About: monensin (unspec.)

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About: monensin (unspec.) Goto Sponge NotDistinct Permalink

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chemical compound

Attributes	Values
rdf:type	Item
description	composto chimico (it) химическое соединение (ru) chemical compound (en) composé chimique (fr) תרכובת (he) kemisk forbindelse (da) compositum chemicum (la) chemische Verbindung (de) քիմիական միացություն (hy) chemická sloučenina (cs) chemická zlúčenina (sk) chemische verbinding (nl) kemia kombinaĵo (eo) związek chemiczny (pl) cheemesch Verbindung (lb) chemical compound (en-ca) chemical compound (en-gb) chemiese verbinding (af) chemische Verbindung (de-ch) component quimic (oc) compost químic (ca) composto químico (gl) composto químico (pt) composto químico (pt-br) compuesto quimico (an) compuestu químicu (ast) compus chimic (ro) kemiallinen yhdiste (fi) kjemisk forbindelse (nb) kjemisk sambinding (nn) komponim kimik (sq) konposatu kimiko (eu) senyawa kimia (id) ķīmisks savienojums (lv) хімічна сполука (uk) مركب كيميائي (ar) রাসায়নিক যৌগ (bn) compuesto químico (es)
rdfs:label	monensin (unspec.) (en)
skos:prefLabel	monensin (unspec.) (en)
name	monensin (unspec.) (en)
isomeric SMILES	wds:Q63393051-532A3CB7-C2EE-4388-8F88-07AFB3973171
stereoisomer of	wds:Q63393051-59805202-A1AC-4F94-B61D-07DF66AB9073
isomeric SMILES	CC[C@]1(CC[C@@H](O1)[C@]2(CC[C@@]3(O2)C[C@@H]([C@H]([C@H](O3)[C@H](C)[C@@H]([C@@H](C)C(=O)O)OC)C)O)C)[C@@H]4[C@@H](C[C@H](O4)[C@@H]5[C@H](C[C@H]([C@@](O5)(CO)O)C)C)C
stereoisomer of	monensin
MassBank accession ID	wds:Q63393051-A8B2D3D8-7A66-4B14-985F-81E295D7DDEE
MassBank accession ID	SM849951
instance of	wds:Q63393051-4FC8490E-4411-42F8-8698-891984FDF083
instance of	type of chemical entity
subclass of	wds:Q63393051-76E2EB81-89A8-4B65-A1E8-54369E315C4C wds:Q63393051-A8345E78-EDE9-4B5B-A46F-A5636D36E4AC
subclass of	monensin (2S,3R,4S)-4-[(2S,7S,8R,9S)-2-[(2S,2'R,3'S,5R,5'R)-2-ethyl-5'-[(2S,3S,5R,6R)-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3'-methyl-[2,2'-bioxolan]-5-yl]-9-hydroxy-2,8-dimethyl-1,6-dioxaspiro[4.5]decan-7-yl]-3-methoxy-2-methylpentanoic acid
found in taxon	wds:Q63393051-5AF912FB-0F8C-41B3-A5F3-0C8C594C6ED0
found in taxon	Streptomyces cinnamonensis
UniChem compound ID	wds:Q63393051-78ECFF85-EC9D-45E1-8FF1-772FD41A994F
Probes And Drugs ID	wds:Q63393051-16A7A7D1-1FD8-4F44-9C7F-C3DAA4D8B1D1
canonical SMILES	wds:Q63393051-436F1089-B56F-4037-9F40-043752572FD9
InChI	wds:Q63393051-32FA19F3-9743-473A-AFBE-ED654F9F6A36
InChIKey	wds:Q63393051-02913B6D-48A0-4101-8129-35B01CF6FB1E
chemical formula	wds:Q63393051-48F2C8DD-0D4E-46EC-AAD7-FA02BC88F521
PubChem CID	wds:Q63393051-DCA5469A-DF80-464E-A21E-7C8F930573D9
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID28263
UniChem compound ID	27307482
Probes And Drugs ID	PD013552
canonical SMILES	O=C(O)C(C)C(OC)C(C)C1OC2(OC(C)(CC2)C3OC(CC)(CC3)C4OC(CC4C)C5OC(O)(CO)C(C)CC5C)CC(O)C1C
InChI	InChI=1S/C36H62O11/c1-10-34(31-20(3)16-26(43-31)28-19(2)15-21(4)36(41,18-37)46-28)12-11-27(44-34)33(8)13-14-35(47-33)17-25(38)22(5)30(45-35)23(6)29(42-9)24(7)32(39)40/h19-31,37-38,41H,10-18H2,1-9H3,(H,39,40)/t19-,20+,21+,22+,23+,24+,25-,26-,27+,28-,29-,30-,31-,33+,34-,35+,36-/m0/s1
