Justicia adhatoda

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff36ca011d889570959
Scientific name	Justicia adhatoda
Authority	L.
First published in	Sp. Pl. : 15 (1753)

Description Top

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Justicia adhatoda, also known as Malabar nut or adulsa, is a shrub native to Asia. Its range includes Afghanistan, the Indian subcontinent, Laos, Myanmar, and Vietnam, and it has been introduced to other regions. The plant has lance-shaped leaves that are bitter-tasting and contain phytochemicals such as alkaloids, tannins, saponins, phenolics, and flavonoids. One of the most important compounds found in the leaves is vasicine, a quinazoline alkaloid. The plant's bark is yellowish in color and its flowers are usually white. Justicia adhatoda has been used for its medicinal properties, and a compound derived from it, bromhexine, is available as a mucolytic medication in Europe.

Synonyms Top

Scientific name	Authority	First published in
Adeloda serrata	Raf.	Fl. Tellur. 4: 61 (1838)
Adhatoda adhatoda	Huth	Helios xi. 132 (1893).
Adatoda arborea	Raf.	Fl. Tellur. 4: 61. 1838 [1836 publ. mid-1838]
Adhatoda pubescens	Moench	Methodus : 431 (1794)
Adhatoda vasica	Nees	Pl. Asiat. Rar. 3: 103 (1832)
Dianthera latifolia	Salisb.	Prodr. Stirp. Chap. Allerton : 103 (1796)
Ecbolium adhatoda	Kuntze	Revis. Gen. Pl. 2: 487 (1891)
Ecbolium latifolium	Kuntze	Revis. Gen. Pl. 2: 980. 1891 [5 Nov 1891]
Gendarussa adhadota	Steud.	Nomencl. Bot. , ed. 2, 1: 668 (1840)
Adhatoda zeylanica	Medik.	Hist. & Commentat. Acad. Elect. Sci. Theod.-Palat. 6: 393 (1790)

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	جوز الكالابار
Arabic	جوز مالابار
Arabic	جوز الكلابار
Assamese	বগা বাহক
Bengali	বাসক
Estonian	vasika justiitsia
Persian	جاستیکا ادهاتدا
Finnish	valkopantterinkita
Gujarati	અરડૂસી
Hebrew	יוסטיציה אדטודה
Hindi	वसाका
ht	adotada
Kannada	ಆಡು ಸೋಗೆ
Malayalam	ആടലോടകം
Marathi	अडुळसा
Burmese	မုရားကြီး
Nepali	असुरो
Punjab	بیکڑ
Sinhala	වං ඇපල
Tamil	ஆடாதோடை
Tamil	ஆடாதொடை
Telugu	అడ్డసరం
Thai	เสนียด
Urdu	وہیکڑ
Vietnamese	xuân tiết
Chinese	鸭嘴花
Chinese	鸭i;紫花
Chinese	大驳骨

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

Africa click to expand
- Northeast Tropical Africa
  - Ethiopia
- Western Indian Ocean
  - Madagascar

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Western Asia
  - Afghanistan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Laos
  - Myanmar
  - Vietnam

Europe click to expand
- Southeastern Europe
  - Sicilia

Southern America click to expand
- Caribbean
  - Cuba
  - Jamaica

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000354128
UNII	9GL9VCO10F
USDA Plants	JUAD
Tropicos	101537
INPN	629968
Flora of Italy	5072
KEW	urn:lsid:ipni.org:names:50237-1
The Plant List	kew-2330223
Open Tree Of Life	410668
Observations.org	119107
NCBI Taxonomy	141317
IUCN Red List	169274250
IPNI	50237-1
iNaturalist	431176
GBIF	3173105
Freebase	/m/02q1hxw
EPPO	IUIAD
EOL	596715
Elurikkus	370054
USDA GRIN	20895
Wikipedia	Justicia_adhatoda
CMAUP	NPO14686

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

Pharmacogenomics of Drugs Used in β-Thalassemia and Sickle-Cell Disease: From Basic Research to Clinical Applications

