Scientific name	Authority	First published in
Arundo saccharifera	Garsault	Fig. Pl. Méd. : t. 111 (1764)
Saccharifera officinalis	Stokes	Bot. Mat. Med. 1: 132 (1812)
Saccharum hybridum	hort. ex R.M.Grey	Rep. Harvard Bot. Gard. Cienfuegos Cuba : 68 (1927)
Saccharum atrorubens	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. : 256 (1892)
Saccharum fragile	Cuzent & Pancher. ex Drake	Fl. Polynésie Franç. : 256 (1892)
Saccharum glabrum	Cuzent & Pancher	Fl. Polynésie Franç. (Drake) (1892) 256. 1893 [Jan-Mar 1893]
Saccharum infirmum	Steud.	Berberid. Amer. Austral. : 56 (1857)
Saccharum luzonicum	Hack.	Monogr. Phan. [A.DC. & C.DC.] 6: 116. 1889 [Apr 1889]
Saccharum monandrum	Rol.	Acta Lit. Univ. Hafn. 1: 285. 1778
Saccharum occidentale	Sw.	Adnot. Bot. : 17 (1829)
Saccharum officinale	Salisb.	Prodr. Stirp. Chap. Allerton : 17 (1796)
Saccharum officinarum var. atrorubens	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. 256. 1892
Saccharum officinarum var. brevipedicellatum	Hack.	Fl. Bras. 2(3): 256 (1883)
Saccharum officinarum var. fragile	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. 256. 1892
Saccharum officinarum var. giganteum	Kunth	Enum. Pl. 1: 474. 1833
Saccharum officinarum var. glabrum	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. 256. 1892
Saccharum officinarum var. jamaicense	Sickenb.	Mém. Inst. Égypt. 4: 302. 1901
Saccharum officinarum var. litteratum	Hassk.	Pl. Jav. Rar. 50. 1848
Saccharum officinarum var. litteratum-breve	Hassk.	Pl. Jav. Rar. 50. 1848
Saccharum officinarum var. luridum	Hassk.	Pl. Jav. Rar. 49. 1848
Saccharum officinarum var. luteum-durum	Hassk.	Pl. Jav. Rar. 47. 1848
Saccharum officinarum var. luzonicum	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. 256. 1892
Saccharum officinarum var. obscurum	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. 256. 1892
Saccharum officinarum var. otaheitense	Roem. & Schult.	Syst. Veg., ed. 15 bis 2: 285. 1817
Saccharum officinarum var. purpureum	Kunth	Enum. Pl. 1: 474. 1833
Saccharum officinarum var. rubicundum	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. 256. 1892
Saccharum officinarum var. rubrum-altum	Hassk.	Pl. Jav. Rar. 48. 1848
Saccharum officinarum var. rubrum-humile	Hassk.	Pl. Jav. Rar. 48. 1848
Saccharum officinarum var. tahitense	Kunth	Enum. Pl. 1: 474. 1833
Saccharum officinarum var. violaceum	Pers.	Syn. Pl. 1: 102. 1805
Saccharum rubicundum	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. : 256 (1892)
Saccharum spontaneum subsp. luzonicum	Hack.	Monogr. Phan. 6: 116. 1889 (1889)
Saccharum violaceum	Tussac	Fl. Antill. 1: 160 (1808)
Saccharum obscurum	Cuzent & Pancher ex Drake	Fl. Polynésie Franç. (Drake) (1892) 256. 1893 [Jan-Mar 1893]
Saccharum officinarum var. litteratum	Hack.	Monogr. Phan. 6: 113 1889

Common names Top

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Filter by language:

