Ostreocin D (CED0024527)

Record Information
Version1.0
Creation Date2014-08-29 06:50:53 UTC
Update Date2026-05-21 00:20:04 UTC
SynCED IDCED0024527
Secondary Accession Numbers
  • CHEM003354
  • T3D4394
Identification
Common NameOstreocin D
ClassSmall Molecule
Description
Ostreocin D is a solid compound with the chemical formula C127H219N3O53. Ostreocin D belongs to the carbohydrates and carbohydrate conjugates, a subclass of organooxygen compounds within the organic compounds. With an average molecular weight of 2,636 g/mol, Ostreocin D is a heavy molecule. This substance is of exogenous origin. The compound is found in or released from 13 recorded sources across several sectors. In the energy, oil & gas and industrial manufacturing & chemical processing sectors, it is found in lubricants. Within healthcare, pharmaceuticals & veterinary products, it is associated with medical devices, while it is found in food packaging within the food, food processing & cookware sector. It is also present in textiles, leather & furnishings, specifically in carpets, rugs, and synthetic textiles. Additionally, it is found in electrical & electronic equipment, including batteries, capacitors, printed circuit boards, wires, cables, and cell phones, as well as one other sector. Recorded exposure routes for Ostreocin D include touch, oral, and inhalation.
Contaminant Type
  • Amine
  • Animal Toxin
  • Ether
  • Food Toxin
  • Marine Toxin
  • Natural Compound
  • Organic Compound
  • PFAS
Chemical Structure
Synonyms
ValueSource
(2S,5R,6E,8R,9S)-10-[(2R,3R,4R,5S,6R)-6-[(1S,2R,3S,5R)-12-[(1R,3S,5S,7R)-5-[(8S)-9-[(2S,4R,5R,6S)-6-[(2S,3S,4E,6S,9R,10R)-10-[(2S,4R,5S,6R)-6-[(2R,3R)-4-[(2R,3S,4R,5R,6S)-6-[(2S,3Z,5E,8R,9S,10R,12Z,17S,18R,19R,20R)-20-{[(2R,3R,4R,5S,6R)-6-[(1Z,3R,4R)-5-[(1S,3R,5R,7R)-7-{2-[(2R,3R,5S)-5-(aminomethyl)-3-hydroxyoxolan-2-yl]ethyl}-2,6-dioxabicyclo[3.2.1]octan-3-yl]-3,4-dihydroxypent-1-en-1-yl]-3,4,5-trihydroxyoxan-2-yl]methyl}-2,8,9,10,17,18,19-heptahydroxy-14-methylidenehenicosa-3,5,12-trien-1-yl]-3,4,5-trihydroxyoxan-2-yl]-2,3-dihydroxybutyl]-4,5-dihydroxyoxan-2-yl]-2,6,9,10-tetrahydroxy-3-methyldec-4-en-1-yl]-4,5,6-trihydroxyoxan-2-yl]-8,9-dihydroxynonyl]-1,3-dimethyl-6,8-dioxabicyclo[3.2.1]octan-7-yl]-1,2,3,5-tetrahydroxydodecyl]-3,4,5-trihydroxyoxan-2-yl]-2,5,8,9-tetrahydroxy-N-[(1E)-2-[(3-hydroxypropyl)-C-hydroxycarbonimidoyl]eth-1-en-1-yl]-7-methyldec-6-enimidateGenerator
Chemical FormulaC127H219N3O53
Average Molecular Mass2636.086 g/mol
Monoisotopic Mass2634.453 g/mol
CAS Registry NumberNot Available
