Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Oman
  - Saudi Arabia
  - Yemen
- Western Asia
  - Afghanistan
  - Iran
  - Iraq

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Pakistan
  - West Himalaya

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000296194
Tropicos	1804251
KEW	urn:lsid:ipni.org:names:81712-1
The Plant List	kew-177985
Open Tree Of Life	618442
NCBI Taxonomy	396313
IPNI	81712-1
iNaturalist	199176
GBIF	3615532
Freebase	/m/0h67k8f
EOL	2900492
USDA GRIN	417560
Wikipedia	Rhazya_stricta

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_001752375.1	RHA1.0	Scaffold	King Abdulaziz University	2016-10-04	112.0x	261.64 Mb

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 assessment of antidiabetic medicinal plants in District Karak, Pakistan

Nazar A, Adnan M, Shah SM, Bari A, Ullah R, Tariq A, Ahmad N

BMC Complement Med Ther

24-Apr-2024

PMCID:	PMC11040872
doi:	10.1186/s12906-024-04462-w
PMID:	38658923

Chromosome-level Alstonia scholaris genome unveils evolutionary insights into biosynthesis of monoterpenoid indole alkaloids

Chen H, Sahu SK, Wang S, Liu J, Yang J, Cheng L, Chiu TY, Liu H

iScience

27-Mar-2024

PMCID:	PMC11033161
doi:	10.1016/j.isci.2024.109599
PMID:	38646178

The Madagascar palm genome provides new insights on the evolution of Apocynaceae specialized metabolism

Cuello C, Jansen HJ, Abdallah C, Zamar Mbadinga DL, Birer Williams C, Durand M, Oudin A, Papon N, Giglioli-Guivarc'h N, Dirks RP, Jensen MK, O'Connor SE, Besseau S, Courdavault V

Heliyon

14-Mar-2024

PMCID:	PMC10963385
doi:	10.1016/j.heliyon.2024.e28078
PMID:	38533072

Camel urine as a potential source of bioactive molecules showing their efficacy against pathogens: A systematic review

Amina R, Habiba R, Abouddihaj B

Saudi J Biol Sci

25-Feb-2024

PMCID:	PMC10940778
doi:	10.1016/j.sjbs.2024.103966
PMID:	38495380

The sustainable use of diverse plants accustomed by different ethnic groups in Sibi District, Balochistan, Pakistan

Maria B, Saeed S, Ahmed A, Ahmed M, Rehman A

PLoS One

21-Feb-2024

PMCID:	PMC10880983
doi:	10.1371/journal.pone.0294989
PMID:	38381718

Phylogenomics and topological conflicts in the tribe Anthospermeae (Rubiaceae)

Thureborn O, Wikström N, Razafimandimbison SG, Rydin C

Ecol Evol

25-Jan-2024

PMCID:	PMC10809029
doi:	10.1002/ece3.10868
PMID:	38274863

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

Silver nanoparticles improve the fungicidal properties of Rhazya stricta decne aqueous extract against plant pathogens

Al-Sahli SA, Al-Otibi F, Alharbi RI, Amina M, Al Musayeib NM

Sci Rep

14-Jan-2024

PMCID:	PMC10788342
doi:	10.1038/s41598-024-51855-5
PMID:	38221517

Conserved untranslated regions of multipartite viruses: Natural markers of novel viral genomic components and tags of viral evolution

Zhang S, Yang C, Qiu Y, Liao R, Xuan Z, Ren F, Dong Y, Xie X, Han Y, Wu D, Ramos-González PL, Freitas-Astúa J, Yang H, Zhou C, Cao M

Virus Evol

12-Jan-2024

PMCID:	PMC10868557
doi:	10.1093/ve/veae004
PMID:	38361819

Structural and Functional Strategies in Cenchrus Species to Combat Environmental Extremities Imposed by Multiple Abiotic Stresses

Basharat S, Ahmad F, Hameed M, Ahmad MS, Asghar A, Fatima S, Ahmad KS, Shah SM, Hashem A, Avila-Quezada GD, Abd_Allah EF, Abbas Z

Plants (Basel)

11-Jan-2024

PMCID:	PMC10818359
doi:	10.3390/plants13020203
PMID:	38256756

The Antifungal Activities of Silver Nano-Aggregates Biosynthesized from the Aqueous Extract and the Alkaline Aqueous Fraction of Rhazya stricta against Some Fusarium Species

