Scientific name	Authority	First published in
Limacia amherstiana	Miers	Contr. Bot. 3: 112 (1871)
Limacia triandra	Miers	Ann. Mag. Nat. Hist. , ser. 2, 7: 43 (1851)
Limacia wallichiana	Miers	Contr. Bot. 3: 113 (1871)
Menispermum triandrum	Roxb.	Fl. Ind. ed. 1832 , 3: 816 (1832)
Tiliacora stipularis	Pierre ex Diels	Pflanzenr. , IV, 94: 65 (1910)
Cocculus triandrus	Colebr.	Trans. Linn. Soc. London 13: 64 (1821)

Common names Top

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Filter by language:

Language	Common/alternative name
Indonesian	cuwing
Korean	야낭
Thai	ย่านาง
Vietnamese	sương sâm
Chinese	香料藤
Chinese	雅囊葉
Chinese	蔘露藤

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-tropical click to expand
- Indian Subcontinent
  - Assam
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Malaya

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000456701
Tropicos	100362031
KEW	urn:lsid:ipni.org:names:581568-1
Open Tree Of Life	6130102
NCBI Taxonomy	527510
IPNI	581568-1
GBIF	3831076
Freebase	/m/07kty3
Wikipedia	Tiliacora_triandra
CMAUP	NPO941

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

Updating the Status quo on the Eco-Friendly Approach for Antioxidants Recovered from Plant Matrices Using Cloud Point Extraction

Travičić V, Cvanić T, Šovljanski O, Erceg T, Perović M, Stupar A, Ćetković G

Antioxidants (Basel)

25-Feb-2024

PMCID:	PMC10967642
doi:	10.3390/antiox13030280
PMID:	38539814

Natural products for the treatment of chemotherapy-related cognitive impairment and prospects of nose-to-brain drug delivery

He YQ, Zhou CC, Jiang SG, Lan WQ, Zhang F, Tao X, Chen WS

Front Pharmacol

29-Jan-2024

PMCID:	PMC10859466
doi:	10.3389/fphar.2024.1292807
PMID:	38348396

Ethnobotanical study of medicinal plants used by the people of Mosop, Nandi County in Kenya

Maiyo ZC, Njeru SN, Toroitich FJ, Indieka SA, Obonyo MA

Front Pharmacol

19-Jan-2024

PMCID:	PMC10834697
doi:	10.3389/fphar.2023.1328903
PMID:	38313073

The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer

Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J

Medicina (Kaunas)

14-Dec-2023

PMCID:	PMC10745032
doi:	10.3390/medicina59122169
PMID:	38138272

Isolation and identification of bioactive compounds from Antrodia camphorata against ESKAPE pathogens

Zhang YD, Liu LY, Wang D, Yuan XL, Zheng Y, Wang Y

PLoS One

27-Oct-2023

PMCID:	PMC10610075
doi:	10.1371/journal.pone.0293361
PMID:	37889913

New Insights into the Latest Advancement in α-Amylase Inhibitors of Plant Origin with Anti-Diabetic Effects

Kashtoh H, Baek KH

Plants (Basel)

14-Aug-2023

PMCID:	PMC10458243
doi:	10.3390/plants12162944
PMID:	37631156

Biologically Active Compounds from Probiotic Microorganisms and Plant Extracts Used as Biopreservatives

Teneva D, Denev P

Microorganisms

27-Jul-2023

PMCID:	PMC10458850
doi:	10.3390/microorganisms11081896
PMID:	37630457

Tiliacora triandra Leaf Powder Ethanolic Extract in Combination with Cisplatin or Gemcitabine Synergistically Inhibits the Growth of Cholangiocarcinoma Cells In Vitro and in Nude Mouse Xenograft Models

Samankul A, Senawong G, Utaiwat S, Prompipak J, Woranam K, Phaosiri C, Sripa B, Senawong T

Medicina (Kaunas)

07-Jul-2023

PMCID:	PMC10386122
doi:	10.3390/medicina59071269
PMID:	37512080

Polysaccharide-Based Hydrogel from Seeds of Artemisia vulgaris: Extraction Optimization by Box–Behnken Design, pH-Responsiveness, and Sustained Drug Release

