Search Results for compounds
Searching compounds for
returned 4373 results.
Displaying compounds 3341 - 3350 of
4373 in total
hederagenin (PAMDB110357)
IUPAC:
(3β)-3,23-dihydroxyolean-12-en-28-oic acid
CAS: Not Available
Description: A sapogenin that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 3 and 23 (the 3β stereoisomer).
soyasapogenol B (PAMDB110358)
IUPAC:
(3β,22β)-olean-12-ene-3,22,24-triol
CAS: 595-15-3
Description: A pentacyclic triterpenoid that is oleanane containing a double bond between positions 12 and 13 and substituted by hydroxy groups at the 3β, 22β and 24-positions.
soyasapogenol E (PAMDB110359)
IUPAC:
(3β)-3,24-dihydroxyolean-12-en-22-one
CAS: 6750-59-0
Description: A pentacyclic triterpenoid that is oleanane containing a double bond between positions 12 and 13, and is substituted by hydroxy groups at the 3β and 24-positions, and by an oxo group at position 22.
pyochelin (PAMDB110360)
IUPAC:
(4R)-
2-[(4R)-2-(2-hydroxyphenyl)-4,5-dihydro-1,3-thiazol-4-yl]-3-methyl-1,3-thiazolidine-4-carboxylic acid
2-[(4R)-2-(2-hydroxyphenyl)-4,5-dihydro-1,3-thiazol-4-yl]-3-methyl-1,3-thiazolidine-4-carboxylic acidCAS: 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 Pseudomonas aeruginosa (via condensation of salicylic acid and two molecules of cysteine) as a mixture of two easily interconvertible diastereoisomers, pyochelin I (major) and pyochelin II (minor). The enantiomeric compounds, enant-pyochelin, are produced by Pseudomonas fluorescens.
Kdo2-(palmitoleoyl)-lipid IVA (PAMDB110362)
IUPAC:
Not Available
CAS: Not Available
Description: A lipid A oxoanion obtained via deprotonation of the carboxy and phosphate OH groups of (KDO)2-(palmitoleoyl)-lipid IVA; major species at pH 7.3.
(Kdo)2-lipid A, cold adapted (PAMDB110363)
IUPAC:
Not Available
CAS: Not Available
Description: A lipid A oxoanion obtained via deprotonation of the carboxy and phosphate OH groups of (KDO)2-(palmitoleoyl-myristoyl)-lipid A; major species at pH 7.3.
α-Kdo-(2->4)-α-Kdo-(2->6)-lipid IVA (PAMDB110364)
IUPAC:
Not Available
CAS: Not Available
Description: (KDO)2-lipid IVA deprotonated at both phosphono groups and at the uronic acid carboxy groups. It is the major species at pH 7.3.
α-D-Kdo-(2→4)-α-D-Kdo-(2→6)-lipid A (PAMDB110365)
IUPAC:
3-deoxy-α-D-manno-oct-2-ulopyranonosyl-(2→4)-3-deoxy-α-D-manno-oct-2-ulopyranonosyl-(2→6)-2-deoxy-2-[(3R)-3-(dodecanoyloxy)tetradecanamido]-4-O-phosphonato-3-O-[(3R)-3-(tetradecanoyloxy)tetradecanoyl]-β-D-glucopyranosyl-(1→6)-2-deoxy-3-O-[(3R)-3-hydroxytetradecanoyl]-2-[(3R)-3-hydroxytetradecanamido]-1-O-phosphonato-α-D-glucopyranose
deoxy-α-D-manno-oct-2-ulopyranonosyl-(2→4)-3-deoxy-α-D-manno-oct-2-ulopyranonosyl-(2→6)-2-deoxy-2-[(3R)-3-(dodecanoyloxy)tetradecanamido]-4-O-phosphonato-3-O-[(3R)-3-(tetradecanoyloxy)tetradecanoyl]-β-D-glucopyranosyl-(1→6)-2-deoxy-3-O-[(3R)-3-hydroxytetradecanoyl]-2-[(3R)-3-hydroxytetradecanamido]-1-O-phosphonato-α-D-glucopyranoseCAS: Not Available
Description: A carbohydrate acid derivative anion that is the hexa-anion of Kdo2-lipid A arising from deprotonation of both the carboxyl and phosphate functions.
α-Kdo-(2->4)-α-Kdo-(2->6)-(lauroyl)-lipid IVA (PAMDB110366)
IUPAC:
Not Available
CAS: Not Available
Description: A lipid A oxoanion obtained via deprotonation of the carboxy and phosphate OH groups of (KDO)2-(lauroyl)-lipid IVA; major species at pH 7.3.