IUPAC Name(2S,5R,6E,8R,9S)-10-[(2R,3R,4R,5S,6R)-6-[(1S,2R,3S,5R)-12-[(1R,3S,5S,7R)-5-[(8S)-9-[(2S,4R,5R,6S)-6-[(2S,3S,4E,6S,9R,10R)-10-[(2S,4R,5S,6R)-6-[(2R,3R)-4-[(2R,3S,4R,5R,6S)-6-[(2S,3Z,5E,8R,9S,10R,12Z,17S,18R,19R,20R)-20-{[(2R,3R,4R,5S,6R)-6-[(1Z,3R,4R)-5-[(1S,3R,5R,7R)-7-{2-[(2R,3R,5S)-5-(aminomethyl)-3-hydroxyoxolan-2-yl]ethyl}-2,6-dioxabicyclo[3.2.1]octan-3-yl]-3,4-dihydroxypent-1-en-1-yl]-3,4,5-trihydroxyoxan-2-yl]methyl}-2,8,9,10,17,18,19-heptahydroxy-14-methylidenehenicosa-3,5,12-trien-1-yl]-3,4,5-trihydroxyoxan-2-yl]-2,3-dihydroxybutyl]-4,5-dihydroxyoxan-2-yl]-2,6,9,10-tetrahydroxy-3-methyldec-4-en-1-yl]-4,5,6-trihydroxyoxan-2-yl]-8,9-dihydroxynonyl]-1,3-dimethyl-6,8-dioxabicyclo[3.2.1]octan-7-yl]-1,2,3,5-tetrahydroxydodecyl]-3,4,5-trihydroxyoxan-2-yl]-2,5,8,9-tetrahydroxy-N-[(1E)-2-[(3-hydroxypropyl)-C-hydroxycarbonimidoyl]eth-1-en-1-yl]-7-methyldec-6-enimidic acid
Traditional Name(2S,5R,6E,8R,9S)-10-[(2R,3R,4R,5S,6R)-6-[(1S,2R,3S,5R)-12-[(1R,3S,5S,7R)-5-[(8S)-9-[(2S,4R,5R,6S)-6-[(2S,3S,4E,6S,9R,10R)-10-[(2S,4R,5S,6R)-6-[(2R,3R)-4-[(2R,3S,4R,5R,6S)-6-[(2S,3Z,5E,8R,9S,10R,12Z,17S,18R,19R,20R)-20-{[(2R,3R,4R,5S,6R)-6-[(1Z,3R,4R)-5-[(1S,3R,5R,7R)-7-{2-[(2R,3R,5S)-5-(aminomethyl)-3-hydroxyoxolan-2-yl]ethyl}-2,6-dioxabicyclo[3.2.1]octan-3-yl]-3,4-dihydroxypent-1-en-1-yl]-3,4,5-trihydroxyoxan-2-yl]methyl}-2,8,9,10,17,18,19-heptahydroxy-14-methylidenehenicosa-3,5,12-trien-1-yl]-3,4,5-trihydroxyoxan-2-yl]-2,3-dihydroxybutyl]-4,5-dihydroxyoxan-2-yl]-2,6,9,10-tetrahydroxy-3-methyldec-4-en-1-yl]-4,5,6-trihydroxyoxan-2-yl]-8,9-dihydroxynonyl]-1,3-dimethyl-6,8-dioxabicyclo[3.2.1]octan-7-yl]-1,2,3,5-tetrahydroxydodecyl]-3,4,5-trihydroxyoxan-2-yl]-2,5,8,9-tetrahydroxy-N-[(1E)-2-[(3-hydroxypropyl)-C-hydroxycarbonimidoyl]eth-1-en-1-yl]-7-methyldec-6-enimidic acid
SMILES[H]\C(C[C@@]([H])(O)[C@]([H])(O)[C@]([H])(O)C\C([H])=C(\[H])C(=C)CC[C@]([H])(O)[C@@]([H])(O)[C@]([H])(O)[C@]([H])(C)C[C@@]1([H])O[C@]([H])(C(\[H])=C(\[H])[C@@]([H])(O)[C@]([H])(O)C[C@]2([H])C[C@]3([H])C[C@]([H])(O2)[C@@]([H])(CC[C@@]2([H])O[C@]([H])(CN)C[C@@]2([H])O)O3)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O)=C(\[H])/C(/[H])=C(/[H])[C@@]([H])(O)C[C@]1([H])O[C@]([H])(C[C@@]([H])(O)[C@]([H])(O)C[C@@]2([H])O[C@@]([H])(C[C@@]([H])(O)[C@]2([H])O)[C@]([H])(O)[C@]([H])(O)CC[C@]([H])(O)C(\[H])=C(/[H])[C@]([H])(C)[C@@]([H])(O)C[C@]2(O)O[C@@]([H])(C[C@@]([H])(O)[C@@]2([H])O)C([H])(O)[C@@]([H])(O)CCCCCCC[C@@]23C[C@@]([H])(C)C[C@@](C)(O2)[C@@]([H])(CCCCCCC[C@@]([H])(O)C[C@]([H])(O)[C@@]([H])(O)[C@]([H])(O)[C@@]2([H])O[C@]([H])(C[C@]([H])(O)[C@]([H])(O)C(\C)=C(/[H])[C@]([H])(O)CC[C@]([H])(O)C(O)=N\C([H])=C(/[H])C(O)=NCCCO)[C@]([H])(O)[C@@]([H])(O)[C@]2([H])O)O3)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O
