Parsonsia alboflavescens - Unknown
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Internal ID UUID643fe6351110a434363186
Scientific name Parsonsia alboflavescens
Authority (Dennst.) Mabb.
First published in Taxon 26: 532 (1977)

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Synonyms Top

Scientific name Authority First published in
Lyonsia sumatrana Ridl. Bull. Misc. Inform. Kew 1925: 84 (1925)
Lyonsia viridiflora F.M.Bailey Queensland Agric. J. 3: 156 (1899)
Apocynum reticulatum L. Sp. Pl. : 214 (1753)
Parsonsia acuminata Wall. Numer. List : n.º 1634 (1829)
Parsonsia aterinervia Elmer ex Merr. Enum. Philipp. Fl. Pl. iii. 338 (1923). in obs., pro syn.; Elmer, Leafl.Philipp. Bot. x. 3695 (1939), descr. angl.
Parsonsia confusa Merr. Philipp. J. Sci. 1(Suppl.): 118 (1906)
Parsonsia cumingiana A.DC. Prodr. 8: 402 (1844)
Parsonsia helicandra Hook. & Arn. Bot. Beechey Voy. : 197 (1837)
Parsonsia howii Tsiang Sunyatsenia 2: 167 (1934)
Parsonsia korthalsiana Boerl. Handl. Fl. Ned. Ind. 2: 397 (1899)
Parsonsia kunstleri King & Gamble J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 74: 457 (1908)
Parsonsia laevigata Alston Ann. Roy. Bot. Gard. (Peradeniya) 11: 203 (1929)
Parsonsia longipedunculata Merr. Univ. Calif. Publ. Bot. 15: 255 (1929)
Parsonsia magnifolia Elmer Leafl. Philipp. Bot. 8: 3071 (1919)
Parsonsia minahassae Koord. Meded. Lands Plantentuin 19: 531 (1898)
Parsonsia momiensis Kaneh. & Hatus. Bot. Mag. (Tokyo) 55: 500 (1941)
Parsonsia oblancifolia Merr. Philipp. J. Sci., C 7: 335 (1921)
Parsonsia oblonga Wall. & G.Don Gen. Hist. 4: 80 (1837)
Parsonsia oblongifolia Merr. Philipp. J. Sci. 27: 50 (1925)
Parsonsia panniculata Pichon Notul. Syst. (Paris) 14: 16 (1950)
Parsonsia pauciflora Wall. Numer. List : n.º 1633 (1829)
Parsonsia spiralis Wall. & G.Don Gen. Hist. 4: 80 (1837)
Periploca alboflavescens Dennst. Schlüssel Hortus Malab. : 12, 23 (1818)
Spirostemon spiralis Griff. Not. Pl. Asiat. 4: 80 (1854)
Chaetosus volubilis Benth. London J. Bot. 2: 226 (1843)
Aganosma concanensis Hook. Hooker's Icon. Pl. 9: t. 841 (1852)
Aganosma laevigata J.Graham Cat. Pl. Bombay : 113 (1839)
Cudicia trichotoma Buch.-Ham. ex G.Don Gen. Hist. iv. 80.
Echites laevigatus Moon Cat. Pl. Ceylon : 20 (1824)
Echites spiralis Blanco Fl. Filip. : 110 (1837)
Helicandra sinensis Hook. & Arn. Bot. Beechey Voy. : 198 (1837)
Heligme javanica Blume Bijdr. Fl. Ned. Ind. : 1043 (1826)
Heligme korthalsiana Miq. Fl. Ned. Ind. 2: 429 (1857)
Heligme minahassae Teijsm. & Binn. Natuurk. Tijdschr. Ned.-Indië 25: 404 (1863)
Heligme spiralis Thwaites Enum. Pl. Zeyl. : 193 (1860)
Helyga javanica Blume Catalogus : 24 (1823)
Parsonsia reticulata Woodson Ann. Missouri Bot. Gard. 1930, xvii. 147.

