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Phenanthrene (Standard)

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Apoptosis (1) Bacterial (2) Biochemical Assay Reagents (1) Drug Metabolite (1) Reference Standards (6)
By Research Areas:	Cancer (1) Infection (1) Inflammation/Immunology (1)

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Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-B1727R

Phenanthrene (Standard)	Reference Standards Apoptosis	Inflammation/Immunology Cancer
Phenanthrene (Standard) is the analytical standard of Phenanthrene. This product is intended for research and analytical applications. Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment .

HY-W007969R

*(8S,13S,14S)-13-Methyl-1,2,6,7,8,12,13,14,15,16-decahydrospiro[cyclopenta[a]phenanthrene-3,2'-[1,3]dioxolan]-17(4H)-one (Standard)*	Reference Standards
(8S,13S,14S)-13-Methyl-1,2,6,7,8,12,13,14,15,16-decahydrospiro[cyclopenta[a]phenanthrene-3,2'-[1,3]dioxolan]-17(4H)-one (Standard) is the analytical standard of (8S,13S,14S)-13-Methyl-1,2,6,7,8,12,13,14,15,16-decahydrospiro[cyclopenta[a]phenanthrene-3,2'-[1,3]dioxolan]-17(4H)-one. This product is intended for research and analytical applications.

HY-103609R

Pyrene (Standard) Benzo[def]Phenanthrene (Standard)	Biochemical Assay Reagents Reference Standards	Others
Pyrene (Standard) is the analytical standard of Pyrene. This product is intended for research and analytical applications. Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

HY-W105644R

*(2'R,7R,8R,10S,13S,14S)-Methyl 10,13-dimethyl-3,5'-dioxo-1,2,3,4',5',6,7,8,10,12,13,14,15,16-tetradecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-7-carboxylate (Standard)*	Reference Standards
(2'R,7R,8R,10S,13S,14S)-Methyl 10,13-dimethyl-3,5'-dioxo-1,2,3,4',5',6,7,8,10,12,13,14,15,16-tetradecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-7-carboxylate (Standard) is the analytical standard of (2'R,7R,8R,10S,13S,14S)-Methyl 10,13-dimethyl-3,5'-dioxo-1,2,3,4',5',6,7,8,10,12,13,14,15,16-tetradecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-7-carboxylate. This product is intended for research and analytical applications.

HY-Y1771R

2-Carboxybenzaldehyde (Standard) Phthalaldehydic acid (Standard)	Reference Standards Drug Metabolite Bacterial	Infection
2-Carboxybenzaldehyde (Standard) is the analytical standard of 2-Carboxybenzaldehyde (HY-Y1771). This product is intended for research and analytical applications. 2-Carboxybenzaldehyde is a key intermediate metabolite in the biodegradation of polycyclic aromatic hydrocarbons (PAHs) such as fluoranthene and phenanthrene. 2-Carboxybenzaldehyde can be produced by the degradation of fluoranthene by Pasteurella sp. IFA and Mycobacterium sp. PYR-1. 2-Carboxybenzaldehyde can also be produced by the degradation of phenanthrene by Pseudomonas sp. PPD .

HY-W016103R

1-Hydroxy-2-naphthoic acid (Standard)	Reference Standards Bacterial	Others
1-Hydroxy-2-naphthoic acid (Standard) is an analytical standard for 1-Hydroxy-2-naphthoic acid (HY-W016103). This product is intended for research and analytical applications. 1-Hydroxy-2-naphthoic acid is a polycyclic aromatic hydrocarbon (PAHs) degradation intermediate, mainly formed during the microbial degradation of aromatic hydrocarbons such as phenanthrene and naphthalene. 1-Hydroxy-2-naphthoic acid can undergo further hydroxylation, resulting in the naphthalene degradation pathway, or direct ring opening, leading to the phthalic acid pathway. 1-Hydroxy-2-naphthoic acid can be eliminated by introducing a heterologous salicylate hydroxylase gene (nahG) into the degrading bacterium.

Cat. No.	Product Name	Type

HY-103609R

Pyrene (Standard) Benzo[def]Phenanthrene (Standard)	Dyes
Pyrene (Standard) is the analytical standard of Pyrene. This product is intended for research and analytical applications. Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

Pyrene (Standard)

Benzo[def]Phenanthrene (Standard)

Dyes

Pyrene (Standard) is the analytical standard of Pyrene. This product is intended for research and analytical applications. Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-Y1771R

2-Carboxybenzaldehyde (Standard) Phthalaldehydic acid (Standard)	Microorganisms Ketones, Aldehydes, Acids Source classification Endogenous metabolite	Reference Standards Drug Metabolite Bacterial
2-Carboxybenzaldehyde (Standard) is the analytical standard of 2-Carboxybenzaldehyde (HY-Y1771). This product is intended for research and analytical applications. 2-Carboxybenzaldehyde is a key intermediate metabolite in the biodegradation of polycyclic aromatic hydrocarbons (PAHs) such as fluoranthene and phenanthrene. 2-Carboxybenzaldehyde can be produced by the degradation of fluoranthene by Pasteurella sp. IFA and Mycobacterium sp. PYR-1. 2-Carboxybenzaldehyde can also be produced by the degradation of phenanthrene by Pseudomonas sp. PPD .

HY-W016103R

1-Hydroxy-2-naphthoic acid (Standard)	Monophenols Ketones, Aldehydes, Acids Source classification Phenols Endogenous metabolite	Reference Standards Bacterial
1-Hydroxy-2-naphthoic acid (Standard) is an analytical standard for 1-Hydroxy-2-naphthoic acid (HY-W016103). This product is intended for research and analytical applications. 1-Hydroxy-2-naphthoic acid is a polycyclic aromatic hydrocarbon (PAHs) degradation intermediate, mainly formed during the microbial degradation of aromatic hydrocarbons such as phenanthrene and naphthalene. 1-Hydroxy-2-naphthoic acid can undergo further hydroxylation, resulting in the naphthalene degradation pathway, or direct ring opening, leading to the phthalic acid pathway. 1-Hydroxy-2-naphthoic acid can be eliminated by introducing a heterologous salicylate hydroxylase gene (nahG) into the degrading bacterium.

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