Naphthalenes

Polycyclic aromatic hydrocarbon compounds that consist of ten carbon atoms and eight hydrogen atoms fused into two benzene rings; it is the simplest polycyclic aromatic hydrocarbon.

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2,701 – 2,715 of 4,900 results

2,701

Chemscene CHEMSCENE

5000577874 4- NAPHTHALEN-1-YL -3 5- 250MG

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2,702

Ambeed AMBEED

5000850054 2- 3-BROMOPHENYL -1-PHE 25G

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2,703

eMolecules 10601-80-6 | Ethyl 3,3-diethoxypropionate | Ambeed | MFCD00009865 | 190.239 | C9H18O4 | 97.000 | CCOC(CC(=O)OCC)OCC | 10g | 521422801

Ethyl 3,3-diethoxypropionate | Ambeed | 10601-80-6 | MFCD00009865 | 190.239 | C9H18O4 | 97.000 | CCOC(CC(=O)OCC)OCC | 10g | 521422801

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2,704

Medchemexpress LLC Bi-847325 | 1207293-36-4 | 98.2% | 10 MG

BI-847325 is an orally bioavailable, ATP-competitive dual inhibitor of MEK and Aurora kinases used in preclinical research to probe MAPK signaling and cell-cycle regulation. The compound has documented biochemical potency and is supplied as a solid research reagent for in vitro and in vivo studies.

Dual MEK and Aurora kinase inhibition for pathway and anticancer research.
Demonstrated in vitro and in vivo activity supporting translational studies.
High purity suitable for research applications.
Solid, light yellow to yellow appearance for easy handling.
Stable under recommended storage conditions to preserve compound integrity.
Provided as a small-scale research quantity for experimental use.

Pricing & Availability

2,705

Medchemexpress LLC Ald-Ph-PEG6-acid | 2055013-55-1 | 95.3% | 50 MG

Ald-Ph-PEG6-acid is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. PROTACs consist of two distinct ligands connected by a linker; one targets an E3 ubiquitin ligase and the other targets a protein of interest. These molecules work by harnessing the intracellular ubiquitin-proteasome system to selectively degrade target proteins. It appears as a colorless to light yellow viscous liquid.

PEG-based PROTAC linker
Used in the synthesis of PROTACs
Targets E3 ubiquitin ligase and a protein of interest
Exploits the intracellular ubiquitin-proteasome system
Selectively degrades target proteins

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2,706

Medchemexpress LLC (±)-BI-D | 1416258-16-6 | 98.1% | 10 MG

(±)-BI-D is an allosteric HIV integrase inhibitor used in research to study integrase function and antiviral activity. It binds the LEDGF/p75 binding site on integrase and has demonstrated inhibition of HIV-Luc infection in cellular assays.

Potent ALLINI mechanism of action.
Binds LEDGF/p75 integrase site to disrupt viral integration.
Demonstrated cellular activity (reported IC50s: 0.16 μM and 2.9 μM).
Available as solid and as a 10 mM solution in DMSO for assay setup flexibility.
High purity and defined molecular weight and formula for reproducible studies.
Intended for biochemical and cellular research use only; not for human use.

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2,707

eMolecules 514844-65-6 | 4-bromo-1-methoxy-2-Naphthalenecarboxaldehyde | 1g

WuXi ChemSupply | 4-bromo-1-methoxy-2-Naphthalenecarboxaldehyde | 1g | 599170784 | LN03282391 | 95.000 | 514844-65-6 | 265.106 | C12H9BrO2

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2,708

Medchemexpress LLC Amiodarone hydrochloride | 19702-44-2 | MFCD00079083 | C25H30ClI2NO3 | 100 MG

Amiodarone hydrochloride is a class III antiarrhythmic agent used in the treatment of various ventricular and supraventricular arrhythmias. It works by prolonging the action potential and refractory period in myocardial tissue.

Acts as an antagonist at α1, β1, and β2 adrenoceptors
Functions as a non-competitive antagonist at muscarinic receptors
Blocks cardiac K+ channels and L-type Ca2+ channels
Displays anti-anginal, anti-fibrillatory, and vasodilator effects

Pricing & Availability

2,709

eMolecules 83-56-7 | Naphthalene-1,5-diol | Oakwood Chemical | MFCD00003980 | 160.172 | C10H8O2 | 98.000 | Oc1cccc2c(O)cccc12 | 1g | 537715483

Naphthalene-1,5-diol | Oakwood Chemical | 83-56-7 | MFCD00003980 | 160.172 | C10H8O2 | 98.000 | Oc1cccc2c(O)cccc12 | 1g | 537715483

Pricing & Availability

2,710

Medchemexpress LLC Rimonabant Hydrochloride | 158681-13-1 | 99.3% | C₂₂H₂₂Cl₄N₄O | 1 ML

Rimonabant Hydrochloride is a highly potent and selective central cannabinoid receptor (CB1) antagonist with a Ki of 1.8 nM. It also inhibits Mycobacterial membrane protein Large 3 (MMPL3). This product is intended for research use only.

