Cleistanthus collinus

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Common Names

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Scientific Literature

Phytochemical Profile

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Details Top

Internal ID	UUID644030f75220a284395214
Scientific name	Cleistanthus collinus
Authority	(Roxb.) Benth. ex Hook.f.
First published in	Fl. Brit. India [J. D. Hooker] 5(14): 274. 1887 [Dec 1887]

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Synonyms Top

Scientific name	Authority	First published in
Lebidieropsis collina	(Roxb.) Müll.Arg.	Linnaea 32: 80 (1863)
Lebidieropsis orbiculata	(Roth) Müll.Arg.	Prodr. [A. P. de Candolle] 15(2): 509. 1866 (1866)
Lebidieropsis orbiculata var. lambertii	Müll.Arg.	Prodr. [A. P. de Candolle] 15(2): 510. 1866
Bridelia collina	(Roxb.) Hook. & Arn.	Bot. Beechey Voy. : 211 (1837)
Clutia collina	Roxb.	Pl. Coromandel 2: 37 (1802)
Emblica palasis	Buch.-Ham.	Trans. Linn. Soc. London 13: 507 (1822)
Amanoa collina	(Roxb.) Baill.	Étude Euphorb. : 582 (1858)
Andrachne cadishaco	Roxb. ex Wall.	Numer. List [Wallich] n. 7877. 1847
Andrachne orbiculata	Roth	Nov. Pl. Sp. : 364 (1821)

Common names Top

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Language	Common/alternative name
English	oduvan
Malayalam	ഒടുക്
Malayalam	ഒടുക്ക്
Chinese	大夜闭花木

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Subvarieties (abbr. subvar.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000875925
KEW	urn:lsid:ipni.org:names:341327-1
The Plant List	kew-42040
Open Tree Of Life	3908429
NCBI Taxonomy	1357584
IUCN Red List	34271
IPNI	341328-1
iNaturalist	190647
GBIF	4940432
EOL	1147912
USDA GRIN	10822
Wikipedia	Cleistanthus_collinus

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

Chemical profiling of bioactive compounds in the methanolic extract of wild leaf and callus of Vitex negundo using gas chromatography-mass spectrometry

Garg G, Bharadwaj A, Chaudhary S, Gupta V

World J Exp Med

20-Mar-2024

PMCID:	PMC10999060
doi:	10.5493/wjem.v14.i1.88064
PMID:	38590309

Bio-mordants: a review

Benli H

Environ Sci Pollut Res Int

23-Feb-2024

PMCID:	PMC10948525
doi:	10.1007/s11356-024-32174-8
PMID:	38396176

Bioactivities and Mechanisms of Action of Diphyllin and Its Derivatives: A Comprehensive Systematic Review

Hou W, Huang LJ, Huang H, Liu SL, Dai W, Li ZM, Zhang ZY, Xin SY, Wang JY, Zhang ZY, Ouyang X, Lan JX

Molecules

30-Nov-2023

PMCID:	PMC10707837
doi:	10.3390/molecules28237874
PMID:	38067601

ECDD-S16 targets vacuolar ATPase: A potential inhibitor compound for pyroptosis-induced inflammation

Ekchariyawat P, Saengfak R, Sanongkiet S, Charoenwongpaiboon T, Khongpraphan S, Mala S, Luangjindarat C, Munyoo B, Chabang N, Charoensutthivarakul S, Borwornpinyo S, Tuchinda P, Ponpuak M, Pudla M, Utaisincharoen P

PLoS One

27-Nov-2023

PMCID:	PMC10681236
doi:	10.1371/journal.pone.0292340
PMID:	38011122

Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity

Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A

Saudi J Biol Sci

26-Nov-2023

PMCID:	PMC10749906
doi:	10.1016/j.sjbs.2023.103877
PMID:	38148949

Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective

Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU

Can J Infect Dis Med Microbiol

28-Oct-2023

PMCID:	PMC10625492
doi:	10.1155/2023/1860084
PMID:	37927532

Silvicultural Practices in the Management of Diospyros melanoxylon (Tendu) Leaf Production: Options and Trade-offs

Date AA, Hiremath AJ, Joshi AA, Lele S

Econ Bot

11-Apr-2023

PMCID:	PMC10088608
doi:	10.1007/s12231-023-09572-z
PMID:	37359048

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Mosquito-Borne Diseases and Their Control Strategies: An Overview Focused on Green Synthesized Plant-Based Metallic Nanoparticles