InChI IdentifierInChI=1S/C127H219N3O53/c1-63(29-34-80(141)110(159)105(154)67(5)47-95-113(162)117(166)112(161)93(177-95)38-37-75(136)82(143)51-72-50-73-53-94(175-72)92(174-73)40-39-91-85(146)52-74(62-128)176-91)22-20-27-77(138)106(155)76(137)25-17-13-15-24-70(134)49-96-114(163)118(167)115(164)99(178-96)55-84(145)83(144)54-97-109(158)88(149)57-98(179-97)107(156)79(140)35-32-68(132)31-30-65(3)90(151)61-127(173)123(171)89(150)58-101(181-127)108(157)78(139)26-16-10-8-12-19-42-126-60-64(2)59-125(6,183-126)102(182-126)28-18-11-7-9-14-23-69(133)48-86(147)111(160)120(169)122-121(170)119(168)116(165)100(180-122)56-87(148)104(153)66(4)46-71(135)33-36-81(142)124(172)130-44-41-103(152)129-43-21-45-131/h13,15,17,20,22,24,30-31,37-38,41,44,46,64-65,67-102,104-123,131-151,153-171,173H,1,7-12,14,16,18-19,21,23,25-29,32-36,39-40,42-43,45,47-62,128H2,2-6H3,(H,129,152)(H,130,172)/b17-13+,22-20-,24-15-,31-30+,38-37-,44-41+,66-46+/t64-,65-,67+,68+,69+,70+,71+,72-,73+,74-,75+,76+,77+,78-,79+,80-,81-,82+,83+,84+,85+,86-,87-,88+,89+,90-,91+,92+,93+,94-,95+,96-,97+,98-,99+,100+,101-,102+,104+,105+,106-,107+,108?,109-,110+,111+,112+,113-,114-,115+,116-,117-,118+,119+,120-,121-,122+,123+,125+,126-,127-/m0/s1
InChI KeyQJZSVGZHSZCZHY-YNRYLGGCSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentC-glycosyl compounds
Alternative Parents
Substituents
  • C-glycosyl compound
  • 1,4-dioxepane
  • Ketal
  • Dioxepane
  • Oxepane
  • Fatty amide
  • Monosaccharide
  • N-acyl-amine
  • Fatty acyl
  • Oxane
  • Meta-dioxolane
  • Acrylic acid or derivatives
  • Vinylogous amide
  • Tetrahydrofuran
  • Secondary carboxylic acid amide
  • Secondary alcohol
  • Amino acid or derivatives
  • Hemiacetal
  • Carboxamide group
  • Polyol
  • Acetal
  • Organoheterocyclic compound
  • Oxacycle
  • Alkanolamine
  • Ether
  • Carboxylic acid derivative
  • Dialkyl ether
  • Alcohol
  • Organic nitrogen compound
  • Organic oxide
  • Carbonyl group
  • Organopnictogen compound
  • Primary aliphatic amine
  • Amine
  • Hydrocarbon derivative
  • Primary amine
  • Organonitrogen compound
  • Primary alcohol
  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Biological Properties
StatusDetected and Not Quantified
OriginExogenous
Cellular Locations
  • Actin Cytoskeleton
  • Actin Filament
  • Cytoskeleton
  • Intermediate Filament
  • Membrane
  • Microtubule
Biofluid LocationsNot Available
Tissue LocationsNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Organoleptic EffectsNot Available
Physical Properties
StateSolid
AppearanceWhite powder.