Language	Common/alternative name
English	sugar cane
English	sugarcane
Arabic	مضار
Arabic	برسوم
Arabic	قصب مص
Arabic	مصان
Arabic	قصب
Arabic	قصب السكر المخزني
Arabic	مزهر
Arabic	قصب سكر
Azerbaijani	dərman şəkərqamışı
azb	شکر قامیشی
ban	tebu
Bulgarian	обикновена захарна тръстика
Bosnian	šećerna trska
Catalan	canya de sucre
Czech	třtinovník cukrový
Czech	cukrová třtina
Danish	almindelig sukkerrør
Greek	Ζαχαροκάλαμο
Esperanto	sukerkano
Estonian	suhkruroog
Basque	azukre-kanabera
Persian	نیشکر خوراکی
Finnish	sokeriruoko
frr	sokerröör
Galician	cana de azucre
gn	takuare'ẽ
guc	ka'ñaruushi
Hausa	rake
Croatian	šećerna trska
Upper Sorbian	prawa cokorina
ht	kann
Armenian	Շաքարեղեգ
Italian	saccharum officinale
Italian	cannamele
Italian	canna da zucchero
Japanese	サトウキビ
Georgian	შაქრის ლერწამი
Korean	사탕수수
li	sókkerreet
Macedonian	шеќерна трска
mrj	Сакыр шуды
Malay	tebu hitam
Malay	tebu
Norwegian Bokmål	sukkerrør
Norwegian Nynorsk	sukkerrøyr
os	Сæкæры хъæз
Punjabi	ਕਮਾਦ
Polish	trzcina cukrowa
Punjab	کماد
Portuguese	cana-de-açúcar
pwn	tjevus
Quechua	misk'i wiru
Romanian	trestie de zahăr
Russian	Сахарный тростник благородный
Russian	сахарный тростник культивируемый
ryu	ウージ
sat	ᱟᱸᱠ
Slovak	cukrová trstina
Slovenian	sladkorni trs
Slovenian	sladkorni trst
Albanian	kallam sheqeri
Swedish	sockerrör
Tamil	செங்கரும்பு
Telugu	సెకారం అఫిష్ననారమ్
Thai	อ้อย
Tonga	tō
Turkish	Şeker kamışı
ty	tō
Ukrainian	цукрова тростина
Chinese	甘蔗
Chinese	秀贵甘蔗
Chinese	红甘蔗
Chinese	秀貴甘蔗
Chinese	斑茅花

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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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
- East Tropical Africa
  - Tanzania
- Macaronesia
  - Canary Islands
  - Madeira
- Northeast Tropical Africa
  - Chad
- Northern Africa
  - Algeria
  - Egypt
  - Morocco
- South Tropical Africa
  - Angola
- West Tropical Africa
  - Benin
  - Burkina
  - Gambia
  - Guinea
  - Guinea-Bissau
  - Ivory Coast
  - Senegal
  - Togo
- West-central Tropical Africa
  - Burundi
  - Cameroon
  - Central African Republic
  - Congo
  - Equatorial Guinea
  - Gulf Of Guinea Islands
  - Rwanda
  - Zaïre
- Western Indian Ocean
  - Aldabra
  - Comoros
  - Madagascar
  - Mauritius
  - Rodrigues
  - Réunion
  - Seychelles

Asia-temperate click to expand
- Arabian Peninsula
  - Oman
  - Yemen
- China
  - China South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Korea
  - Nansei-shoto
  - Taiwan
- Western Asia
  - Cyprus
  - Iraq
  - Lebanon-Syria
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Maldives
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Australasia click to expand
- New Zealand
  - New Zealand North

Europe click to expand
- Southwestern Europe
  - Spain

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Florida
  - Louisiana
  - Mississippi

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
  - Marianas
  - Marshall Islands
- South-central Pacific
  - Cook Islands
  - Easter Island
  - Line Islands
  - Marquesas
  - Pitcairn Islands
  - Society Islands
  - Tuamotu
  - Tubuai Islands
- Southwestern Pacific
  - Fiji
  - Gilbert Islands
  - Nauru
  - New Caledonia
  - Niue
  - Samoa
  - Santa Cruz Island
  - Tonga
  - Tuvalu
  - Vanuatu

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Bahamas
  - Bermuda
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Venezuelan Antilles
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - Venezuela
- Western South America
  - Colombia
  - Ecuador
  - Galápagos

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000896660
UNII	3Z20C92XNB
Florida Plant Atlas	1544
USDA Plants	SAOF
Tropicos	25512479
INPN	446334
Flora of Italy	11486
KEW	urn:lsid:ipni.org:names:419977-1
The Plant List	kew-439977
Missouri Botanical Garden	285293
PFAF	Saccharum officinarum
Open Tree Of Life	1079465
Observations.org	136438
NCBI Taxonomy	4547
Nature Serve	2.154512
IPNI	419977-1
iNaturalist	128270
GBIF	2703912
Freebase	/m/0n48fnp
EPPO	SACOF
EOL	1115140
US Library of Congress	sh85129721
USDA GRIN	32617
Wikipedia	Saccharum_officinarum

