It is used in traditional medicine for the treatment of a variety of ailments, including fever, headache, and stomachache.

Arisaema erubescens is a flowering plant species in the genus Arisaema, endemic to Nepal. It has a globose tuber which is 2-7 cm wide and 3 cataphylls which are dark green and carry white spots. Its petiole is 2 cm long and its peduncle is 75 cm long with a free part of 9 cm. The spathe is green and cylindrical with tubes of 6-7 cm by 1.5 cm and sometimes stripeless. The limb of its throat is deep green but can sometimes be with purple coloured outside margin and pale green inside. It is used in traditional medicine for the treatment of a variety of ailments, including fever, headache, and stomachache.

Synonyms Top

Scientific name	Authority	First published in
Arum erubescens	Wall.	Pl. Asiat. Rar. 2: 30 (1831)

Common names Top

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Language	Common/alternative name
Bulgarian	червенееща аризема
Russian	Аризема красноватая
Thai	โหราน้ำเต้า
Chinese	长行南星
Chinese	短柄南星
Chinese	一把伞
Chinese	山蕃芋
Chinese	打蛇棒
Chinese	法夏
Chinese	粉南星
Chinese	虎掌南星
Chinese	蛇子麦
Chinese	蛇舌草
Chinese	血南星
Chinese	都士不礼
Chinese	铁骨伞
Chinese	麻芋杆
Chinese	麻蛇饭
Chinese	黄狗卵
Chinese	狗爪半夏
Chinese	胆星
Chinese	蛇芋
Chinese	刀口药
Chinese	虎掌
Chinese	野磨芋
Chinese	麻芋子
Chinese	青脚莲
Chinese	半夏
Chinese	山磨芋
Chinese	天南星
Chinese	独角莲
Chinese	蛇包谷
Chinese	山包谷
Chinese	闹狗药
Chinese	白南星
Chinese	蛇芋头
Chinese	一把伞南星
Chinese	南星一把伞

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-tropical click to expand
- Indian Subcontinent
  - Nepal

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000270688
UNII	SF6XYE1WTC
Tropicos	2101483
KEW	urn:lsid:ipni.org:names:85637-1
The Plant List	kew-15355
Open Tree Of Life	49726
NCBI Taxonomy	228806
IPNI	85637-1
iNaturalist	556029
GBIF	2867313
Freebase	/m/0j7lzz6
EOL	1134767
USDA GRIN	429280
Wikipedia	Arisaema_erubescens
CMAUP	NPO5621

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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

Efficacy and safety of Wuhu oral liquid in treating acute soft tissue injuries: a multicenter, randomized, double-blind, double-dummy, parallel-controlled trial

Zhu WH, Shen Y, Xiao Y, Shi Q, Fan ZX, Feng YQ, Wan HB, Qu B, Zhao J, Zhang WQ, Xu GH, Wu XQ, Tang DZ

Front Pharmacol

23-Feb-2024

PMCID:	PMC10921885
doi:	10.3389/fphar.2024.1335182
PMID:	38464733

The Potentiality of Natural Products and Herbal Medicine as Novel Medications for Parkinson’s Disease: A Promising Therapeutic Approach

So YJ, Lee JU, Yang GS, Yang G, Kim SW, Lee JH, Kim JU

Int J Mol Sci

15-Jan-2024

PMCID:	PMC10816678
doi:	10.3390/ijms25021071
PMID:	38256144

The complete chloroplast genome sequence of Amorphophallus konjac (Araceae) from Yunnan, China and its phylogenetic analysis in the family Araceae

Li L, Qi Y, Gao P, Yang S, Zhao Y, Guo J, Liu J, Huang F, Yu L

Mitochondrial DNA B Resour

08-Jan-2024

PMCID:	PMC10776074
doi:	10.1080/23802359.2023.2300471
PMID:	38197049

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Application of digital-intelligence technology in the processing of Chinese materia medica