Common names Top

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Language Common/alternative name
Chinese 海南同心结
Chinese 爬森藤

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000264703
Tropicos 1805996
KEW urn:lsid:ipni.org:names:80868-1
The Plant List kew-147819
Open Tree Of Life 5793920
NCBI Taxonomy 2126282
IPNI 80868-1
iNaturalist 427336
GBIF 7317262
Wikipedia Parsonsia_alboflavescens

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_028571225.1 ASM2857122v1 Scaffold Iridian Genomes 2023-02-09 110.0x 366.48 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Taxonomic re-examination of Japanese isolates of the genus Lasiodiplodia Hattori Y, Nakano L, Nakashima C Mycoscience 20-Feb-2023
PMCID:PMC10165170
doi:10.47371/mycosci.2022.12.004
PMID:37168245
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
HPLC‐MS detection of pyrrolizidine alkaloids and their N‐oxides in herbarium specimens dating back to the 1850s Tasca JA, Smith CR, Burzynski EA, Sundberg BN, Lagalante AF, Livshultz T, Minbiole KP Appl Plant Sci 08-May-2018
PMCID:PMC5947603
doi:10.1002/aps3.1143
PMID:30131885
Evolution of pyrrolizidine alkaloid biosynthesis in Apocynaceae: revisiting the defence de‐escalation hypothesis Livshultz T, Kaltenegger E, Straub SC, Weitemier K, Hirsch E, Koval K, Mema L, Liston A New Phytol 26-Feb-2018
PMCID:PMC5873419
doi:10.1111/nph.15061
PMID:29479722
Parsonine, a Pyrrolizidine Alkaloid from <I>Parsonsia laevigata</I> FUMIKO ABE, TATSUO YAMAUCHI Pharmaceutical Society of Japan 18-Mar-2017
doi:10.1248/CPB.35.4661
Pyrrolizidine Alkaloids from Parsonsia laevigata in Okinawa Island (Studies on Parsonsia. V). Fumiko ABE, Tatsuo YAMAUCHI, Shiryo YAGA, Kazuo MINATO Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.39.1576
Parsonsianine, a macrocyclic pyrrolizidine alkaloid from the leaves of Parsonsia laevigata(Studies on Parsonsia. III). Fumiko ABE, Tsuneatsu NAGAO, Hikaru OKABE, Tatsuo YAMAUCHI, Nobuhiro MARUBAYASHI, Ikuhiko UEDA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.38.2127
Macrocyclic pyrrolizidine alkaloids from Parsonsia laevigata Fumiko Abe, Tsuneatsu Nagao, Hikaru Okabe, Tatsuo Yamauchi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)84253-O
Triterpenes from the leaves of parsonsia laevigata Kazuhito Ogihara, Matsutake Higa, Kozo Hokama, Takayuki Suga Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84786-X
Lignan glycosides from Parsonsia laevigata Fumiko Abe, Tatsuo Yamauchi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97835-X

