-8
Lenvatinib (E7080) is a multi-target receptor tyrosine kinase inhibitor that inhibits VEGFR1-3, FGFR1-4, KIT, PDGFR, and RET, and has oral activity. Lenvatinib has the strongest inhibitory activity on VEGFR2 and VEGFR3 (IC50=4 5.2 nM). Lenvatinib has strong anti-tumor activity.
  • $40
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Corticosterone
Kendall's compound B, Corticosterone (From plants), 17-Deoxycortisol, 11β,21-Dihydroxyprogesterone
T0948L50-22-6
Corticosterone (Kendall's compound B) is an adrenocortical steroid with salocorticoid and glucocorticoid activity that is orally active. Corticosterone is involved in the regulation of energy, immune responses, and stress responses in the body.
  • $30
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Dxd
UNII-OQM5SD32BQ, OQM5SD32BQ, Exatecan derivative for ADC
T11249L1599440-33-1
Dxd (OQM5SD32BQ) is a potent inhibitor of DNA topoisomerase I with an IC50 of 0.31 μM. It is used as a conjugated drug of HER2-targeting ADC.
  • $39
In Stock
Size
QTY
TargetMol | Inhibitor Hot
osmi-4
T123282260791-14-6In house
OSMI-4 is a low nanomolar O-GlcNAc transferase (OGT) inhibitor (EC50 of 3 μM in cells) that can be used to study OGT inhibition in different human cell lines.
  • $215
In Stock
Size
QTY
TargetMol | Inhibitor Hot
deoxynivalenol
Vomitoxin, 4-Deoxynivalenol
T1509751481-10-8
Deoxynivalenol (Vomitoxin) is a mycotoxin produced by Fusarium spp. of the single trichothecene family and is commonly found in contaminated food and feed.Deoxynivalenol crosses the intestinal mucosa via a cellular bypass at the tight junctions.Deoxynivalenol transporters are unaffected by inhibitors of P-glycoprotein (PgP) or multidrug resistance-associated protein (MRP). Deoxynivalenol commonly causes diarrhea, vomiting, and gastrointestinal inflammation in humans and animals.
  • $89
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Resveratrol
trans-Resveratrol, SRT 501
T1558501-36-0
Resveratrol (SRT 501) is a polyphenolic natural product, a plant antitoxin with antioxidant and chemopreventive activities. Resveratrol has a wide range of targets including COX, SIRT, LOC, etc. Resveratrol induces autophagy and apoptosis.
  • $36
In Stock
Size
QTY
TargetMol | Inhibitor Hot
ONC206
T163921638178-87-6
ONC206, an analogue of the TRAIL inducer ONC201, acts as a selective antagonist of the D2-like dopamine receptors (DRD2 3 4) at nanomolar concentrations and possesses broad-spectrum anti-tumor activity.
  • $29
In Stock
Size
QTY
TargetMol | Inhibitor Hot
3-Methyladenine
NSC 66389, 3-MA
T18795142-23-4
3-Methyladenine (3-MA) is a PI3K inhibitor that selectively inhibits class IB PI3Kγ (IC50 = 60 μM) and class III VPS34 (IC50 = 25 μM). 3-Methyladenine inhibits autophagy.
  • $35
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Dinaciclib
SCH 727965, PS-095760
T1912779353-01-4
Dinaciclib (SCH 727965) is a selective CDK inhibitor targeting CDK1, CDK2, CDK5, and CDK9 (IC50 = 3 1 1 4 nM). It exhibits potential antitumor activity by inhibiting the incorporation of thoracic glycan (dThd) DNA.
  • $47
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Puromycin dihydrochloride
Puromycin 2HCl, CL13900 dihydrochloride
T221958-58-2
Puromycin dihydrochloride (CL13900 dihydrochloride) is a cinnamamide adenosine antibiotic and an inhibitor of protein synthesis. Puromycin dihydrochloride inhibits protein synthesis by binding to RNA and has antitumor and antitrypanosomal activity.
  • $39
In Stock
Size
QTY
TargetMol | Inhibitor Hot
SKLB-163
SKLB163
T261931255099-06-9In house
SKLB-163 acts by downregulating RhoGDI, activating JNK-1 signaling pathway and caspase-3, and reducing phosphorylated Akt and p44 42 MAPK.
  • $137
In Stock
Size
QTY
TargetMol | Inhibitor Hot
(E)-Daporinad
FK866, Daporinad, APO866, (E)-N-[4-(1-BENZOYL-PIPERIDIN-4-YL)-BUTYL]-3-PYRIDIN-3-YL-ACRYLAMIDE
T2644658084-64-1
(E)-Daporinad (FK866) is a highly specific, non-competitive small molecule inhibitor of nicotinamide phosphoribosyltransferase (NAMPT) with potential anti-tumor and anti-angiogenic activities with an IC50 value of 0.09 nM.
  • $36
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Palmatine chloride
T271810605-02-4
Palmatine chloride an isoquinoline alkaloid, is an important medicinal herbal extract with diverse pharmacological and biological properties.
  • $39
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Citronellol
dihydrogeraniol
T3240106-22-9
Citronellol ((±)-β-Citronellol) is used in insect repellents and perfumes and as a mite attractant.
  • $30
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Punicalagin
T392165995-63-3
Punicalagin is a major ellagitannin found in pomegranates that is reported to produce antioxidant, anti-inflammatory, and anticancer effects. It has been shown to prevent high-fat diet-induced obesity-associated accumulation of cardiac triglyceride and ch
  • $30
In Stock
Size
QTY
TargetMol | Inhibitor Hot
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
  • $50
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Dehydrocorydaline
Dehydrocorydalin, 13-Methylpalmatine
T5S235830045-16-0
1. Dehydrocorydaline (13-Methylpalmatine) exerts anti-metastatic potential via suppression of MMPs and Bcl-2 signaling in NSC-LC cells. 2. Dehydrocorydaline stimulates p38 MAPK activation, which can enhance heterodimerization of MyoD and E proteins, thus resulting in MyoD activation and myoblast differentiation. 3. Dehydrocorydaline shows antiplatelet effects, it inhibits thrombin-induced platelet aggregation in a low dose ( IC50= 34.914 ug mL). 4. Dehydrocorydaline has anti-inflammatory and antinociceptive effects. 5. Dehydrocorydaline inhibits MCF-7 cell proliferation by inducing apoptosis mediated by regulating Bax Bcl-2, activating caspases as well as cleaving PARP.
  • $52
In Stock
Size
QTY
TargetMol | Inhibitor Hot