Tabernaemontana catharinensis is a type of plant that belongs to the Apocynaceae family and is commonly found in the southern region of South America.

Synonyms Top

Scientific name	Authority	First published in
Peschiera acuminata	Miers	Apocyn. S. Amer. : 43 (1878)
Peschiera affinis	(Müll.Arg.) Miers	Apocyn. S. Amer. : 40 (1878)
Peschiera albidiflora	Miers	Apocyn. S. Amer. : 39 (1878)
Peschiera australis	(Müll.Arg.) Miers	Apocyn. S. Amer. : 46 (1878)
Peschiera australis var. hilariana	(Müll.Arg.) L.Allorge	Mém. Mus. Natl. Hist. Nat., B, Bot. 30: 148 (1985)
Peschiera catharinensis	(A.DC.) Miers	Apocyn. S. Amer. : 42 (1878)
Peschiera hilariana	(Müll.Arg.) Miers	Apocyn. S. Amer. : 41 (1878)
Tabernaemontana acuminata	Müll.Arg.	Linnaea 30: 406 (1860)
Tabernaemontana affinis	Müll.Arg.	Fl. Bras. 6(1): 83 (1860)
Tabernaemontana albiflora	Rojas Acosta	Cat. Hist. Nat. Corrientes : 71 (1897)
Tabernaemontana australis	Müll.Arg.	Fl. Bras. 6(1): 84 (1860)
Tabernaemontana hilariana	Müll.Arg.	Fl. Bras. 6(1): 85 (1860)
Tabernaemontana hybrida	Hand.-Mazz.	Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 79: 9, tab. 33, fig. 1. 1910 Advance separate Denkschr. Akad. Wissensch. Wien 79: 384, tab. 33, fig. 1, 1931
Tabernaemontana affinis var. lanceolata	Müll.Arg.	Fl. Bras. 6(1): 84 (1860)
Peschiera affinis var. acuminata	L.Allorge

Common names Top

Add a new one! Suggest a correction!

No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Southern America click to expand
- Brazil
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Southern South America
  - Argentina Northeast
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000319766
Tropicos	1800579
KEW	urn:lsid:ipni.org:names:82043-1
The Plant List	kew-200611
Open Tree Of Life	94844
NCBI Taxonomy	403124
IUCN Red List	58920120
IPNI	82043-1
iNaturalist	479950
GBIF	3618496
Freebase	/m/012cf32m
EPPO	TAECA
EOL	5327478
USDA GRIN	464349
Wikipedia	Tabernaemontana_catharinensis

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

Style head in Apocynaceae: a very complex secretory activity performed by one tissue

Maximo D, Demarco D

Eur J Histochem

02-Apr-2024

PMCID:	PMC11017725
doi:	10.4081/ejh.2024.4027
PMID:	38568208

Phytochemistry Profile, Antimicrobial and Antitumor Potential of the Methanolic Extract of Tabernaemontana catharinensis A DC and Eragrostis plana NEES

da Rosa E, Stopiglia CD, Machado MM, Filho AC, Soci UP, Mendez AS, Fernandes T, de Oliveira EM, Moreira CM

Evid Based Complement Alternat Med

03-Jan-2024

PMCID:	PMC10781527
doi:	10.1155/2024/5513141
PMID:	38213844

How Scarification, GA3 and Graphene Oxide Influence the In Vitro Establishment and Development of Strelitzia

Paiva PD, da Silva DP, da Silva BR, de Sousa IP, Paiva R, dos Reis MV

Plants (Basel)

29-May-2023

PMCID:	PMC10255328
doi:	10.3390/plants12112142
PMID:	37299121

Natural Products as Anticancer Agents: Current Status and Future Perspectives

Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q

Molecules

30-Nov-2022

PMCID:	PMC9737905
doi:	10.3390/molecules27238367
PMID:	36500466

Hydrolyzable Tannins in the Management of Th1, Th2 and Th17 Inflammatory-Related Diseases

Piazza S, Fumagalli M, Martinelli G, Pozzoli C, Maranta N, Angarano M, Sangiovanni E, Dell’Agli M

Molecules

05-Nov-2022

PMCID:	PMC9655852
doi:	10.3390/molecules27217593
PMID:	36364420

Virtual Screening of Alkaloid and Terpenoid Inhibitors of SMT Expressed in Naegleria sp.

