Scientific name	Authority	First published in
Tithymalus wallichii	(Hook.f.) Soják	Cas. Nár. Mus., Odd. Prír. 140: 177 (1972)
Euphorbia duclouxii	H.Lév. & Vaniot	Repert. Spec. Nov. Regni Veg. 6: 113 (1908)
Euphorbia wallichii subsp. duclouxii	(H.Lév. & Vaniot) R.Turner	New Pl. 1(3): 169 (1994)
Euphorbia yunnanensis	Radcl.-Sm.	Kew Bull. 45: 569 (1990)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	euphorbia duclouxii
Spanish	euphorbia wallichii subsp. duclouxii
Spanish	euphorbia yunnanensis
Spanish	tithymalus wallichii
Chinese	大果大戟
Chinese	云南大戟
Chinese	长虫山大戟

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

Asia-temperate click to expand
- China
  - China South-central
  - Qinghai
  - Tibet
- Western Asia
  - Afghanistan

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Laos

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000965397
Tropicos	50105978
KEW	urn:lsid:ipni.org:names:348725-1
The Plant List	kew-82801
Open Tree Of Life	3912272
NCBI Taxonomy	1333960
IPNI	348725-1
iNaturalist	603037
GBIF	3065773
EOL	1143639
Wikipedia	Euphorbia_wallichii
CMAUP	NPO8770

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

The local medicinal plant knowledge in Kashmir Western Himalaya: a way to foster ecological transition via community-centred health seeking strategies

Manzoor M, Ahmad M, Zafar M, Gillani SW, Shaheen H, Pieroni A, Al-Ghamdi AA, Elshikh MS, Saqib S, Makhkamov T, Khaydarov K

J Ethnobiol Ethnomed

30-Nov-2023

PMCID:	PMC10688143
doi:	10.1186/s13002-023-00631-2
PMID:	38037066

Antibacterial Efficacy of Green Synthesized Silver Nanoparticles Using Salvia nubicola Extract against Ralstonia solanacearum, the Causal Agent of Vascular Wilt of Tomato

Dilbar S, Sher H, Ali H, Ullah R, Ali A, Ullah Z

ACS Omega

17-Aug-2023

PMCID:	PMC10468922
doi:	10.1021/acsomega.3c03164
PMID:	37663485

Antimicrobial activity of phytofabricated silver nanoparticles using Carica papaya L. against Gram-negative bacteria

Arsene MM, Viktorovna PI, Alla M, Mariya M, Davares AK, Carime BZ, Anatolievna GO, Vyacheslavovna YN, Vladimirovna ZA, Andreevna SL, Aleksandrovna VE, Alekseevich BL, Nikolaïevna BM, Parfait K, Andrey V

Vet World

13-Jun-2023

PMCID:	PMC10421558
doi:	10.14202/vetworld.2023.1301-1311
PMID:	37577189

A cross-cultural study of high-altitude botanical resources among diverse ethnic groups in Kashmir Himalaya, India

Haq SM, Waheed M, Khoja AA, Amjad MS, Bussmann RW, Ali K

J Ethnobiol Ethnomed

13-Apr-2023

PMCID:	PMC10100632
doi:	10.1186/s13002-023-00582-8
PMID:	37055855

Keeping Healthy in Your Skin—Plants and Fungi Used by Indigenous Himalayan Communities to Treat Dermatological Ailments

Haq SM, Khoja AA, Lone FA, Waheed M, Bussmann RW, Casini R, Mahmoud EA, Elansary HO

Plants (Basel)

06-Apr-2023

PMCID:	PMC10097107
doi:	10.3390/plants12071575
PMID:	37050200

A Novel Based Synthesis of Silver/Silver Chloride Nanoparticles from Stachys emodi Efficiently Controls Erwinia carotovora, the Causal Agent of Blackleg and Soft Rot of Potato

Dilbar S, Sher H, Binjawhar DN, Ali A, Ali I

Molecules

09-Mar-2023

PMCID:	PMC10058436
doi:	10.3390/molecules28062500
PMID:	36985472

Pattern of β-Diversity and Plant Species Richness along Vertical Gradient in Northwest Himalaya, India

Wani ZA, Khan S, Bhat JA, Malik AH, Alyas T, Pant S, Siddiqui S, Moustafa M, Ahmad AE

Biology (Basel)

18-Jul-2022

PMCID:	PMC9312975
doi:	10.3390/biology11071064
PMID:	36101443

Green Synthesis of Silver Nanoparticles Using Euphorbia wallichii Leaf Extract: Its Antibacterial Action against Citrus Canker Causal Agent and Antioxidant Potential

Arif M, Ullah R, Ahmad M, Ali A, Ullah Z, Ali M, Al-Joufi FA, Zahoor M, Sher H

Molecules

30-May-2022

PMCID:	PMC9182241
doi:	10.3390/molecules27113525
PMID:	35684463

A Critical Review of the Antimicrobial and Antibiofilm Activities of Green-Synthesized Plant-Based Metallic Nanoparticles

