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Vassobia breviflora

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644041fc7739b844210211
Scientific name Vassobia breviflora
Authority (Sendtn.) Hunz.
First published in Kurtziana 10: 23. 1977.

Description Top

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Synonyms Top

Scientific name Authority First published in
Acnistus bornmuelleri Dammer Repert. Spec. Nov. Regni Veg. 15: 391. 1919
Acnistus glabratus Hassl. Hassl. et al., Repert. Spec. Nov. Regni Veg. 15: 242. 1918, 1918.
Acnistus indutus Hassl. Hassl. et al., Repert. Spec. Nov. Regni Veg. 15: 242. 1918, 1918.
Acnistus pubescens Hassl. Hassl. et al., Repert. Spec. Nov. Regni Veg. 15: 242. 1918, 1918.
Acnistus tomentosus Hassl. Hassl. et al., Repert. Spec. Nov. Regni Veg. 15: 242. 1918, 1918.
Acnistus breviflorus var. glabratus Sendtn. Fl. Bras. (Martius) 10: 152. 1846
Acnistus breviflorus var. spinescens Sendtn. Fl. Bras. (Martius) 10: 132. 1846
Acnistus galanderi Dammer Repert. Spec. Nov. Regni Veg. 15: 389. 1919
Acnistus glabratus (Sendtn.) Dammer Repert. Spec. Nov. Regni Veg. 15: 388. 1919
Acnistus hauthalii Dammer Repert. Spec. Nov. Regni Veg. 15: 391. 1919
Acnistus lycioides Dammer Repert. Spec. Nov. Regni Veg. 15: 388. 1919
Acnistus mollis Dammer Repert. Spec. Nov. Regni Veg. 15: 388. 1919
Acnistus parviflorus var. arboreus (Griseb.) Griseb. Abh. Königl. Ges. Wiss. Göttingen 24: 247. 1879.
Acnistus schunckii Dammer Repert. Spec. Nov. Regni Veg. 15: 392. 1919
Acnistus sellowii Dammer Repert. Spec. Nov. Regni Veg. 15: 388. 1919
Acnistus spinescens (Sendtn.) Dammer Repert. Spec. Nov. Regni Veg. 15: 390. 1919
Acnistus spinosus Dammer Bot. Jahrb. Syst. 37: 636. 1906
Acnistus ulei Dammer Repert. Spec. Nov. Regni Veg. 15: 392. 1919
Bassovia pyraster var. glabriusculum Dunal Prodr. [A.P. de Candolle] 13(1): 408. 1852.
Bassovia spina-alba Griseb. Abh. Königl. Ges. Wiss. Göttingen 24: 248. 1879.
Capsicum breviflorum (Sendtn.) Hunz. Huitieme Congr. Int. Bot. Paris. Comptes Rend. Seances Rapp. & Commun. sect.4: 73 (1954 publ. 1956).
Capsicum glandulosum Dunal Prodr. [A. P. de Candolle] 13(1): 417. 1852 [10 May 1852]
Capsicum pyraster (Dunal) Kuntze Rev. Gen. Pl. 2: 450. 1891.
Capsicum spina-alba (Dunal) Kuntze Rev. Gen. Pl. 2: 448. 1891.
Dierbachia breviflora (Sendtn.) Kuntze Revis. Gen. Pl. 3[3]: 220. 1898 [28 Sep 1898]
Dierbachia parviflora (Griseb.) Kuntze Revis. Gen. Pl. 3[3]: 221. 1898 [28 Sep 1898]
Dierbachia senticosa (Miers) Kuntze Revis. Gen. Pl. 2: 451. 1891
Dunalia breviflora var. glabrata (Sendtn. ex Mart.) Sleumer Lilloa 23: 131. 1950
Dunalia senticosa Miers London J. Bot. 7: 340. 1848
Fregirardia spina-alba Dunal Prodr. [A. P. de Candolle] 13(1): 507. 1852 [10 May 1852]
Acnistus breviflorus f. glabratus Hassl.
Acnistus breviflorus f. indutus Hassl.
Acnistus breviflorus subf. pubescens Hassl. Repert. Spec. Nov. Regni Veg. 15: 242 (1918)
Acnistus breviflorus subf. tomentosus Hassl. Repert. Spec. Nov. Regni Veg. 15: 242 (1918)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001032708
Tropicos 29603756
KEW urn:lsid:ipni.org:names:821660-1
The Plant List kew-2461997
Open Tree Of Life 950238
NCBI Taxonomy 126907
IUCN Red List 146113380
IPNI 821660-1
iNaturalist 626809
GBIF 3801366
USDA GRIN 465539