Onen H, Luzala MM, Kigozi S, Sikumbili RM, Muanga CJ, Zola EN, Wendji SN, Buya AB, Balciunaitiene A, Viškelis J, Kaddumukasa MA, Memvanga PB

Insects

23-Feb-2023

PMCID:	PMC10059804
doi:	10.3390/insects14030221
PMID:	36975906

Activities against Lung Cancer of Biosynthesized Silver Nanoparticles: A Review

Mejía-Méndez JL, López-Mena ER, Sánchez-Arreola E

Biomedicines

28-Jan-2023

PMCID:	PMC9953519
doi:	10.3390/biomedicines11020389
PMID:	36830926

Functional silver nanoparticles synthesis from sustainable point of view: 2000 to 2023 ‒ A review on game changing materials

Hasan KM, Xiaoyi L, Shaoqin Z, Horváth PG, Bak M, Bejó L, Sipos G, Alpár T

Heliyon

10-Dec-2022

PMCID:	PMC9800342
doi:	10.1016/j.heliyon.2022.e12322
PMID:	36590481

Cleistanthins A and B Ameliorate Testosterone-Induced Benign Prostatic Hyperplasia in Castrated Rats by Regulating Apoptosis and Cell Differentiation

S C SK, R R, Nachiappa Ganesh R

Cureus

02-Dec-2022

PMCID:	PMC9805890
doi:	10.7759/cureus.32141
PMID:	36601166

Green Nano-Biotechnology: A New Sustainable Paradigm to Control Dengue Infection

Zohra T, Khalil AT, Saeed F, Latif B, Salman M, Ikram A, Ayaz M, Murthy HC

Bioinorg Chem Appl

08-Aug-2022

PMCID:	PMC9377959
doi:	10.1155/2022/3994340
PMID:	35979184

Rapid Preparative Isolation of Cleistanthin A from the Leaves of Cleistanthus Collinus Using Reverse-Phase Flash Chromatography