Luzala MM, Muanga CK, Kyana J, Safari JB, Zola EN, Mbusa GV, Nuapia YB, Liesse JM, Nkanga CI, Krause RW, Balčiūnaitienė A, Memvanga PB

Nanomaterials (Basel)

27-May-2022

PMCID:	PMC9182092
doi:	10.3390/nano12111841
PMID:	35683697

Green synthesis and characterization of iron-oxide nanoparticles using Moringa oleifera: a potential protocol for use in low and middle income countries

Kiwumulo HF, Muwonge H, Ibingira C, Lubwama M, Kirabira JB, Ssekitoleko RT

BMC Res Notes

25-Apr-2022

PMCID:	PMC9036744
doi:	10.1186/s13104-022-06039-7
PMID:	35468836

A Cross-Cultural Analysis of Plant Resources among Five Ethnic Groups in the Western Himalayan Region of Jammu and Kashmir

Haq SM, Hassan M, Bussmann RW, Calixto ES, Rahman IU, Sakhi S, Ijaz F, Hashem A, Al-Arjani AB, Almutairi KF, Abd_Allah EF, Aziz MA, Ali N

Biology (Basel)

23-Mar-2022

PMCID:	PMC9032642
doi:	10.3390/biology11040491
PMID:	35453691

Antimicrobial Diterpenes: Recent Development From Natural Sources

Saha P, Rahman FI, Hussain F, Rahman SM, Rahman MM

Front Pharmacol

28-Feb-2022

PMCID:	PMC8918777
doi:	10.3389/fphar.2021.820312
PMID:	35295739

Gold Nanoparticles: Biosynthesis and Potential of Biomedical Application

Mikhailova EO

J Funct Biomater

03-Dec-2021

PMCID:	PMC8708476
doi:	10.3390/jfb12040070
PMID:	34940549

Fruit Derived Potentially Bioactive Bioengineered Silver Nanoparticles

Baker A, Iram S, Syed A, Elgorban AM, Bahkali AH, Ahmad K, Sajid Khan M, Kim J

Int J Nanomedicine

18-Nov-2021

PMCID:	PMC8612025
doi:	10.2147/IJN.S330763
PMID:	34848956

Seed bank characteristics in a Pinus densata forest and its relationship with vegetation diversity in Southeast Tibet, China

