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Salvia bucharica

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

Internal ID UUID643feb9d072fa438436872
Scientific name Salvia bucharica
Authority Popov
First published in Trudy Turkestansk. Nauchn. Obshch. 1: 40 (1923)

Description Top

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Synonyms Top

Scientific name Authority First published in
Arischrada bucharica (Popov) Pobed. Novosti Sist. Vyssh. Rast. 9: 247 (1972)
Salvia honigbergeri Rech.f. Ann. Naturhist. Mus. Wien 51: 418 (1941)
Schraderia bucharica (Popov) Nevski Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast. 4: 327 (1937)
Stiefia bucharica (Popov) Soják Cas. Nár. Mus., Odd. Prír. 152: 22 (1983)

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
  • Asia-temperate
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000300515
Tropicos 50312006
KEW urn:lsid:ipni.org:names:455829-1
The Plant List kew-182199
Open Tree Of Life 448587
Observations.org 121728
NCBI Taxonomy 49209
IPNI 455829-1
iNaturalist 1005354
GBIF 3883069
Elurikkus 432995

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
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
Buchariate: An Aromatic Ester from Salvia bucharica V. U. Ahmad, M. Zahid, M. S. Ali, S. Ahmad, Z. Ali, M. Z. Iqbal, R.B. Tareen MDPI AG 03-May-2019
doi:10.3797/SCIPHARM.AUT-00-39
Applications of Friedel–Crafts reactions in total synthesis of natural products Heravi MM, Zadsirjan V, Saedi P, Momeni T RSC Adv 03-Dec-2018
PMCID:PMC9091380
doi:10.1039/c8ra07325b
PMID:35558228
Ethnomedicines and anti-parasitic activities of Pakistani medicinal plants against Plasmodia and Leishmania parasites Tariq A, Adnan M, Amber R, Pan K, Mussarat S, Shinwari ZK Ann Clin Microbiol Antimicrob 20-Sep-2016
PMCID:PMC5029062
doi:10.1186/s12941-016-0170-0
PMID:27647140
Isoperadione: A New Triterpenoid from Salvia bucharica Viqar Uddin Ahmad, Muhammad Zahid, Muhammad Shaiq Ali, Zulfiqar Ali, Naseer Alam, Rasool Bakhsh Tareen, Muhammad Zafar Iqbal Walter de Gruyter GmbH 17-Feb-2015
doi:10.1515/ZNB-1999-0320
Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione Majetich G, Zhang Y, Tian X, Zou G, Li Y, Wang Y, Hu S, Huddleston E Molecules 14-Jun-2013
PMCID:PMC6269985
doi:10.3390/molecules18066969
PMID:23771059
Terpenoids from Cleome droserifolia (Forssk.) Del. El-Askary HI Molecules 31-Aug-2005
PMCID:PMC6147721
doi:10.3390/10080971
PMID:18007365
Salvadiones-A and -B:  Two Terpenoids Having Novel Carbon Skeleta from <i>Salvia bucharica</i> Viqar Uddin Ahmad, M. Zahid, M. Shaiq Ali, Z. Ali, A. R. Jassbi, M. Abbas, J. Clardy, E. Lobkovsky, R. B. Tareen, M. Zafar Iqbal American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/JO990024S
Salvadiol: A novel triterpenoid from Salvia bucharica Viqar Uddin Ahmad, Muhammad Zahid, Muhammad Shaiq Ali, Muhammad Iqbal Choudhary, Farzana Akhtar, Zulfiqar Ali, Muhammad Zafar Iqbal Elsevier BV 26-Jul-2002
doi:10.1016/S0040-4039(99)01603-2
Bucharioside and buchariol from Salvia bucharica. Ahmad VU, Zahid M, Ali MS, Jassbi AR, Abbas M, Ali Z, Iqbal MZ Phytochemistry 01-Dec-1999
doi:10.1016/S0031-9422(99)00389-1
PMID:10691324