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
1-O-[(1S,8R)-7-[[(2S,3S)-2-ethyl-2,3-dihydroxybutanoyl]oxymethyl]-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl] 4-O-methyl (2R)-2-hydroxy-2-propan-2-ylbutanedioate 162858494 Click to see CCC(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C(CC(=O)OC)(C(C)C)O)O 457.50 unknown https://doi.org/10.1248/CPB.39.1576
1-O-[7-[(2-ethyl-2,3-dihydroxybutanoyl)oxymethyl]-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl] 4-O-methyl 2-hydroxy-2-propan-2-ylbutanedioate 162858493 Click to see CCC(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C(CC(=O)OC)(C(C)C)O)O 457.50 unknown https://doi.org/10.1248/CPB.39.1576
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3S,4S,5R,6S)-6-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-2-(hydroxymethyl)oxane-3,4-diol 14309783 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)OC6C(C(CO6)(CO)O)O)OC)O 652.60 unknown https://doi.org/10.1016/S0031-9422(00)97835-X
(2R,3S,4S,5S,6R)-2-[4-[(2R,3R)-2,3-bis(hydroxymethyl)-4-[3-methoxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]butyl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 162983695 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)CC(CO)C(CC3=CC(=C(C=C3)OC4C(C(C(C(O4)C)O)O)O)OC)CO)OC)O)O)O 654.70 unknown https://doi.org/10.1016/S0031-9422(00)97835-X
(2R,3S,4S,5S,6R)-2-[4-[[(3R,4R,5S)-4-(hydroxymethyl)-5-[3-methoxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]oxolan-3-yl]methyl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 162985854 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)CC3COC(C3CO)C4=CC(=C(C=C4)OC5C(C(C(C(O5)C)O)O)O)OC)OC)O)O)O 652.70 unknown https://doi.org/10.1016/S0031-9422(00)97835-X
(2R,3S,4S,5S,6R)-2-[4-[[(3R,4R,5S)-5-[3,5-dimethoxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]-4-(hydroxymethyl)oxolan-3-yl]methyl]-2,6-dimethoxyphenoxy]-6-methyloxane-3,4,5-triol 162902817 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2OC)CC3COC(C3CO)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)C)O)O)O)OC)OC)O)O)O 712.70 unknown https://doi.org/10.1016/S0031-9422(00)97835-X
2-[4-[[4-(Hydroxymethyl)-5-[3-methoxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]oxolan-3-yl]methyl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 14309774 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)CC3COC(C3CO)C4=CC(=C(C=C4)OC5C(C(C(C(O5)C)O)O)O)OC)OC)O)O)O 652.70 unknown https://doi.org/10.1016/S0031-9422(00)97835-X
2-[4-[[5-[3,5-Dimethoxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]-4-(hydroxymethyl)oxolan-3-yl]methyl]-2,6-dimethoxyphenoxy]-6-methyloxane-3,4,5-triol 14309776 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2OC)CC3COC(C3CO)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)C)O)O)O)OC)OC)O)O)O 712.70 unknown https://doi.org/10.1016/S0031-9422(00)97835-X
2-[4-[2,3-Bis(hydroxymethyl)-4-[3-methoxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]butyl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 14309780 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)CC(CO)C(CC3=CC(=C(C=C3)OC4C(C(C(C(O4)C)O)O)O)OC)CO)OC)O)O)O 654.70 unknown https://doi.org/10.1016/S0031-9422(00)97835-X
5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[4-[3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-2-(hydroxymethyl)oxane-3,4-diol 14309782 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)OC6C(C(CO6)(CO)O)O)OC)O 652.60 unknown https://doi.org/10.1016/S0031-9422(00)97835-X
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4S,4aR,6aR,6aS,8aR,12aR,14aR,14bR)-4-(hydroxymethyl)-4,6a,6a,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 162994505 Click to see CC1(CCC2(CC=C3C4(CCC5C(C4CCC3(C2C1)C)(CCC(C5(C)CO)O)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)84786-X
4-(Hydroxymethyl)-4,6a,6a,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 162994504 Click to see CC1(CCC2(CC=C3C4(CCC5C(C4CCC3(C2C1)C)(CCC(C5(C)CO)O)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)84786-X
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84786-X
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84786-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84786-X
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84786-X
> Organoheterocyclic compounds / Pyrrolizines
(7-oxo-5,6-dihydropyrrolizin-1-yl)methyl (2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate 13946372 Click to see CC(C)C(C(C)O)(C(=O)OCC1=C2C(=O)CCN2C=C1)O 295.33 unknown https://doi.org/10.1248/CPB.35.4661