Al-Otibi F

Nanomaterials (Basel)

28-Dec-2023

PMCID:	PMC10780319
doi:	10.3390/nano14010088
PMID:	38202544

Diversity, Distribution, and applications of arbuscular mycorrhizal fungi in the Arabian Peninsula

Alrajhi K, Bibi S, Abu-Dieyeh M

Saudi J Biol Sci

25-Dec-2023

PMCID:	PMC10805673
doi:	10.1016/j.sjbs.2023.103911
PMID:	38268781

Intrageneric structural variation in organelle genomes from the genus Dystaenia (Apiaceae): genome rearrangement and mitochondrion-to-plastid DNA transfer

Park S, Park S

Front Plant Sci

05-Dec-2023

PMCID:	PMC10728875
doi:	10.3389/fpls.2023.1283292
PMID:	38116150

Ethnomedicinal evaluation of medicinal plants used for therapies by men and women in rural and urban communities in Makkah district

Qari SH, Alqethami A, Qumsani AT

Saudi Pharm J

02-Dec-2023

PMCID:	PMC10733703
doi:	10.1016/j.jsps.2023.101881
PMID:	38130903

The Rauvolfia tetraphylla genome suggests multiple distinct biosynthetic routes for yohimbane monoterpene indole alkaloids

Stander EA, Lehka B, Carqueijeiro I, Cuello C, Hansson FG, Jansen HJ, Dugé De Bernonville T, Birer Williams C, Vergès V, Lezin E, Lorensen MD, Dang TT, Oudin A, Lanoue A, Durand M, Giglioli-Guivarc’h N, Janfelt C, Papon N, Dirks RP, O’connor SE, Jensen MK, Besseau S, Courdavault V

