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Periploca calophylla

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64404b99c227c165780922
Scientific name Periploca calophylla
Authority (Wight) Falc.
First published in Proc. Linn. Soc. London 1: 115 (1841)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Streptocaulon calophyllum Wight Contr. Bot. India : 65 (1834)

Common names Top

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Language Common/alternative name
Chinese 乌骚风
Chinese 美叶杠柳
Chinese 青蛇藤
Chinese 黑骨头
Chinese 宽叶凤仙藤
Chinese 管人香
Chinese 铁夹藤
Chinese 鸡骨头

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Periploca calophylla var. calophylla
Periploca calophylla var. mucronata P.T.Li Acta Phytotax. Sin. 23: 467 (1985)

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-temperate
    • China
      • China South-central
      • China Southeast
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Myanmar
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001102782
Tropicos 2604001
KEW urn:lsid:ipni.org:names:100435-1
The Plant List tro-2604001
Open Tree Of Life 270066
NCBI Taxonomy 413293
IPNI 100435-1
GBIF 6022628
USDA GRIN 454139
CMAUP NPO10437

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
“A Review of Parquetina nigrescens (Afzel.) Bullock, A Plant for Traditional Medicine: Phytochemical and Pharmacological Properties” Adase E, Ankutse P, Kumadoh D, Archer MA, Kyene MO, Yeboah GN, Asamoah Agyare DO Evid Based Complement Alternat Med 16-Nov-2022
PMCID:PMC9683991
doi:10.1155/2022/6076707
PMID:36437836
RNA-dependent RNA polymerase (RdRp) natural antiviral inhibitors: a review Leite DR, Mantovani KM, Cordeiro SP, Maia FB, Betim FC, de Bona Sartor E, Montrucchio DP, de Fátima Gaspari Dias J, Miguel OG, Miguel MD Med Chem Res 29-Sep-2022
PMCID:PMC9520115
doi:10.1007/s00044-022-02963-2
PMID:36193545
Comparative morpho-anatomical standardization and chemical profiling of root drugs for distinction of fourteen species of family Apocynaceae Kumar P, Bhushan A, Gupta P, Gairola S Bot Stud 25-Apr-2022
PMCID:PMC9038984
doi:10.1186/s40529-022-00342-z
PMID:35467168
Periplocin and cardiac glycosides suppress the unfolded protein response Tokugawa M, Inoue Y, Ishiuchi K, Kujirai C, Matsuno M, Ri M, Itoh Y, Miyajima C, Morishita D, Ohoka N, Iida S, Mizukami H, Makino T, Hayashi H Sci Rep 04-May-2021
PMCID:PMC8097017
doi:10.1038/s41598-021-89074-x
PMID:33947921
Antiparasitic Efficacy of Herbal Extracts and Active Compound Against Gyrodactylus kobayashii in Carassius auratus Zhou S, Dong J, Liu Y, Yang Q, Xu N, Yang Y, Ai X Front Vet Sci 06-Apr-2021
PMCID:PMC8056006
doi:10.3389/fvets.2021.665072
PMID:33889606
Ethnomedicine study on traditional medicinal plants in the Wuliang Mountains of Jingdong, Yunnan, China Gao L, Wei N, Yang G, Zhang Z, Liu G, Cai C J Ethnobiol Ethnomed 19-Aug-2019
PMCID:PMC6699132
doi:10.1186/s13002-019-0316-1
PMID:31426826
Ethnomedicinal Uses of Plant Resources in the Machhapuchchhre Rural Municipality of Kaski District, Nepal Adhikari M, Thapa R, Kunwar RM, Devkota HP, Poudel P Medicines (Basel) 23-Jun-2019
PMCID:PMC6630641
doi:10.3390/medicines6020069
PMID:31234605
Prioritizing fodder species based on traditional knowledge: a case study of mithun (Bos frontalis) in Dulongjiang area, Yunnan Province, Southwest China Geng Y, Hu G, Ranjitkar S, Wang Y, Bu D, Pei S, Ou X, Lu Y, Ma X, Xu J J Ethnobiol Ethnomed 04-May-2017
PMCID:PMC5418811
doi:10.1186/s13002-017-0153-z
PMID:28472968
An Update on Oligosaccharides and Their Esters from Traditional Chinese Medicines: Chemical Structures and Biological Activities Chen XY, Wang RF, Liu B Evid Based Complement Alternat Med 15-Mar-2015
PMCID:PMC4377491
doi:10.1155/2015/512675
PMID:25861364
Triterpenoids of Periploca calophylla Om P. Srivastava, Anakshi Khare, Maheshwari P. Khare American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50028A003
A pregnane ester glycoside from Periploca calophylla Desh Deepak, Maheshwari P. Khare, Anakshi Khare Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83178-7
A pregnane ester diglycoside from periploca calophylla Desh Deepak, Maheshwari P. Khare, Anakshi Khare Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(85)80047-9

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1021/NP50028A003
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1021/NP50028A003
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
3-(3,5,14-trihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2H-furan-5-one 608378 Click to see 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
[(3S,8R,9S,10R,11S,12S,13S,14S,17S)-17-[(1S)-1-benzoyloxyethyl]-11,14-dihydroxy-3-[(2R,3S,4R,5S)-4-[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-3-methoxy-5-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-12-yl] benzoate 163030245 Click to see CC1COC(C(C1OC2CC(C(C(O2)C)O)OC)OC)OC3CCC4(C5C(CC=C4C3)C6(CCC(C6(C(C5O)OC(=O)C7=CC=CC=C7)C)C(C)OC(=O)C8=CC=CC=C8)O)C 863.00 unknown https://doi.org/10.1016/S0031-9422(00)83178-7
[(3S,8S,9R,10R,12R,13R,14R,17S)-8,14,17-trihydroxy-3-[(2S,4S,5S,6S)-5-[(2S,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-17-[(1S)-1-[(E)-3-phenylprop-2-enoyl]oxyethyl]-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] (E)-3-phenylprop-2-enoate 163189219 Click to see 931.10 unknown https://doi.org/10.1016/0031-9422(85)80047-9
[17-(1-Benzoyloxyethyl)-11,14-dihydroxy-3-[4-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-3-methoxy-5-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-12-yl] benzoate 163030244 Click to see CC1COC(C(C1OC2CC(C(C(O2)C)O)OC)OC)OC3CCC4(C5C(CC=C4C3)C6(CCC(C6(C(C5O)OC(=O)C7=CC=CC=C7)C)C(C)OC(=O)C8=CC=CC=C8)O)C 863.00 unknown https://doi.org/10.1016/S0031-9422(00)83178-7
[8,14,17-Trihydroxy-3-[5-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-17-[1-(3-phenylprop-2-enoyloxy)ethyl]-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] 3-phenylprop-2-enoate 163039806 Click to see 931.10 unknown https://doi.org/10.1016/0031-9422(85)80047-9
Locin 590475 Click to see 480.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Melilotoside 5280759 Click to see 326.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
O-Coumaric Acid 637540 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Morin 5281670 Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Trifolin 5282149 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 3,7-diglucoside 6325460 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown via CMAUP database
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database

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