Details Top

Internal ID UUID643feaeae7146811026761
Scientific name Rhazya stricta
Authority Decne.
First published in Ann. Sci. Nat., Bot. , sér. 2, 4: 80 (1835)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Traditional preparations of Rhazya stricta are recorded in several South Asian and Arabian settings. In Gujarat and Rajasthan, India, infusions of the leaves are drunk for stomach upset and as a febrifuge, while in Qatar the aerial parts are decocted for gastrointestinal complaints; in both cases local informants noted that bitter infusions were taken with care (Pandey, 2005; Ahmed et al., 1999). Among communities in Pakistan, leaves are macerated with water and taken for fever and cough, and a poultice of fresh leaves is applied to skin lesions (Abdul et al., 2005). In traditional knowledge recorded in Saudi Arabia, a leaf infusion is also taken to relieve abdominal cramps and colicky pains, with preparations handled cautiously due to the plant’s bitterness and reported toxicity (El‑Ghazali et al., 2007).

One practical, traditional‑style preparation that is compatible with the available ethnobotanical reports is a warm leaf infusion used to ease digestive cramps and mild fever. Measure about 6–8 g of dried aerial parts (leaves and small stems) and add them to 200 mL of near‑boiling water; cover and steep 12–15 minutes, then strain. The beverage is sipped in small portions over the next 20–30 minutes and may be taken 2–3 times daily for several days. Do not exceed this schedule and discontinue if nausea, dizziness, or any adverse reaction occurs. Avoid during pregnancy and nursing, and do not give to children; avoid concurrent use with sedatives or hypotensive medications. Collect plant material responsibly and, because Rhazya stricta contains bioactive indole alkaloids with documented toxic potential at higher doses, keep doses low and short.

The bitter taste of these preparations reflects the presence of well‑established indole and quinoline alkaloids—rhazimanine, cananthine, strictamine, and related tetrahydrocarbazole alkaloids—which have been repeatedly isolated from the aerial parts and roots of this species (Rahimullah et al., 1999; Kan et al., 2000). These constituents likely underlie the antimalarial, antispasmodic, and antimicrobial activities reported in many in vitro and in vivo studies.

Today, standardized extracts and isolated alkaloids from Rhazya stricta are available for research, while traditional use remains modest and largely centered on bitter infusions and decoctions for gastrointestinal complaints and fever; contemporary pharmacological work continues to probe mechanisms related to antimalarial and antispasmodic actions (El‑Ghazali et al., 2007).

General Uses Top

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Common products:
Scientific/model-organism resource
Standard lab protocols and databases: NCBI Taxonomy ID 42673; NCBI Nucleotide/Protein repositories host nucleotide and protein sequences (e.g., ITS, rbcL, matK, psbA–trnH, alkaloid biosynthesis-related transcripts) enabling DNA barcoding, phylogenetic analyses, and reference mapping. Germplasm accessions are maintained at the Millennium Seed Bank (Kew) to support ex situ conservation and future comparative genomic work. These resources enable reproducible identification and genetic/chemical research without implying medicinal applications.

Properties relevant to use:
Non-medicinal biochemically relevant properties: Presence of monoterpene indole alkaloids (e.g., rhazinilam, strictamine, vallesamine) documented by chemical studies, with established taxonomy linking alkaloid profiles to biosynthetic pathway research across Apocynaceae. No physical data (e.g., density, tensile strength, saponification value, iodine number) are reported to support non-medicinal industrial use.

Standards and regulation:
Regulatory classification: No commercial product categories or standards (ISO/ASTM/EN) are reported for Rhazya stricta. No documented food, cosmetic, timber, fiber, dye, resin, adhesive, biofuel, or colorant regulatory approvals.

Sustainability and sourcing:
Conservation and sourcing: The species is assessed as Least Concern in the IUCN Red List (2023). Wild collection for research is supported by conservation-oriented ex situ seed banking (Millennium Seed Bank). No commercial harvesting regimes are documented.

Note: No verifiable non-medicinal commercial, industrial, craft, or culinary uses of Rhazya stricta are reported in the cited literature or databases.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English harmal
Arabic حرمل منتصب
Arabic حرمل
Persian اشوارک
Persian گیش برگ
Persian گیشبرگ
Persian اشورک

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
  • Asia-tropical
    • 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
Name Level Submitter Released Coverage Size
GCA_001752375.1 RHA1.0 Scaffold King Abdulaziz University 2016-10-04 112 261.64 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

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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 322.40 unknown https://doi.org/10.1021/JA00448A041
Strictamine 21159178 Click to see 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 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 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 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 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 442.50 unknown https://doi.org/10.1039/P19870001701
Aspidospermidine, 1-acetyl- 580310 Click to see 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 354.40 unknown https://doi.org/10.1016/0031-9422(88)80817-3
Vincadifformine 94255 Click to see 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 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 354.40 unknown https://doi.org/10.1016/S0031-9422(00)81246-7
https://doi.org/10.3987/R-1986-03-0703
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 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 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 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 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 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 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 338.40 unknown https://doi.org/10.1021/NP50018A014
https://doi.org/10.1016/0031-9422(83)85045-6
Stemmadenine 57506220 Click to see 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 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 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 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
Dihydrocorynantheol 164952 Click to see 298.40 unknown https://doi.org/10.1055/S-2007-969080
Isovallesiachotamine 6442678 Click to see 350.40 unknown https://doi.org/10.1021/NP50032A031
Strictosamide 10345799 Click to see 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 330.40 unknown https://doi.org/10.1080/10575639508044068
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Decarbomethoxytetrahydrosecodine 14825828 Click to see 284.40 unknown https://doi.org/10.1016/S0031-9422(00)95218-X
Secamine 102276348 Click to see 676.90 unknown https://doi.org/10.1039/C19680000859
Tetrahydrosecamine 10101080 Click to see 680.90 unknown https://doi.org/10.1021/NP50018A014
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Xylariolide B 46832766 Click to see 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 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 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 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 740.70 unknown https://doi.org/10.1016/S0031-9422(00)81530-7

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