Kumar SC, Raveendran R, Achari KM

J Pharm Bioallied Sci

18-Jul-2022

PMCID:	PMC9416109
doi:	10.4103/jpbs.jpbs_723_21
PMID:	36034488

Effects of Cleistanthus collinus on the reproductive system of male Wistar rats

Umamaheswari S, Girish C, Basu D

JBRA Assist Reprod

01-Jul-2022

PMCID:	PMC9355444
doi:	10.5935/1518-0557.20210114
PMID:	35234024

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
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
(3S)-9-(1,3-benzodioxol-5-yl)-4-hydroxy-3,6,7-trimethoxy-3H-benzo[f][2]benzofuran-1-one	154496353	Click to see COC1C2=C(C3=CC(=C(C=C3C(=C2C(=O)O1)C4=CC5=C(C=C4)OCO5)OC)OC)O	410.40	unknown	https://doi.org/10.1248/CPB.51.1299
Cleistanone(rac)	10409277	Click to see COC1C2=C(C3=CC(=C(C=C3C(=C2C(=O)O1)C4=CC5=C(C=C4)OCO5)OC)OC)O	410.40	unknown	https://doi.org/10.1248/CPB.51.1299
Diphyllin	100492	Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2O)COC3=O)C4=CC5=C(C=C4)OCO5)OC	380.30	unknown	https://doi.org/10.1016/S0021-9673(01)96081-9 https://doi.org/10.1016/0379-0738(92)90170-2 https://doi.org/10.1016/0040-4020(69)80025-6 https://doi.org/10.1093/JAT/8.4.182 https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1248/CPB.51.1299
Taiwanin C	363127	Click to see C1C2=C(C(=C3C=C4C(=CC3=C2)OCO4)C5=CC6=C(C=C5)OCO6)C(=O)O1	348.30	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
Taiwanin E	493164	Click to see C1C2=C(C3=CC4=C(C=C3C(=C2C(=O)O1)C5=CC6=C(C=C5)OCO6)OCO4)O	364.30	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Dihydrocubebin	193042	Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO	358.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Paulownin	3321512	Click to see C1C2C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6	370.40	unknown	https://doi.org/10.1016/0040-4020(69)80025-6 https://doi.org/10.1016/S0040-4020(01)98893-3
(3aS,6aS)-3,6-bis(1,3-benzodioxol-5-yl)-1,3,4,6-tetrahydrofuro[3,4-c]furan-3a,6a-diol	138112870	Click to see C1C2(C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6)O	386.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
(3S,3aS,4S,6S,6aR)-3,6-bis(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-4-ol	21722917	Click to see C1C2C(C(O1)C3=CC4=C(C=C3)OCO4)C(OC2C5=CC6=C(C=C5)OCO6)O	370.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
3,6-Bis(1,3-benzodioxol-5-yl)-1,3,4,6-tetrahydrofuro[3,4-c]furan-3a,6a-diol	15143182	Click to see C1C2(C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6)O	386.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
3,6-Bis(2H-1,3-benzodioxol-5-yl)tetrahydro-1H,3H-furo[3,4-c]furan-1-ol	14032964	Click to see C1C2C(C(O1)C3=CC4=C(C=C3)OCO4)C(OC2C5=CC6=C(C=C5)OCO6)O	370.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
4-Hydroxysesamin	53321864	Click to see C1C2C(C(O1)C3=CC4=C(C=C3)OCO4)C(OC2C5=CC6=C(C=C5)OCO6)O	370.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
Episesamin	5204	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
Paulownin	3084131	Click to see C1C2C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6	370.40	unknown	https://doi.org/10.1016/0040-4020(69)80025-6 https://doi.org/10.1016/S0040-4020(01)98893-3
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
Wodeshiol	10927155	Click to see C1C2(C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6)O	386.40	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
> Lignans, neolignans and related compounds / Lignan glycosides
9-(1,3-benzodioxol-5-yl)-4-[(2R,3R,4R,5R)-3-hydroxy-4,5-dimethoxyoxan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one	9915257	Click to see COC1COC(C(C1OC)O)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6	540.50	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1248/CPB.51.1299
9-(1,3-benzodioxol-5-yl)-4-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one	102533446	Click to see COC1C(C(OC(C1O)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6)CO)O	556.50	unknown	https://doi.org/10.1248/CPB.51.1299
9-(1,3-benzodioxol-5-yl)-4-[(3R,4R,5R)-3-hydroxy-4,5-dimethoxy-tetrahydropyran-2-yl]oxy-6,7-dimethoxy-3H-benzo[f]isobenzofuran-1-one	442833	Click to see COC1COC(C(C1OC)O)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6	540.50	unknown	https://doi.org/10.1248/CPB.51.1299 https://doi.org/10.1016/S0021-9673(01)96081-9 https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1093/JAT/8.4.182 https://doi.org/10.1016/0379-0738(92)90170-2
9-(1,3-benzodioxol-5-yl)-4-[3,4-dihydroxy-5-(5-hydroxy-3,4-dimethoxyoxan-2-yl)oxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one	163055067	Click to see COC1C(COC(C1OC)OC2C(OC(C(C2O)O)OC3=C4COC(=O)C4=C(C5=CC(=C(C=C53)OC)OC)C6=CC7=C(C=C6)OCO7)CO)O	702.70	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1248/CPB.51.1299
9-(1,3-benzodioxol-5-yl)-4-[3,4-dimethoxy-5-(methoxymethyl)oxolan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one	163086021	Click to see COCC1C(C(C(O1)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6)OC)OC	554.50	unknown	https://doi.org/10.1248/CPB.51.1299 https://doi.org/10.1016/S0040-4020(01)98893-3