Gambari R, Waziri AD, Goonasekera H, Peprah E

Int J Mol Sci

12-Apr-2024

PMCID:	PMC11050010
doi:	10.3390/ijms25084263
PMID:	38673849

A Systematic Analysis of COVID-19 Clinical Trials Registered in the Clinical Trials Registry of India

Dutta S, Singhal S, Shah R

Cureus

09-Apr-2024

PMCID:	PMC11082480
doi:	10.7759/cureus.57939
PMID:	38738059

Unraveling the role of HIF-1α in sepsis: from pathophysiology to potential therapeutics—a narrative review

Ruan H, Zhang Q, Zhang YP, Li SS, Ran X

Crit Care

27-Mar-2024

PMCID:	PMC10976824
doi:	10.1186/s13054-024-04885-4
PMID:	38539163

Impact of Heavy Metal Pollution in the Environment on the Metabolic Profile of Medicinal Plants and Their Therapeutic Potential

Asiminicesei DM, Fertu DI, Gavrilescu M

Plants (Basel)

21-Mar-2024

PMCID:	PMC10976221
doi:	10.3390/plants13060913
PMID:	38592933

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

Safety and efficacy of COROPROTECT kit as an add-on therapy in the management of mild-to-moderate COVID-19: A randomized, placebo-controlled trial

Savaliya C, Pandya S, Thumar K, Nagore D

Ayu

21-Feb-2024

PMCID:	PMC10946664
doi:	10.4103/ayu.ayu_92_22
PMID:	38505111

An appraisal of traditional knowledge of plant poisoning of livestock and its validation through acute toxicity assay in rats

Rasool F, Nizamani ZA, Ahmad KS, Parveen F, Khan SA, Sabir N

Front Pharmacol

14-Feb-2024

PMCID:	PMC10900104
doi:	10.3389/fphar.2024.1328133
PMID:	38420196

Beneficial Effects of Natural Alkaloids from Berberis glaucocarpa as Antidiabetic Agents: An In Vitro, In Silico, and In Vivo Approach

Alamzeb M, Shah SW, Hussain H, Zahoor M, Ahmad S, Mughal EU, Ahmad S, Ullah I, Khan S, Ullah A, Ghias M, Ullah R, Ali EA

ACS Omega

12-Feb-2024

PMCID:	PMC10905588
doi:	10.1021/acsomega.3c10232
PMID:	38434828

Exploring the pharmacological and chemical aspects of pyrrolo-quinazoline derivatives in Adhatoda vasica

Khandelwal P, Wadhwani BD, Rao RS, Mali D, Vyas P, Kumar T, Nair R

Heliyon

08-Feb-2024

PMCID:	PMC10877266
doi:	10.1016/j.heliyon.2024.e25727
PMID:	38379997

Dynamic Adsorption of a Cationic Dye onto Wool Fibers as Column-Filling Media: Response Surface Optimization and Fixed-Bed Adsorption Modeling

Condurache BC, Cojocaru C, Bargan A, Samoila P, Harabagiu V

Materials (Basel)

06-Feb-2024

PMCID:	PMC10890706
doi:	10.3390/ma17040790
PMID:	38399041

Silica/Annona muricata nano-hybrid: Synthesis and anticancer activity against breast cancer

Perinbarajan GK, Sinclair BJ, Mossa AT, Ohja N, Jeelani PG

Heliyon

24-Jan-2024

PMCID:	PMC10844132
doi:	10.1016/j.heliyon.2024.e25048
PMID:	38322972

Blood proteins self-assembly, staphylococcal enterotoxins-interaction, antibacterial synergistic activities of biogenic carbon/FeSO4/Cu/CuO nanocomposites modified with three antibiotics

Alavi M, Karimi N

BMC Chem

23-Jan-2024

PMCID:	PMC10804493
doi:	10.1186/s13065-024-01115-4
PMID:	38263198

Phytochemical screening, antioxidant activity of selected methanolic plant extracts and their detoxification capabilities against AFB1 toxicity

