lambertianin D
group of stereoisomers
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lambertianin D
Summary
lambertianin D is a group of stereoisomers[1]. It draws 2 Wikipedia views per month (group_of_stereoisomers category, ranking #216 of 1,063).[2]
Key Facts
- lambertianin D's instance of is recorded as group of stereoisomers[3].
- lambertianin D's chemical structure is recorded as Lambertianin D.png[4].
- lambertianin D's CAS Registry Number is recorded as 152617-89-5[5].
- lambertianin D's canonical SMILES is recorded as O=C1OCC2OC(OC(=O)C3=CC(O)=C(O)C(OC=4C(O)=C(O)C(O)=C5C4C(=O)OC6C(OC(OC(=O)C7=CC(O)=C(O)C(OC=8C(O)=C(O)C(O)=C9C8C(=O)OC%10C(OC(OC(=O)C%11=CC(O)=C(O)C(OC=%12C(O)=C(O)C(O)=C%13C%12C(=O)OC%14C(OC(OC(=O)C%15=CC(O)=C(O)C(O)=C%15)C%16OC(=O)C%17=CC(O)=C(O)C(O)=C%17C%18=C(O)C(O)=C(O)C=C%18C(=O)OC%16%14)COC(=O)C%19=CC(O)=C(O)C(O)=C%19%13)=C%11)C%20OC(=O)C%21=CC(O)=C(O)C(O)=C%21C%22=C(O)C(O)=C(O)C=C%22C(=O)OC%20%10)COC(=O)C%23=CC(O)=C(O)C(O)=C%239)=C7)C%24OC(=O)C%25=CC(O)=C(O)C(O)=C%25C%26=C(O)C(O)=C(O)C=C%26C(=O)OC%246)COC(=O)C%27=CC(O)=C(O)C(O)=C%275)=C3)C%28OC(=O)C%29=CC(O)=C(O)C(O)=C%29C%30=C(O)C(O)=C(O)C=C%30C(=O)OC%28C2OC(=O)C%31=CC(O)=C(O)C(O)=C%31C%32=C(O)C(O)=C(O)C=C1%32[6].
- lambertianin D's InChI is recorded as InChI=1S/C164H106O104/c165-43-1-26(2-44(166)87(43)183)141(222)265-161-138-134(258-151(232)36-15-54(176)94(190)107(203)71(36)75-40(155(236)262-138)19-58(180)98(194)111(75)207)127-65(250-161)23-243-146(227)31-10-49(171)101(197)114(210)78(31)81-84(158(239)254-127)130(123(219)120(216)117(81)213)247-62-7-28(4-46(168)89(62)185)143(224)267-163-140-136(260-153(234)38-17-56(178)96(192)109(205)73(38)77-42(157(238)264-140)21-60(182)100(196)113(77)209)129-67(252-163)25-245-148(229)33-12-51(173)103(199)116(212)80(33)83-86(160(241)256-129)132(125(221)122(218)119(83)215)248-63-8-29(5-47(169)90(63)186)144(225)268-164-139-135(259-152(233)37-16-55(177)95(191)108(204)72(37)76-41(156(237)263-139)20-59(181)99(195)112(76)208)128-66(251-164)24-244-147(228)32-11-50(172)102(198)115(211)79(32)82-85(159(240)255-128)131(124(220)121(217)118(82)214)246-61-6-27(3-45(167)88(61)184)142(223)266-162-137-133(257-150(231)35-14-53(175)93(189)106(202)70(35)74-39(154(235)261-137)18-57(179)97(193)110(74)206)126-64(249-162)22-242-145(226)30-9-48(170)91(187)104(200)68(30)69-34(149(230)253-126)13-52(174)92(188)105(69)201/h1-21,64-67,126-129,133-140,161-221H,22-25H2[7].
- lambertianin D's InChIKey is recorded as WZQCGDLPTFKQNG-UHFFFAOYSA-N[8].
- lambertianin D's chemical formula is recorded as C₁₆₄H₁₀₆O₁₀₄[9].
- lambertianin D's subclass of is recorded as ellagitannin[10].
- lambertianin D's Freebase ID is recorded as /m/0jt02vh[11].
- lambertianin D's ChemSpider ID is recorded as 58993330[12].
- lambertianin D's PubChem CID is recorded as 44460483[13].
- lambertianin D's found in taxon is recorded as Rubus corchorifolius[14].
- lambertianin D's found in taxon is recorded as Rubus palmatus[15].
- lambertianin D's found in taxon is recorded as Rubus chingii[16].
- lambertianin D's found in taxon is recorded as Rubus idaeus[17].
- lambertianin D's found in taxon is recorded as Rubus parvifolius[18].
- lambertianin D's found in taxon is recorded as Rubus crataegifolius[19].
- lambertianin D's found in taxon is recorded as Rubus sieboldii[20].
- lambertianin D's found in taxon is recorded as Rubus phoenicolasius[21].
- lambertianin D's found in taxon is recorded as Rubus lambertianus[22].
- lambertianin D's found in taxon is recorded as Rubus calycinoides[23].
- lambertianin D's Human Metabolome Database ID is recorded as HMDB0302936[24].
- lambertianin D's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+3738.300573872'}[25].
- lambertianin D's FooDB compound ID is recorded as FDB006960[26].
- lambertianin D's UniChem compound ID is recorded as 111604[27].
Why It Matters
lambertianin D draws 2 Wikipedia views per month (group_of_stereoisomers category, ranking #216 of 1,063).[2]