InChIKey	GAOZTHIDHYLHMS-GDMSFIFLSA-N
chemical formula	C₃₆H₆₂O₁₁
PubChem CID	28263
mass	wds:Q63393051-FB03DA68-9921-4EC9-A195-82FAD2583C92
mass	670.429212804 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q63393051
is stereoisomer of of	monensin
is stereoisomer of of	wds:Q3493048-5EEF19E5-3555-46BB-B145-57DEFD346F44
is main subject of	Insights into polyether biosynthesis from analysis of the nigericin biosynthetic gene cluster in Streptomyces sp. DSM4137. Analysis of the biosynthetic gene cluster for the polyether antibiotic monensin in Streptomyces cinnamonensis and evidence for the role of monB and monC genes in oxidative cyclization Multiple pathways for acetate assimilation in Streptomyces cinnamonensis MeaA, a putative coenzyme B12-dependent mutase, provides methylmalonyl coenzyme A for monensin biosynthesis in Streptomyces cinnamonensis. Enhancing macrolide production in Streptomyces by coexpressing three heterologous genes. Role of Crotonyl Coenzyme A Reductase in Determining the Ratio of Polyketides Monensin A and Monensin B Produced byStreptomyces cinnamonensis Insertional Inactivation of Methylmalonyl Coenzyme A (CoA) Mutase and Isobutyryl-CoA Mutase Genes in Streptomyces cinnamonensis: Influence on Polyketide Antibiotic Biosynthesis Characterisation of actI-homologous DNA encoding polyketide synthase genes from the monensin producer Streptomyces cinnamonensis High titer production of tetracenomycins by heterologous expression of the pathway in a Streptomyces cinnamonensis industrial monensin producer strain. Biosynthesis of monensins A and B Biosynthesis of monensins A and B: the role of isoleucine Effect of precursors on biosynthesis of monensins A and B Production of 26-deoxymonensins A and B by Streptomyces cinnamonensis in the presence of Metyrapone Determination of monensins A and B in the fermentation broth ofStreptomyces cinnamonensis by high performance liquid chromatography Biosynthesis of monensins and 3-O-demethylmonensins in Streptomyces cinnamonensis in the presence of methylation inhibitors Propionate and the production of monensins in Streptomyces cinnamonensis 2-Demethylmonensins A and B. Novel minor congeners of monensins from Streptomyces cinnamonensis Terrosamycins A and B, Bioactive Polyether Ionophores from Streptomyces sp. RKND004 from Prince Edward Island Sediment Identification and disruptional analysis of the Streptomyces cinnamonensis msdA gene, encoding methylmalonic acid semialdehyde dehydrogenase The biosynthesis of monensin-A: thymine, beta-aminoisobutyrate and methacrylate metabolism in Streptomyces cinnamonensis Polyether biosynthesis. 2. Origin of the oxygen atoms of monensin A Resistance of Streptomyces cinnamonensis to butyrate and isobutyrate: production and properties of a new anti-isobutyrate (AIB) factor Characterization of three pathway-specific regulators for high production of monensin in Streptomyces cinnamonensis. Biosynthesis of the polyether antibiotic monensin A: incorporation of a polyketide chain elongation intermediate

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