Abraham J, Chauhan N, Ray S

Molecules

05-Sep-2022

PMCID:	PMC9457665
doi:	10.3390/molecules27175727
PMID:	36080504

Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review

Salazar-Gómez A, Alonso-Castro AJ

Pharmaceuticals (Basel)

31-Aug-2022

PMCID:	PMC9505834
doi:	10.3390/ph15091095
PMID:	36145316

Functional trade-offs in volume allocation to xylem cell types in 75 species from the Brazilian savanna Cerrado

Dória LC, Sonsin-Oliveira J, Rossi S, Marcati CR

Ann Bot

22-Jul-2022

PMCID:	PMC9486921
doi:	10.1093/aob/mcac095
PMID:	35863898

Plant-Derived Toxin Inhibitors as Potential Candidates to Complement Antivenom Treatment in Snakebite Envenomations

Adrião AA, dos Santos AO, de Lima EJ, Maciel JB, Paz WH, da Silva FM, Pucca MB, Moura-da-Silva AM, Monteiro WM, Sartim MA, Koolen HH

Front Immunol

09-May-2022

PMCID:	PMC9126284
doi:	10.3389/fimmu.2022.842576
PMID:	35615352

Flavonoids as Potential Anti-Inflammatory Molecules: A Review

Al-Khayri JM, Sahana GR, Nagella P, Joseph BV, Alessa FM, Al-Mssallem MQ

Molecules

02-May-2022

PMCID:	PMC9100260
doi:	10.3390/molecules27092901
PMID:	35566252

Research progress of Chinese herbal medicine compounds and their bioactivities: Fruitful 2020

Gu X, Hao D, Xiao P

Chin Herb Med

17-Mar-2022

PMCID:	PMC9476823
doi:	10.1016/j.chmed.2022.03.004
PMID:	36117669

An update of label-free protein target identification methods for natural active products

Cui Z, Li C, Chen P, Yang H

Theranostics

24-Jan-2022

PMCID:	PMC8825594
doi:	10.7150/thno.68804
PMID:	35198076

Secretory Patterns in Colleters of Apocynaceae

Ribeiro JC, Tölke ED, Demarco D

Plants (Basel)

15-Dec-2021

PMCID:	PMC8703501
doi:	10.3390/plants10122770
PMID:	34961240

Evaluation of Protection by Caffeic Acid, Chlorogenic Acid, Quercetin and Tannic Acid against the In Vitro Neurotoxicity and In Vivo Lethality of Crotalus durissus terrificus (South American Rattlesnake) Venom

Oliveira IC, Yoshida EH, Dini MM, Paschoal AB, Cogo JC, da Cruz-Höfling MA, Hyslop S, Oshima-Franco Y

Toxins (Basel)

13-Nov-2021

PMCID:	PMC8623703
doi:	10.3390/toxins13110801
PMID:	34822584

Analgesic effects of medicinal plants and phytochemicals on chemotherapy‐induced neuropathic pain through glial modulation

