Searching compounds for returned 4373 results.
Displaying compounds 3031 - 3040 of 4373 in total

2,5-dihydroxy-3-methanesulfinylbenzyl alcohol  (PAMDB100057)

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IUPAC: 2-(hydroxymethyl)-6-(methylsulfinyl)benzene-1,4-diol
CAS: Not Available
Description: A benzyl alcohol with hydroxy substituents at positions 2 and 5 and a methanesulfinyl group at position 3. It is a fungal secondary metabolite from Ampelomyces sp. SC0307 and has antibacterial activity against Escherichia coli, Pseudomona

spiruchostatin  (PAMDB100058)

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IUPAC: Not Available
CAS: Not Available
Description: A class of cyclodepsipeptides with a bicyclic skeleton containing a disulfide linkage originally isolated from a Pseudomonas culture broth. The class also includes semi-synthetic derivatives, and synthetic analogues.

pyochelin  (PAMDB100059)

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IUPAC: (4R)-3-methyl-2-[(2E,4R)-2-(6-oxocyclohexa-2,4-dien-1-ylidene)-1,3-thiazolidin-4-yl]-1,3-thiazolidine-4-carboxylic acid
CAS: Not Available
Description: A member of the class of thiazolidines that is (4R)-3-methyl-1,3-thiazolidine-4-carboxylic acid which is substituted at position 2 by a (4R)-2-(2-hydroxyphenyl)-4,5-dihydro-1,3-thiazol-4-yl group. A siderophore, it is it is produced by Ps

4-chloro-3,5-dimethylphenol  (PAMDB100060)

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IUPAC: 4-chloro-3,5-dimethylphenol
CAS: Not Available
Description: A member of the class of phenols that is 3,5-xylenol which is substituted at position 4 by chlorine. It is bactericidal against most Gram-positive bacteria but less effective against staphylococci and Gram-negative bacteria, and often inactive against

colistimethate sodium  (PAMDB100061)

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IUPAC: Not Available
CAS: Not Available
Description: A mixture where R = H or Me. Colistin in which each of the primary amino groups is converted to the corresponding aminomethanesulfonic acid sodium salt, commonly by the action of formaldehyde followed by sodium bisulfite. A polymyxin antibiotic derivative

asphodelin A  (PAMDB100062)

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IUPAC: 3-(2,4-dihydroxyphenyl)-4,7-dihydroxy-2H-chromen-2-one
CAS: Not Available
Description: A hydroxycoumarin that is 4,7-dihydroxy-2H-chromen-2-one substituted by a 2,4-dihydroxyphenyl group at position 3. It is isolated from the roots of Asphodelus microcarpus and exhibits antimicrobial activity against bacteria like Staphyloc

pederin  (PAMDB100063)

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IUPAC: (2S)-N-[(S)-[(2S,4R,6R)-6-[(2S)-2,3-dimethoxypropyl]-4-hydroxy-5,5-dimethyloxan-2-yl]-methoxymethyl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]acetamide
CAS: Not Available
Description: A polyketide and carboxamide produced by a (Pseudomonas) bacterial endosymbiont of certain rove beetles (genus Paederus). Pederin is the agent responsible for the vesicant effects (linear or Paederus dermatitis) when the beetle is crushed ag

finafloxacin  (PAMDB100064)

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IUPAC: 7-[(4aS,7aS)-3,4,4a,5,7,7a-hexahydro-2H-pyrrolo[3,4-b][1,4]oxazin-6-yl]-8-cyano-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid
CAS: Not Available
Description: A quinolone that is 4-oxo-1,4-dihydroquinoline-3-carboxylic acid which is substituted at positions 1, 6, 7 and 8 by cyclopropyl, fluoro, hexahydropyrrolo[3,4-b][1,4]oxazin-6-yl and cyano groups respectively; an antibiotic used for treatment of acut

asphodelin A-4'-O-beta-glucoside  (PAMDB100065)

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IUPAC: 4,7-dihydroxy-3-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-2-one
CAS: Not Available
Description: A β-D-glucoside in which a β-D-glucopyranosyl residue is attached at position 4' of asphodelin A via a glycosidic linkage. It is isolated from the roots of Asphodelus microcarpus and exhibits antimicrobial ac

mupirocin  (PAMDB100066)

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IUPAC: 9-({(2E)-4-[(2
CAS: Not Available
Description: An α,β-unsaturated ester resulting from the formal condensation of the alcoholic hydroxy group of 9-hydroxynonanoic acid with the carboxy group of (2E)-4-[(2S)-tetrahydro-2H-pyran-2-yl]-3-methylbut-2-enoic acid in which the