Camellia crassicolumna

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Internal ID	UUID64400f0286556149016582
Scientific name	Camellia crassicolumna
Authority	Hung T.Chang
First published in	Taxonomy of the genus Camellia : 113 (1981)

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Synonyms Top

Scientific name	Authority	First published in
Camellia atrothea	Chang, H.S.Wang & B.H.Chen	Tea Sci. Res. J. (China) 1983: 8 (1983)
Camellia crassicolumna var. shangbaensis	F.C.Zhang	Acta Bot. Yunnan. 19: 437 (1997)
Camellia crispula	Hung T.Chang	Taxonomy of the genus Camellia : 115 (1981)
Camellia haaniensis	Chang, H.S.Wang & B.H.Chen	Tea Sci. Res. J. (China) 1983: 5 (1983)
Camellia makuanica	Chang, Y.J.Tan & P.S.Wang	Tea Sci. Res. J. (China) 1983: 4 (1983)
Camellia purpurea	Chang, H.S.Wang & B.H.Chen	Tea Sci. Res. J. (China) 1983: 16 (1983)
Camellia rotundata	Chang, Y.J.Tan & P.S.Wang	Tea Sci. Res. J. (China) 1983: 6 (1983)
Camellia makuanica	Hung T.Chang & Tang	Acta Sci. Nat. Univ. Sunyatseni 1984(1): 6 (1984).
Camellia haaniensis	Hung T.Chang & Yu	Acta Sci. Nat. Univ. Sunyatseni 1984(1): 7 (1984).

Common names Top

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Language	Common/alternative name
Chinese	厚轴茶
Chinese	圆基茶
Chinese	皱叶茶
Chinese	老黑茶

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Camellia crassicolumna var. multiplex	(Chang & Tan) T.L.Ming	Acta Bot. Yunnan. 14: 121 (1992)

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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 click to expand
- China
  - China South-central

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000582301
Tropicos	31600449
KEW	urn:lsid:ipni.org:names:897214-1
The Plant List	kew-2694516
Open Tree Of Life	5264064
NCBI Taxonomy	1407748
IUCN Red List	61858758
IPNI	897214-1
GBIF	7313877
EOL	2905886

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)!
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Title

Authors

Publication

Released

IDs

Species delimitation of tea plants (Camellia sect. Thea) based on super-barcodes

Jiang Y, Yang J, Folk RA, Zhao J, Liu J, He Z, Peng H, Yang S, Xiang C, Yu X

BMC Plant Biol

11-Mar-2024

PMCID:	PMC10926627
doi:	10.1186/s12870-024-04882-3
PMID:	38468197

CsMYB184 regulates caffeine biosynthesis in tea plants

Li P, Ye Z, Fu J, Xu Y, Shen Y, Zhang Y, Tang D, Li P, Zuo H, Tong W, Wang S, Fernie AR, Zhao J

Plant Biotechnol J

06-Apr-2022

PMCID:	PMC9129078
doi:	10.1111/pbi.13814
PMID:	35332639

Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica

Chen J, Xu H, Zhang J, Dong S, Liu Q, Wang R

PeerJ

20-Oct-2021

PMCID:	PMC8541319
doi:	10.7717/peerj.12349
PMID:	34722001

Climate change‐induced migration patterns and extinction risks of Theaceae species in China

Zhang Y, Meng Q, Wang Y, Zhang X, Wang W

Ecol Evol

31-Mar-2020

PMCID:	PMC7246209
doi:	10.1002/ece3.6202
PMID:	32489602

Thirteen Camellia chloroplast genome sequences determined by high-throughput sequencing: genome structure and phylogenetic relationships

Huang H, Shi C, Liu Y, Mao SY, Gao LZ

BMC Evol Biol

07-Jul-2014

PMCID:	PMC4105164
doi:	10.1186/1471-2148-14-151
PMID:	25001059

Phenolic antioxidants from green tea produced from Camellia crassicolumna Var. multiplex.

Liu Q, Zhang YJ, Yang CR, Xu M

J Agric Food Chem

28-Jan-2009

doi:	10.1021/JF802974M
PMID:	19128040

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1021/JF802974M
> Benzenoids / Phenols / Methoxyphenols
3,4-Dimethoxyphenol	16251	Click to see COC1=C(C=C(C=C1)O)OC	154.16	unknown	https://doi.org/10.1021/JF802974M
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Putranjivadione	634915	Click to see CC1C(=O)CCC2C1(CC(=O)C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	440.70	unknown	https://doi.org/10.1021/JF802974M
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1021/JF802974M
4-Caffeoylquinic acid;4-O-Caffeoylquinic acid	58427569	Click to see C1C(C(C(CC1(C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O	354.31	unknown	https://doi.org/10.1021/JF802974M
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1021/JF802974M
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4,5-triol	3496897	Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O	342.34	unknown	https://doi.org/10.1021/JF802974M
Coniferin	5280372	Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O	342.34	unknown	https://doi.org/10.1021/JF802974M
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1021/JF802974M
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1021/JF802974M
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate	107905	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	https://doi.org/10.1021/JF802974M
[(2R,3S)-7-hydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate	162954411	Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	610.50	unknown	https://doi.org/10.1021/JF802974M
[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate	367141	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	https://doi.org/10.1021/JF802974M
[7-hydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate	3349592	Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	610.50	unknown	https://doi.org/10.1021/JF802974M
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate	1287	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	458.40	unknown	https://doi.org/10.1021/JF802974M
Epigallocatechin Gallate	65064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	458.40	unknown	https://doi.org/10.1021/JF802974M
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF802974M
Afzelin	5316673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JF802974M
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF802974M
kaempferol 3-O-beta-D-allopyranoside	12358430	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF802974M
Kaempferol-3-O-rhamnoside	5835713	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JF802974M
Myricetin 3-rhamnoside	5352000	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JF802974M
Myricitrin	5281673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JF802974M
Quercetin 3-O-rhamnoside	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF802974M
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF802974M
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1021/JF802974M
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1021/JF802974M
> Phenylpropanoids and polyketides / Tannins
[(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-4,5,6-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-3-yl] 3,4,5-trihydroxybenzoate	5321843	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)CO	788.60	unknown	https://doi.org/10.1021/JF802974M
[2-(Hydroxymethyl)-4,5,6-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-3-yl] 3,4,5-trihydroxybenzoate	5153916	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)CO	788.60	unknown	https://doi.org/10.1021/JF802974M
[3,5-Dihydroxy-2-(hydroxymethyl)-6-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate	85372017	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2O)OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O	484.40	unknown	https://doi.org/10.1021/JF802974M
galloyl(-3)Glc(b)-O-galloyl	11027295	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2O)OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O	484.40	unknown	https://doi.org/10.1021/JF802974M
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,4,5,11,12,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl) 3,4,5-trihydroxybenzoate	13917511	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1021/JF802974M
[(10R,11R,12S,13S,15R)-3,4,5,11,12,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxybenzoate	163060083	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1021/JF802974M

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Camellia crassicolumna

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top