Details Top

Internal ID UUID643fe4195b600628487445
Scientific name Nauclea latifolia
Authority Sm.
First published in Cycl. 24: n.º 5 (1813)

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.

Ethnobotanical Uses

Among the Yoruba of southwestern Nigeria, Nauclea latifolia is used as a fever‑reducing and antimalarial medicine. Here, the bark is decocted in water—often in combination with other bitter plants—and the liquid is taken in modest doses as a short‑course decoction. The Gbaya of the Central African Republic have long prepared infusions of the leaves for abdominal complaints and diarrhea, with infusions of young shoots occasionally taken to reduce fever. Among Bakola and other forest peoples of southern Cameroon, fresh leaf poultices are applied to wounds and sore skin; the inner bark is also macerated in cold water and the liquid drunk to treat fevers and stomach pains. These practices were recorded in community surveys by Betti (2004) and by traditional‑use documentation in the African Herbal Pharmacopoeia (2009), and they have been corroborated by participatory studies in the Congo by Loumeto (1999). Across West and Central Africa, decoctions of the roots are commonly made for diarrhea and related gut complaints and are used in several regions as a tonic after childbirth. These observations, along with the plant’s presence in regional pharmacopoeias, were summarized by Iwu (2014).

One practical recipe is a mild bark decoction for fever and malaria‑type symptoms in adults. Simmer 20 g of dried Nauclea latifolia bark in 1 L of water for 20 minutes, then cool, strain, and take 200–250 ml, once or twice daily, for no more than 7 days. A 1:5 tincture on 45% ethanol—maceroating 1 part bark with 5 parts ethanol for 2–4 weeks in the dark, shaking daily, and then straining—can be used as a modest gastro‑intestinal aid; adults may take 2–3 ml up to three times daily for short periods. Safety: do not use during pregnancy or breastfeeding; avoid exceeding stated doses; stop if vomiting or diarrhoea worsens; consult a qualified clinician if you are on antimalarials, anticoagulants, or other medicines.

The plant is rich in indole alkaloids (notably strictosamide), quinovic acid glycosides, and tannins—constituents consistently reported in the chemical profile of Nauclea latifolia and likely responsible for its antimicrobial, astringent, and antipyretic properties. These compounds also underpin many of the documented uses in wound care and gastrointestinal upset.

Modern relevance: Nauclea latifolia remains widely used in community medicine across West and Central Africa, and its extracts have been examined in recent studies for antimalarial and antimicrobial activities, while standardized bark products and tinctures continue to be produced by herbal suppliers in the region.

General Uses Top

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Common products:
The fruit of Nauclea latifolia (wild African peach) is eaten locally. Fully ripe infructescences are collected from the wild and sold in markets; they may be eaten fresh or cooked in water and sweetened, without medicinal claims.

Food and beverages (non-medicinal):
Fruit pulp is consumed as a fresh snack or dessert. Ripe infructescences are sometimes boiled with water and sugar to make a sweetened drink; the pulp is then eaten. No health or efficacy claims are implied.

Scientific/model-organism use:
The species is documented in ethnobotanical and phytochemical literature as an object of study for fruit composition, native-range ecology, and genetic resources. It is maintained as living collections in botanical gardens and germplasm networks in West and Central Africa (e.g., genetic-resource collections referenced by PROTA and regional herbaria).

Properties relevant to use:
Fully ripe fruit pulp has soft, sweet tissue typical of mature Rubiaceae infructescences; flesh is easily separated for fresh consumption or processing. The pulp yields a clear to lightly colored juice when boiled; boiled fruit produces a translucent syrup suitable for sweetening without intensive purification.

Standards and regulation:
No specific international standards for Nauclea latifolia fruit products were identified; trade is区域性 and informal. Regulatory status varies by country and would be governed by general food-composition or food-safety frameworks where applicable.

Sustainability and sourcing:
Fruit is collected from wild trees; overharvesting can occur where local demand is high. There is some evidence of domestication attempts and improved management of wild stands to stabilize supply. Sustainable harvesting practices—selective, non-destructive collection and promotion of regeneration—are recommended to maintain wild populations.

Synonyms Top

Scientific name Authority First published in
Nauclea esculenta Merr. J. Washington Acad. Sci. 5: 535 (1915)
Sarcocephalus esculentus Afzel. ex Sabine Trans. Hort. Soc. London 5: 442 (1824)
Sarcocephalus esculentus var. amarissima A.Chev. Rev. Bot. Appl. Agric. Trop. 18: 179. 1938
Sarcocephalus esculentus var. velutina A.Chev. Rev. Bot. Appl. Agric. Trop. 18: 181. 1938
Sarcocephalus latifolius (Sm.) E.A.Bruce Kew Bull. 2: 31 (1947)
Sarcocephalus russeggeri Kotschy ex Schweinf. Reliq. Kotschy. : 49 (1868)
Sarcocephalus sambucinus K.Schum. Nat. Pflanzenfam. 4(4): 59 (1891)
Cephalina esculenta Schumach. & Thonn. Beskr. Guin. Pl. : 105 (1827)
Nauclea sambucina T.Winterb. Account Sierra Leone 2: 45 (1803)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000249572
CMAUP NPO13017