Highly potent and selective central cannabinoid receptor (CB1) antagonist
Inhibits mycobacterial membrane protein Large 3 (MMPL3)
Soluble in DMSO at 33.33 mg/mL (66.63 mM)
Store solid at 4°C, sealed, away from moisture
Store in solvent at -80°C for 1 year or -20°C for 6 months, sealed, away from moisture
For research use only

Pricing & Availability

2,711

eMolecules 38858-90-1 | 4-Methyl-3-nitro-1H-pyrazole | Ambeed | MFCD09701703 | 127.103 | C4H5N3O2 | 97.000 | Cc1c[nH]nc1[N+]([O-])=O | 250mg | 490529939

4-Methyl-3-nitro-1H-pyrazole | Ambeed | 38858-90-1 | MFCD09701703 | 127.103 | C4H5N3O2 | 97.000 | Cc1c[nH]nc1[N+]([O-])=O | 250mg | 490529939

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2,712

Apexbio Technology LLC BI 2536(Synonyms: BI-2536, BI2536, Plk1 inhibitor BI 2536), 50mg, CAS: 755038-02-9.

BI 2536 (CAS number 755038-02-9) is an ATP-competitive inhibitor selectively targeting human polo-like kinase 1 (PLK1) exhibiting an IC50 value of approximately 0 83 nM Comparatively BI 2536 shows substantially less affinity towards other kinases In vitro studies demonstrate that BI 2536 inhibits proliferation of various human tumor cell lines (EC50 values ranging from 2 to 25 nM) and induces G2/M cell cycle arrest accompanied by apoptosis as evidenced in HeLa cervical cancer cells In vivo data from xenograft tumor models indicate that BI 2536 administered intravenously on a weekly or biweekly schedule possesses antitumor efficacy

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2,713

Medchemexpress LLC Scavenger receptor class B member 1 (SR-BI/SCARB1), recombinant human | >95.0% | 10 UG

Recombinant human scavenger receptor class B member 1 (SR-BI/SCARB1) expressed in HEK293 cells and supplied as a lyophilized C-terminal His-tagged protein. Supplied as a 10 μg lyophilized vial, the product runs at ~70-90 kDa and is >95% pure, suitable for biochemical and cell biology assays requiring recombinant human SR-BI.

Human sequence P33-Y443, accession Q8WTV0-1.
C-terminal His tag facilitates purification and detection.
Expressed in HEK293 for mammalian post-translational modifications.
Lyophilized with stabilizers (trehalose or mannitol, and Tween 80) for stability.
Purity >95.0% by reducing SDS-PAGE for consistent performance.
Reconstitute to ≥100 μg/mL; avoid concentrations below 100 μg/mL in ddH2O.

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2,714

Medchemexpress LLC SR-BI/SCARB1 protein (human, HEK293, C-His tag) | >95.0% | 100 UG

Recombinant human SR-BI/SCARB1 protein produced in HEK293 mammalian cells and supplied as a lyophilized C-terminal His-tagged protein for biochemical and cell-based studies of HDL-mediated cholesterol transport and lipid/receptor interactions.

Expressed in HEK293 mammalian cells.
C-terminal His tag for purification and detection.
Purity >95% by reducing SDS-PAGE.
Molecular weight 70-90 kDa (approx.).
Lyophilized formulation with stabilizers (trehalose or mannitol, and Tween 80).
Store at -20°C; after reconstitution stable at 4°C for 1 week.

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2,715

Medchemexpress LLC Lincomycin hydrochloride | 859-18-7 | 99.3% | 1 G

Lincomycin hydrochloride is the salt form of the antibiotic lincomycin. It inhibits protein synthesis in gram-positive and, to a lesser extent, gram-negative bacteria by binding to the 50S subunits of bacterial ribosomes and acting on aminoacyl-tRNA binding and the transpeptidation reaction.

Inhibits protein synthesis in bacteria
Binds to 50S subunits of bacterial ribosomes
Active against gram-positive and some gram-negative bacteria
Soluble in H2O at 100 mg/mL
Transported at room temperature
Store at 4°C in sealed storage, away from moisture
Can be stored at -80°C for 6 months or -20°C for 1 month when dissolved in solvent

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Naphthalenes

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Chemscene CHEMSCENE Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Bi-847325 | 1207293-36-4 | 98.2% | 10 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Ald-Ph-PEG6-acid | 2055013-55-1 | 95.3% | 50 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC (±)-BI-D | 1416258-16-6 | 98.1% | 10 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Amiodarone hydrochloride | 19702-44-2 | MFCD00079083 | C25H30ClI2NO3 | 100 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Rimonabant Hydrochloride | 158681-13-1 | 99.3% | C₂₂H₂₂Cl₄N₄O | 1 ML Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Apexbio Technology LLC BI 2536(Synonyms: BI-2536, BI2536, Plk1 inhibitor BI 2536), 50mg, CAS: 755038-02-9. Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Scavenger receptor class B member 1 (SR-BI/SCARB1), recombinant human | >95.0% | 10 UG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC SR-BI/SCARB1 protein (human, HEK293, C-His tag) | >95.0% | 100 UG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Lincomycin hydrochloride | 859-18-7 | 99.3% | 1 G Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More