Pyridines and derivatives
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- (1)
- (1)
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- (1)
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- (1)
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- (128)
- (55)
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- (1)
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- (1)
- (1)
- (63)
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- (1)
- (1)
- (29)
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- (1)
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- (1)
- (1)
- (1)
- (1)
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- (15)
- (1)
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- (1)
- (1)
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- (1)
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- (1)
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- (4)
- (1)
- (1)
- (1)
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- (2)
- (1)
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- (4)
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- (2)
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- (1)
- (1)
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- (1)
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- (1)
- (1)
- (1)
- (1)
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- (2)
- (16)
- (7)
- (5)
- (1)
- (1)
- (3)
- (5)
- (10)
- (2)
- (1)
- (6)
- (6)
- (7)
- (12)
- (1)
- (1)
- (39)
- (1)
- (12)
- (11)
- (4)
- (2)
- (2)
- (15)
- (15)
- (1)
- (1)
- (1)
- (2)
- (9)
- (3)
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- (1)
- (1)
- (1)
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- (6)
- (3)
- (3)
- (1)
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- (1)
- (1)
- (1)
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- (3)
- (1)
- (6)
- (5)
- (2)
- (1)
- (19)
- (9)
- (1)
- (2)
- (1)
- (1)
- (1)
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- (24)
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- (1)
- (1)
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Filtered Search Results
Medchemexpress LLC LY3509754 | 2452464-73-0 | 99.4% | 586.51 | 100 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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LY3509754, also known as IL-17A inhibitor 1, is a potent IL-17A inhibitor with demonstrated IC50 values of less than 9.45 nM in alphalisa assay and 9.3 nM in HT-29 cells. It exhibits high oral bioavailability (F=107%), making it a promising candidate for research.
- Potent IL-17A inhibitor
- High oral bioavailability (F=107%)
- Effective in alphalisa assay and HT-29 cells
- Supplied as 100 MG
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Lunresertib | 2719793-90-3 | 100.0% | C18H20N4O2 | 1 ML
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Lunresertib (RP-6306) is a potent, selective, and orally active PKMYT1 inhibitor with an IC50 of 14 nM. It demonstrates high selectivity over other kinases in cellular binding assays and exhibits anticancer effects by inducing pan-γH2AX in HCC1569 breast cancer cell lines, making them vulnerable to DNA damage. Lunresertib also causes unscheduled activation of CDK1 in CCNE1-overexpressing cells, promoting early mitosis.
- Potent and selective PKMYT1 inhibitor
- Orally active with an IC50 of 14 nM
- High selectivity over other kinases in cellular binding assays
- Exhibits anticancer effects
- Induces pan-γH2AX in HCC1569 breast cancer cell line
- Causes unscheduled activation of CDK1 in CCNE1-overexpressing cells
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Piperacillin | 61477-96-1 | 98.1% | 1 ML
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Piperacillin is a semisynthetic broad-spectrum β-lactam antibiotic. It exhibits potent bactericidal activity against Gram-negative bacteria and selected Gram-positive strains by targeting penicillin-binding proteins. It is commonly combined with the β-lactamase inhibitor Tazobactam for enhanced efficacy.
- Semisynthetic broad-spectrum β-lactam antibiotic
- Potent bactericidal activity against Gram-negative bacteria
- Effective against selected Gram-positive strains
- Functions by targeting penicillin-binding proteins
- Frequently used in combination with β-lactamase inhibitors
- Demonstrates in vitro inhibition against various bacteria including Pseudomonas aeruginosa and Escherichia coli
- Prolongs survival in animal models of infection when combined with Tazobactam
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eMolecules 330645-87-9 | HCTU | Combi-Blocks | MFCD04973268 | 413.690 | C11H15ClF6N5OP | 98.000 | F[P-](F)(F)(F)(F)F.CN(C)C(On1nnc2ccc(Cl)cc12)=[N+](C)C | 5g | 117535827
HCTU | Combi-Blocks | 330645-87-9 | MFCD04973268 | 413.690 | C11H15ClF6N5OP | 98.000 | F[P-](F)(F)(F)(F)F.CN(C)C(On1nnc2ccc(Cl)cc12)=[N+](C)C | 5g | 117535827
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Medchemexpress LLC CC-671 | 1618658-88-0 | 99.1% | 512.56 | 1 ML
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CC-671 is a dual TTK protein kinase/CDC2-like kinase (CLK2) inhibitor, demonstrating potent inhibitory activity against both enzymes. It exhibits cytotoxicity against human BT474 and CAL51 cells and shows significant tumor growth inhibition in vivo. This compound also selectively binds to kinases such as CLK2, CAMKK2, PIP4K22, and JNK.
- Dual TTK protein kinase/CDC2-like kinase (CLK2) inhibitor
- Exhibits cytotoxicity against human BT474 and CAL51 cells
- Demonstrates significant tumor growth inhibition in vivo
- Selectively binds to CLK2, CAMKK2, PIP4K22, and JNK
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Medchemexpress LLC (E)-2-((1,4-dimethylpiperazin-2-ylidene)amino)-5-nitro-N-phenylbenzamide | 1613465-33-0 | 99.7% | 367.40 g/mol | C19H21N5O3 | 5 MG
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ML336 is a quinazolinone-based small-molecule inhibitor of Venezuelan equine encephalitis virus (VEEV) that potently inhibits VEEV-induced cytopathic effects in multiple strains in the low-nanomolar range. It is supplied for research use only and is typically provided as a powder for biochemical and antiviral assays.
