Lipoxygenase, general
Lipoxygenase, general structure
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Common Name | Lipoxygenase, general | ||
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| CAS Number | 9029-60-1 | Molecular Weight | N/A | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | N/A | Melting Point | N/A | |
| MSDS | USA | Flash Point | N/A | |
Use of Lipoxygenase, generalLipoxygenase, general (LOX) is a dioxygenase, is often used in biochemical studies. Lipoxygenase, general catalyzes the formation of corresponding hydroperoxides from polyunsaturated fatty acids such as linoleic acid and arachidonic acid[1]. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | Lipoxydase from Soybean |
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| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | Lipoxygenase, general (LOX) is a dioxygenase, is often used in biochemical studies. Lipoxygenase, general catalyzes the formation of corresponding hydroperoxides from polyunsaturated fatty acids such as linoleic acid and arachidonic acid[1]. |
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| Related Catalog | |
| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| InChIKey | AUMCYORTVSBJGW-UHFFFAOYSA-N |
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| SMILES | CC1(C)c2ccccc2-c2ccc(-c3cccc(-c4ccc5c6c(n(C(C=C(N)c7ccc(-c8ccccc8)cc7)c7ccccc7)c5c4)CCc4ccccc4-6)c3)cc21 |
This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |
This table lists relevant public references with title, journal and publication metadata for this compound.
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Synthesis, characterization, DNA binding properties and antioxidant activity of a manganese(II) complex with NO6 chromophore.
J. Inorg. Biochem. 118 , 48-58, (2013) The mononuclear complex [Mn(thiophenyl-2-carboxylate)(2)(H(3)tea)] (1), where H(3)tea=triethanolamine has been synthesized, characterized, while the DNA binding properties and the antioxidant activity... |
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Study of anti-inflammatory activities of α-D-glucosylated eugenol.
Arch. Pharm. Res. 36(1) , 109-15, (2013) Inflammation is an immune response against a variety of noxious stimuli, such as infection, chemicals, and physical injury. Eugenol, a natural phenolic extract, has drawn much attention for its variou... |
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Probing conformational changes in lipoxygenases upon membrane binding: fine-tuning by the active site inhibitor ETYA.
Biochim. Biophys. Acta 1841(1) , 1-10, (2014) Lipoxygenases (LOXs) are lipid-peroxidizing enzymes that are involved in the metabolism of polyunsaturated fatty acids. Their biological activity includes a membrane binding process whose molecular de... |
This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| MFCD00131527 |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What is the InChIKey of Lipoxydase from Soybean? |
| A: InChIKey of Lipoxydase from Soybean is AUMCYORTVSBJGW-UHFFFAOYSA-N. |
| Q: What is the CAS number of Lipoxydase from Soybean? |
| A: CAS number of Lipoxydase from Soybean is 9029-60-1. |
| Q: What English synonyms does Lipoxydase from Soybean have? |
| A: English synonyms of Lipoxydase from Soybean: MFCD00131527. |
| Q: What is the English name of Lipoxydase from Soybean? |
| A: The English name of Lipoxydase from Soybean is Lipoxydase from Soybean. |
| Q: What is the SMILES notation of Lipoxydase from Soybean? |
| A: SMILES notation of Lipoxydase from Soybean is CC1(C)c2ccccc2-c2ccc(-c3cccc(-c4ccc5c6c(n(C(C=C(N)c7ccc(-c8ccccc8)cc7)c7ccccc7)c5c4)CCc4ccccc4-6)c3)cc21. |
| Q: What are the uses of Lipoxydase from Soybean? |
| A: Main uses of Lipoxydase from Soybean: Lipoxygenase, general (LOX) is a dioxygenase, is often used in biochemical studies. Lipoxygenase, general catalyzes the formation of corresponding hydroperoxides from polyunsaturated fatty acids such as linoleic acid and arachidonic acid[1]. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |