Antibiotics and Antimycotics

2,5-Di-tert-butyl-1,4-benzoquinone (DTBBQ) is an 2,5-disubstituted quinone. It is an antibacterial compound. It has been isolated from marine Streptomyces sp. VITVSK1. Pressure dependance on the intramolecular and intermolecular migration rates of

2,5-Di-tert-butyl-1,4-benzoquinone (DTBBQ) is an 2,5-disubstituted quinone. It is an antibacterial compound. It has been isolated from marine Streptomyces sp. VITVSK1. Pressure dependance on the intramolecular and intermolecular migration rates of

2,5-Di-tert-butyl-1,4-benzoquinone (DTBBQ) is an 2,5-disubstituted quinone. It is an antibacterial compound. It has been isolated from marine Streptomyces sp. VITVSK1. Pressure dependance on the intramolecular and intermolecular migration rates of

2,5-Di-tert-butyl-1,4-benzoquinone (DTBBQ) is an 2,5-disubstituted quinone. It is an antibacterial compound. It has been isolated from marine Streptomyces sp. VITVSK1. Pressure dependance on the intramolecular and intermolecular migration rates of

2,5-Di-tert-butyl-1,4-benzoquinone (DTBBQ) is an 2,5-disubstituted quinone. It is an antibacterial compound. It has been isolated from marine Streptomyces sp. VITVSK1. Pressure dependance on the intramolecular and intermolecular migration rates of

2,5-Dibromo-6-isopropyl-3-methyl-1,4-benzoquinone, is also known as DBMIB. Research shows DBMIB can act as an inhibitor by residing at the Qo site of the cytochrome b6f complex. DBMIB can stimulate antimycin-insensitive reduction of cytochrome c

2,5-Dibromo-6-isopropyl-3-methyl-1,4-benzoquinone, is also known as DBMIB. Research shows DBMIB can act as an inhibitor by residing at the Qo site of the cytochrome b6f complex. DBMIB can stimulate antimycin-insensitive reduction of cytochrome c

Synonyms: Gentisaldehyde Chemical Formula: ₂,₅-(OH)₂C₆H₃CHO Hill Formula: C₇H₆O₃ CAS Number: 1194-98-5

Synonyms: Gentisaldehyde Chemical Formula: ₂,₅-(OH)₂C₆H₃CHO Hill Formula: C₇H₆O₃ CAS Number: 1194-98-5

2,6-Dichloro-3-nitropyridine undergoes macrocyclic condensation reaction with resorcinol derivatives to yield chiral tetraoxacalix[2]arene[2]pyridines.

2,6-Dichloro-3-nitropyridine undergoes macrocyclic condensation reaction with resorcinol derivatives to yield chiral tetraoxacalix[2]arene[2]pyridines.

2,6-Dichloro-3-nitropyridine undergoes macrocyclic condensation reaction with resorcinol derivatives to yield chiral tetraoxacalix[2]arene[2]pyridines.