Hussain MA, Ali A, Alsahli TG, Khan N, Sharif A, Haseeb MT, Alsaidan OA, Tayyab M, Bukhari SN

Gels

28-Jun-2023

PMCID:	PMC10379781
doi:	10.3390/gels9070525
PMID:	37504404

Antiviral and Immunomodulatory Activities of Clinacanthus nutans (Burm. f.) Lindau

Lin CM, Chen HH, Lung CW, Chen HJ

Int J Mol Sci

28-Jun-2023

PMCID:	PMC10342181
doi:	10.3390/ijms241310789
PMID:	37445964

Natural products targeting inflammation-related metabolic disorders: A comprehensive review

Nainu F, Frediansyah A, Mamada SS, Permana AD, Salampe M, Chandran D, Emran TB, Simal-Gandara J

Heliyon

02-Jun-2023

PMCID:	PMC10279840
doi:	10.1016/j.heliyon.2023.e16919
PMID:	37346355

Antioxidant properties and cytotoxic effects of selected edible plants in Southeast Asia for further use as phytogenic antioxidant additives

Pasri P, Mermillod P, Khempaka S

Saudi J Biol Sci

31-Mar-2023

PMCID:	PMC10123259
doi:	10.1016/j.sjbs.2023.103631
PMID:	37101816

Multi-drug resistant ESKAPE pathogens and the uses of plants as their antimicrobial agents

Idris FN, Nadzir MM

Arch Microbiol

14-Mar-2023

PMCID:	PMC10013289
doi:	10.1007/s00203-023-03455-6
PMID:	36917278

Effect of hot water, ultrasound, microwave, and pectinase-assisted extraction of anthocyanins from black goji berry for food application

Vidana Gamage GC, Choo WS

Heliyon

10-Mar-2023

PMCID:	PMC10024101
doi:	10.1016/j.heliyon.2023.e14426
PMID:	36942215

Medicinal Plants as Therapeutic Alternatives to Combat Mycobacterium tuberculosis: A Comprehensive Review

Gautam S, Qureshi KA, Jameel Pasha SB, Dhanasekaran S, Aspatwar A, Parkkila S, Alanazi S, Atiya A, Khan MM, Venugopal D

Antibiotics (Basel)