Lu J, Li Z, Gao T, Tang X

Ecol Evol

20-Aug-2020

PMCID:	PMC7487222
doi:	10.1002/ece3.6603
PMID:	32953056

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 / Benzene and substituted derivatives / Phenylpropanes
Butylated Hydroxytoluene	31404	Click to see CC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C	220.35	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
(2S,3S,3aS,4'aS,4'bS,6S,7aR,8'aR,10'aS)-2,6-dihydroxy-3a,4'a,6',6',7,7,8'a,10'a-octamethylspiro[1,2,4,5,6,7a-hexahydroindene-3,2'-3,4,4b,5,7,8,9,10-octahydrophenanthrene]-1'-one	163035768	Click to see CC1(CCC2(CCC3(C(=O)C4(CCC3(C2C1)C)C(CC5C4(CCC(C5(C)C)O)C)O)C)C)C	458.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245439/
2,6-Dihydroxy-3a,4'a,6',6',7,7,8'a,10'a-octamethylspiro[1,2,4,5,6,7a-hexahydroindene-3,2'-3,4,4b,5,7,8,9,10-octahydrophenanthrene]-1'-one	163035767	Click to see CC1(CCC2(CCC3(C(=O)C4(CCC3(C2C1)C)C(CC5C4(CCC(C5(C)C)O)C)O)C)C)C	458.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245439/
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane	11636	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC	380.70	unknown	via CMAUP database
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	via CMAUP database
Pentadecane	12391	Click to see CCCCCCCCCCCCCCC	212.41	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Dodecanoate	4149208	Click to see CCCCCCCCCCCC(=O)[O-]	199.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(10E)-16-hydroxy-4,8,8,11,15-pentamethyl-12-oxo-3-oxatetracyclo[11.3.0.02,4.07,9]hexadec-10-en-13-yl] (E)-3-phenylprop-2-enoate	56680640	Click to see CC1CC2(C(C1O)C3C(O3)(CCC4C(C4(C)C)C=C(C2=O)C)C)OC(=O)C=CC5=CC=CC=C5	464.60	unknown	via CMAUP database
Retene	10222	Click to see CC1=C2C=CC3=C(C2=CC=C1)C=CC(=C3)C(C)C	234.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4S,9S,10R,12R,13S,14S)-5,5,9-trimethyl-6-oxopentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-13-carboxylic acid	162896887	Click to see CC1(C2CCC34CC5C(C5(C3)C(=O)O)CC4C2(CCC1=O)C)C	316.40	unknown	https://doi.org/10.1021/OL0608552
5,5,9-Trimethyl-6-oxopentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-13-carboxylic acid	73023507	Click to see CC1(C2CCC34CC5C(C5(C3)C(=O)O)CC4C2(CCC1=O)C)C	316.40	unknown	https://doi.org/10.1021/OL0608552
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids / Phorbol esters
Phorbol 12-myristate 13-acetate	27924	Click to see CCCCCCCCCCCCCC(=O)OC1C(C2(C(C=C(CC3(C2C=C(C3=O)C)O)CO)C4C1(C4(C)C)OC(=O)C)O)C	616.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1S,4S,6R,9S,10R,12R,13S,15R)-5,5,9-trimethylpentacyclo[11.3.1.01,10.04,9.012,15]heptadecane-6,13-diol	163061274	Click to see CC1(C2CCC34CC5CC(C3)(C5CC4C2(CCC1O)C)O)C	304.50	unknown	https://doi.org/10.1021/OL0608552
(1S,4S,6S,9S,10R,12R,13S,15R)-6,13-dihydroxy-5,5,9-trimethylpentacyclo[11.3.1.01,10.04,9.012,15]heptadecan-7-one	162990595	Click to see CC1(C2CCC34CC5CC(C3)(C5CC4C2(CC(=O)C1O)C)O)C	318.40	unknown	https://doi.org/10.1021/OL0608552
5,5,9-Trimethylpentacyclo[11.3.1.01,10.04,9.012,15]heptadecane-6,13-diol	73030846	Click to see CC1(C2CCC34CC5CC(C3)(C5CC4C2(CCC1O)C)O)C	304.50	unknown	https://doi.org/10.1021/OL0608552
6,13-Dihydroxy-5,5,9-trimethylpentacyclo[11.3.1.01,10.04,9.012,15]heptadecan-7-one	73047792	Click to see CC1(C2CCC34CC5CC(C3)(C5CC4C2(CC(=O)C1O)C)O)C	318.40	unknown	https://doi.org/10.1021/OL0608552
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(Z)-alpha-Bisabolene	5352653	Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Helioscopinolide A	10245246	Click to see CC1=C2C=C3CCC4C(C(CCC4(C3CC2OC1=O)C)O)(C)C	316.40	unknown	via CMAUP database
helioscopinolide B	10335933	Click to see CC1=C2C=C3CCC4C(C(CCC4(C3CC2OC1=O)C)O)(C)C	316.40	unknown	via CMAUP database
Helioscopinolide E	11565893	Click to see CC1=C2C=C3CCC4C(C(=O)CCC4(C3CC2OC1=O)C)(C)C	314.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(17alpha,23E)-5alpha-Dammara-20,23-diene-3beta,25-diol	9955042	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CC=CC(C)(C)O)C)C)C	442.70	unknown	via CMAUP database
(3S,5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	12312929	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C	440.70	unknown	https://doi.org/10.1055/S-0028-1097206
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Euphorbol	634628	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C	440.70	unknown	https://doi.org/10.1055/S-0028-1097206
Lanosta-8,24-dien-3-ol	856	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1055/S-0028-1097206
Tirucallol	101257	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1055/S-0028-1097206
Yamogenin	441900	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25R)-3beta-[4-O-[4-O-(alpha-L-Rhamnopyranosyl)-alpha-L-rhamnopyranosyl]-beta-D-glucopyranosyloxy]spirosta-5-ene	21603983	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	21603986	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1015.20	unknown	via CMAUP database
Borassoside A	16204068	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Borassoside B	102155844	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O	901.00	unknown	via CMAUP database
Borassoside C	102155845	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O	901.00	unknown	via CMAUP database
Borassoside D	16204180	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Borassoside E	16204181	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Borassoside F	16204183	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1015.20	unknown	via CMAUP database
Collettinside III	10653210	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Dioscin	119245	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Disogluside	11827970	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	576.80	unknown	via CMAUP database
Methylprotodioscin	11263254	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC	1063.20	unknown	via CMAUP database
Progenin II	44429638	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Prosapogenin A	11061578	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Protodioscin	441891	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	via CMAUP database
Pseudoprotodioscin	21637110	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O	1031.20	unknown	via CMAUP database
Trigonelloside C	441899	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	via CMAUP database
Yamogenin 3-O-neohesperidoside	441901	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
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	via CMAUP database
> Organic acids and derivatives / Carbothioic S-acids
Pentadecanethioic acid	18413781	Click to see CCCCCCCCCCCCCCC(=O)S	258.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose	5288769	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Gal(a1-6)a-Man	11724912	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp	5287808	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O	504.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
17-hydroxyjolkinolide A	6712606	Click to see CC1(CCCC2(C1CCC34C2C=C5C(=C(C(=O)O5)CO)C3O4)C)C	330.40	unknown	via CMAUP database

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Euphorbia wallichii

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