Kongolo Kalemba MR, Makhuvele R, Njobeh PB

Heliyon

11-Jan-2024

PMCID:	PMC10835242
doi:	10.1016/j.heliyon.2024.e24435
PMID:	38312698

Thespesia lampas mediated green synthesis of silver and gold nanoparticles for enhanced biological applications

Nath S, Shyanti RK, Singh RP, Mishra M, Pathak B

Front Microbiol

05-Jan-2024

PMCID:	PMC10832436
doi:	10.3389/fmicb.2023.1324111
PMID:	38304863

Investigating the phenology and interactions of competitive plant species co-occurring with invasive Lantana camara in Indian Himalayan Region

Kumar A, Singh S, Kumar D, Singh RK, Gupta AK, Premkumar K, Chand HB, Kewat AK

Sci Rep

03-Jan-2024

PMCID:	PMC10764828
doi:	10.1038/s41598-023-50287-x
PMID:	38172161

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 / Aniline and substituted anilines
(3R)-1-[(2-aminophenyl)methyl]-3-hydroxypyrrolidin-2-one	92470596	Click to see C1CN(C(=O)C1O)CC2=CC=CC=C2N	206.24	unknown	https://doi.org/10.1055/S-2007-969891 https://doi.org/10.1055/S-2007-971226 https://doi.org/10.1021/NP50109A012
(3S)-1-[(2-aminophenyl)methyl]-3-hydroxypyrrolidin-2-one	642668	Click to see C1CN(C(=O)C1O)CC2=CC=CC=C2N	206.24	unknown	https://doi.org/10.1016/0031-9422(81)85115-1
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines
Ambroxol	2132	Click to see C1CC(CCC1NCC2=C(C(=CC(=C2)Br)Br)N)O	378.10	unknown	https://doi.org/10.1016/0378-8741(95)01331-8
Bromhexine	2442	Click to see CN(CC1=C(C(=CC(=C1)Br)Br)N)C2CCCCC2	376.13	unknown	https://doi.org/10.1016/0378-8741(95)01331-8
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	https://doi.org/10.1016/0031-9422(91)80114-G
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(37R)-37-hydroxyhentetracontan-19-one	162848691	Click to see CCCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCCCCC(CCCC)O	607.10	unknown	https://doi.org/10.1016/0031-9422(91)80114-G
(37S)-37-hydroxyhexatetracont-1-en-15-one	163006727	Click to see CCCCCCCCCC(CCCCCCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCC=C)O	675.20	unknown	https://doi.org/10.1016/0031-9422(91)80114-G
37-Hydroxyhentetracontan-19-one	85626343	Click to see CCCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCCCCC(CCCC)O	607.10	unknown	https://doi.org/10.1016/0031-9422(91)80114-G
37-Hydroxyhexatetracont-1-en-15-one	15714517	Click to see CCCCCCCCCC(CCCCCCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCC=C)O	675.20	unknown	https://doi.org/10.1016/0031-9422(91)80114-G
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aR,6aR,6aS,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol	137705053	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	https://doi.org/10.1007/BF00366025
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)83845-5
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)83845-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Diapid	53477739	Click to see C1CC(N(C1)C(=O)C2CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2)CC(=O)N)CCC(=O)N)CC3=CC=CC=C3)CC4=CC=C(C=C4)O)N)C(=O)NC(CCCCN)C(=O)NCC(=O)N	1056.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Eleutheroside C	9859136	Click to see CCOC1C(C(C(C(O1)CO)O)O)O	208.21	unknown	https://doi.org/10.1016/S0031-9422(00)83845-5
Ethyl glucoside	428040	Click to see CCOC1C(C(C(C(O1)CO)O)O)O	208.21	unknown	https://doi.org/10.1016/S0031-9422(00)83845-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Androsin	164648	Click to see CC(=O)C1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC	328.31	unknown	https://doi.org/10.1055/S-2006-959787