08-Mar-2023

PMCID:	PMC10044459
doi:	10.3390/antibiotics12030541
PMID:	36978408

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
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
(1S,2S,3S)-1,8-Dihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-2,3-dihydroa nthracene-2-carboperoxoic acid	146415	Click to see CC1C(C(C2=C(C1=O)C=C3C=CC=C(C3=C2)O)(CCC(C)C)O)C(=O)OO	372.40	unknown	https://doi.org/10.1002/ARDP.19863190912 https://doi.org/10.1071/CH9812001 https://doi.org/10.1002/ARDP.19863190207
> Lignans, neolignans and related compounds
(7S,8S,21S)-16,27-dimethoxy-7,22-dimethyl-7-oxido-29,31-dioxa-22-aza-7-azoniaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25,27,32-dodecaen-13-ol	163195497	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CC[N+]7(C)[O-])O4)O)OC	592.70	unknown	https://doi.org/10.1071/CH9812001
(8R,21R)-16,27-dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25,27,32-dodecaen-13-ol	124511658	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)O)C6=C(C=CC(=C6)CC7C8=C(O4)C(=C(C=C8CCN7C)OC)O3)OC	576.70	unknown	https://doi.org/10.1071/CH9812001 https://doi.org/10.1002/PTR.2650030514
(8R,21S)-13,27-dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25(33),26,28(32)-dodecaene-16,26-diol	162986615	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=C(CCN7C)C(=C(C(=C8O4)O3)OC)O)O	592.70	unknown	https://doi.org/10.1002/ARDP.19863191003
(8R,21S)-16,27-dimethoxy-22-methyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25(33),26,28(32)-dodecaene-13,26-diol	163083141	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4)OC)C5=C(C=CC(=C5)CC6C7=CC8=C(C=C7CCN6)OC(=C3O8)C(=C2O)OC)O	578.70	unknown	https://doi.org/10.1055/S-2006-962491
(8S,21R)-16,27-dimethoxy-22-methyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25,27,32-dodecaen-13-ol	162895441	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC	562.70	unknown	https://doi.org/10.1055/S-2006-962491
(8S,21R)-16,27-dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25,27,32-dodecaen-13-ol	14527218	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)O)C6=C(C=CC(=C6)CC7C8=C(O4)C(=C(C=C8CCN7C)OC)O3)OC	576.70	unknown	https://doi.org/10.1002/ARDP.19863190207 https://doi.org/10.1071/CH9812001 https://doi.org/10.1002/ARDP.19863190912
(8S,21S)-13,27-dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25(33),26,28(32)-dodecaene-16,26-diol	162986614	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=C(CCN7C)C(=C(C(=C8O4)O3)OC)O)O	592.70	unknown	https://doi.org/10.1002/ARDP.19863191003
(8S,21S)-16,27-dimethoxy-22-methyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25(33),26,28(32)-dodecaene-13,26-diol	163083140	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4)OC)C5=C(C=CC(=C5)CC6C7=CC8=C(C=C7CCN6)OC(=C3O8)C(=C2O)OC)O	578.70	unknown	https://doi.org/10.1055/S-2006-962491
(8S,21S)-16,27-dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25(33),26,28(32)-dodecaene-13,26-diol	162878517	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)O)C6=C(C=CC(=C6)CC7C8=C(CCN7C)C(=C(C(=C8O4)O3)OC)O)OC	592.70	unknown	https://doi.org/10.1002/ARDP.19863190912
(8S,21S)-16,27-dimethoxy-7,22-dimethyl-7-oxido-29,31-dioxa-22-aza-7-azoniaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25,27,32-dodecaen-13-ol	101428568	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CC[N+]7(C)[O-])O4)O)OC	592.70	unknown	https://doi.org/10.1071/CH9812001
(8S)-16,27-dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25,27,32-dodecaen-13-ol	101670430	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)O)C6=C(C=CC(=C6)CC7C8=C(O4)C(=C(C=C8CCN7C)OC)O3)OC	576.70	unknown	https://doi.org/10.1071/CH9812001 https://doi.org/10.1002/PTR.2650030514
13,27-Dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25,27,32-dodecaen-16-ol	78173028	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=C(O4)C(=C(C=C8CCN7C)OC)O3)O	576.70	unknown	https://doi.org/10.1002/ARDP.19863190912 https://doi.org/10.1002/ARDP.19863190207
13,27-Dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25(33),26,28(32)-dodecaene-16,26-diol	162986613	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=C(CCN7C)C(=C(C(=C8O4)O3)OC)O)O	592.70	unknown	https://doi.org/10.1002/ARDP.19863191003
13'-Bromo-tiliacorinine	57404336	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)C6=C(C(=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)Br)O)OC	655.60	unknown	via CMAUP database
2'-Nortiliacorinine	14527219	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC	562.70	unknown	https://doi.org/10.1071/CH9812001 https://doi.org/10.1002/ARDP.19863191003 https://doi.org/10.1002/ARDP.19863190207
Dinklacorine	181286	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=C(O4)C(=C(C=C8CCN7C)OC)O3)O	576.70	unknown	https://doi.org/10.1002/ARDP.19863191003 https://doi.org/10.1002/ARDP.19863190912
Isotiliarine	630659	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC	562.70	unknown	https://doi.org/10.1002/ARDP.19863190207 https://doi.org/10.1071/CH9812001 https://doi.org/10.1002/ARDP.19863191003
