About: (2R)-N-[(4S,4aS,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-hexahydropyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]ethanimidic acid

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About: (2R)-N-[(4S,4aS,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-hexahydropyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]ethanimidic acid Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

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) 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) payvastagii khimiyaviy (tg-latn) пайвастагии химиявӣ (tg-cyrl) chemesch Verbindung (lb)
rdfs:label	(2R)-N-[(4S,4aS,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-hexahydropyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]ethanimidic acid (en)
skos:prefLabel	(2R)-N-[(4S,4aS,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-hexahydropyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]ethanimidic acid (en)
name	(2R)-N-[(4S,4aS,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-hexahydropyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]ethanimidic acid (en)
isomeric SMILES	wds:Q105113870-6F4BB9E8-A9B2-40E2-BC93-0F4A20926677
stereoisomer of	wds:Q105113870-163CD2EF-9FE5-4806-9F4F-F79086968A4A wds:Q105113870-4EBC4581-3ABB-4A11-95E4-DAB0DDD31761
isomeric SMILES	C=C1C[C@](OC)([C@H](O)C(=O)N[C@H]2OCO[C@H]3[C@@H]2O[C@H](C[C@H](O)CO)C(C)(C)[C@@H]3OC)O[C@H](C)[C@@H]1C
stereoisomer of	(2S)-N-[(4S,4aR,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-4a,6,8,8a-tetrahydro-4H-pyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]acetamide (2S)-N-[(4R,4aS,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-4a,6,8,8a-tetrahydro-4H-pyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]acetamide
instance of	wds:Q105113870-A55EA6D0-C3B5-4DBC-9141-0143EDD02194
instance of	type of chemical entity
subclass of	wds:Q105113870-5E52F2CA-8D15-4376-9CB4-2F3BB4471312 wds:Q105113870-F5B88BE0-C89C-4E44-9210-8B7A772A29A5
subclass of	(2R)-N-[(4aS,6R,8S,8aR)-6-(2,3-dihydroxypropyl)-8-methoxy-7,7-dimethyl-hexahydropyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]ethanimidic acid N-[6-(2,3-dihydroxypropyl)-8-methoxy-7,7-dimethyl-4a,6,8,8a-tetrahydro-4H-pyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-(2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl)acetamide
found in taxon	wds:Q105113870-A56ED779-24E2-4383-8A94-428EBA28A404 wds:Q105113870-C7AEC673-123A-41D9-A99F-4F3696905AE4 wds:Q105113870-D6B82017-8CDC-4197-85D6-91E232007A1A
found in taxon	Hymeniacidon Mycale Mycale hentscheli
UniChem compound ID	wds:Q105113870-6FD29905-E27F-49D7-B09E-3B2182795C0C
CAS Registry Number	wds:Q105113870-AB74AF40-8803-47C1-8C53-07F1A9A369F5
canonical SMILES	wds:Q105113870-F94DF556-FD3A-444C-86A3-815F9B599529
InChI	wds:Q105113870-A4597455-CC26-4059-AC01-F22AE411FCBA
InChIKey	wds:Q105113870-5BC09CEE-6022-48A4-972F-12BC477F9C9E
chemical formula	wds:Q105113870-F2452ECB-B216-4362-8FF3-D4B81A7C6E62
PubChem CID	wds:Q105113870-23C9856D-C807-4E7B-922C-A72E77BE6831
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10345974
UniChem compound ID	280824
CAS Registry Number	115185-92-7
canonical SMILES	C=C1CC(OC)(C(O)C(=O)NC2OCOC3C2OC(CC(O)CO)C(C)(C)C3OC)OC(C)C1C
InChI	InChI=1S/C24H41NO10/c1-12-9-24(31-7,35-14(3)13(12)2)19(28)21(29)25-22-18-17(32-11-33-22)20(30-6)23(4,5)16(34-18)8-15(27)10-26/h13-20,22,26-28H,1,8-11H2,2-7H3,(H,25,29)/t13-,14-,15+,16-,17+,18+,19-,20-,22+,24-/m1/s1
InChIKey	IJASURGZDJYQGF-GBNRTHSESA-N
chemical formula	C₂₄H₄₁NO₁₀
PubChem CID	10345974
mass	wds:Q105113870-790ADE6E-B0A4-4A46-8FAC-26CEFAEAF336
mass	503.273046512 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q105113870
is stereoisomer of of	(2S)-N-[(4S,4aR,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-4a,6,8,8a-tetrahydro-4H-pyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]acetamide (2S)-N-[(4R,4aS,6R,8S,8aR)-6-[(2S)-2,3-dihydroxypropyl]-8-methoxy-7,7-dimethyl-4a,6,8,8a-tetrahydro-4H-pyrano[3,2-d][1,3]dioxin-4-yl]-2-hydroxy-2-[(2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]acetamide
is stereoisomer of of	wds:Q76614173-CF65CA25-0BD1-4709-8E03-275E68BB34C2 wds:Q104396206-7AEF668B-224B-47C6-95A7-6909E24B32D2
is main subject of	Peloruside A enhances apoptosis in H-ras-transformed cells and is cytotoxic to proliferating T cells. Peloruside A: a potent cytotoxic macrolide isolated from the new zealand marine sponge Mycale sp Mycalamides C and D, cytotoxic compounds from the marine sponge Stylinos n. species Mycalamide D, a new cytotoxic amide from the New Zealand marine sponge Mycale species Mycalamide A, an antiviral compound from a New Zealand sponge of the genus Mycale Antiviral and antitumor agents from a New Zealand sponge, Mycale sp. 2. Structures and solution conformations of mycalamides A and B Peloruside B, a potent antitumor macrolide from the New Zealand marine sponge Mycale hentscheli: isolation, structure, total synthesis, and bioactivity
is main subject of	wds:Q105113871-9EB34F2B-8F43-46C1-9BE4-28CB5C59E933 wds:Q30492926-C0AD0E37-B512-4F4A-B60F-BD478EFFD7A5 wds:Q73868599-C488FAEC-76BD-49D6-800C-9A184331458F wds:Q73868604-BE84D8C1-1876-4A28-ADDF-79FE75B80054 wds:Q73798692-E81D11EF-A7A7-438B-A5F8-73CDB132BC89 wds:Q58863062-9D2914AE-4DC4-4CB3-B7CB-3160A9C37D65 wds:Q40499838-D8C41CD7-FF85-47B5-8FC9-D6BAA232B41B

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