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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2,026 – 2,040 of 4,900 results

2,026

eMolecules 395-47-1 | (2-(trifluoromethyl)phenyl)magnesium bromide, 0.50 M in THF | Synthonix | MFCD18253606 | 249.313 | C7H4BrF3Mg | 0.000 | [Br-].FC(F)(F)c1ccccc1[Mg+] | 100ml | 702445989

(2-(trifluoromethyl)phenyl)magnesium bromide, 0.50 M in THF | Synthonix | 395-47-1 | MFCD18253606 | 249.313 | C7H4BrF3Mg | 0.000 | [Br-].FC(F)(F)c1ccccc1[Mg+] | 100ml | 702445989

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2,027

Sigma Aldrich Fine Chemicals Biosciences 3-Bromo-2-naphthol 99% | 30478-88-7 | MFCD10000951 | 1G

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2,028

eMolecules 312693-19-9 | 2-Methylbenzylzinc chloride, 0.50 M in THF | Synthonix205.990 | C8H9ClZn | 0.000 | [Cl-].Cc1ccccc1C[Zn+] | 50ml | 702445951

2-Methylbenzylzinc chloride, 0.50 M in THF | Synthonix | 312693-19-9205.990 | C8H9ClZn | 0.000 | [Cl-].Cc1ccccc1C[Zn+] | 50ml | 702445951

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2,029

Medchemexpress LLC 1-piperazinedodecanamide, phthalazinyl-fluorobenzoyl isoindole piperidinyl amide | 2523016-96-6 | 99.9% | C47H53FN8O8 | 10MG

SK-575 is a proteolysis-targeting chimera (PROTAC) that selectively induces degradation of PARP1. It is supplied as a research-grade small molecule for biochemical and cellular studies of PARP1 biology and targeted protein degradation.

Selective PARP1 degradation via PROTAC mechanism.
Potent activity with low-nanomolar efficacy.
High chemical purity (~99.9%) suitable for biological assays.
Available in research-friendly quantities for assay development.
Datasheet and certificate of analysis available for batch verification.

Pricing & Availability

2,030

eMolecules 41242-25-5 | 2,3,4,5,6-Pentafluorophenylzinc bromide, 0.50 M in THF | Synthonix312.340 | C6BrF5Zn | 97.000 | [Br-].Fc1c(F)c(F)c([Zn+])c(F)c1F | 25ml | 795399116

2,3,4,5,6-Pentafluorophenylzinc bromide, 0.50 M in THF | Synthonix | 41242-25-5312.340 | C6BrF5Zn | 97.000 | [Br-].Fc1c(F)c(F)c([Zn+])c(F)c1F | 25ml | 795399116

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2,031

Medchemexpress LLC Sch-1473759 hydrochloride | 1094067-13-6 | 99.2% | 463.00 | C20H27ClN8OS | 1 ML

SCH-1473759 hydrochloride is a small-molecule aurora kinase inhibitor with potent activity against aurora A (IC50 4 nM) and aurora B (IC50 13 nM). It shows antiproliferative activity across multiple tumor cell lines and has demonstrated tumor growth inhibition in xenograft models. Available as solid material and as a ready-to-use 10 mM solution in DMSO for research applications.

Potent inhibition of aurora A and aurora B (IC50 4 nM and 13 nM).
Demonstrated antiproliferative activity in diverse tumor cell lines.
Shown in vivo tumor growth inhibition in xenograft models.
Available as solid and as a convenient DMSO solution for experiments.
High purity suitable for research applications.
Documented solubility and formulation protocols for in vitro and in vivo use.

Pricing & Availability

2,032

Medchemexpress LLC NNC-711 hydrochloride | 145645-62-1 | MFCD00153853 | 99.8% | 386.87 g/mol | C21H23ClN2O3 | 50 MG

NNC-711 hydrochloride is a potent, selective inhibitor of the GABA transporter GAT-1 used as a research reagent in neuroscience. It exhibits anticonvulsant and analgesic effects in vivo and is commonly used to study GABA uptake and synaptic inhibition.

Potent, selective inhibitor of GAT-1 with an IC50 of 0.04 μM (hGAT-1).
Hydrochloride salt provided as a solid for laboratory use.
Molecular weight 386.87 g/mol and formula C21H23ClN2O3.
High purity (~99.8% as listed by the supplier).
Supplied as a 50 MG research quantity suitable for in vitro and in vivo studies.

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2,033

Sigma Aldrich Fine Chemicals Biosciences 1,8-Naphthalic anhydride | 81-84-5 | MFCD00006925 | 500G

1,8-Naphthalic anhydride | Mol Wt: 198.17 | 81-84-5 | MFCD00006925 | 500G

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2,034

Medchemexpress LLC Bi-78d3 | 883065-90-5 | MFCD12912396 | 99.9% | 379.37 g/mol | C13H9N5O5S2 | 10 MG

BI-78D3 is a substrate-competitive inhibitor of c-Jun N-terminal kinase (JNK) used as a research tool to probe JNK-mediated signaling. It inhibits JNK kinase activity with an IC50 of approximately 280 nM and is supplied in solid and solution formats for in vitro and cell-based studies. For research use only.