Tiliacorine	442369	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)O)C6=C(C=CC(=C6)CC7C8=C(O4)C(=C(C=C8CCN7C)OC)O3)OC	576.70	unknown	https://doi.org/10.1002/ARDP.19863190912 https://doi.org/10.1002/PTR.2650030514 https://doi.org/10.1002/ARDP.19863190207 https://doi.org/10.1071/CH9812001
Yanangcorinin	190390	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)C6=C(C=CC(=C6)CC7C8=C(O4)C(=C(C=C8CCN7C)OC)O3)O	576.70	unknown	https://doi.org/10.1002/ARDP.19863190912 https://doi.org/10.1002/ARDP.19863190207
Yanangin	184528	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)O)C6=C(C=CC(=C6)CC7C8=C(CCN7C)C(=C(C(=C8O4)O3)OC)O)OC	592.70	unknown	https://doi.org/10.1002/ARDP.19863190912
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aS,1bS,3R,4R,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1,1b,2,3,4,5,6,6a-octahydrocyclopropa[a]inden-4-ol	57394792	Click to see CC12CC3CC3(C1CC(C(C2)O)C(C)(C)O)C	238.37	unknown	via CMAUP database
(1aS,1bS,3R,4S,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1,1b,2,3,4,5,6,6a-octahydrocyclopropa[a]inden-4-ol	57396552	Click to see CC12CC3CC3(C1CC(C(C2)O)C(C)(C)O)C	238.37	unknown	via CMAUP database
(1aS,1bS,3S,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1b,2,3,5,6,6a-hexahydro-1H-cyclopropa[a]inden-4-one	57398335	Click to see CC12CC3CC3(C1CC(C(=O)C2)C(C)(C)O)C	236.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(2R,4aR,8aR)-8-(hydroxymethyl)-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	57391287	Click to see CC12CCC=C(C1CC(CC2)C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)CO	400.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	57396551	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	via CMAUP database
1-oxo-3beta,23-dihydroxyolean-12-en-28-oic acid 28-O-beta-D-glucopyranoside	52952751	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	648.80	unknown	via CMAUP database
3beta,22alpha-dihydroxyurs-12-en-28-oic acid 28-O-beta-D-glucopyranoside	52950912	Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)O	634.80	unknown	via CMAUP database
3beta,23-dihydroxyurs-12-en-28-oic acid 28-O-beta-D-glucopyranoside	52950911	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	634.80	unknown	via CMAUP database
Arjunglucoside II	52951052	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	650.80	unknown	via CMAUP database
hederagenin 28-O-beta-D-glucopyranosyl ester	21120798	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	634.80	unknown	via CMAUP database
quadranoside IV	10372074	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3S,4aS,6aS,6aR,6bR,8aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicene-1,3-diol	57391286	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C)C)C	442.70	unknown	via CMAUP database
1-Oxo-3beta-hydroxyolean-18-ene	52950910	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C)C)C	440.70	unknown	via CMAUP database
1-Oxo-3beta,23-dihydroxyolean-12-en-28-oic acid	11134679	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C	486.70	unknown	via CMAUP database
23-Hydroxyursolic Acid	14136881	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
3-Oxo-23-hydroxyurs-12-en-28-oic acid	14396856	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C2C1C)C)C(=O)O	470.70	unknown	via CMAUP database
3beta-Acetoxyolean-18-en-28-oic acid	21594125	Click to see CC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C(=O)O)(C)C)C	498.70	unknown	via CMAUP database
Arjunolic acid	73641	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	via CMAUP database
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
Esculentic acid	9898760	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Maslinic Acid	73659	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
Virgatic acid	14489125	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	470.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(1S,14S)-9,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.13,7.18,12.114,18.027,31.022,33]pentatriaconta-3(35),4,6,8,10,12(34),18,20,22(33),24,26,31-dodecaene-6,21-diol	163010937	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)C5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6)OC)O3)O)O)OC	594.70	unknown	https://doi.org/10.1055/S-2006-962534
Tiliageine	76315750	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)C5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)O)OC	608.70	unknown	https://doi.org/10.1055/S-2006-962534
Tilitriandrin	149348	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)C5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6)OC)O3)O)O)OC	594.70	unknown	https://doi.org/10.1055/S-2006-962534
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,para-diphenylether diarylheptanoids
Juglanin A	70697839	Click to see COC1=C2C=C(CCC(=O)CCCCC3=C(C(=C(O2)C=C3)OC)O)C=C1	356.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(5R)-1-(4-Hydroxyphenyl)-5-hydroxy-7-(3-methoxy-4-hydroxyphenyl)heptane-3-one	637003	Click to see COC1=C(C=CC(=C1)CCC(CC(=O)CCC2=CC=C(C=C2)O)O)O	344.40	unknown	via CMAUP database

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Tiliacora triandra

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