Zhang W, Zhang C, Cao L, Liang F, Xie W, Tao L, Chen C, Yang M, Zhong L

Front Pharmacol

24-Aug-2023

PMCID:	PMC10484343
doi:	10.3389/fphar.2023.1208055
PMID:	37693890

Efficacy of Chinese herbal medicine on nasal itching in children with allergic rhinitis: a systematic review and meta-analysis

Chen Y, Wang J, Wu L, Zhang Y, Chen H, Zhang Z

Front Pharmacol

23-Aug-2023

PMCID:	PMC10482051
doi:	10.3389/fphar.2023.1240917
PMID:	37680707

Insight into Nephrotoxicity and Processing Mechanism of Arisaema erubescens (Wall.) Schott by Metabolomics and Network Analysis

Wang M, Yang N, Wu X, Zou T, Zheng J, Zhu H, Zhao C, Wang J

Drug Des Devel Ther

19-Jun-2023

PMCID:	PMC10289099
doi:	10.2147/DDDT.S406551
PMID:	37360574

Gastrodia elata BI.:A Comprehensive Review of Its Traditional Use, Botany, Phytochemistry, Pharmacology, and Pharmacokinetics

Wu YN, Wen SH, Zhang W, Yu SS, Yang K, Liu D, Zhao CB, Sun J

Evid Based Complement Alternat Med

18-Apr-2023

PMCID:	PMC10129437
doi:	10.1155/2023/5606021
PMID:	37114145

Naoxin’an capsules protect brain function and structure in patients with vascular cognitive impairment

Lu H, Dang M, Chen K, Shang H, Wang B, Zhao S, Li X, Zhang Z, Zhang J, Chen Y

Front Pharmacol

05-Apr-2023

PMCID:	PMC10113453
doi:	10.3389/fphar.2023.1129125
PMID:	37089924

Insights of Chinese herbal medicine for mitochondrial dysfunction in chronic cerebral hypoperfusion induced cognitive impairment: Existed evidences and potential directions

Wang Y, Wang Y, Li S, Jin H, Duan J, Lu X, Qin Y, Song J, Li X, Jin X

Front Pharmacol

10-Feb-2023

PMCID:	PMC9950122
doi:	10.3389/fphar.2023.1138566
PMID:	36843941

Targeting bacterial pathogenesis by inhibiting virulence-associated Type III and Type IV secretion systems

Blasey N, Rehrmann D, Riebisch AK, Mühlen S

Front Cell Infect Microbiol

10-Jan-2023

PMCID:	PMC9872159
doi:	10.3389/fcimb.2022.1065561
PMID:	36704108

Uniting the Role of Endophytic Fungi against Plant Pathogens and Their Interaction

Akram S, Ahmed A, He P, He P, Liu Y, Wu Y, Munir S, He Y

J Fungi (Basel)

03-Jan-2023

PMCID:	PMC9860820
doi:	10.3390/jof9010072
PMID:	36675893

A narrative review on traditional Chinese medicine prescriptions and bioactive components in epilepsy treatment

Tao F, Cai Y, Deng C, Chen Z, Shen Y, Sun H

Ann Transl Med

13-Dec-2022

PMCID:	PMC9929833
doi:	10.21037/atm-22-3306
PMID:	36819494

The Effects of Adding Di-Tan Decoction (DTD) and/or Electroacupuncture (EA) to Standard Swallowing Rehabilitation Training (SRT) for Improving Poststroke Dysphagia (PSD): A Pilot, Single-Centred, Randomized Trial

Shao X, Chen B, Zhu L, Zhu L, Zheng J, Pu X, Chen J, Xia J, Wu X, Zhang J, Wu D

Evid Based Complement Alternat Med

08-Dec-2022

PMCID:	PMC9754838
doi:	10.1155/2022/2011597
PMID:	36532853

Cangfudaotan decoction inhibits mitochondria-dependent apoptosis of granulosa cells in rats with polycystic ovarian syndrome

Jiang XL, Tai H, Xiao XS, Zhang SY, Cui SC, Qi SB, Hu DD, Zhang LN, Kuang JS, Meng XS, Li SM