Commun Biol

24-Nov-2023

PMCID:	PMC10673892
doi:	10.1038/s42003-023-05574-8
PMID:	38001233

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 / Akuammilan and related alkaloids
Strictamin	5324377	Click to see CC=C1CN2CCC34C(C1CC2C3=NC5=CC=CC=C45)C(=O)OC	322.40	unknown	https://doi.org/10.1021/JA00448A041
Strictamine	21159178	Click to see CC=C1CN2CCC34C(C1CC2C3=NC5=CC=CC=C45)C(=O)OC	322.40	unknown	https://doi.org/10.1021/JA00448A041 https://doi.org/10.1016/0031-9422(83)85045-6
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
(1S,9S,10S,12R,19R)-12-ethyl-10-hydroxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-triene-8-carbaldehyde	163028438	Click to see CCC12CCCN3C1C4(CC3)C(C(C2)O)N(C5=CC=CC=C45)C=O	326.40	unknown	https://doi.org/10.1016/S0031-9422(00)81467-3
(2R,4S,5R,6S)-6-[(1S,9S,12S,19S)-12-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-trien-8-yl]-2,4,5-trihydroxyoxan-3-one	163067498	Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=CC=CC=C45)C6C(C(C(=O)C(O6)O)O)O	428.50	unknown	https://doi.org/10.1016/S0031-9422(00)81246-7
1-[(1R,9R,12R,19R)-12-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-trien-8-yl]ethanone	13943056	Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=CC=CC=C45)C(=O)C	324.50	unknown	https://doi.org/10.1016/S0031-9422(00)95218-X
12-Ethyl-10-hydroxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-triene-8-carbaldehyde	163028437	Click to see CCC12CCCN3C1C4(CC3)C(C(C2)O)N(C5=CC=CC=C45)C=O	326.40	unknown	https://doi.org/10.1016/S0031-9422(00)81467-3
6-(12-Ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-trien-8-yl)-2,4,5-trihydroxyoxan-3-one	163067497	Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=CC=CC=C45)C6C(C(C(=O)C(O6)O)O)O	428.50	unknown	https://doi.org/10.1016/0031-9422(88)80488-6
6-(12-Ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-trien-8-yl)-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-one	13875466	Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=CC=CC=C45)C6C(C(C(=O)C(O6)CO)O)O	442.50	unknown	https://doi.org/10.1039/P19870001701
Aspidospermidine, 1-acetyl-	580310	Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=CC=CC=C45)C(=O)C	324.50	unknown	https://doi.org/10.1016/S0031-9422(00)95218-X
methyl (1R,12S,13R,19R)-12-ethyl-13-hydroxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	11530478	Click to see CCC12CC(=C3C4(C1N(CCC2O)CC4)C5=CC=CC=C5N3)C(=O)OC	354.40	unknown	https://doi.org/10.1016/0031-9422(88)80817-3
Vincadifformine	94255	Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC	338.40	unknown	https://doi.org/10.1515/ZNC-1986-0403
> Alkaloids and derivatives / Corynanthean-type alkaloids
(1S,10S,12S,13Z,18S)-13-ethylidene-18-(hydroxymethyl)-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylic acid	101986486	Click to see CC=C1CN2CCC34C5=CC=CC=C5N=C3C2CC1C4(CO)C(=O)O	338.40	unknown	https://doi.org/10.1055/S-2007-969080
methyl (13Z)-13-ethylidene-18-formyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate	5324378	Click to see CC=C1CN2CCC34C5=CC=CC=C5N=C3C2CC1C4(C=O)C(=O)OC	350.40	unknown	https://doi.org/10.1016/S0031-9422(00)85265-6
methyl (1S,10S,12S,13Z,18S)-13-ethylidene-18-formyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate	101967159	Click to see CC=C1CN2CCC34C5=CC=CC=C5N=C3C2CC1C4(C=O)C(=O)OC	350.40	unknown	https://doi.org/10.1016/0031-9422(83)85045-6
methyl (2R)-2-[(2R,3Z,12bR)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate	14109838	Click to see CC=C1CN2CCC3=C(C2CC1C(CO)C(=O)OC)NC4=CC=CC=C34	354.40	unknown	https://doi.org/10.3987/R-1986-03-0703 https://doi.org/10.1016/S0031-9422(00)81246-7
methyl (9R,12S,13Z,16S,17R)-13-ethylidene-18-oxo-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-17-carboxylate	101607204	Click to see CC=C1CN2C3CC1C4(C2CC5(C3NC6=CC=CC=C65)C4=O)C(=O)OC	350.40	unknown	https://doi.org/10.1016/S0031-9422(00)95218-X
methyl (Z)-2-[(3E)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxyprop-2-enoate	10043592	Click to see CC=C1CN2CCC3=C(C2CC1C(=CO)C(=O)OC)NC4=CC=CC=C34	352.40	unknown	https://doi.org/10.1016/S0031-9422(00)85265-6
> Alkaloids and derivatives / Harmala alkaloids