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility0.27 g/LALOGPS
logP-0.17ALOGPS
logP-13ChemAxon
logS-4ALOGPS
pKa (Strongest Acidic)0.3ChemAxon
pKa (Strongest Basic)9.22ChemAxon
Physiological Charge2ChemAxon
Hydrogen Acceptor Count56ChemAxon
Hydrogen Donor Count44ChemAxon
Polar Surface Area1012.93 ŲChemAxon
Rotatable Bond Count80ChemAxon
Refractivity658.63 m³·mol⁻¹ChemAxon
Polarizability283.89 ųChemAxon
Number of Rings10ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Spectra
SpectraNot Available
Toxicity Profile
Toxicity ValuesNot Available
Toxicity / Toxin ClassNot Available
Mechanism of ToxicityNot Available
Carcinogenicity (IARC Classification)No indication of carcinogenicity to humans (not listed by IARC).
Minimum Risk LevelNot Available
SymptomsNot Available
TreatmentNot Available
Health Effects
Health EffectRelationshipDirectionDescriptionReference
Exposure Sources
Source IDSourceSectorReference
CEDs000007Pesticides?Pesticides are synthetic chemicals designed to prevent, destroy, or control pests that threaten crops and agricultural productivity.Agriculture & land managementNot Available
CEDs000120Wires and cables?Wires and cables are integral components in the transmission of electrical power and signals.Electrical & Electronic EquipmentNot Available
CEDs000121Printed circuit boards?Printed circuit boards (PCBs) are essential components in the manufacturing of electronic devices, serving as the backbone for electrical connections and circuit pathways.Electrical & Electronic EquipmentNot Available
CEDs000125Batteries?Batteries are devices that store and release electrical energy through electrochemical reactions.Electrical & Electronic EquipmentNot Available
CEDs000130Semiconductors?Semiconductors are materials that possess electrical conductivity between that of conductors and insulators, making them essential for various electronic applications, including transistors, diodes, and integrated circuits.Electrical & Electronic EquipmentNot Available
CEDs000138Lubricants?Lubricants are synthetic or petroleum-derived substances used to reduce friction between surfaces in machinery and equipment, enhancing operational efficiency and longevity.Energy, oil & gasNot Available
CEDs000147Food packaging?Food packaging often utilizes synthetic chemicals, such as plastics and coatings, to enhance durability, moisture resistance, and shelf life.Food, food processing & cookwareNot Available
CEDs000174Lubricants?Lubricants are synthetic or petroleum-based substances used to reduce friction and wear between moving parts in machinery and equipment.Industrial manufacturing & chemical processingNot Available
CEDs000234Medical devices?Medical devices often incorporate synthetic chemicals in their manufacturing processes, which can contribute to contamination in healthcare settings.Healthcare, pharmaceuticals & veterinary productsNot Available
CEDs000451Carpets and Rugs?Carpets and rugs are commonly manufactured using synthetic fibers such as nylon, polyester, and polypropylene, which can be derived from petrochemical sources.Textiles, leather & furnishingsNot Available
CEDs000454Synthetic textiles?Synthetic textiles are materials derived from man-made fibers, such as polyester, nylon, and acrylic, which are produced through chemical processes involving petrochemicals.Textiles, leather & furnishingsNot Available
CEDs000490Personal care & cosmeticsNot Available
CEDs000492Cell phones?Cell phones contain a variety of synthetic chemicals and materials, including plastics, metals, and glass, which can contribute to environmental contamination.Electrical & Electronic EquipmentNot Available
CEDs000493Capacitors?Capacitors are electronic components that store and release electrical energy, often using dielectric materials that can include synthetic chemicals.Electrical & Electronic EquipmentNot Available
Pathways
1 pathwayPathway Source: PathBank