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_020631735.1	ASM2063173v1	Chromosome	Fujian Agriculture and Forestry University	2021-10-27	66.0x	6.34 Gb

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

Leveraging the sugarcane CRISPR/Cas9 technique for genetic improvement of non-cultivated grasses

Li C, Iqbal MA

Front Plant Sci

27-Mar-2024

PMCID:	PMC11004347
doi:	10.3389/fpls.2024.1369416
PMID:	38601306

Photoperiodic and lighting treatments for flowering control and its genetic regulation in sugarcane breeding

Wickramasinghe KP, Kong CY, Lin XQ, Zhao PF, Mehdi F, Li XJ, Liu XL, Mao J, Lu X

Heliyon

26-Mar-2024

PMCID:	PMC10998108
doi:	10.1016/j.heliyon.2024.e28531
PMID:	38586380

Biosynthesis, characterization and study of the application of silver nanoparticle for 4-nitrophenol reduction, and antimicrobial activities

Mulu M, Tefera M, Guadie A, Basavaiah K

Biotechnol Rep (Amst)

21-Mar-2024

PMCID:	PMC10999826
doi:	10.1016/j.btre.2024.e00838
PMID:	38590717

Establishment of an Efficient Sugarcane Transformation System via Herbicide-Resistant CP4-EPSPS Gene Selection

Wang W, Javed T, Shen L, Sun T, Yang B, Zhang S

Plants (Basel)

15-Mar-2024

PMCID:	PMC10975096
doi:	10.3390/plants13060852
PMID:	38592870

The effect of biopolymer gel derived from sugarcane on healing of traumatic oral ulcers: an experimental study

Barbosa LM, de Oliveira LM, Queiroz CP, Freitas BA, de Lima TM, Aguiar JL, Medeiros MD Júnior, Perez DE, Godoy GP

Acta Cir Bras

11-Mar-2024

PMCID:	PMC10926972
doi:	10.1590/acb390724
PMID:	38477784

Using Machine Learning Methods Combined with Vegetation Indices and Growth Indicators to Predict Seed Yield of Bromus inermis

Ou C, Jia Z, Sun S, Liu J, Ma W, Wang J, Mi C, Mao P

Plants (Basel)

08-Mar-2024

PMCID:	PMC10974845
doi:	10.3390/plants13060773
PMID:	38592838

Pb uptake, accumulation, and translocation in plants: Plant physiological, biochemical, and molecular response: A review

Ur Rahman S, Qin A, Zain M, Mushtaq Z, Mehmood F, Riaz L, Naveed S, Ansari MJ, Saeed M, Ahmad I, Shehzad M

Heliyon

07-Mar-2024

PMCID:	PMC10945279
doi:	10.1016/j.heliyon.2024.e27724
PMID:	38500979

Heavy Metal Bioaccumulation in Peruvian Food and Medicinal Products

Tejada-Purizaca TR, Garcia-Chevesich PA, Ticona-Quea J, Martínez G, Martínez K, Morales-Paredes L, Romero-Mariscal G, Arenazas-Rodríguez A, Vanzin G, Sharp JO, McCray JE

Foods

29-Feb-2024

PMCID:	PMC10931273
doi:	10.3390/foods13050762
PMID:	38472875

Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia

Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW

J Ethnobiol Ethnomed

28-Feb-2024

PMCID:	PMC10900619
doi:	10.1186/s13002-024-00666-z
PMID:	38419092

Current perspectives on the regulatory mechanisms of sucrose accumulation in sugarcane

Mehdi F, Galani S, Wickramasinghe KP, Zhao P, Lu X, Lin X, Xu C, Liu H, Li X, Liu X

Heliyon

28-Feb-2024

PMCID:	PMC10923725
doi:	10.1016/j.heliyon.2024.e27277
PMID:	38463882

Polyploidization of Indotyphlops braminus: evidence from isoform-sequencing

Zhu F, Lu J, Sun K, Deng C, Xu Y

BMC Genom Data

26-Feb-2024

PMCID:	PMC10895795
doi:	10.1186/s12863-024-01208-y
PMID:	38408920

The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil

da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC

J Ethnobiol Ethnomed

26-Feb-2024

PMCID:	PMC10895823
doi:	10.1186/s13002-024-00667-y
PMID:	38409039

Secretory molecules from secretion systems fine-tune the host-beneficial bacteria (PGPRs) interaction