Front Endocrinol (Lausanne)

09-Nov-2022

PMCID:	PMC9716878
doi:	10.3389/fendo.2022.962154
PMID:	36465612

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[[(3S,5R,7S,8R,9R,10S,13R,14R,17S)-7-hydroxy-17-[(E,2R)-2-hydroxy-6-methoxy-6-methylhept-4-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11158610	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6C(CCC6(C5(C(CC4C3(C)C)O)C)C)C(C)(CC=CC(C)(C)OC)O)C)CO)O)O)O)O)O	799.00	unknown	via CMAUP database
Sapinmusaponin O	21607566	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6C(CCC6(C5(C(CC4C3(C)C)O)C)C)C(C)(CCC=C(C)C)O)C)CO)O)O)O)O)O	769.00	unknown	via CMAUP database
Sapinmusaponin P	24866793	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6C(CCC6(C5(C(CC4C3(C)C)O)C)C)C(C)(CCC=C(C)C)O)C)CO)O)O)O)O)O	769.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(3S,5R,9R,10R,13S,14S,17S)-17-[(2R,3S,5S)-2-methoxy-5-(2-methylprop-1-enyl)oxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	11542343	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C5CCC6(C(CCC6(C5=CCC4C3(C)C)C)C7CC(OC7OC)C=C(C)C)C)C)O)O)O)O)O)O	779.00	unknown	via CMAUP database
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(3S,5R,9R,10R,13S,14S,17S)-17-[(2S,3S,5S)-2-methoxy-5-(2-methylprop-1-enyl)oxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	11672254	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C5CCC6(C(CCC6(C5=CCC4C3(C)C)C)C7CC(OC7OC)C=C(C)C)C)C)O)O)O)O)O)O	779.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(3S,5R,9R,10R,13S,14S,17S)-17-[(2R,3S,5S)-2-methoxy-5-(2-methylprop-1-enyl)oxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11527893	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6(C(CCC6(C5=CCC4C3(C)C)C)C7CC(OC7OC)C=C(C)C)C)C)CO)O)O)O)O)O	779.00	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5R)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	102316696	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O	925.10	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-3,4-diacetyloxy-5-hydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	24866958	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)OC(=O)C)OC(=O)C)O	967.10	unknown	via CMAUP database
3beta-(2-O-alpha-L-Rhamnopyranosyl-3-O-beta-D-xylopyranosyl-alpha-L-arabinopyranosyloxy)-23-hydroxyoleana-12-ene-28-oic acid	101682283	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(CO8)O)O)O)O)O)O	883.10	unknown	via CMAUP database
3beta-[2-O-(3-O-alpha-L-Arabinopyranosyl-alpha-L-rhamnopyranosyl)-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	21637697	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	via CMAUP database
3beta-[2-O-[3-O-(2-O-Acetyl-beta-D-xylopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	101118028	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)OC(=O)C)O	925.10	unknown	via CMAUP database
3beta-[2-O-[3-O-(2-O,4-O-Diacetyl-alpha-L-arabinopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	101749122	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)OC(=O)C)O	967.10	unknown	via CMAUP database
3beta-[2-O-[3-O-(3-O-Acetyl-beta-D-xylopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	21637699	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)OC(=O)C)O)O	925.10	unknown	via CMAUP database
3beta-[2-O-[3-O-(3-O,4-O-Diacetyl-alpha-L-arabinopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	102316698	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O	967.10	unknown	via CMAUP database
3beta-[2-O-[3-O-(3-O,4-O-Diacetyl-beta-D-xylopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	21637700	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O	967.10	unknown	via CMAUP database
alpha-Hederin	73296	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)O)O	751.00	unknown	via CMAUP database
Cauloside A	441928	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C	604.80	unknown	via CMAUP database
Hederagenin	73299	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Rarasaponin II	24866957	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)OC(=O)C)O)O	925.10	unknown	via CMAUP database
Rarasaponin III	24866792	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O	925.10	unknown	via CMAUP database
Rarasaponin VI	24866959	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)OC(=O)C)O	967.10	unknown	via CMAUP database
Sapimukoside E	101412373	Click to see CCOC1C(CC(O1)C=C(C)C)C2CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(C(O8)C)O)OC9C(C(C(CO9)O)O)O)O)C)C)C	1057.30	unknown	via CMAUP database
Sapimukoside F	101412374	Click to see CCOC1C(CC(O1)C=C(C)C)C2CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(C(O8)C)O)OC9C(C(C(CO9)O)O)O)O)C)C)C	1057.30	unknown	via CMAUP database
Sapimukoside G	101412375	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6(C(CCC6(C5=CCC4C3(C)C)C)C7CC(OC7OC)C=C(C)C)C)C)CO)O)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(CO9)O)O)O)O	1043.20	unknown	via CMAUP database
Sapimukoside H	101412376	Click to see CCOC1C(CC(O1)C=C(C)C)C2CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)C)O)OC9C(C(C(CO9)O)O)O)O)C)C)C	1071.30	unknown	via CMAUP database
Sapimukoside I	101412377	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)O)OC4C(C(C(CO4)O)O)O)O)OC5CCC6(C7CCC8(C(CCC8(C7=CCC6C5(C)C)C)C9CC(OC9OC)C=C(C)C)C)C)CO)O)O)O)O	1057.30	unknown	via CMAUP database
Sapimukoside J	101412378	Click to see CCOC1C(CC(O1)C=C(C)C)C2CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)COC7C(C(C(C(O7)C)O)O)O)O)O)O)C)C)C	793.00	unknown	via CMAUP database
Sapindoside B	161686	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	via CMAUP database
Sapinmusaponin Q	70697764	Click to see CC(=CC1CC(C(O1)OC)C2CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)C	795.00	unknown	via CMAUP database
Sapinmusaponin R	70697842	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(C(C(OC3OC4CCC5(C6CCC7(C(CCC7(C6=CCC5C4(C)C)C)C8CC(OC8OC)C=C(C)C)C)C)CO)O)O)O)O)O)O)O)O	941.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids / Simple glycosylceramides / Glycosyl-N-acylsphingosines
beta-D-glucosyl-N-(dodecanoyl)sphingosine	20057354	Click to see CCCCCCCCCCCCCC=CC(C(COC1C(C(C(C(O1)CO)O)O)O)NC(=O)CCCCCCCCCCC)O	643.90	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one	6802	Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N	283.24	unknown	via CMAUP database
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine	6029	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
[(2R)-2-[[[(2S)-2-benzamido-3-phenylpropanoyl]amino]methyl]-3-phenylpropyl] acetate	5321123	Click to see CC(=O)OCC(CC1=CC=CC=C1)CNC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	458.50	unknown	https://doi.org/10.1055/S-2006-957878
Asperglaucide	10026486	Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	444.50	unknown	https://doi.org/10.1055/S-2006-957878
Aurantiamide acetate	124319	Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	444.50	unknown	https://doi.org/10.1055/S-2006-957878
Tifentai	9832120	Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	444.50	unknown	https://doi.org/10.1055/S-2006-957878
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eugenol rutinoside	15101911	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C(C=C3)CC=C)OC)O)O)O)O)O)O	472.50	unknown	via CMAUP database
Geoside	25087713	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O	458.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Paeonol	11092	Click to see CC(=O)C1=C(C=C(C=C1)OC)O	166.17	unknown	https://doi.org/10.1055/S-2006-959390
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine	190	Click to see C1=NC2=NC=NC(=C2N1)N	135.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
CID 790	790	Click to see C1=NC2=C(N1)C(=O)N=CN2	136.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Xanthine	1188	Click to see C1=NC2=C(N1)C(=O)NC(=O)N2	152.11	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Apigenin 6-C-alpha-L-arabinopyranoside-8-C-beta-D-glucopyranoside	44257699	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	via CMAUP database
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	via CMAUP database
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	via CMAUP database

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Arisaema erubescens

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