Substrate-competitive inhibitor of JNK.
Reported IC50 of 280 nM against JNK.
High purity (99.85%).
Available as solid (10 mg) and as 10 mM solution in DMSO.
Powder storage: -20°C for long-term stability.

Pricing & Availability

2,035

Medchemexpress LLC BI 224436 | 1155419-89-8 | 99.7% | 442.51 | 50 MG

BI 224436 is a novel HIV-1 noncatalytic site integrase inhibitor. It exhibits EC50 values of less than 15 nM against different HIV-1 laboratory strains. Originally designed by Boehringer Ingelheim, this compound is suitable for various laboratory research applications.

Novel HIV-1 noncatalytic site integrase inhibitor
Effective against different HIV-1 laboratory strains with EC50 values less than 15 nM
Displays an additive effect in combination with most approved antiretrovirals
Retains full antiviral activity against recombinant viruses encoding INSTI resistance substitutions
Exhibits excellent pharmacokinetic profiles in rat, monkey, and dog

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2,036

eMolecules 119-79-9 | 5-Amino-2-naphthalenesulfonic acid | Combi-Blocks, Inc. | MFCD00004030 | 223.250 | C10H9NO3S | 97.000 | Nc1cccc2cc(ccc12)S(O)(=O)=O | 25g | 603136858

5-Amino-2-naphthalenesulfonic acid | Combi-Blocks, Inc. | 119-79-9 | MFCD00004030 | 223.250 | C10H9NO3S | 97.000 | Nc1cccc2cc(ccc12)S(O)(=O)=O | 25g | 603136858

Pricing & Availability

2,037

eMolecules 32018-89-6 | 6-AMINO-1-NAPHTHOIC ACID | AstaTech | MFCD11847894 | 187.198 | C11H9NO2 | 95.000 | Nc1ccc2c(cccc2c1)C(O)=O | 0.1g | 517263200

6-AMINO-1-NAPHTHOIC ACID | AstaTech | 32018-89-6 | MFCD11847894 | 187.198 | C11H9NO2 | 95.000 | Nc1ccc2c(cccc2c1)C(O)=O | 0.1g | 517263200

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2,038

ROWLEY BIOCHEMICAL INSTITUTE INC 4-CHLORO-1-NAPHTHOL SOL 8OZ

NC3344252 4-CHLORO-1-NAPHTHOL SOL 8OZ

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2,039

Medchemexpress LLC 2-(3,5-difluoro-4-hydroxyphenylamino)-8-isopentyl-5,7-dimethyl-7,8-dihydropteridin-6(5H)-one | 501437-28-1 | MFCD11223662 | >98.0% | 391.42 g·mol⁻¹ | C19H23F2N5O2 | 500 MG

BI-D1870 is a potent, ATP-competitive inhibitor of the p90 ribosomal S6 kinase (RSK) family. It is cell permeable and reported to penetrate the brain, making it suitable for cellular and in vivo studies of RSK-mediated signaling and related biological processes.

Selective ATP-competitive inhibitor of RSK isoforms.
Low nanomolar potency against RSK1-RSK4 (IC50s: 31, 24, 18, 15 nM).
Cell permeable for use in cellular assays.
Reported brain penetration supports in vivo applications.
Useful for studying MAPK/ERK-RSK signaling pathways.
Available as a solid suitable for storage and formulation.

Pricing & Availability

2,040

Medchemexpress LLC (±)-BI-D | 1416258-16-6 | 98.06% | 405.49 | 50 MG

(±)-BI-D is a potent allosteric integrase inhibitor (ALLINI). It operates by binding to integrase at the LEDGF/p75 binding site, effectively inhibiting HIV-Luc infection in cellular assays.

Potent allosteric integrase inhibitor.
Binds integrase at the LEDGF/p75 binding site.
Inhibits HIV-Luc infection in cells.
For research use only.

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Naphthalenes

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Medchemexpress LLC 1-piperazinedodecanamide, phthalazinyl-fluorobenzoyl isoindole piperidinyl amide | 2523016-96-6 | 99.9% | C47H53FN8O8 | 10MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Sch-1473759 hydrochloride | 1094067-13-6 | 99.2% | 463.00 | C20H27ClN8OS | 1 ML Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC NNC-711 hydrochloride | 145645-62-1 | MFCD00153853 | 99.8% | 386.87 g/mol | C21H23ClN2O3 | 50 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Bi-78d3 | 883065-90-5 | MFCD12912396 | 99.9% | 379.37 g/mol | C13H9N5O5S2 | 10 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC BI 224436 | 1155419-89-8 | 99.7% | 442.51 | 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 | 98.06% | 405.49 | 50 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More