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
Novel land uses shape meta-community structures in neighbouring native forests: Dataset across Uruguay Säumel I, Ramírez LR Data Brief 16-May-2022
PMCID:PMC9130530
doi:10.1016/j.dib.2022.108267
PMID:35647241
Withaferin A: From Ancient Remedy to Potential Drug Candidate Sultana T, Okla MK, Ahmed M, Akhtar N, Al-Hashimi A, Abdelgawad H, Haq IU Molecules 20-Dec-2021
PMCID:PMC8705790
doi:10.3390/molecules26247696
PMID:34946778
Evaluation of the geroprotective effects of withaferin A in Drosophila melanogaster Koval L, Zemskaya N, Aliper A, Zhavoronkov A, Moskalev A Aging (Albany NY) 26-Jan-2021
PMCID:PMC7880378
doi:10.18632/aging.202572
PMID:33498013
Intrinsic and extrinsic drivers of intraspecific variation in seed dispersal are diverse and pervasive Schupp EW, Zwolak R, Jones LR, Snell RS, Beckman NG, Aslan C, Cavazos BR, Effiom E, Fricke EC, Montaño-Centellas F, Poulsen J, Razafindratsima OH, Sandor ME, Shea K AoB Plants 14-Dec-2019
PMCID:PMC6914678
doi:10.1093/aobpla/plz067
PMID:31857875
Natural Products as Modulators of the Proteostasis Machinery: Implications in Neurodegenerative Diseases Cuanalo-Contreras K, Moreno-Gonzalez I Int J Mol Sci 20-Sep-2019
PMCID:PMC6801507
doi:10.3390/ijms20194666
PMID:31547084
A Review of Promising Natural Chemopreventive Agents for Head and Neck Cancer Crooker K, Aliani R, Ananth M, Arnold L, Anant S, Thomas SM Cancer Prev Res (Phila) 30-Mar-2018
PMCID:PMC6072563
doi:10.1158/1940-6207.CAPR-17-0419
PMID:29602908
Exploring fungal mega-diversity: Pseudocercospora from Brazil Silva M, Barreto RW, Pereira OL, Freitas NM, Groenewald JZ, Crous PW Persoonia 12-Feb-2016
PMCID:PMC5315286
doi:10.3767/003158516X691078
PMID:28232763
Antiproliferative withanolides from several Solanaceous species Zhang H, Cao CM, Gallagher RJ, Timmermann BN Nat Prod Res 28-May-2014
PMCID:PMC4177291
doi:10.1080/14786419.2014.919286
PMID:24871278
Cytotoxicity of withaferin A in glioblastomas involves induction of an oxidative stress-mediated heat shock response while altering Akt/mTOR and MAPK signaling pathways Grogan PT, Sleder KD, Samadi AK, Timmermann BN, Cohen MS Invest New Drugs 06-Nov-2012
PMCID:PMC3677827
doi:10.1007/s10637-012-9888-5
PMID:23129310
Reciprocal Loss of CArG-Boxes and Auxin Response Elements Drives Expression Divergence of MPF2-Like MADS-Box Genes Controlling Calyx Inflation Khan MR, Hu J, Ali GM PLoS One 10-Aug-2012
PMCID:PMC3416756
doi:10.1371/journal.pone.0042781
PMID:22900049
Anti-proliferative withanolides from the Solanaceae: a structure-activity study Zhang H, Samadi AK, Cohen MS, Timmermann BN Pure Appl Chem 15-Apr-2012
PMCID:PMC3789375
doi:10.1351/PAC-CON-11-10-08
PMID:24098060
Checklist of vascular plants of the Department of Ñeembucú, Paraguay Egea JD, Peña-Chocarro M, Espada C, Knapp S PhytoKeys 30-Jan-2012
PMCID:PMC3281576
doi:10.3897/phytokeys.9.2279
PMID:22371688
Minor Withanolides of Physalis longifolia: Structure and Cytotoxicity Zhang H, Motiwala H, Samadi A, Day V, Aubé J, Cohen M, Kindscher K, Gollapudi R, Timmermann B Chem Pharm Bull (Tokyo) 01-Jan-2012
PMCID:PMC3762585
doi:10.1248/cpb.c12-00305
PMID:23036966
Withaferin A, a Cytotoxic Steroid from Vassobia breviflora, Induces Apoptosis in Human Head and Neck Squamous Cell Carcinoma Samadi AK, Tong X, Mukerji R, Zhang H, Timmermann BN, Cohen MS J Nat Prod 24-Sep-2010
PMCID:PMC2945430
doi:10.1021/np100112p
PMID:20726569
Withaferin A, a cytotoxic steroid from Vassobia breviflora, induces apoptosis in human head and neck squamous cell carcinoma. Samadi AK, Tong X, Mukerji R, Zhang H, Timmermann BN, Cohen MS J Nat Prod 24-Sep-2010
PMCID:PMC2945430
doi:10.1021/NP100112P
PMID:20726569