methyl 9H-pyrido[3,4-b]indole-1-carboxylate	597266	Click to see COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23	226.23	unknown	https://doi.org/10.1016/0031-9422(88)80488-6
> Alkaloids and derivatives / Macroline alkaloids
19-(Z)-Akuammidine	138113962	Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC	352.40	unknown	https://doi.org/10.1016/0031-9422(83)85045-6
methyl (12S,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate	134716693	Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC	352.40	unknown	https://doi.org/10.1021/NP50018A014
> Alkaloids and derivatives / Pleiocarpaman alkaloids
Methyl 13-acetyl-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17),12-pentaene-18-carboxylate	162980424	Click to see CC(=O)C1=CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC	336.40	unknown	https://doi.org/10.1016/0031-9422(83)85045-6 https://doi.org/10.3987/R-1987-08-2125
> Alkaloids and derivatives / Quebrachamine alkaloids
2H-3,7-Methanoazacycloundecino(5,4-b)indole-9-carboxylic acid, 7-ethyl-1,4,5,6,7,8,9,10-octahydro-, methyl ester, (7S-(7R,9S))-	12444819	Click to see CCC12CCCN(C1)CCC3=C(C(C2)C(=O)OC)NC4=CC=CC=C34	340.50	unknown	https://doi.org/10.1021/NP50037A040
Quebrachamine	92990	Click to see CCC12CCCN(C1)CCC3=C(CC2)NC4=CC=CC=C34	282.40	unknown	https://doi.org/10.1016/0031-9422(83)85045-6
> Alkaloids and derivatives / Strychnos alkaloids
(+)-Condylocarpine	10914255	Click to see CC=C1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC	322.40	unknown	https://doi.org/10.1021/NP50048A033
(1R,11R,12Z,17S)-12-ethylidene-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carbaldehyde	129317219	Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C=O	292.40	unknown	https://doi.org/10.1021/JA00448A041
Methyl (1S,2S,16Z)-16-ethylidene-2-(hydroxymethyl)-4,14-diazatetracyclo[12.2.2.03,11.05,10]octadeca-3(11),5,7,9-tetraene-2-carboxylate	20839798	Click to see CC=C1CN2CCC1C(C3=C(CC2)C4=CC=CC=C4N3)(CO)C(=O)OC	354.40	unknown	https://doi.org/10.1021/NP50055A036
Methyl 3'-methylspiro[8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-12,2'-oxirane]-10-carboxylate	13820696	Click to see CC1C2(O1)CN3CCC45C3CC2C(=C4NC6=CC=CC=C56)C(=O)OC	338.40	unknown	https://doi.org/10.1016/S0040-4039(00)95548-5 https://doi.org/10.1016/0031-9422(83)85045-6
Nor-C-fluorocurarine	139292102	Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C=O	292.40	unknown	https://doi.org/10.1016/0031-9422(83)85045-6
Sewarine	44559355	Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=C4C=C(C=C5)O)C(=O)OC	338.40	unknown	https://doi.org/10.1016/0031-9422(83)85045-6 https://doi.org/10.1021/NP50018A014
Stemmadenin	57506220	Click to see CC=C1CN2CCC1C(C3=C(CC2)C4=CC=CC=C4N3)(CO)C(=O)OC	354.40	unknown	https://doi.org/10.1021/NP50055A036
> Alkaloids and derivatives / Yohimbine alkaloids
Tetrahydroalstonine	72340	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1055/S-2007-969707
> Benzenoids
Rhazinilam	11312435	Click to see CCC12CCCN3C1=C(C=C3)C4=CC=CC=C4NC(=O)CC2	294.40	unknown	https://doi.org/10.1016/S0031-9422(00)85265-6 https://doi.org/10.1016/S0040-4039(01)84472-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-(8-Methyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-2-yl)propan-2-ol	142113479	Click to see CC1=CCCC2C1CC(CC2)C(C)(C)O	208.34	unknown	https://doi.org/10.1016/0031-9422(88)80488-6
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
10-Ethenyl-1-ethyl-3,13-diazatetracyclo[11.3.1.02,11.04,9]heptadeca-2,4,6,8,10-pentaene	163192324	Click to see CCC12CCCN(C1)CC3=C(C4=CC=CC=C4N=C23)C=C	278.40	unknown	https://doi.org/10.1080/10575639608043240
> Organoheterocyclic compounds / Indoles and derivatives
methyl (13E)-13-ethylidene-15-oxido-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-3,5,7,9-tetraene-18-carboxylate	101407506	Click to see CC=C1C[N+]2(CCC34C5C=CC=CC5=NC3=C2CC1C4C(=O)OC)[O-]	338.40	unknown	https://doi.org/10.1016/S0031-9422(00)80424-0
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(4R,15S)-15-ethyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-5,7,9,11-tetraen-4-ol	163097335	Click to see CCC12CCCN(C1)CCC3(C(=NC4=CC=CC=C43)CC2)O	298.40	unknown	https://doi.org/10.1016/S0031-9422(00)81467-3
