Bioactive Small Molecules
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Filtered Search Results
Medchemexpress LLC O=[N+](C1=CC2=C(N(CC3=CC=CC=C3)N=C2OCC4CCCCC4)C=C1)[O-] | 1564253-75-3 | 99.7% | 365.43 | C21H23N3O3 | 5 MG
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PGN36 is a selective cannabinoid CB2 receptor antagonist used as a research tool in neurobiology and bone biology. It shows high affinity for CB2R and is reported to cross the blood-brain barrier, making it suitable for in vivo and in vitro studies of neurodegeneration and collagen type I regulation.
- Selective CB2 receptor antagonist (Ki 0.09 μM)
- Marked selectivity over CB1 receptor (>40 μM)
- Used in studies of frontotemporal dementia and bone-related assays
- Molecular formula C21H23N3O3; molecular weight 365.43 g·mol-1
- Purity 99.74%
- Appearance light yellow solid
- Storage: powder -20°C; in solvent -80°C for 6 months or -20°C for 1 month
- Available in small research pack sizes such as 5 mg
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Medchemexpress LLC Benzoic acid, 4-[(3aS,4R,9bR)-6-ethoxy-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinolin-4-yl]- | 1357248-83-9 | 98.7% | 335.40 | 5 MG
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Benzoic acid, 4-[(3aS,4R,9bR)-6-ethoxy-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinolin-4-yl]- | 1357248-83-9 | 98.7% | 335.40 | 5 MG
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Cayman Chemical MLN0905, Purity: ≥98%, CAS: 1228960-69-7, 5 mg
A Plk1 inhibitor (IC50 = 2 nM); inhibits 95% of Plk1 activity but also inhibits the activity of 10 additional kinases by greater than or equal to 90% in a panel of 359 kinases at 1 µM; reduces H3S10Ph in HT-29 colorectal cancer cells (EC30 = 9 nM); inhibits proliferation in a panel of six human lymphoma cell lines (IC50 = 3.2-24 nM)
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Medchemexpress LLC Methyl 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)acetate | 15991-13-6 | MFCD01463811 | 97.4% | 234.20 g/mol | C12H10O5 | 25 MG
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Methyl 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)acetate is a coumarin-class small molecule used as a fluorescent probe and synthetic intermediate in chemical and biological research. Supplied as a solid with high listed purity, it is intended for analytical assays, fluorescence-based applications, and lab-scale synthesis.
- Solid, white to light yellow appearance.
- High purity suitable for analytical and synthetic use.
- Coumarin-derived structure with fluorescent properties.
- Available in multiple milligram packaging sizes for lab-scale work.
- Provided with standard chemical identifiers for reproducibility.
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Medchemexpress LLC 2H-Dipyrido[1,2-a:2',3'-d]pyrimidine-3-carboxamide, 1,5-dihydro-2-imino-10-methyl-N-[3-(4-morpholinyl)propyl]- | 99.7% | 573.51 | 50 MG
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SPOP-IN-6b dihydrochloride is a potent speckle-type POZ protein (SPOP) inhibitor with an IC50 of 3.58 μM. It can suppress SPOP activity, which then increases the suppression of cancer substrate protein PTEN and DUSP7 content. In vivo, it can slow down tumor growth by suppressing SPOP. For research use only. We do not sell to patients.
- In vitro, SPOP-IN-6b shows IC50s of 2-10.2 μM for A498, Caki-2, Ketr-3, 769-P, OS-RC-2, and 786-0 cells.
- In vitro, SPOP-IN-6b can suppress SPOP activity, leading to an increase in suppression cancer substrate protein PTEN and DUSP7 content.
- In vivo, SPOP-IN-6b can slow down the growth of tumor by suppressing SPOP.
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AG Scientific Inc TCEP Hydrochloride, 5 G
TCEP hydrochloride is a non-thiol reducing agent used to reduce and break disulfide bonds. TCEP HCl is widely preferred to the similar reducing agent DTT because of its greater effectiveness and resistance to oxidation from air exposure.CAS Number: 51805-45-9Molecular Weight: 286.6 DaChemical Formula: C9H15O6P HClSolubility: Soluble in waterStorage Temperature: -20CResearch or further manufacturing use only, not for food or drug use.