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal	3037556	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)83845-5
L-Galactose	24749	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)83845-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetosyringone	17198	Click to see CC(=O)C1=CC(=C(C(=C1)OC)O)OC	196.20	unknown	https://doi.org/10.1055/S-2006-959787
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
(3R)-3-[2-(dimethylamino)phenyl]-3-hydroxy-1,2-dihydropyrrolo[2,1-b]quinazolin-9-one	101995827	Click to see CN(C)C1=CC=CC=C1C2(CCN3C2=NC4=CC=CC=C4C3=O)O	321.40	unknown	https://doi.org/10.1016/0031-9422(96)00120-3
(3R)-3-hydroxy-5-methoxy-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-9-one	92470595	Click to see COC1=CC=CC2=C1N=C3C(CCN3C2=O)O	232.23	unknown	https://doi.org/10.1016/0031-9422(96)00120-3
(3R)-3-hydroxy-7-methoxy-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-9-one	101995828	Click to see COC1=CC2=C(C=C1)N=C3C(CCN3C2=O)O	232.23	unknown	https://doi.org/10.1016/0031-9422(96)00120-3
(3R)-5-methoxy-9-methylidene-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-3-ol	163186285	Click to see COC1=CC=CC2=C1N=C3C(CCN3C2=C)O	230.26	unknown	https://doi.org/10.1016/0031-9422(85)80070-4
(3R)-9-methylidene-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-3-ol	162985110	Click to see C=C1C2=CC=CC=C2N=C3N1CCC3O	200.24	unknown	https://doi.org/10.1016/0031-9422(85)80070-4
(3S,3aS)-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazoline-3,3a-diol	162956801	Click to see C1CN2CC3=CC=CC=C3NC2(C1O)O	206.24	unknown	https://doi.org/10.1016/0031-9422(81)85115-1
(3S)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-ol	667496	Click to see C1CN2CC3=CC=CC=C3N=C2C1O	188.23	unknown	https://doi.org/10.1081/JLC-100001478 https://doi.org/10.1016/0031-9422(96)00120-3 https://doi.org/10.1021/NP50109A012 https://doi.org/10.1159/000235378 https://doi.org/10.1055/S-2007-971226 https://doi.org/10.3109/13880209209053998 https://doi.org/10.1016/S0021-9673(00)96410-0 https://doi.org/10.1055/S-2007-969891 https://doi.org/10.1016/S0944-7113(97)80061-X
1-(3-Hydroxy-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-9-yl)propan-2-one	14391707	Click to see CC(=O)CC1C2=CC=CC=C2N=C3N1CCC3O	244.29	unknown	https://doi.org/10.1007/BF00366025
1-[(3S,9R)-3-hydroxy-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-9-yl]propan-2-one	154497166	Click to see CC(=O)CC1C2=CC=CC=C2N=C3N1CCC3O	244.29	unknown	https://doi.org/10.1080/10575639708043737
1,2,3,9-Tetrahydropyrrolo(2,1-B)Quinazolin-3-Ol	72610	Click to see C1CN2CC3=CC=CC=C3N=C2C1O	188.23	unknown	https://doi.org/10.1016/0031-9422(96)00120-3
1H-Pyrrolo[2,1-b]quinazolin-9-one, 3-hydroxy-2,3-dihydro-	10242	Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O	202.21	unknown	https://doi.org/10.1016/0031-9422(96)00120-3 https://doi.org/10.1007/BF00366025 https://doi.org/10.1016/0031-9422(81)85115-1
2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazoline-3,3a-diol	101255920	Click to see C1CN2CC3=CC=CC=C3NC2(C1O)O	206.24	unknown	https://doi.org/10.1016/0031-9422(81)85115-1
3-[2-(Dimethylamino)phenyl]-3-hydroxy-1,2-dihydropyrrolo[2,1-b]quinazolin-9-one	162924682	Click to see CN(C)C1=CC=CC=C1C2(CCN3C2=NC4=CC=CC=C4C3=O)O	321.40	unknown	https://doi.org/10.1016/0031-9422(96)00120-3
3-Hydroxy-5-methoxy-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one	21769547	Click to see COC1=CC=CC2=C1N=C3C(CCN3C2=O)O	232.23	unknown	https://doi.org/10.1016/0031-9422(96)00120-3
3-hydroxy-7-methoxy-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-9-one	23872051	Click to see COC1=CC2=C(C=C1)N=C3C(CCN3C2=O)O	232.23	unknown	https://doi.org/10.1016/0031-9422(96)00120-3