Targets
StructureProteinUniProt IDOrganismRelationshipDetails
Sialic acid-binding Ig-like lectin 7 structureClick to view 3D structureSialic acid-binding Ig-like lectin 7Q9Y286HumansPredicted (SEA)
Prediction Confidence Score
0.143
Applicability Domain
0.143 Low confidence
Statistical Significance
0.0024
Supporting Reference Compounds
1
E-value
18.6838
Click to view 3D structureE-selectinP98105Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.132
Applicability Domain
0.132 Low confidence
Statistical Significance
0.0067
Supporting Reference Compounds
1
E-value
52.3925
Phospho-N-acetylmuramoyl-pentapeptide-transferase structureClick to view 3D structurePhospho-N-acetylmuramoyl-pentapeptide-transferaseO66465Aquifex aeolicus (strain VF5)Predicted (SEA)
Prediction Confidence Score
0.131
Applicability Domain
0.131 Low confidence
Statistical Significance
0.0553
Supporting Reference Compounds
1
E-value
430.818
Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform structureClick to view 3D structureSerine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoformQ15172HumansPredicted (SEA)
Prediction Confidence Score
0.13
Applicability Domain
0.141 Low confidence
Statistical Significance
0.0204
Supporting Reference Compounds
3
E-value
159.202
Click to view 3D structurePhospho-N-acetylmuramoyl-pentapeptide-transferaseQ03521Bacillus subtilis (strain 168)Predicted (SEA)
Prediction Confidence Score
0.127
Applicability Domain
0.127 Low confidence
Statistical Significance
0.1057
Supporting Reference Compounds
1
E-value
822.788
Click to view 3D structurecAMP-dependent protein kinase type II-beta regulatory subunitP31323HumansPredicted (SEA)
Prediction Confidence Score
0.126
Applicability Domain
0.126 Low confidence
Statistical Significance
0.1256
Supporting Reference Compounds
1
E-value
977.475
Fanconi anemia group F protein structureClick to view 3D structureFanconi anemia group F proteinQ9NPI8HumansPredicted (SEA)
Prediction Confidence Score
0.124
Applicability Domain
0.124 Low confidence
Statistical Significance
0.1139
Supporting Reference Compounds
1
E-value
886.703
Tyrosine-protein phosphatase non-receptor type 1 structureClick to view 3D structureTyrosine-protein phosphatase non-receptor type 1P18031HumansPredicted (SEA)
Prediction Confidence Score
0.123
Applicability Domain
0.141 Low confidence
Statistical Significance
0.9906
Supporting Reference Compounds
197
E-value
7711.43
Serine/threonine-protein phosphatase 5 structureClick to view 3D structureSerine/threonine-protein phosphatase 5P53041HumansPredicted (SEA)
Prediction Confidence Score
0.122
Applicability Domain
0.141 Low confidence
Statistical Significance
0.2057
Supporting Reference Compounds
12
E-value
1601.51
Click to view 3D structureSerine-threonine protein phosphatase 2A regulatory subunitQ8AWE3Gallus gallusPredicted (SEA)
Prediction Confidence Score
0.122
Applicability Domain
0.141 Low confidence
Statistical Significance
0.2971
Supporting Reference Compounds
12
E-value
2312.74
Serine/threonine-protein phosphatase PP1-gamma catalytic subunit structureClick to view 3D structureSerine/threonine-protein phosphatase PP1-gamma catalytic subunitP36873HumansPredicted (SEA)
Prediction Confidence Score
0.122
Applicability Domain
0.141 Low confidence
Statistical Significance
0.3138
Supporting Reference Compounds
10
E-value
2443.3
Click to view 3D structureHistone acetyltransferase GCN5Q245K9Tetrahymena thermophila (strain SB210)Predicted (SEA)
Prediction Confidence Score
0.122
Applicability Domain
0.122 Low confidence
Statistical Significance
0.0749
Supporting Reference Compounds
2
E-value
583.324
Click to view 3D structurePhospho-N-acetylmuramoyl-pentapeptide-transferaseP9WMW7Mycobacterium tuberculosisPredicted (SEA)
Prediction Confidence Score
0.119
Applicability Domain
0.119 Low confidence
Statistical Significance
0.1585
Supporting Reference Compounds
1
E-value
1234.3