Gupta G, Chauhan PS, Jha PN, Verma RK, Singh S, Yadav VK, Sahoo DK, Patel A

Front Microbiol

26-Feb-2024

PMCID:	PMC10925705
doi:	10.3389/fmicb.2024.1355750
PMID:	38468848

Carbon-Based Nanostructures as Emerging Materials for Gene Delivery Applications

Yazdani S, Mozaffarian M, Pazuki G, Hadidi N, Villate-Beitia I, Zárate J, Puras G, Pedraz JL

Pharmaceutics

18-Feb-2024

PMCID:	PMC10891563
doi:	10.3390/pharmaceutics16020288
PMID:	38399344

Use of Various Sugarcane Byproducts to Produce Lipid Extracts with Bioactive Properties: Physicochemical and Biological Characterization

Pereira JO, Oliveira D, Faustino M, Vidigal SS, Pereira AM, Ferreira CM, Oliveira AS, Durão J, Rodríguez-Alcalá LM, Pintado ME, Madureira AR, Carvalho AP

Biomolecules

17-Feb-2024

PMCID:	PMC10886787
doi:	10.3390/biom14020233
PMID:	38397470

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
> Benzenoids / Phenols / Methoxyphenols
Coniferyl alcohol	1549095	Click to see COC1=C(C=CC(=C1)C=CCO)O	180.20	unknown	https://doi.org/10.1271/BBB.60.1714
Sinapyl alcohol	5280507	Click to see COC1=CC(=CC(=C1O)OC)C=CCO	210.23	unknown	https://doi.org/10.1271/BBB.60.1714
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3aR,6aS)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol	138113862	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	388.40	unknown	https://doi.org/10.1271/BBB.60.1714
4-[(3S,3aR,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol	332425	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	388.40	unknown	https://doi.org/10.1271/BBB.60.1714
Syringaresinol	100067	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1271/BBB.60.1714
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1271/BBB.60.1714
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 4-methoxybenzoate	14039831	Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)OC)(C(C)C)O)C	372.50	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(+)-Abscisic acid	5375200	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C	264.32	unknown	https://doi.org/10.1007/BF02042234
(4E)-5-[(1S)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid	131954763	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C	264.32	unknown	https://doi.org/10.1007/BF02042234
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Sawamilletin	609451	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)OC)(C)C)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(00)94579-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Arundoin	12308619	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(00)94579-5
Cylindrin	189045	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(00)94579-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
cis-Aconitic acid	643757	Click to see C(C(=CC(=O)O)C(=O)O)C(=O)O	174.11	unknown	https://doi.org/10.3136/NSKKK1962.33.10_740
trans-Aconitic acid	444212	Click to see C(C(=CC(=O)O)C(=O)O)C(=O)O	174.11	unknown	https://doi.org/10.3136/NSKKK1962.33.10_740
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Malic Acid	525	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.3136/NSKKK1962.33.10_740
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
4,5-Dihydroxy-3-methoxy-6-(2,4,5-trihydroxyoxan-3-yl)oxyoxane-2-carboxylic acid	14078718	Click to see COC1C(C(C(OC1C(=O)O)OC2C(C(COC2O)O)O)O)O	340.28	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
Qchfhxzdzvjvjc-ifwyrxgasa-	21635776	Click to see COC1C(C(C(OC1C(=O)O)OC2C(C(COC2O)O)O)O)O	340.28	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R,4S,5R)-2-[(3R,4R,5R,6S)-4,5,6-trihydroxyoxan-3-yl]oxyoxane-3,4,5-triol	5289596	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)O)O)O)O	282.24	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
1,4-beta-D-Xylobiose;1,4-D-Xylobiose	552964	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)O)O)O)O	282.24	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3 https://doi.org/10.3136/NSKKK1962.33.10_740
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose	5984	Click to see C(C(C(C(C(=O)CO)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
D-Fructose	2723872	Click to see C1C(C(C(C(O1)(CO)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
(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/S0021-9673(01)88498-3
D-Galactose	6036	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
(2S,3R,4R)-2,3,4,5-tetrahydroxypentanal	66308	Click to see C(C(C(C(C=O)O)O)O)O	150.13	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
D-Xylose	135191	Click to see C1C(C(C(C(O1)O)O)O)O	150.13	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
DL-Xylose	644160	Click to see C(C(C(C(C=O)O)O)O)O	150.13	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