- Potent VEEV inhibitor exhibiting low-nanomolar antiviral activity.
- Quinazolinone-based small molecule for antiviral research and probe development.
- High purity (≈99.65%) for consistent experimental results.
- Available in small mass vials suitable for screening and assay optimization.
- Powder stable at -20°C for long-term storage; solutions stable at -80°C.
- Intended for research use only; not for human or veterinary use.
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Medchemexpress LLC CP-316819 | 186392-43-8 | 99.0% | 415.87 | 100 MG
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CP-316819 is a potent glycogen phosphorylase (GPase) inhibitor with antihyperglycemic effect. It has IC50 values of 17 nM against human skeletal muscle glycogen phosphorylase (huSMGPa) and 34 nM against liver glycogen phosphorylase (huLGPa). CP-316819 causes glycogen accumulation under normoglycemic conditions but permits glycogen utilization when glucose concentrations are low. It also prevents neuronal cell death and maintains brain electrical currents.
- Molecular weight: 415.87
- Formula: C21H22ClN3O4
- Appearance: Solid
- Color: White to off-white
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Apexbio Technology LLC Triciribine 35943-35-2 50mg
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Triciribine also known as API-2 is a selective inhibitor of Akt kinase activity targeting Akt1 Akt2 and Akt3 without affecting upstream regulators PDK1 and PI3K It suppresses Akt phosphorylation at Thr308 and Ser473 sites triggering apoptosis and growth inhibition in multiple cancer cell models with an IC50 of approximately 130 nM Additionally Triciribine exhibits antiviral activity against HIV-1 inhibiting viral replication and syncytia formation at an IC50 of 20 nM In biomedical research Triciribine is employed to investigate Akt-associated signaling pathways and evaluate potential therapeutic strategies targeting Akt-dependent tumors and HIV infections
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Medchemexpress LLC MS023 | 1831110-54-3 | 99.9% | 287.40 | 100 MG
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MS023 is a chemical probe and a potent, selective, and cell-active inhibitor of human type I protein arginine methyltransferases (PRMTs), with IC50s of 30, 119, 83, 4, and 5 nM for PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8. It is utilized for research in epigenetics, particularly in studies involving histone methyltransferases, and demonstrates antiproliferative effects against human A549, HCC4006, and SK-LU-1 cells.
- Potent, selective, and cell-active inhibitor of human type I protein arginine methyltransferases (PRMTs)
- Inhibits PRMT1 methyltransferase activity in MCF7 cells
- Inhibits PRMT6 methyltransferase activity in HEK293 cells
- Blocks MLL-r acute lymphoblastic leukemia (ALL) propagation in animal models
- Extends survival of leukemic mice in combination treatments
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Medchemexpress LLC NNC 63-0532 | 50MG
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NNC 63-0532 | 50MG
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Cayman Chemical SBromoenol lactoned7
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An internal standard for the quantification of (S)-BEL by GC- or LC-MS
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Medchemexpress LLC 3-hydroxypropionic acid-13C3 sodium | 115.04 | 13C3H5NaO3 | 500ug
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3-Hydroxypropionic acid-13C3 sodium is the 13C labeled 3-Hydroxypropionic acid sodium (HY-W095705A) 3-Hydroxypropionic acid sodium an endogenous metabolite is a building block in the chemical synthesis[1]
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Medchemexpress LLC GE11 | 875142-25-9 | 99.6% | 1540.68 | 100 MG
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GE11 is an active peptide suitable for cancer studies and targeted drug delivery. It acts as a smart carrier for antitumor drugs by combining with colloidal drug delivery systems. As a potent EGFR ligand, this dodecapeptide specifically binds to EGFR with high affinity and selectivity, making it valuable for the diagnosis and targeted delivery of drugs in radiotherapy, gene therapy, and chemotherapy against EGFR-positive tumors.
- Active peptide for cancer studies
- Combines with colloidal drug delivery systems as smart carriers
- Potent EGFR ligand with high affinity and selectivity
- Used in diagnosis and targeted drug delivery
- Applicable for radiotherapy, gene therapy, and chemotherapy against EGFR-positive tumors
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Medchemexpress LLC PF-4989216 | 1276553-09-3 | 99.4% | 380.40 | 50 MG
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PF-4989216 is a potent and selective PI3Kα inhibitor with a Ki of 0.6 nM. It is for research use only.
- Potent and selective PI3Kα inhibitor (Ki of 0.6 nM)
- Excellent selectivity against mTOR (Ki=1440 nM) and other kinases
- Demonstrates dose-responsive tumor growth inhibitory activity in xenograft models
- Available as white to off-white solid
- Suitable for research use only
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Medchemexpress LLC WAY-600 | 1062159-35-6 | MFCD22419019 | C28H30N8O | 50 MG
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WAY-600 is a potent, ATP-competitive, and selective mTOR inhibitor with an IC50 of 9 nM for the recombinant mTOR enzyme. It effectively blocks mTOR complex 1/2 (mTORC1/2) assembly and activation, demonstrating significant anti-cancer activity in vitro against HepG2 and Huh-7 cells and in vivo by inhibiting HepG2 tumor growth in nude mice.
- Potent, ATP-competitive, and selective mTOR inhibitor
- Blocks mTOR complex 1/2 assembly and activation
- Inhibits HepG2 and Huh-7 cell viability
- Decreases HepG2 cell colonies
- Increases caspase-3 and caspase-9 activity in HepG2 cells
- Inhibits HepG2 tumor growth in nude mice
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