Lee JH, Kim N, Park S, Kim SK

Pharmacol Res Perspect

22-Oct-2021

PMCID:	PMC8532132
doi:	10.1002/prp2.819
PMID:	34676990

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 / Ajmaline-sarpagine alkaloids
(1R,10S,13E,16S)-13-ethylidene-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-trien-18-ol	118701737	Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=CC=CC=C65)C)C4O	308.40	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
> Alkaloids and derivatives / Ibogan-type alkaloids
(-)-20S-Heyneanine	432336	Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)88971-2 https://doi.org/10.1016/S0031-9422(00)80552-X
(-)-Voacangine	10361692	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC	368.50	unknown	https://doi.org/10.1021/JA01490A031 https://doi.org/10.5935/0103-5053.19960018
(1R,15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene	51055165	Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45	280.40	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3 https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y
(1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene	137628544	Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC	310.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y https://doi.org/10.1016/S0021-9673(98)00084-3
(1S)-1-[(1R,15R,17R,18R)-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-17-yl]ethanol	44566758	Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O	296.40	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
19-Epivoacristine	56842093	Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O	384.50	unknown	https://doi.org/10.5935/0103-5053.19960018
6,9-Methano-5H-pyrido[1',2':1,2]azepino[4,5-b]indole, 7-ethyl-6,6a,7,8,9,10,12,13-octahydro-, [6R-(6alpha,6abeta,7beta,9alpha)]-	500053	Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45	280.40	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3 https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y
CID 442136	442136	Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC	310.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y https://doi.org/10.1016/S0021-9673(98)00084-3
Conodurine	5387837	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC	704.90	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
Conodurine B640243K102	5477056	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC	704.90	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
Coronardine	278173	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC	338.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC90472/
Coronaridine	73489	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC	338.40	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC90472/ https://doi.org/10.1016/S0031-9422(00)80552-X https://doi.org/10.5935/0103-5053.19960018 https://doi.org/10.1016/S0021-9673(97)00723-1 https://doi.org/10.1016/S0031-9422(00)80552-X https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y https://www.ncbi.nlm.nih.gov/pmc/articles/PMC90472/ https://doi.org/10.3109/13880209309082955
Ibogamine-18-carboxylic acid, 12-methoxy-, methyl ester	363270	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC	368.50	unknown	https://doi.org/10.1016/S0021-9673(97)00723-1 https://doi.org/10.1016/S0021-9673(98)00084-3 https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y
Ibogamine-18-carboxylic acid, 13-methoxy-, methyl ester	99199	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC	368.50	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
Ibogamine-18-carboxylic acid, 19-hydroxy-12-methoxy-, methyl ester, (19R)-	157784	Click to see CCC1CC2CC3(C1N(C2O)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC	384.50	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
Iboxygaine	71656190	Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)O	326.40	unknown	https://doi.org/10.1590/1809-43921985152197
Isovoacangine	44393473	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC	368.50	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
methyl (12R,15E)-12-[(1R,15S,17S,18S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-6-yl]-15-ethylidene-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate	118701524	Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC	616.80	unknown	https://doi.org/10.3109/13880209309082955
methyl (15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	137628478	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC	338.40	unknown	https://doi.org/10.3109/13880209309082955 https://doi.org/10.5650/JOS1956.25.561 https://doi.org/10.1016/S0021-9673(98)00084-3 https://doi.org/10.1016/S0031-9422(00)80552-X https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y https://doi.org/10.1016/S0021-9673(97)00723-1 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC90472/ https://doi.org/10.1590/1809-43921985152197
Methyl (1R,15R)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8,16-pentaene-1-carboxylate	13993928	Click to see CCC1=CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC	336.40	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
methyl (1R,15S,17R,18R)-17-[(1S)-1-hydroxyethyl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	21598351	Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)88971-2
methyl (1R,15S,17R,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate	134688048	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC	368.50	unknown	https://doi.org/10.1016/S0021-9673(97)00723-1 https://doi.org/10.1016/S0021-9673(98)00084-3 https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y https://doi.org/10.1590/1809-43921985152197
methyl (1S,12R,14R,15Z,18R)-15-ethylidene-12-[(1R,15R,17S,18S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-5-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate	163186246	Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC	646.90	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