Methyl 1,4-dihydrocyclopenta[b]indole-1-carboxylate	85702936	Click to see COC(=O)C1C=CC2=C1C3=CC=CC=C3N2	213.23	unknown	https://doi.org/10.1016/0031-9422(88)80488-6
Strictanol	12314913	Click to see CCC12CCCN(C1)CCC3(C(=NC4=CC=CC=C43)CC2)O	298.40	unknown	https://doi.org/10.1016/S0031-9422(00)81467-3 https://doi.org/10.1016/0031-9422(88)80488-6
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
methyl (8'Z)-8'-ethylidene-2-hydroxy-5'-oxospiro[1,2-dihydroindole-3,4'-1-azatricyclo[5.2.2.02,6]undecane]-6'-carboxylate	13890386	Click to see CC=C1CN2CCC1C3(C2CC4(C3=O)C(NC5=CC=CC=C45)O)C(=O)OC	368.40	unknown	https://doi.org/10.3987/R-1987-02-0405
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
methyl (2R)-2-[3-[2-[(3S)-3-ethylpiperidin-1-yl]ethyl]-1H-indol-2-yl]propanoate	162891111	Click to see CCC1CCCN(C1)CCC2=C(NC3=CC=CC=C32)C(C)C(=O)OC	342.50	unknown	https://doi.org/10.1515/ZNC-1986-0403
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Antirhine	5462421	Click to see C=CC(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34	296.40	unknown	https://doi.org/10.1016/S0031-9422(00)85265-6
Corynan-17-ol	164952	Click to see CCC1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34	298.40	unknown	https://doi.org/10.1055/S-2007-969080
Isovallesiachotamine	6442678	Click to see CC=C(C=O)C1CC2C3=C(CCN2C=C1C(=O)OC)C4=CC=CC=C4N3	350.40	unknown	https://doi.org/10.1021/NP50032A031
Strictosamide	10345799	Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4	498.50	unknown	https://doi.org/10.1016/S0031-9422(00)95218-X
Vallesiachotamine	5384527	Click to see CC=C(C=O)C1CC2C3=C(CCN2C=C1C(=O)OC)C4=CC=CC=C4N3	350.40	unknown	https://doi.org/10.1021/NP50018A014
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
14-Ethyl-14-(2-hydroxyethyl)-16-oxa-8,10-diazatetracyclo[8.6.2.01,9.02,7]octadeca-2,4,6-trien-15-one	163192604	Click to see CCC1(CCCN2CCC3(C2NC4=CC=CC=C43)OC1=O)CCO	330.40	unknown	https://doi.org/10.1080/10575639508044068
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Decarbomethoxytetrahydrosecodine	14825828	Click to see CCC1CCCN(C1)CCC2=C(NC3=CC=CC=C32)CC	284.40	unknown	https://doi.org/10.1016/S0031-9422(00)95218-X
dimethyl (6R,9R)-10-[2-(3-ethylpiperidin-1-yl)ethyl]-6-[3-[2-(3-ethylpiperidin-1-yl)ethyl]-1H-indol-2-yl]-8,9-dihydro-7H-pyrido[1,2-a]indole-6,9-dicarboxylate	10101080	Click to see CCC1CCCN(C1)CCC2=C(NC3=CC=CC=C32)C4(CCC(C5=C(C6=CC=CC=C6N54)CCN7CCCC(C7)CC)C(=O)OC)C(=O)OC	680.90	unknown	https://doi.org/10.1021/NP50018A014
dimethyl (6R,9R)-10-[2-(5-ethyl-3,6-dihydro-2H-pyridin-1-yl)ethyl]-6-[3-[2-(5-ethyl-3,6-dihydro-2H-pyridin-1-yl)ethyl]-1H-indol-2-yl]-8,9-dihydro-7H-pyrido[1,2-a]indole-6,9-dicarboxylate	102276348	Click to see CCC1=CCCN(C1)CCC2=C(NC3=CC=CC=C32)C4(CCC(C5=C(C6=CC=CC=C6N54)CCN7CCC=C(C7)CC)C(=O)OC)C(=O)OC	676.90	unknown	https://doi.org/10.1039/C19680000859
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Xylariolide B	46832766	Click to see CCC(C)(C(C1(C(C(C(=O)O1)C)O)C)O)O	232.27	unknown	https://doi.org/10.1021/NP50018A014
> Organoheterocyclic compounds / Piperidines / Piperidinecarboxylic acids and derivatives / Piperidinecarboxamides
Bis(3-ethylpiperidin-1-yl)methanone	86260418	Click to see CCC1CCCN(C1)C(=O)N2CCCC(C2)CC	252.40	unknown	https://doi.org/10.3987/R-1984-09-2023
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Rhazimine	6443646	Click to see CC=C1CN2CCC34C5=CC=CC=C5N=CC3(C1CC2C4=O)C(=O)OC	350.40	unknown	https://doi.org/10.1016/S0040-4039(01)91202-X https://doi.org/10.1055/S-2006-959765
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
4',5,7,8-Tetra-hydroxyflavanonol	11722549	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O	304.25	unknown	https://doi.org/10.1016/S0040-4039(01)91202-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Robinin	5281693	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O	740.70	unknown	https://doi.org/10.1016/S0031-9422(00)81530-7

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Rhazya stricta

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