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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 / Methoxybenzenes / Dimethoxybenzenes
(e)-4-(3,4-Dimethoxy-phenyl)but-3-en-1-yl palmitate 21668972 Click to see CCCCCCCCCCCCCCCC(=O)OCCC=CC1=CC(=C(C=C1)OC)OC 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see 152.23 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids / Simple glycosylceramides / Glycosyl-N-acylsphingosines
(2R)-2-hydroxy-N-[(2S,3R,4E,8E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]tetradecanamide 10818374 Click to see CCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O 686.00 unknown via CMAUP database
(2R)-2-hydroxy-N-[(E,2S,3R)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-4-en-2-yl]hexadecanamide 101948670 Click to see 716.00 unknown via CMAUP database
(2S,3R,4E,8E)-1-(beta-D-Glucopyranosyloxy)-2-[[(2R)-2-hydroxypentadecanoyl]amino]-4,8-octadecadiene-3-ol 10628502 Click to see CCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O 700.00 unknown via CMAUP database
Soyacerebroside I 11104507 Click to see CCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O 714.00 unknown via CMAUP database
Soyacerebroside II 15599558 Click to see 714.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,6R,7S,8R,9S,12S,13R,15R,16R,18S,19R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,19-triol 59052452 Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O 1277.40 unknown via CMAUP database
(1R,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18S,19R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,19-triol 101584207 Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O 1277.40 unknown via CMAUP database
(1S,2S,4S,6R,7S,8R,9S,12S,13R,15R,16R,18R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,18-triol 59052451 Click to see 1277.40 unknown via CMAUP database
(1S,2S,4S,6R,7S,8R,9S,12S,13R,15R,16R,18R)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,18-triol 59052312 Click to see 1439.50 unknown via CMAUP database
(1S,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,18-triol 101584206 Click to see CC1C2C(CC3C2(CCC4C3CCC5(C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O 1277.40 unknown via CMAUP database
(1S,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18R)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,18-triol 101584205 Click to see 1439.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19R)-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 13787750 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)O)C)C)OC1 1081.20 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101932450 Click to see 1081.20 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101826551 Click to see 1197.30 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2R)-2-amino-3-[(R)-prop-2-enylsulfinyl]propanoic acid 51399534 Click to see C=CCS(=O)CC(C(=O)O)N 177.22 unknown via CMAUP database
(2R)-2-ammonio-3-(methylselanyl)propanoate 45266674 Click to see C[Se]CC(C(=O)[O-])[NH3+] 182.09 unknown via CMAUP database
(2R)-2-azaniumyl-3-[(S)-methylsulfinyl]propanoate 40528043 Click to see 151.19 unknown via CMAUP database
L-Selenomethionine 105024 Click to see 196.12 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
gamma-L-Glutamyl-L-phenylalanine 111299 Click to see 294.30 unknown via CMAUP database
Phenylalanine 6140 Click to see C1=CC=C(C=C1)CC(C(=O)O)N 165.19 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives / L-cysteine-S-conjugates
(2R)-2-azaniumyl-3-[(prop-2-en-1-yl)sulfanyl]propanoate 40424388 Click to see 161.22 unknown via CMAUP database
(2R)-2-azaniumyl-3-propylsulfanylpropanoate 40565896 Click to see 163.24 unknown via CMAUP database
3-(Methyldithio)-L-alanine 3080775 Click to see 167.30 unknown via CMAUP database
S-allylmercapto-L-cysteine 9794159 Click to see 193.30 unknown via CMAUP database
S-trans-1-propenyl-L-cysteine 91820358 Click to see CC=CSCC(C(=O)[O-])[NH3+] 161.22 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
gamma-Glutamyl-S-1-propenyl cysteine 87289205 Click to see 290.34 unknown via CMAUP database
gamma-Glutamyl-S-allylcysteine 11346811 Click to see 290.34 unknown via CMAUP database
gamma-glutamyl-S-allylmercaptocysteine 101630431 Click to see 322.40 unknown via CMAUP database
L-gamma-Glutamyl-S-propyl-L-cysteine 54090099 Click to see 292.35 unknown via CMAUP database
Methylseleno carboxyethylglutamine 20807051 Click to see C[Se]CC(C(=O)O)NC(=O)CCC(C(=O)O)N 311.20 unknown via CMAUP database
Methylseleno carboxypropylglutamine 16128830 Click to see C[Se]CCC(C(=O)O)NC(=O)CCC(C(=O)O)N 325.23 unknown via CMAUP database
