Cryptocarya chinensis, also known as the Chinese cryptocarya, is a type of medium-sized evergreen tree that can be found in subtropical forests in Taiwan, southern China, and Japan. It is commonly found in regions such as Fujian, Guangdong, Guangxi, Hainan, and Sichuan. This tree is known for its unique appearance and is a popular species in these areas.

Synonyms Top

Scientific name	Authority	First published in
Beilschmiedia chinensis	Hance	J. Bot. 20: 79 (1882)

Common names Top

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Language	Common/alternative name
Chinese	硬壳槁
Chinese	香果
Chinese	厚壳桂
Chinese	厚殼桂
Chinese	华厚壳桂
Chinese	山饼斗
Chinese	铜锣桂
Chinese	香花桂

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Japan
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000627835
Tropicos	17800433
KEW	urn:lsid:ipni.org:names:463847-1
The Plant List	kew-2745896
Open Tree Of Life	445161
NCBI Taxonomy	128609
IUCN Red List	159080211
IPNI	463847-1
iNaturalist	632420
GBIF	4177857
Freebase	/m/0271hvv
EOL	5397992
Wikipedia	Cryptocarya_chinensis
CMAUP	NPO15311

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

Cryptocaryone induces apoptosis in human hepatocellular carcinoma cells by inhibiting aerobic glycolysis through Akt and c-Src signaling pathways

Yu CL, Lai YW, Chen JJ, Lee JJ, Chou TH, Huang CC, Liu SC, Chen GW, Tsai CH, Wang SW

J Food Drug Anal

15-Dec-2023

PMCID:	PMC10962672
doi:	10.38212/2224-6614.3480
PMID:	38526828

Cryptocarya chinensis from the Upper Pleistocene of South China and its biogeographic and paleoecological implications

Huang LL, Li SF, Huang WY, Jin JH, Oskolski AA

iScience

10-Jul-2023

PMCID:	PMC10405060
doi:	10.1016/j.isci.2023.107313
PMID:	37554461

Dynamic changes of the contents of photoprotective substances and photosynthetic maturation during leaf development of evergreen tree species in subtropical forests

Yu ZC, Lin W, He W, Yan GZ, Zheng XT, Luo YN, Zhu H, Peng CL

Tree Physiol

02-Mar-2023

PMCID:	PMC10785039
doi:	10.1093/treephys/tpad026
PMID:	36864631

Distinct Responses of Abundant and Rare Soil Bacteria to Nitrogen Addition in Tropical Forest Soils

He J, Tan X, Nie Y, Ma L, Liu J, Lu X, Mo J, Leloup J, Nunan N, Ye Q, Shen W

Microbiol Spectr

09-Jan-2023

PMCID:	PMC9927163
doi:	10.1128/spectrum.03003-22
PMID:	36622236

Comprehensive Review of Recent Advances in Chiral A-Ring Flavonoid Containing Compounds: Structure, Bioactivities, and Synthesis

Zhang C, Liu Y, Liu X, Chen X, Chen R

Molecules

02-Jan-2023

PMCID:	PMC9822200
doi:	10.3390/molecules28010365
PMID:	36615559

Genetic Diversity and Population Structure of an Arctic Tertiary Relict Tree Endemic to China (Sassafras tzumu) Revealed by Novel Nuclear Microsatellite (nSSR) Markers

Wang S, Wang Y, Zhou J, Li P, Lin H, Peng Y, Yu L, Zhang Y, Wang Z

Plants (Basel)

13-Oct-2022

PMCID:	PMC9610890
doi:	10.3390/plants11202706
PMID:	36297730

Promising Antimycobacterial Activities of Flavonoids against Mycobacterium sp. Drug Targets: A Comprehensive Review

Rabaan AA, Alhumaid S, Albayat H, Alsaeed M, Alofi FS, Al-Howaidi MH, Turkistani SA, Alhajri SM, Alahmed HE, Alzahrani AB, Mashraqi MM, Alwarthan S, Alhajri M, Alshahrani FS, Almuthree SA, Alsubki RA, Abuzaid AA, Alfaresi M, Al Fares MA, Mutair AA

Molecules

22-Aug-2022

PMCID:	PMC9415813
doi:	10.3390/molecules27165335
PMID:	36014572

Photoprotection Differences between Dominant Tree Species at Mid- and Late-Successional Stages in Subtropical Forests in Different Seasonal Environments

Lin W, Yu Z, Luo Y, He W, Yan G, Peng C

Int J Mol Sci

12-May-2022

PMCID:	PMC9140998
doi:	10.3390/ijms23105417
PMID:	35628227

Natural Products Targeting Liver X Receptors or Farnesoid X Receptor

She J, Gu T, Pang X, Liu Y, Tang L, Zhou X

Front Pharmacol

05-Jan-2022

PMCID:	PMC8766425
doi:	10.3389/fphar.2021.772435
PMID:	35069197

Variations in airborne pollen and spores in urban Guangzhou and their relationships with meteorological variables

Rahman A, Khan MH, Luo C, Yang Z, Ke J, Jiang W

Heliyon

13-Nov-2021

PMCID:	PMC8605060
doi:	10.1016/j.heliyon.2021.e08379
PMID:	34825088

Adaptation of Soil Fungal Community Structure and Assembly to Long- Versus Short-Term Nitrogen Addition in a Tropical Forest

He J, Jiao S, Tan X, Wei H, Ma X, Nie Y, Liu J, Lu X, Mo J, Shen W

Front Microbiol

25-Aug-2021

PMCID:	PMC8424203
doi:	10.3389/fmicb.2021.689674
PMID:	34512567

Influences of temperature and moisture on abiotic and biotic soil CO2 emission from a subtropical forest

Chen X, Liu M, Xu Z, Wei H

Carbon Balance Manag

25-May-2021

PMCID:	PMC8152076
doi:	10.1186/s13021-021-00181-8
PMID:	34032935

Light-driven selective aerobic oxidation of (iso)quinoliniums and related heterocycles

Zhou M, Yu K, Liu J, Shi W, Pan Y, Tang H, Peng X, Liu Q, Wang H

RSC Adv

04-May-2021

PMCID:	PMC9031974
doi:	10.1039/d1ra01226f
PMID:	35479138

Co-ordination between leaf biomechanical resistance and hydraulic safety across 30 sub-tropical woody species

Wang YQ, Ni MY, Zeng WH, Huang DL, Xiang W, He PC, Ye Q, Cao KF, Zhu SD

Ann Bot

30-Apr-2021

PMCID:	PMC8324032
doi:	10.1093/aob/mcab055
PMID:	33930116

Nitrogen deposition accelerates soil carbon sequestration in tropical forests

Lu X, Vitousek PM, Mao Q, Gilliam FS, Luo Y, Turner BL, Zhou G, Mo J

Proc Natl Acad Sci U S A

12-Apr-2021

PMCID:	PMC8072245
doi:	10.1073/pnas.2020790118
PMID:	33846252

Phytochemical Profile Top

Add a new one!

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
> Alkaloids and derivatives / Aporphines
(-)-Isoboldine	6971182	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	https://doi.org/10.1248/CPB.49.1292
(6R,6aR)-2,10-dimethoxy-6-methyl-6-oxido-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1,9-diol	101140028	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC)[O-]	343.40	unknown	via CMAUP database
(6R,6aS)-2,10-dimethoxy-6-methyl-6-oxido-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1,9-diol	163189286	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC)[O-]	343.40	unknown	https://doi.org/10.1021/NP010258I
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol	98369	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	https://doi.org/10.1248/CPB.49.1292
Glaucine	16754	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC	355.40	unknown	https://doi.org/10.1021/NP010258I
Isoboldine	133323	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	https://doi.org/10.1248/CPB.49.1292
Isoboldine beta-N-oxide	163184385	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC)[O-]	343.40	unknown	https://doi.org/10.1021/NP010258I
Norisoboldine	14539911	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)O	313.30	unknown	via CMAUP database
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine	442168	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC	355.40	unknown	https://doi.org/10.1021/NP010258I
(-)-Caryachine	13895183	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4	325.40	unknown	https://doi.org/10.1248/CPB.49.1292 https://doi.org/10.1021/NP010258I https://doi.org/10.1248/CPB.50.157
(+)-Caryachine	12305286	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O	325.40	unknown	https://doi.org/10.1248/CPB.49.1292 https://doi.org/10.1021/NP010258I https://doi.org/10.1248/CPB.50.157 https://doi.org/10.1248/YAKUSHI1947.86.3_177
(+)-Eschscholtzidine N-oxide	11024673	Click to see C[N+]1(C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)OC)OC)OCO4)[O-]	355.40	unknown	https://doi.org/10.1021/NP010258I
(1R,12R,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol	102304442	Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-]	341.40	unknown	https://doi.org/10.1021/NP010258I
(1R,12R,20S)-15,16-dimethoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaene	162822881	Click to see C[N+]1(C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)OC)OC)OCO4)[O-]	355.40	unknown	https://doi.org/10.1021/NP010258I
(1R,12R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol	10925883	Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-]	341.40	unknown	https://doi.org/10.1021/NP010258I
(1R,12R)-16-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol	3082467	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4	325.40	unknown	https://doi.org/10.1021/NP010258I https://doi.org/10.1248/CPB.49.1292 https://doi.org/10.1021/NP50071A020
(1R,12R)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol	101148425	Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC6=C(C=C25)OCO6)O)OCO4	339.30	unknown	via CMAUP database
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol	10948236	Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC(=C(C=C25)OC)OC)O)OCO4	355.40	unknown	https://doi.org/10.1021/NP010258I
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol	11110561	Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC6=C(C=C25)OCO6)O)OCO4	339.30	unknown	https://doi.org/10.1021/NP010258I
(1R,9R)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol	11869664	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O	327.40	unknown	via CMAUP database
(1S,12S,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol	102304441	Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-]	341.40	unknown	via CMAUP database
(1S,12S,20R)-16-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol	102304443	Click to see C[N+]1(C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4)[O-]	341.40	unknown	via CMAUP database
(1S,12S,20S)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol	102304444	Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-]	341.40	unknown	via CMAUP database
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol	11823545	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O	325.40	unknown	https://doi.org/10.1248/CPB.49.1292
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-14-ol	102317578	Click to see CN1C2CC3=C(C1CC4=CC5=C(C=C24)OCO5)C(=C(C=C3)OC)O	325.40	unknown	via CMAUP database
(1S,12S)-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene	11012304	Click to see C1C2C3=CC4=C(C=C3CC(N2)C5=CC6=C(C=C51)OCO6)OCO4	309.30	unknown	https://doi.org/10.1021/NP010258I
(1S,9S)-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaene-3,12-diol	92856799	Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O	327.40	unknown	https://doi.org/10.1248/CPB.49.1292
(1S,9S)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol	12300156	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O	327.40	unknown	https://doi.org/10.1248/CPB.49.1292
(1S)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol	44558921	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O	327.40	unknown	via CMAUP database
15-Methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol	85318036	Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-]	341.40	unknown	https://doi.org/10.1248/CPB.50.157
15-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-14-ol	14753611	Click to see CN1C2CC3=C(C1CC4=CC5=C(C=C24)OCO5)C(=C(C=C3)OC)O	325.40	unknown	https://doi.org/10.1021/NP010258I https://doi.org/10.1248/CPB.50.157 https://doi.org/10.1021/NP50071A020
15,16-Dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol	85341939	Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC(=C(C=C25)OC)OC)O)OCO4	355.40	unknown	https://doi.org/10.1021/NP010258I
23-Methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol	85402438	Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC6=C(C=C25)OCO6)O)OCO4	339.30	unknown	https://doi.org/10.1021/NP010258I
5,7,16,18-Tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene	19034001	Click to see C1C2C3=CC4=C(C=C3CC(N2)C5=CC6=C(C=C51)OCO6)OCO4	309.30	unknown	https://doi.org/10.1021/NP010258I
Argemonine	98569	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC	355.40	unknown	https://doi.org/10.1021/NP010258I
Benzo(5,6)cycloocta(1,2-f)-1,3-benzodioxol-5,11-imine, 5,6,11,12-tetrahydro-8,9-dimethoxy-14-methyl-, (5S)-	15559171	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)OC)OC)OCO4	339.40	unknown	https://doi.org/10.1021/NP010258I
Bisnorargemonine	288120	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O	327.40	unknown	https://doi.org/10.1248/CPB.49.1292
Californine	421259	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4	323.30	unknown	https://doi.org/10.1021/NP50092A007 https://doi.org/10.1248/YAKUSHI1947.86.4_296
Caryachine	44575219	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4	325.40	unknown	https://doi.org/10.1021/NP010258I https://doi.org/10.1248/CPB.49.1292 https://doi.org/10.1248/YAKUSHI1947.86.4_296 https://doi.org/10.1248/CPB.50.157 https://doi.org/10.1021/NP50071A020
Crychine	193382	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4	323.30	unknown	https://doi.org/10.1021/NP010258I https://doi.org/10.1111/J.2042-7158.1993.TB07093.X
Escholtzine	12304178	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4	323.30	unknown	https://doi.org/10.1021/NP010258I https://doi.org/10.1248/YAKUSHI1947.86.4_296 https://doi.org/10.1111/J.2042-7158.1993.TB07093.X
Eschscholtzidine	442222	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)OC)OC)OCO4	339.40	unknown	https://doi.org/10.1021/NP50092A007 https://doi.org/10.1248/CPB.50.157
Munitagine	12313000	Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O	327.40	unknown	https://doi.org/10.1248/CPB.49.1292
Munitagine, (-)-	288123	Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O	327.40	unknown	https://doi.org/10.1248/CPB.49.1292
> Alkaloids and derivatives / Proaporphines
(+)-8,9-Dihydrostepharine	13819281	Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC	299.40	unknown	https://doi.org/10.1021/NP010258I
(1'R,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol	101140029	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC	301.40	unknown	https://doi.org/10.1248/CPB.49.1292 https://doi.org/10.1248/CPB.50.157
(1'S,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol	10870351	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC	301.40	unknown	https://doi.org/10.1248/CPB.49.1292
(1'S,2S,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-ol	162945444	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)OC)OC	315.40	unknown	https://doi.org/10.1021/NP50092A007 https://doi.org/10.1021/NP010258I
(2R,4R)-10,11-dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one	13819282	Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC	299.40	unknown	https://doi.org/10.1021/NP010258I
(2R,4S)-10,11-dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one	163036016	Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC	299.40	unknown	https://doi.org/10.1021/NP010258I
10-Methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol	73804870	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC	301.40	unknown	https://doi.org/10.1248/CPB.49.1292
10,11-Dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-ol	12306121	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)OC)OC	315.40	unknown	https://doi.org/10.1021/NP50092A007 https://doi.org/10.1021/NP010258I
10,11-Dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one	12306125	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(=O)C=C4)OC)OC	313.40	unknown	https://doi.org/10.1021/NP010258I
10,11-Dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one	13819280	Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC	299.40	unknown	https://doi.org/10.1021/NP010258I
Isoamuronine	12306127	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(=O)C=C4)OC)OC	313.40	unknown	https://doi.org/10.1021/NP010258I
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine	2353	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC	336.40	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
8-iso PROSTAGLANDIN E2	158	Click to see CCCCCC(C=CC1C(CC(=O)C1CC=CCCCC(=O)O)O)O	352.50	unknown	https://doi.org/10.1248/CPB.49.1292 https://doi.org/10.1248/CPB.50.157 https://doi.org/10.1248/YAKUSHI1947.86.3_177
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-(3-Hydroxy-3,7,11,15-tetramethylhexadecyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione	24205	Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C	446.70	unknown	https://doi.org/10.1021/NP100014J
alpha-Tocopherolquinone	2734086	Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C	446.70	unknown	https://doi.org/10.1021/NP100014J
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	https://doi.org/10.1021/NP100014J
Super Squalene; trans-Squalene;AddaVax	1105	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	https://doi.org/10.1021/NP100014J
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterone	9801811	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Quinomethanes / O-quinomethanes
Infectocaryone	10379922	Click to see COC(=O)CC1CC=CC(=O)C1=C(C=CC2=CC=CC=C2)O	298.30	unknown	https://doi.org/10.1021/NP100014J
methyl 2-[(6Z)-6-[(E)-1-hydroxy-3-phenylprop-2-enylidene]-5-oxocyclohex-3-en-1-yl]acetate	21588497	Click to see COC(=O)CC1CC=CC(=O)C1=C(C=CC2=CC=CC=C2)O	298.30	unknown	https://doi.org/10.1021/NP100014J
> Organoheterocyclic compounds / Benzofurans
4-(1-hydroxy-3-phenylprop-2-enylidene)-3a,7a-dihydro-3H-1-benzofuran-2,5-dione	582990	Click to see C1C2C(C=CC(=O)C2=C(C=CC3=CC=CC=C3)O)OC1=O	282.29	unknown	https://doi.org/10.1002/CBDV.201000367
Cryptocaryone	10379026	Click to see C1C2C(C=CC(=O)C2=C(C=CC3=CC=CC=C3)O)OC1=O	282.29	unknown	https://doi.org/10.1002/CBDV.201000367
> Organoheterocyclic compounds / Isoquinolines and derivatives
(2R,6'S)-6',11-dihydroxy-10-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),4,6,8,10-pentaene-2,3'-cyclohexene]-3-one	162961396	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C24CCC(C=C4)O)O	297.30	unknown	https://doi.org/10.1021/NP010258I
(2S,6'R)-6',11-dihydroxy-10-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),4,6,8,10-pentaene-2,3'-cyclohexene]-3-one	162961394	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C24CCC(C=C4)O)O	297.30	unknown	https://doi.org/10.1021/NP010258I
(2S)-6',11-dihydroxy-10-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),4,6,8,10-pentaene-2,3'-cyclohexene]-3-one	10968491	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C24CCC(C=C4)O)O	297.30	unknown	via CMAUP database
6-Methyl-[1,3]dioxolo[4,5-g]isoquinolin-6-ium	2753983	Click to see C[N+]1=CC2=CC3=C(C=C2C=C1)OCO3	188.20	unknown	via CMAUP database
6',11-Dihydroxy-10-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),4,6,8,10-pentaene-2,3'-cyclohexene]-3-one	85349739	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C24CCC(C=C4)O)O	297.30	unknown	https://doi.org/10.1021/NP010258I
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
1,2,3,4-Tetrahydro-1-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methyl-6,7-(methylenedioxy)isoquinoline	101872780	Click to see CN1CCC2=CC3=C(C=C2C1CC4=CC(=C(C=C4)O)OC)OCO3	327.40	unknown	https://doi.org/10.1021/NP010258I
2-methoxy-4-[[(5S)-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]phenol	162955228	Click to see CN1CCC2=CC3=C(C=C2C1CC4=CC(=C(C=C4)O)OC)OCO3	327.40	unknown	https://doi.org/10.1021/NP010258I
4-(6,7-Dimethoxyisoquinoline-1-ylmethyl)phenol	21814573	Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC=C(C=C3)O)OC	295.30	unknown	https://doi.org/10.1248/CPB.50.157
Cinnamolaurine	22294346	Click to see CN1CCC2=CC3=C(C=C2C1CC4=CC=C(C=C4)O)OCO3	297.30	unknown	https://doi.org/10.1248/CPB.50.157
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Doryanin	12998814	Click to see CN1C=CC2=CC3=C(C=C2C1=O)OCO3	203.19	unknown	https://doi.org/10.1021/NP010258I
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
4-hydroxy-7-phenyl-3a,4,5,7,8,9b-hexahydro-1H-furo[3,2-f]chromene-2,9-dione	75244783	Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O	300.30	unknown	https://doi.org/10.1021/NP100014J
4-methoxy-7-phenyl-3a,4,5,7,8,9b-hexahydro-1H-furo[3,2-f]chromene-2,9-dione	75244784	Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4	314.30	unknown	https://doi.org/10.1021/NP100014J
7-O-Methylcryptochinone A	46939685	Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4	314.30	unknown	https://doi.org/10.1021/NP100014J
7-phenyl-3a,7,8,9b-tetrahydro-1H-furo[3,2-f]chromene-2,9-dione	85100737	Click to see C1C2C(C=CC3=C2C(=O)CC(O3)C4=CC=CC=C4)OC1=O	282.29	unknown	https://doi.org/10.1021/NP100014J
Cryptocaryanone A	10356404	Click to see C1C2C(C=CC3=C2C(=O)CC(O3)C4=CC=CC=C4)OC1=O	282.29	unknown	https://doi.org/10.1021/NP100014J
Cryptochinone A	46939683	Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O	300.30	unknown	https://doi.org/10.1021/NP100014J
Cryptochinone B	46939684	Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O	300.30	unknown	https://doi.org/10.1021/NP100014J
Cryptochinone D	46939686	Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4	314.30	unknown	https://doi.org/10.1021/NP100014J
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1'S,2R,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol	10914050	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC	315.40	unknown	https://doi.org/10.1021/NP010258I
10,11-Dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol	85313421	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC	315.40	unknown	https://doi.org/10.1021/NP010258I
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate	5318033	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	558.90	unknown	https://doi.org/10.1002/CBDV.201000367
Hexacosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	20980932	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	558.90	unknown	https://doi.org/10.1002/CBDV.201000367
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-5,7-dimethyl-2-phenyl-2,3-dihydrochromen-4-one	162937491	Click to see CC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)C	252.31	unknown	https://doi.org/10.1002/CBDV.201000367
(2S)-7-hydroxyflavanone	688857	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3	240.25	unknown	https://doi.org/10.1021/NP100014J
7-Hydroxyflavanone	1890	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3	240.25	unknown	https://doi.org/10.1021/NP100014J
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin	712318	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1002/CBDV.201000367
(+/-)-Taxifolin	471	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1002/CBDV.201000367
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl-	5748697	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O	298.29	unknown	https://doi.org/10.1021/NP100014J
5-Hydroxy-7-methoxy-2-phenylchroman-4-one	73201	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1021/NP100014J
5-Hydroxy-7-methoxyflavanone	4101463	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1021/NP100014J
Mosloflavone	471722	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC	298.29	unknown	https://doi.org/10.1021/NP100014J
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxyflavone	21632881	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=CC=C3)OC)OC	328.30	unknown	https://doi.org/10.1021/NP100014J
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxy-3-methoxyphenyl)-3-phenylprop-2-en-1-one	71407261	Click to see COC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O	270.28	unknown	https://doi.org/10.1021/NP100014J
Larrein	9993268	Click to see COC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O	270.28	unknown	https://doi.org/10.1021/NP100014J

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Cryptocarya chinensis

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