L-Arabinose	439195	Click to see C1C(C(C(C(O1)O)O)O)O	150.13	unknown	https://doi.org/10.1016/S0021-9673(01)88498-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(1,4)-beta-Xylotetraose	5289594	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)OC4COC(C(C4O)O)O)O)O)O	546.50	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
alpha-D-GlcpA4Me-(1->2)-beta-D-Xylp-(1->4)-beta-D-Xylp-(1->4)-beta-D-Xylp	5288379	Click to see COC1C(C(C(OC1C(=O)O)OC2C(C(COC2OC3COC(C(C3O)O)OC4COC(C(C4O)O)O)O)O)O)O	604.50	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose	5289598	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)O)O)O)O	414.36	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
HexA4Me(?1-2)Pen(?1-4)Pen(?1-4)Pen	78382736	Click to see COC1C(C(C(OC1C(=O)O)OC2C(C(COC2OC3COC(C(C3O)O)OC4COC(C(C4O)O)O)O)O)O)O	604.50	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
Pen(?1-4)Pen(?1-4)Pen(?1-4)Pen	13872868	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)OC4COC(C(C4O)O)O)O)O)O	546.50	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
Pen(?1-4)Pen(?1-4)Pen(?1-4)Pen(?1-4)Pen	13872870	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)OC4COC(C(C4O)O)OC5COC(C(C5O)O)O)O)O)O	678.60	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
Pen(?1-4)Pen(?1-4)Pen(?1-4)Pen(?1-4)Pen(?1-4)Pen	13872872	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)OC4COC(C(C4O)O)OC5COC(C(C5O)O)OC6COC(C(C6O)O)O)O)O)O	810.70	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
Xyl(b1-4)Xyl(b1-4)Xyl(b1-4)Xyl(b1-4)b-Xyl	5289597	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)OC4COC(C(C4O)O)OC5COC(C(C5O)O)O)O)O)O	678.60	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
Xyl(b1-4)Xyl(b1-4)Xyl(b1-4)Xyl(b1-4)Xyl(b1-4)b-Xyl	24857495	Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)OC4COC(C(C4O)O)OC5COC(C(C5O)O)OC6COC(C(C6O)O)O)O)O)O	810.70	unknown	https://doi.org/10.1016/0008-6215(88)80064-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/0021-9673(93)80317-2
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/0021-9673(93)80317-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
6-beta-D-glucopyranosyl-3',4',5-trihydroxy-7-methoxyflavone	44258368	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1016/0021-9673(93)80317-2
6-beta-D-Glucopyranosyl-4',5-dihydroxy-7-methoxyflavone	369636	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1021/NP50031A018
Isoorientin	114776	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/0021-9673(93)80317-2
Swertiajaponin	442659	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1016/0021-9673(93)80317-2
Swertisin	124034	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1021/NP50031A018
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one	138454316	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	https://doi.org/10.1016/0021-9673(93)80317-2 https://doi.org/10.1021/NP50031A018
Homo-orientin	5382105	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.01.015
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/0021-9673(93)80317-2 https://doi.org/10.1021/NP50031A018
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.01.015 https://doi.org/10.1016/0021-9673(93)80317-2
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	https://doi.org/10.1016/0021-9673(93)80317-2 https://doi.org/10.1021/NP50031A018
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-3-(4-methoxyphenyl)prop-2-enoate	16656544	Click to see COC1=CC=C(C=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O	652.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.01.015
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-methoxyphenyl)prop-2-enoate	73299661	Click to see COC1=CC=C(C=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O	652.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.01.015
5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44258267	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	492.40	unknown	https://doi.org/10.1021/NP50031A018
7-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromen-4-one	162927840	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C(=C5)OC)O)OC)O)CO)O)O)O)O)O	638.60	unknown	https://doi.org/10.1016/0031-9422(74)80088-9
Tricin 7-neohesperidoside	74977750	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C(=C5)OC)O)OC)O)CO)O)O)O)O)O	638.60	unknown	https://doi.org/10.1002/PCA.923
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin	5281702	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	330.29	unknown	https://doi.org/10.1016/0021-9673(93)80317-2
> Phenylpropanoids and polyketides / Stilbenes
Piceatannol	667639	Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O	244.24	unknown	https://doi.org/10.1016/0031-9422(91)83181-J

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Saccharum officinarum

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