N5-((R)-1-Carboxy-3-(methylthio)propyl)-L-glutamine 87315837 Click to see CSCCC(C(=O)O)NC(=O)CCC(C(=O)O)N 278.33 unknown via CMAUP database
> Organic acids and derivatives / Organic sulfuric acids and derivatives / Sulfuric acid esters / Sulfuric acid diesters
(E)-2-Propenyl (3-(2-propenylthio)-2-propenyl) sulfate 10977885 Click to see 250.30 unknown via CMAUP database
> Organic acids and derivatives / Organic thiosulfuric acids and derivatives / S-alkyl thiosulfates
3-Sulfonatosulfanylprop-1-ene 59479946 Click to see 153.20 unknown via CMAUP database
> Organic acids and derivatives / Thiosulfinic acid esters
3-[(S)-prop-2-enylsulfinyl]sulfanylprop-1-ene 51380898 Click to see 162.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Allyl Alcohol 7858 Click to see 58.08 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eugenol gentiobioside 10390778 Click to see 488.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Pentanal 8063 Click to see 86.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated aldehydes / Enals
(E)-3-(prop-2-enyldisulfanyl)prop-2-enal 5317516 Click to see C=CCSSC=CC=O 160.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Enols
1-Propen-2-ol 141483 Click to see 58.08 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Aminopyrimidines and derivatives
Allithiamine 3037212 Click to see 354.50 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
2(5H)-Furanone, 4-bromo-5-(bromomethylene)-, (5Z)- 10131246 Click to see C1=C(C(=CBr)OC1=O)Br 253.88 unknown via CMAUP database
> Organoheterocyclic compounds / Dithioles / 1,2-dithioles
4-Methyl-1,2-dithiacyclopentene 5319597 Click to see 118.20 unknown via CMAUP database
5-methyl-3H-dithiole 5319596 Click to see CC1=CCSS1 118.20 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Allixin 86374 Click to see CCCCCC1=C(C(=O)C(=C(O1)C)OC)O 226.27 unknown via CMAUP database
> Organosulfur compounds / Allyl sulfur compounds
Allyl methyl disulfide 62434 Click to see 120.20 unknown via CMAUP database
Allyl methyl sulfide 66282 Click to see 88.17 unknown via CMAUP database
Allyl methyl tetrasulfide 525329 Click to see 184.40 unknown via CMAUP database
Allyl prop-1-enyl disulfide 5352855 Click to see CC=CSSCC=C 146.30 unknown via CMAUP database
Allyl propyl disulfide 16591 Click to see CCCSSCC=C 148.30 unknown via CMAUP database
Diallyl disulfide 16590 Click to see C=CCSSCC=C 146.30 unknown via CMAUP database
Diallyl Sulfide 11617 Click to see 114.21 unknown via CMAUP database
Diallyl tetrasulfide 75552 Click to see C=CCSSSSCC=C 210.40 unknown via CMAUP database
Methyl 2-propenyl pentasulfide 528713 Click to see CSSSSSCC=C 216.40 unknown via CMAUP database
Npc247380 5352907 Click to see 146.30 unknown via CMAUP database
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
Dimethyl Disulfide 12232 Click to see 94.20 unknown via CMAUP database
Dipropyl disulfide 12377 Click to see 150.30 unknown via CMAUP database
Methyl propyl disulfide 16592 Click to see 122.30 unknown via CMAUP database
> Organosulfur compounds / Organic trisulfides
6-ethenyl-4H-trithiine 5315241 Click to see C=CC1=CCSSS1 162.30 unknown via CMAUP database
Diallyl trisulfide 16315 Click to see C=CCSSSCC=C 178.30 unknown via CMAUP database
Dimethyl trisulfide 19310 Click to see CSSSC 126.30 unknown via CMAUP database
Methyl propyl trisulfide 5319765 Click to see 154.30 unknown via CMAUP database
Methylallyl trisulfide 61926 Click to see 152.30 unknown via CMAUP database
> Organosulfur compounds / Sulfonyls
S-2-Propenyl 2-propene-1-sulfonothioate 85776791 Click to see C=CCSS(=O)(=O)CC=C 178.30 unknown via CMAUP database
> Organosulfur compounds / Sulfonyls / Sulfones
(E)-3-(prop-2-enyldisulfanyl)-1-prop-2-enylsulfonylprop-1-ene 5322033 Click to see 250.40 unknown via CMAUP database
> Organosulfur compounds / Sulfoxides
(E)-1-(prop-2-enyldisulfanyl)-3-[(R)-prop-2-enylsulfinyl]prop-1-ene 76962524 Click to see 234.40 unknown via CMAUP database
(Z)-1-(prop-2-enyldisulfanyl)-3-[(R)-prop-2-enylsulfinyl]prop-1-ene 76960957 Click to see 234.40 unknown via CMAUP database
> Organosulfur compounds / Thioacetals / Dithioacetals
1,3-Dithiole 5316944 Click to see 104.20 unknown via CMAUP database
> Organosulfur compounds / Thioethers / Dialkylthioethers
Dimethyl Sulfide 1068 Click to see 62.14 unknown via CMAUP database
> Organosulfur compounds / Thioethers / Thioenol ethers
Ethene, 1,1'-thiobis- 12321 Click to see 86.16 unknown via CMAUP database

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