Benzenoids

Medchemexpress LLC HY-117549 10mg Medchemexpress, Ibrolipim CAS:133208-93-2 Purity:>98%

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Medchemexpress, HY-117549 10mg Ibrolipim CAS:133208-93-2 Ibrolipim (NO-1886) is an orally active lipoprotein lipase (LPL)-promoting agent. Ibrolipim decreases plasma triglycerides, increases high-density lipoprotein cholesterol levels. Ibrolipim has renoprotective and hypolipidemic effects[3]. 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 HY-112668 5mg Medchemexpress, Retagliptin Phosphate CAS:1256756-88-3 Purity:>98%

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Medchemexpress, HY-112668 5mg Retagliptin Phosphate CAS:1256756-88-3 Retagliptin Phosphate is pharmaceutical composition of DPP-4 inhibitor for treating type-2 diabetes. 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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eMolecules​ Medchem Express / AZD-5069 / 1mg / 446270466 / HY-19855 / / 878385-84-3 / [null] / 476.510 / C18H22F2N4O5S2

Medchem Express / AZD-5069 / 1mg / 446270466 / HY-19855 / / 878385-84-3 / [null] / 476.510 / C18H22F2N4O5S2

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Medchemexpress LLC 4-Chloro-2-fluorobenzeneboronic acid | 160591-91-3 | 174.37 | 5 G

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4-Chloro-2-fluorobenzeneboronic acid is a biochemical reagent. It can be used as a biological material or organic compound for life science related research.

• For research use only
• Not sold to patients
• Can be used as a biological material
• Can be used as an organic compound for life science related research

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eMolecules​ Medchem Express / GSK2643943A / 5mg / 441681837 / HY-111458 / / 2449301-27-1 / [null] / 277.302 / C17H12FN3

Medchem Express / GSK2643943A / 5mg / 441681837 / HY-111458 / / 2449301-27-1 / [null] / 277.302 / C17H12FN3

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Apexbio Technology LLC Escitalopram Oxalate 219861-08-2 50mg

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Escitalopram Oxalate (CAS 219861-08-2) is the S-( )-enantiomer of citalopram and functions as a selective serotonin reuptake inhibitor (SSRI) It exhibits high affinity for the human serotonin transporter (5-HTT) inhibiting [3H]-5-HT uptake with a Ki of 6 6 nM in COS-1 cells expressing 5-HTT and displacing [125I]-RTI-55 with a Ki of 3 9 nM In rat brain synaptosomes Escitalopram Oxalate blocks the accumulation of [3H]-serotonin (IC50 2 1 nM) with markedly lower activity against norepinephrine and dopamine uptake It also shows in vitro affinity for rat histamine H1 receptors and 1 sites Escitalopram Oxalate is widely utilized in neuropharmacological research related to depression and anxiety mechanisms

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Medchemexpress LLC PKG inhibitor peptide | 82801-73-8 | 99.8% | 943.11 | 10 MG

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PKG inhibitor peptide is an ATP-competitive inhibitor of cGMP-dependent protein kinase (PKG), with a Ki of 86 μM. This peptide is for research use only and not intended for patient use. It is provided as a white to off-white solid with a purity of 99.8%.

• ATP-competitive inhibitor of cGMP-dependent protein kinase (PKG)
• Ki of 86 μM (PKG)
• Purity of 99.8%
• White to off-white solid appearance
• Stable under recommended storage conditions
• For research use only

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Medchemexpress LLC L-826266 | 244101-03-9 | 98.0% | 570.88 | 50 MG

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L-826266 is a selective and competitive EP3 receptor antagonist that can be used for convulsive disorders research. It also prevents PGE2-induced decrease of Na+,K+-ATPase activity in adult rat hippocampal slices and delays and increases the latency for clonic and generalized tonic-clonic seizures induced by PTZ in animal models.

• Selective and competitive EP3 receptor antagonist
• Can be used for convulsive disorders research
• Prevents PGE2-induced decrease of Na+,K+-ATPase activity in adult rat hippocampal slices
• Delays and increases the latency for clonic and generalized tonic-clonic seizures induced by PTZ in animal models

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Medchemexpress LLC KKI-5 TFA | 99.3% | 887.90 | 10 MG

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KKI-5 TFA is a specific inhibitor of tissue kallikrein. It has been shown to attenuate breast cancer cell invasion and is intended for research use only.

• Specific inhibitor of tissue kallikrein
• Attenuates breast cancer cell invasion
• Target: Kallikrein
• For research use only

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Medchemexpress LLC Sting agonist-16 | 652142-94-4 | ≥99.0% | 396.23 | C19H11Cl2N5O | 5 MG

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STING agonist-16 is a small-molecule activator of the STING (stimulator of interferon genes) pathway used as a research tool to study innate immune signaling, antiviral responses, and antitumor immunity. It is supplied as a high-purity solid suitable for biochemical and cellular assays.

• Activates STING signaling in vitro.
• High purity ≥99.0%.
• Molecular formula C19H11Cl2N5O; molecular weight 396.23.
• Off-white to light brown solid appearance.
• Powder storage: -20°C for long-term stability.
• Available in small research-sized quantities for laboratory use.

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Medchemexpress LLC HY-100209 5mg Medchemexpress, Sufugolix CAS:308831-61-0 Purity:>98%

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Medchemexpress, HY-100209 5mg Sufugolix CAS:308831-61-0 Sufugolix (TAK-013) is a highly potent and orally available luteinizing hormone-releasing hormone ( LHRH ) receptor antagonist with an IC 50 of 0.1 nM. 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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eMolecules​ ChemScene / ethyl 5-(4-fluorophenyl)-134-oxadiaZole-2-carboxylate / 100mg / 714125953 / CS-0236207 / 0.000 / 950259-82-2 / MFCD14716324 / 236.202 / C11H9FN2O3

ChemScene / ethyl 5-(4-fluorophenyl)-134-oxadiaZole-2-carboxylate / 100mg / 714125953 / CS-0236207 / 0.000 / 950259-82-2 / MFCD14716324 / 236.202 / C11H9FN2O3

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eMolecules​ Medchem Express / Itanapraced / 5mg / 446264139 / HY-14399 / / 749269-83-8 / MFCD18633206 / 325.160 / C16H11Cl2FO2

Medchem Express / Itanapraced / 5mg / 446264139 / HY-14399 / / 749269-83-8 / MFCD18633206 / 325.160 / C16H11Cl2FO2

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eMolecules​ Medchem Express / NCGC00092410 / 5mg / 572596557 / HY-114043 / / 442898-34-2 / [null] / 353.466 / C21H27N3O2

Medchem Express / NCGC00092410 / 5mg / 572596557 / HY-114043 / / 442898-34-2 / [null] / 353.466 / C21H27N3O2

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Apexbio Technology LLC ML161 423735-93-7 10mg

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ML161 (CAS 423735-93-7) is a selective small-molecule inhibitor targeting protease-activated receptor-1 (PAR1) a G protein-coupled receptor implicated in signal transduction pathways associated with tumor progression ML161 exhibits potent inhibitory activity against PAR1 with an IC of 0 26 M In human platelet assays ML161 suppresses thrombin-induced platelet activation in a dose-dependent manner as evidenced by reduced P-selectin expression Additionally ML161 inhibits P-selectin surface expression during granule secretion (EC 0 3 M) and blocks SFLLRN-stimulated platelet aggregation This compound is utilized in studies of PAR1-mediated signaling and platelet function

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