methyl (1S,15R,17R,18S)-17-[(1R)-1-hydroxyethyl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	162988186	Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O	354.40	unknown	https://doi.org/10.1590/1809-43921983132409
methyl (1S,15R,17R,18S)-17-[(1S)-1-hydroxyethyl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	102067253	Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
methyl (1S,15R,17R,18S)-17-ethyl-16-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	102428240	Click to see CCC1C(C2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O	354.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<60::AID-PCA446>3.0.CO;2-Y https://doi.org/10.1016/S0021-9673(97)00723-1 https://doi.org/10.1016/S0021-9673(98)00084-3
methyl (1S,15R,17R,18S)-17-ethyl-16-oxo-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	102121234	Click to see CCC1C2C3(CC(C1=O)CN2CCC4=C3NC5=CC=CC=C45)C(=O)OC	352.40	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
methyl (1S,15S,17S,18S)-17-ethyl-5-[(1S,12R,14S,15E)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate	134714950	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC	704.90	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
methyl (1S,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate	163188392	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC	368.50	unknown	https://doi.org/10.1021/JA01490A031 https://doi.org/10.5935/0103-5053.19960018
Methyl 15-ethylidene-12-(17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-5-yl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate	162925404	Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC	646.90	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
Methyl 17-ethyl-5-(15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl)-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate	431073	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC	704.90	unknown	https://doi.org/10.3109/13880209309082955 https://doi.org/10.1016/S0031-9422(00)80552-X
Voacristine	196982	Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O	384.50	unknown	https://doi.org/10.1590/1809-43921985152197
> Alkaloids and derivatives / Macroline alkaloids
[(1S,12S,13R,15E)-15-ethylidene-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methanol	163194567	Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO	308.40	unknown	https://doi.org/10.1590/1809-43921983132409
[(1S,14R,15Z)-15-ethylidene-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methanol	101286222	Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO	308.40	unknown	https://doi.org/10.1590/1809-43921985152197
> Alkaloids and derivatives / Plumeran-type alkaloids
Tabersonine	20485	Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC	336.40	unknown	https://doi.org/10.3109/13880209309082955 https://doi.org/10.5650/JOS1956.25.561
> Alkaloids and derivatives / Vobasan alkaloids
(14R,15Z)-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one	163195333	Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
(1S,14R,15Z,18R)-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one	101926661	Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
15-Ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one	5087853	Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
Affinine	5281345	Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
methyl (1S,14R,15Z,18S)-15-ethylidene-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate	101281359	Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C	352.40	unknown	https://doi.org/10.1590/1809-43921985152197
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate	162901456	Click to see CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4CC(=C3)C=O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC	521.60	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol	145706026	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
[(1R,3As,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate	12900948	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1590/S0100-40421998000600005
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
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/10.1016/S0021-9673(98)00084-3
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
Lupeol Acetate	92157	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0021-9673(98)00084-3
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
1,5-dimethyl-6H-pyrido[4,3-b]carbazole	5281407	Click to see CC1=C2C=CN=C(C2=CC3=C1NC4=CC=CC=C43)C	246.31	unknown	https://doi.org/10.1055/S-0028-1097929 https://doi.org/10.3109/13880209309082955
Olivacine	96364	Click to see CC1=C2C=CNC(=C2C=C3C1=NC4=CC=CC=C43)C	246.31	unknown	https://doi.org/10.3109/13880209309082955 https://doi.org/10.1055/S-0028-1097929 https://doi.org/10.1590/1809-43921985152197
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
methyl 2-[(3R,6'R,7'R,8'aR)-6'-ethyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]prop-2-enoate	162925311	Click to see CCC1CN2CCC3(C2CC1C(=C)C(=O)OC)C4=CC=CC=C4NC3=O	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X
> Organoheterocyclic compounds / Indolizidines
methyl 2-(6'-ethyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl)prop-2-enoate	14164958	Click to see CCC1CN2CCC3(C2CC1C(=C)C(=O)OC)C4=CC=CC=C4NC3=O	354.40	unknown	https://doi.org/10.3109/13880209309082955 https://doi.org/10.1016/S0031-9422(00)80552-X
> Organoheterocyclic compounds / Quinolizidines
methyl 9'-ethyl-3-oxospiro[1H-indole-2,6'-3-azatricyclo[5.3.1.03,8]undecane]-7'-carboxylate	163009889	Click to see CCC1CC2CC3(C1N(C2)CCC34C(=O)C5=CC=CC=C5N4)C(=O)OC	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)88971-2
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
salvianolic acid C	13991590	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C=C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)O)O	492.40	unknown	https://doi.org/10.1016/S0031-9422(00)80552-X

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Tabernaemontana catharinensis

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