9-(1,3-benzodioxol-5-yl)-4-[3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one	162963990	Click to see COC1C(C(OC(C1O)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6)CO)O	556.50	unknown	https://doi.org/10.1248/CPB.51.1299
9-(1,3-benzodioxol-5-yl)-5-(3-hydroxy-4,5-dimethoxyoxan-2-yl)oxy-6H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one	162851727	Click to see COC1COC(C(C1OC)O)OC2=C3COC(=O)C3=C(C4=CC5=C(C=C42)OCO5)C6=CC7=C(C=C6)OCO7	524.50	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
9-(1,3-benzodioxol-5-yl)-5-[(2R,3R,4R,5R)-3-hydroxy-4,5-dimethoxyoxan-2-yl]oxy-6H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one	162851728	Click to see COC1COC(C(C1OC)O)OC2=C3COC(=O)C3=C(C4=CC5=C(C=C42)OCO5)C6=CC7=C(C=C6)OCO7	524.50	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
Cleistanthin	4485134	Click to see COC1COC(C(C1OC)O)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6	540.50	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1248/CPB.51.1299
Cleistanthin A	44563408	Click to see COC1COC(C(C1OC)O)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6	540.50	unknown	https://doi.org/10.1016/0379-0738(92)90170-2 https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1016/S0021-9673(01)96081-9 https://doi.org/10.1248/CPB.51.1299 https://doi.org/10.1093/JAT/8.4.182
Cleistanthin B	119458	Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(C(C(O4)CO)O)O)O)COC3=O)C5=CC6=C(C=C5)OCO6)OC	542.50	unknown	https://doi.org/10.1093/JAT/8.4.182 https://doi.org/10.1016/S0021-9673(01)96081-9 https://doi.org/10.1016/0379-0738(92)90170-2
Cleistanthin C	86583367	Click to see COC1C(COC(C1OC)OC2C(OC(C(C2O)O)OC3=C4COC(=O)C4=C(C5=CC(=C(C=C53)OC)OC)C6=CC7=C(C=C6)OCO7)CO)O	702.70	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1248/CPB.51.1299
Cleistanthin D	86583368	Click to see COCC1C(C(C(O1)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6)OC)OC	554.50	unknown	https://doi.org/10.1248/CPB.51.1299 https://doi.org/10.1016/0040-4020(69)80025-6 https://doi.org/10.1016/S0040-4020(01)98893-3
> Lignans, neolignans and related compounds / Lignan lactones
(8aR)-5-(1,3-benzodioxol-5-yl)-8a,9-dihydro-8H-[2]benzofuro[6,5-f][1,3]benzodioxol-6-one	92161701	Click to see C1C2COC(=O)C2=C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6	350.30	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
(9aR)-4-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-9,9a-dihydro-1H-benzo[f][2]benzofuran-3-one	167687	Click to see COC1=C(C=C2C(=C1)CC3COC(=O)C3=C2C4=CC5=C(C=C4)OCO5)OC	366.40	unknown	https://doi.org/10.1016/0379-0738(92)90170-2 https://doi.org/10.1016/S0021-9673(01)96081-9
5-(1,3-Benzodioxol-5-yl)-8a,9-dihydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(8h)-one	270045	Click to see C1C2COC(=O)C2=C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6	350.30	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
Collinusin	11760310	Click to see COC1=C(C=C2C(=C1)CC3COC(=O)C3=C2C4=CC5=C(C=C4)OCO5)OC	366.40	unknown	https://doi.org/10.1016/S0021-9673(01)96081-9 https://doi.org/10.1016/0379-0738(92)90170-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	https://doi.org/10.1016/0040-4020(69)80025-6
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1016/0040-4020(69)80025-6
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	https://doi.org/10.1016/0040-4020(69)80025-6
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1016/0040-4020(69)80025-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1016/0040-4020(69)80025-6
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3 https://doi.org/10.1016/0040-4020(69)80025-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Cleistanone	54762610	Click to see CC1(CCC(=C)C12CCC3(C(C2)CCC4C3(CC(C5C4(CCC(=O)C5(C)C)C)O)C)C)C	440.70	unknown	https://doi.org/10.1248/CPB.51.1299
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
9-(1,3-benzodioxol-5-yl)-4-[5-[5-[3,4-dimethoxy-5-(methoxymethyl)oxolan-2-yl]oxy-3,4-dimethoxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one	163036098	Click to see COCC1C(C(C(O1)OC2COC(C(C2OC)OC)OC3C(OC(C(C3O)O)OC4=C5COC(=O)C5=C(C6=CC(=C(C=C64)OC)OC)C7=CC8=C(C=C7)OCO8)CO)OC)OC	876.80	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
cleistanthin E	86583369	Click to see COCC1C(C(C(O1)OC2COC(C(C2OC)OC)OC3C(OC(C(C3O)O)OC4=C5COC(=O)C5=C(C6=CC(=C(C=C64)OC)OC)C7=CC8=C(C=C7)OCO8)CO)OC)OC	876.80	unknown	https://doi.org/10.1016/S0040-4020(01)98893-3
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
(R)-dyphylline	688353	Click to see CN1C2=C(C(=O)N(C1=O)C)N(C=N2)CC(CO)O	254.24	unknown	https://doi.org/10.1248/CPB.51.1299

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Cleistanthus collinus

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