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Medchemexpress LLC HY-105040C 5mg Medchemexpress, Pomaglumetad methionil (hydrochloride) CAS:635318-26-2 Purity:>98%
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Medchemexpress, HY-105040C 5mg Pomaglumetad methionil (hydrochloride) CAS:635318-26-2 Pomaglumetad methionil hydrochloride (LY2140023 hydrochloride) is an orally active, methionine prodrug of the selective mGlu2/3 receptor agonist LY404039. Pomaglumetad methionil hydrochloride has the potential for schizophrenia research. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Ccx-777 | 1226686-36-7 | 98.5% | 593.78 g/mol | C31H43N7O3S | 10MG
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CCX-777 is a small-molecule partial agonist of β-arrestin-2 recruitment to ACKR3 (atypical chemokine receptor 3), provided as a purified research compound for in vitro and preclinical studies. The compound has formula C31H43N7O3S and a molecular weight of 593.78 g/mol.
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Cayman Chemical DC-05, Purity: ≥98%, CAS: 890643-16-0, 10 mg
A non-nucleoside DNMT1 inhibitor (IC50 = 10.3 µM); selective for DNMT1 over DNMT3A and DNMT3B (IC50s = >200 µM), as well as G9a, SUV39H1, MLL1, SET7/9, and PRMT1 (IC50s = >150, >150, >150, >150, and 37.1 µM, respectively); reduces proliferation of HCT116 colon cancer cells from 2.5-10 µM
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Cayman Chemical Arylquin 1, Purity: ≥98%, CAS: 1630743-73-5, 5 mg
A Par-4 secretagogue; binds to vimentin to displace Par-4 for secretion; induces Par-4 secretion from MEFs and prostate cancer cells in vitro; induces paracrine apoptosis of H1299, HOP92, and H460 cancer cells when co-cultured with Par-4+/+ MEFs
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Selleck Chemical LLC Marinopyrrole A (Maritoclax) 5mg 1227962-62-0
Marinopyrrole A (Maritoclax) is a selective Mcl-1 antagonist. It binds to Mcl-1, but not Bcl-XL, and targets Mcl-1 for proteasomal degradation. Maritoclax disrupts the interaction between Bim and Mcl-1 with an IC50 of 10.1 ?M. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Amsbio LLC Stemolecule Doxycycline hyclate (10 mg)
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Stemolecule Doxycycline hyclate (10 mg)
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Cayman Chemical Dehydrocannabifuran, Purity: ≥95%, CAS: 56154-59-7, 5 mg
An analytical reference standard that is structurally similar to known phytocannabinoids; has been found in Cannabis and marijuana smoke condensate; intended for research and forensic applications
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Medchemexpress LLC Quipazine (maleate) | 5786-68-5 | 98.0% | 25 MG
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Quipazine maleate is a chemical compound that acts as a 5-HT agonist, known to cause behavioral changes like hyperactivity. It also exhibits weak reversible MAO inhibitory activity.
- 5-HT receptor agonist
- Causes behavioral changes such as hyperactivity
- Shows weak reversible MAO inhibitory activity
- For research use only
- Store at 4°C in sealed container, away from moisture and light
- In solvent, store at -80°C for 6 months or -20°C for 1 month
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Apexbio Technology LLC Dacomitinib (PF299804, PF299), 5mg. Cas: 1110813-31-4 MFCD: MFCD19443734. HER inhibitor
IC50: 6 nM (EGFR); 45.7 nM (ERBB2); 73.7 nM (ERBB4)The epidermal growth factor receptor (EGFR; ErbB-1; HER1 in humans) is the cell-surface receptor for members of the epidermal growth factor family (EGF-family) of extracellular protein ligands. Other sizes are available. Please inqury us for quote.
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