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
17-Hydroxygutiesolbriolide 163184465 Click to see CC(=CCCC1=CC(=O)OC1)CCC=C(CCC=C(C)CO)C(=O)O 348.40 unknown https://doi.org/10.1016/0031-9422(81)85277-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R,4S,5R)-4,5-dimethyl-6-oxooxan-2-yl]ethyl]-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 23266166 Click to see CC1CC(OC(=O)C1C)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C 456.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R,4S,5R)-4,5-dimethyl-6-oxooxan-2-yl]ethyl]-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one 162904936 Click to see CC1CC(OC(=O)C1C)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6O)C)O5)C 458.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 23266155 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)C 454.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one 131877047 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6O)C)O5)C)C 456.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
(1S,2R,7S,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one 162905721 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6)C)O5)C)CO 456.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
(2R)-2-[(1S)-1-[(4S,8S,9S,10R,13S,14S,17R)-4-hydroxy-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 162878562 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(=O)CCC5O)C)C)CO 456.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
(2R)-2-[(1S)-1-[(4S,8S,9S,10R,13S,14S,17R)-4-hydroxy-10,13-dimethyl-1-oxo-4,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 90670439 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)CO 454.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
https://doi.org/10.1016/S0031-9422(00)82554-6
(2R)-2-[(1S)-1-[(5R,6R,8S,9S,10R,13S,14S,17R)-5-ethoxy-6-hydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 162902159 Click to see CCOC12CC=CC(=O)C1(C3CCC4(C(C3CC2O)CCC4C(C)C5CC(=C(C(=O)O5)CO)C)C)C 500.70 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
(2R)-2-[(1S)-1-[(5R,6R,8S,9S,10R,13S,14S,17R)-6-hydroxy-5-methoxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 162895266 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)OC)O)C)CO 486.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
(2R)-2-[(1S)-1-[(5R,6R,8S,9S,10S,13S,14S,17R)-5-chloro-6-hydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 12304662 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)Cl)O)C)CO 491.10 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
(2S)-2-[(1S)-1-[(4S,5R,6S,8S,9S,10R,13S,14S,17R)-6-chloro-4,5-dihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 162959413 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5O)C)O)Cl)C)CO 507.10 unknown https://doi.org/10.1016/0031-9422(81)83091-9
15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 301758 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)C 454.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
15-[1-(4,5-Dimethyl-6-oxooxan-2-yl)ethyl]-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one 162904935 Click to see CC1CC(OC(=O)C1C)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6O)C)O5)C 458.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
15-[1-[5-(Hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one 162905720 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6)C)O5)C)CO 456.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
2-[1-(4-Hydroxy-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 162878561 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(=O)CCC5O)C)C)CO 456.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
2-[1-(4-Hydroxy-10,13-dimethyl-1-oxo-4,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 163009498 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)CO 454.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
https://doi.org/10.1016/S0031-9422(00)82554-6