Relaxin-3 receptor 2 structureClick to view 3D structureRelaxin-3 receptor 2Q8TDU9HumansPredicted (SEA)
Prediction Confidence Score
0.118
Applicability Domain
0.121 Low confidence
Statistical Significance
0.0683
Supporting Reference Compounds
3
E-value
531.866
Hemagglutinin structureClick to view 3D structureHemagglutininP03452Influenza A virus (A/Puerto Rico/8/1934(H1N1))Predicted (SEA)
Prediction Confidence Score
0.117
Applicability Domain
0.13 Low confidence
Statistical Significance
0.1647
Supporting Reference Compounds
2
E-value
1282.1
Serine/threonine-protein phosphatase 2A catalytic subunit alpha isoform structureClick to view 3D structureSerine/threonine-protein phosphatase 2A catalytic subunit alpha isoformP67775HumansPredicted (SEA)
Prediction Confidence Score
0.115
Applicability Domain
0.141 Low confidence
Statistical Significance
0.2929
Supporting Reference Compounds
8
E-value
2280.13
Click to view 3D structureSolute carrier organic anion transporter family member 2B1Q9JHI3Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.114
Applicability Domain
0.114 Low confidence
Statistical Significance
0.097
Supporting Reference Compounds
2
E-value
755.527
Prostacyclin receptor structureClick to view 3D structureProstacyclin receptorP43119HumansPredicted (SEA)
Prediction Confidence Score
0.114
Applicability Domain
0.115 Low confidence
Statistical Significance
0.9884
Supporting Reference Compounds
63
E-value
7694.38
Caveolin-1 structureClick to view 3D structureCaveolin-1Q03135HumansPredicted (SEA)
Prediction Confidence Score
0.114
Applicability Domain
0.114 Low confidence
Statistical Significance
0.1479
Supporting Reference Compounds
1
E-value
1151.31
Prostaglandin E2 receptor EP2 subtype structureClick to view 3D structureProstaglandin E2 receptor EP2 subtypeP43116HumansPredicted (SEA)
Prediction Confidence Score
0.114
Applicability Domain
0.115 Low confidence
Statistical Significance
0.9944
Supporting Reference Compounds
95
E-value
7741.56
Neuropeptide Y receptor type 4 structureClick to view 3D structureNeuropeptide Y receptor type 4P50391HumansPredicted (SEA)
Prediction Confidence Score
0.114
Applicability Domain
0.141 Low confidence
Statistical Significance
0.9109
Supporting Reference Compounds
23
E-value
7091.05
Prostaglandin E2 receptor EP3 subtype structureClick to view 3D structureProstaglandin E2 receptor EP3 subtypeP43115HumansPredicted (SEA)
Prediction Confidence Score
0.113
Applicability Domain
0.115 Low confidence
Statistical Significance
0.9939
Supporting Reference Compounds
102
E-value
7737.43
Click to view 3D structureProstaglandin E2 receptor EP1 subtypeP34995HumansPredicted (SEA)
Prediction Confidence Score
0.113
Applicability Domain
0.115 Low confidence
Statistical Significance
0.991
Supporting Reference Compounds
78
E-value
7714.86
GDNF family receptor alpha-like structureClick to view 3D structureGDNF family receptor alpha-likeQ6UXV0HumansPredicted (SEA)
Prediction Confidence Score
0.113
Applicability Domain
0.113 Low confidence
Statistical Significance
0.1424
Supporting Reference Compounds
1
E-value
1108.88
Isoleucine--tRNA ligase structureClick to view 3D structureIsoleucine--tRNA ligaseP56690Thermus thermophilus (strain HB8 / ATCC 27634 / DSM 579)Predicted (SEA)
Prediction Confidence Score
0.113
Applicability Domain
0.113 Low confidence
Statistical Significance
0.0633
Supporting Reference Compounds
1
E-value
492.863
Concentrations
Not Available
External Links
DrugBank IDNot Available
HMDB IDNot Available
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider IDNot Available
ChEBI IDNot Available
PubChem Compound ID56928159
Kegg Compound IDC20028
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
  1. Ares IR, Cagide E, Louzao MC, Espina B, Vieytes MR, Yasumoto T, Botana LM: Ostreocin-D impact on globular actin of intact cells. Chem Res Toxicol. 2009 Feb;22(2):374-81. doi: 10.1021/tx800273f. [PubMed: 19154108]