3,7-Dihydroxy-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one	13970119	Click to see C1CN2C(=NC3=C(C2=O)C=C(C=C3)O)C1O	218.21	unknown	https://doi.org/10.1055/S-2007-971226
5-methoxy-9-methylidene-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-3-ol	162932387	Click to see COC1=CC=CC2=C1N=C3C(CCN3C2=C)O	230.26	unknown	https://doi.org/10.1016/0031-9422(85)80070-4
9-methylidene-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-3-ol	162985109	Click to see C=C1C2=CC=CC=C2N=C3N1CCC3O	200.24	unknown	https://doi.org/10.1016/0031-9422(85)80070-4
Anisotine	442884	Click to see CNC1=C(C=C(C=C1)C2CCN3C2=NC4=CC=CC=C4C3=O)C(=O)OC	349.40	unknown	https://doi.org/10.1002/HLCA.19710540307 https://doi.org/10.1021/NP50109A012
CID 776133	776133	Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O	202.21	unknown	https://doi.org/10.1081/JLC-100001478 https://doi.org/10.1016/0031-9422(96)00120-3 https://doi.org/10.1055/S-2007-971226 https://doi.org/10.1016/0031-9422(81)85115-1 https://doi.org/10.1016/S0021-9673(00)96410-0 https://doi.org/10.1055/S-2007-969891 https://doi.org/10.1016/S0944-7113(97)80061-X https://doi.org/10.1007/BF00366025 https://doi.org/10.3109/03639048209022128
Deoxyvasicinone	68261	Click to see C1CC2=NC3=CC=CC=C3C(=O)N2C1	186.21	unknown	https://doi.org/10.1016/S0031-9422(00)83845-5
methyl 2-(methylamino)-5-[(3S)-9-oxo-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-3-yl]benzoate	92143160	Click to see CNC1=C(C=C(C=C1)C2CCN3C2=NC4=CC=CC=C4C3=O)C(=O)OC	349.40	unknown	https://doi.org/10.1002/HLCA.19710540307
methyl 2-[(9-oxo-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-3-yl)amino]benzoate	9997066	Click to see COC(=O)C1=CC=CC=C1NC2CCN3C2=NC4=CC=CC=C4C3=O	335.40	unknown	https://doi.org/10.1021/NP50109A012
methyl 2-[[(3S)-9-oxo-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-3-yl]amino]benzoate	162981297	Click to see COC(=O)C1=CC=CC=C1NC2CCN3C2=NC4=CC=CC=C4C3=O	335.40	unknown	https://doi.org/10.1021/NP50109A012
Methyl 5-(3-hydroxy-9-oxo-1,2-dihydropyrrolo[2,1-b]quinazolin-3-yl)-2-(methylamino)benzoate	101670821	Click to see CNC1=C(C=C(C=C1)C2(CCN3C2=NC4=CC=CC=C4C3=O)O)C(=O)OC	365.40	unknown	https://doi.org/10.1021/NP50109A012
Peganine	442929	Click to see C1CN2CC3=CC=CC=C3N=C2C1O	188.23	unknown	https://doi.org/10.1081/JLC-100001478 https://doi.org/10.1016/0031-9422(96)00120-3 https://doi.org/10.1159/000235378 https://doi.org/10.1055/S-2007-971226 https://doi.org/10.3109/13880209209053998 https://doi.org/10.1016/S0021-9673(00)96410-0 https://doi.org/10.1055/S-2007-969891 https://doi.org/10.1016/S0944-7113(97)80061-X
Pyrrolo(2,1-b)quinazolin-9(1H)-one, 2,3-dihydro-3,7-dihydroxy-, (3S)-	158720	Click to see C1CN2C(=NC3=C(C2=O)C=C(C=C3)O)C1O	218.21	unknown	https://doi.org/10.1055/S-2007-971226
Pyrrolo(2,1-b)quinazoline-3,7-diol, 1,2,3,9-tetrahydro-, (R)-	6452262	Click to see C1CN2CC3=C(C=CC(=C3)O)N=C2C1O	204.22	unknown	via CMAUP database
Pyrrolo[2,1-b]quinazolin-9(1H)-one, 3-[2-(dimethylamino)phenyl]-2,3-dihydro-	627712	Click to see CN(C)C1=CC=CC=C1C2CCN3C2=NC4=CC=CC=C4C3=O	305.40	unknown	via CMAUP database
Vasicinol	442934	Click to see C1CN2CC3=C(C=CC(=C3)O)N=C2C1O	204.22	unknown	https://doi.org/10.1055/S-2007-971226
Vasicinone	442935	Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O	202.21	unknown	https://doi.org/10.1016/S0021-9673(00)96410-0 https://doi.org/10.1055/S-2007-969891 https://doi.org/10.3109/03639048209022128 https://doi.org/10.1081/JLC-100001478 https://doi.org/10.1016/0031-9422(96)00120-3 https://doi.org/10.1016/S0944-7113(97)80061-X https://doi.org/10.1055/S-2007-971226