2-[1-(5-chloro-6-hydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl)ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 12304661 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)Cl)O)C)CO 491.10 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
2-[1-(5-ethoxy-6-hydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl)ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 162902158 Click to see CCOC12CC=CC(=O)C1(C3CCC4(C(C3CC2O)CCC4C(C)C5CC(=C(C(=O)O5)CO)C)C)C 500.70 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
2-[1-(5,6-dihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl)ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 3808690 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)O)O)C)CO 472.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
2-[1-(6-hydroxy-5-methoxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl)ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 14019837 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)OC)O)C)CO 486.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
2,3-dihydro-3beta-methoxy withaferin A 10767792 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)CO 502.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
2,3-Dihydrowithaferin A 15411208 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6O)C)O5)C)CO 472.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
https://doi.org/10.1016/0031-9422(81)85277-6
27-Hydroxy-5,6:22,26-diepoxyergosta-2,24-diene-1,26-dione 268945 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)C)CO 454.60 unknown https://doi.org/10.1016/S0031-9422(00)80671-8
https://doi.org/10.1016/S0031-9422(00)90640-X
https://doi.org/10.1016/S0031-9422(00)82554-6
3-Methoxy-2,3-dihydrowithaferin-A 433363 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)CO 502.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
4-Hydroxy-5,6:22,26-diepoxyergost-24-ene-1,26-dione 263436 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6O)C)O5)C)C 456.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
6alpha-Chloro-5beta-hydroxywithaferin A 70686220 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5O)C)O)Cl)C)CO 507.10 unknown https://doi.org/10.1016/0031-9422(81)85277-6
https://doi.org/10.1016/S0031-9422(00)82554-6
6alpha-Chloro-5beta-hydroxywithaferinA 77911828 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5O)C)O)Cl)C)CO 507.10 unknown https://doi.org/10.1016/0031-9422(81)85277-6
https://doi.org/10.1016/S0031-9422(00)82554-6
https://doi.org/10.1016/0031-9422(81)83091-9
CID 23266164 23266164 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)Cl)O)C)CO 491.10 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
Jaborosalactone A 12304656 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)C)CO 454.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
https://doi.org/10.1016/S0031-9422(00)80671-8
https://doi.org/10.1016/S0031-9422(00)90640-X
Jaborosalactone D 268947 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)O)O)C)CO 472.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
https://doi.org/10.1016/S0031-9422(00)80671-8
https://doi.org/10.1016/S0031-9422(00)90640-X
Withaferin A 265237 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)CO 470.60 unknown https://doi.org/10.1016/S0031-9422(00)80671-8
https://doi.org/10.1016/S0031-9422(00)82554-6
https://doi.org/10.1016/0031-9422(81)85277-6
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945430/
https://doi.org/10.1016/S0031-9422(00)90640-X
Withaferin A, dihydro- 418033 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6O)C)O5)C)CO 472.60 unknown https://doi.org/10.1016/0031-9422(81)85277-6
https://doi.org/10.1016/S0031-9422(00)82554-6
Withaferine A 580064 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)CO 470.60 unknown https://doi.org/10.1016/S0031-9422(00)82554-6
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945430/
https://doi.org/10.1016/0031-9422(81)85277-6

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