(7-Oxo-5,6-dihydropyrrolizin-1-yl)methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 13946371 Click to see CC(C)C(C(C)O)(C(=O)OCC1=C2C(=O)CCN2C=C1)O 295.33 unknown https://doi.org/10.1248/CPB.35.4661
> Phenylpropanoids and polyketides / Macrolides and analogues
(16R)-25-Methyl-16-hydroxyparsonsine 14845642 Click to see CCC(C)C1(C(C(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C(C)C)O)C)O)O 469.50 unknown https://doi.org/10.1016/0031-9422(91)84253-O
(1R,4R,5R,8R,9S,19R)-4-[(2S)-butan-2-yl]-4,5,9-trihydroxy-8-methyl-9-propan-2-yl-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 163074236 Click to see CCC(C)C1(C(C(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C(C)C)O)C)O)O 469.50 unknown https://doi.org/10.1016/0031-9422(91)84253-O
(1R,4R,5R,8R,9S,19R)-4-[(2S)-butan-2-yl]-9-ethyl-4,5,9-trihydroxy-8-methyl-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 162935577 Click to see CCC(C)C1(C(C(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CC)O)C)O)O 455.50 unknown https://doi.org/10.1016/0031-9422(91)84253-O
(1R,4R,5S,8R,9S,19R)-9-ethyl-4,5,9-trihydroxy-8-methyl-4-propan-2-yl-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 14680172 Click to see CCC1(C(OC(=O)C(C(C(=O)OC2CCN3C2C(=CC3)COC1=O)(C(C)C)O)O)C)O 441.50 unknown https://doi.org/10.1248/CPB.38.2127
(1R,4S,8R,9S,19R)-4-[(2S)-butan-2-yl]-4,9-dihydroxy-8-methyl-9-propan-2-yl-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 163035077 Click to see CCC(C)C1(CC(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C(C)C)O)C)O 453.50 unknown https://doi.org/10.1248/CPB.39.1576
(1R,4S,8R,9S,19R)-4-[(2S)-butan-2-yl]-9-ethyl-4,9-dihydroxy-8-methyl-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 163031585 Click to see CCC(C)C1(CC(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CC)O)C)O 439.50 unknown https://doi.org/10.1248/CPB.39.1576
(1R,4S,8R,9S,19R)-9-ethyl-4,9-dihydroxy-8-methyl-4-propan-2-yl-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 15060935 Click to see CCC1(C(OC(=O)CC(C(=O)OC2CCN3C2C(=CC3)COC1=O)(C(C)C)O)C)O 425.50 unknown https://doi.org/10.1248/CPB.39.1576
17-Methylparsonsianidine 134714993 Click to see CCC(C)C1(C(C(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C(C)C)O)C)O)O 469.50 unknown https://doi.org/10.1248/CPB.39.1576
4-Butan-2-yl-4,9-dihydroxy-8-methyl-9-propan-2-yl-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 163035076 Click to see CCC(C)C1(CC(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C(C)C)O)C)O 453.50 unknown https://doi.org/10.1248/CPB.39.1576
4-Butan-2-yl-9-ethyl-4,9-dihydroxy-8-methyl-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 163031584 Click to see CCC(C)C1(CC(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CC)O)C)O 439.50 unknown https://doi.org/10.1248/CPB.39.1576
4,5,9-Trihydroxy-8-methyl-4,9-di(propan-2-yl)-2,7,11-trioxa-16-azatricyclo[11.5.1.016,19]nonadec-13-ene-3,6,10-trione 78302634 Click to see CC1C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C(C(C(=O)O1)O)(C(C)C)O)(C(C)C)O 455.50 unknown https://doi.org/10.1248/CPB.39.1576
CID 14680171 14680171 Click to see CCC1(C(OC(=O)C(C(C(=O)OC2CCN3C2C(=CC3)COC1=O)(C(C)C)O)O)C)O 441.50 unknown https://doi.org/10.1016/0031-9422(91)84253-O
https://doi.org/10.1248/CPB.38.2127
CID 14845640 14845640 Click to see CCC(C)C1(C(C(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CC)O)C)O)O 455.50 unknown https://doi.org/10.1016/0031-9422(91)84253-O
Parsonsianidine 134714989 Click to see CCC(C)C1(C(C(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CC)O)C)O)O 455.50 unknown https://doi.org/10.1016/0031-9422(91)84253-O
https://doi.org/10.1248/CPB.39.1576
Parsonsianine 14680173 Click to see CCC1(C(OC(=O)C(C(C(=O)OC2CCN3C2C(=CC3)COC1=O)(C(C)C)O)O)C)O 441.50 unknown https://doi.org/10.1248/CPB.39.1576
https://doi.org/10.1248/CPB.38.2127
https://doi.org/10.1016/0031-9422(91)84253-O
Parsonsine 15060933 Click to see CC1C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C(CC(=O)O1)(C(C)C)O)(C(C)C)O 439.50 unknown https://doi.org/10.1248/CPB.39.1576
Spiraline 3086069 Click to see CC1C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C(C(C(=O)O1)O)(C(C)C)O)(C(C)C)O 455.50 unknown https://doi.org/10.1248/CPB.39.1576
Spiranine 14845643 Click to see CCC(C)C1(C(C(=O)OC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C(C)C)O)C)O)O 469.50 unknown https://doi.org/10.1016/0031-9422(91)84253-O

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