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1-(3,4-Dihydropyrido[3,4-b]indol-9-yl)ethanone	21586650	Click to see CC(=O)N1C2=CC=CC=C2C3=C1C=NCC3	212.25	unknown	https://doi.org/10.1016/S0031-9422(00)83845-5
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
Benzenamine, N,N-dimethyl-2-(1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-yl)-	626005	Click to see CN(C)C1=CC=CC=C1C2CCN3C2=NC4=CC=CC=C4C3	291.40	unknown	https://doi.org/10.1002/HLCA.19710540307
Methyl 2-(methylamino)-5-(1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-yl)benzoate	5316460	Click to see CNC1=C(C=C(C=C1)C2CCN3C2=NC4=CC=CC=C4C3)C(=O)OC	335.40	unknown	https://doi.org/10.1002/HLCA.19710540307
methyl 2-(methylamino)-5-[(3S)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-yl]benzoate	154496105	Click to see CNC1=C(C=C(C=C1)C2CCN3C2=NC4=CC=CC=C4C3)C(=O)OC	335.40	unknown	https://doi.org/10.1002/HLCA.19710540307
N,N-dimethyl-2-[(3R)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-yl]aniline	154497653	Click to see CN(C)C1=CC=CC=C1C2CCN3C2=NC4=CC=CC=C4C3	291.40	unknown	https://doi.org/10.1002/HLCA.19710540307
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-5-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one	101326868	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C(C=C4)OC)O)O)C	436.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
ent-Gallocatechin 4'-methyl ether	10087345	Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O	320.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-4-benzopyrone	442396	Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O	300.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
3,5,7-trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	101713180	Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	508.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
1-(2-hydroxyphenyl)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	162996121	Click to see C1=CC=C(C(=C1)C(=O)C=CC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O	402.40	unknown	https://doi.org/10.1016/0031-9422(82)80064-2
4,2'-Dihydroxychalcone 4-glucoside	42607583	Click to see C1=CC=C(C(=C1)C(=O)C=CC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O	402.40	unknown	https://doi.org/10.1016/0031-9422(82)80064-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(2R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one	12310452	Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O	302.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Hydroxygenistein	5282074	Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O	286.24	unknown	via CMAUP database
6-(1,1-Dimethylallyl)genistein	44257285	Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O	338.40	unknown	via CMAUP database
Genistein	5280961	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzin	107971	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O	416.40	unknown	via CMAUP database
Genistin	5281377	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxy-3-(p-methoxyphenyl)-propiophenone	578444	Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)O)O	272.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4-[3-(4-Hydroxy-3-methoxyphenyl)propyl]benzene-1,3-diol	44130318	Click to see COC1=C(C=CC(=C1)CCCC2=C(C=C(C=C2)O)O)O	274.31	unknown	via CMAUP database

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Justicia adhatoda

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