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
3-Oxooctyl 4-hydroxybenzoate 162876771 Click to see CCCCCC(=O)CCOC(=O)C1=CC=C(C=C1)O 264.32 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
(1S,3R,5S,6R,8R,10S,15S,16S)-10-hydroxy-14,14,17-trimethyl-6-(2-methylprop-1-enyl)-3-propan-2-yl-4-oxahexacyclo[14.3.1.15,8.01,8.03,5.010,15]henicos-17-ene-2,21-dione 100970221 Click to see CC1=CCC23CC1C4C(CCCC4(CC25CC(C6(C5=O)C(C3=O)(O6)C(C)C)C=C(C)C)O)(C)C 466.70 unknown https://doi.org/10.1515/ZNB-1999-0320
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,2R,3S,4R,7R,9R)-7,9-dimethyl-4-propan-2-yl-8-oxatricyclo[5.4.0.02,9]undecan-3-ol 101009028 Click to see CC(C)C1CCC2(C3CCC(C3C1O)(O2)C)C 238.37 unknown https://doi.org/10.1016/S0031-9422(99)00389-1
7,9-Dimethyl-4-propan-2-yl-8-oxatricyclo[5.4.0.02,9]undecan-3-ol 76024921 Click to see CC(C)C1CCC2(C3CCC(C3C1O)(O2)C)C 238.37 unknown https://doi.org/10.1016/S0031-9422(99)00389-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1R,4S,9S,11S,12R)-18-ethenyl-12-hydroxy-15-(2-hydroxypropan-2-yl)-5,5-dimethyl-14-propan-2-yl-21-oxahexacyclo[12.5.1.19,12.01,11.04,9.011,16]henicos-17-ene-13,20-dione 10743410 Click to see CC(C)C12C(C3C=C(CC4(C1=O)C35CC6(CCCC(C6CC4)(C)C)OC5(C2=O)O)C=C)C(C)(C)O 482.60 unknown https://doi.org/10.1016/S0040-4039(99)01603-2
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(1R,9S,11S,12R,16R)-5,5,15,15,19-pentamethyl-23-propan-2-yl-14,24-dioxaheptacyclo[11.8.2.19,12.01,11.04,9.011,18.012,16]tetracosa-13(23),19-dien-22-one 101629488 Click to see CC1=CCC23CCC4C(CCCC45CC26C1CC7C6(O5)C(=C(C3=O)C(C)C)OC7(C)C)(C)C 450.70 unknown https://doi.org/10.1515/ZNB-1999-0320
(1S,2S,8S,10R,14R,16S,21S,23R)-7,7,11,17,17-pentamethyl-4-propan-2-yl-6,22-dioxaheptacyclo[19.2.1.01,10.02,14.05,23.08,23.016,21]tetracosa-4,11-dien-3-one 162846090 Click to see CC1=CCC2CC3C(CCCC34CC56C1CC7C5(O4)C(=C(C(=O)C62)C(C)C)OC7(C)C)(C)C 450.70 unknown https://doi.org/10.1515/ZNB-1999-0320
(1S,3S,5S,10S,13R,17S,18S,20R)-5-hydroxy-9,9,16-trimethyl-18-(2-methylprop-1-enyl)-20-propan-2-yl-19-oxahexacyclo[11.5.3.01,20.03,13.03,17.05,10]henicos-15-ene-2,21-dione 100970222 Click to see CC1=CCC23CCC4C(CCCC4(CC25C1C(C6(C5=O)C(C3=O)(O6)C(C)C)C=C(C)C)O)(C)C 466.70 unknown https://doi.org/10.1515/ZNB-1999-0320
(4S,9S,11S,12R,14R,15R,16S)-12-hydroxy-5,5,17-trimethyl-15-(2-methylprop-1-enyl)-14-propan-2-yl-21-oxahexacyclo[12.5.1.19,12.01,11.04,9.011,16]henicos-17-ene-13,20-dione 101008508 Click to see CC1=CCC23CCC4C(CCCC45CC26C1C(C(C3=O)(C(=O)C6(O5)O)C(C)C)C=C(C)C)(C)C 466.70 unknown https://doi.org/10.1021/JO990024S
7,7,11,17,17-Pentamethyl-4-propan-2-yl-6,22-dioxaheptacyclo[19.2.1.01,10.02,14.05,23.08,23.016,21]tetracosa-4,11-dien-3-one 162846089 Click to see CC1=CCC2CC3C(CCCC34CC56C1CC7C5(O4)C(=C(C(=O)C62)C(C)C)OC7(C)C)(C)C 450.70 unknown https://doi.org/10.1515/ZNB-1999-0320
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1beta,3beta)-Olean-18-ene-1,3-diol 15380487 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C)C)C 442.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73072970 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.3797/SCIPHARM.AUT-00-39
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 https://doi.org/10.3797/SCIPHARM.AUT-00-39
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,4S,6R)-1,3,3-Trimethyl-2-oxabicyclo[2.2.2]oct-6-yl I(2)-D-glucopyranoside 100917677 Click to see CC1(C2CCC(O1)(C(C2)OC3C(C(C(C(O3)CO)O)O)O)C)C 332.39 unknown https://doi.org/10.1016/S0031-9422(99)00389-1
(1S,2S,4R)-1,8-Epoxy-p-menthan-2-ol glucoside 73815050 Click to see CC1(C2CCC(O1)(C(C2)OC3C(C(C(C(O3)CO)O)O)O)C)C 332.39 unknown https://doi.org/10.1016/S0031-9422(99)00389-1
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,4R,6R)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-6-yl]oxy]oxane-3,4,5-triol 21630950 Click to see CC1(C2CCC(O1)(C(C2)OC3C(C(C(C(O3)CO)O)O)O)C)C 332.39 unknown https://doi.org/10.1016/S0031-9422(99)00389-1
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,4R,6S)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-6-yl]oxy]oxane-3,4,5-triol 21630948 Click to see CC1(C2CCC(O1)(C(C2)OC3C(C(C(C(O3)CO)O)O)O)C)C 332.39 unknown https://doi.org/10.1016/S0031-9422(99)00389-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetyl-4-isopropylpyridine 529345 Click to see CC(C)C1=CC(=NC=C1)C(=O)C 163.22 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
> Organoheterocyclic compounds / Naphthofurans
(1S,4R,9R,11R,13S,16S,17S,22S)-19-ethenyl-9,13-dihydroxy-5,5,15,15-tetramethyl-22-propan-2-yl-14-oxahexacyclo[11.7.2.01,11.04,9.011,17.016,22]docos-18-ene-12,21-dione 162982004 Click to see CC(C)C12C3C4C=C(CC5(C1=O)C4(CC6(CCCC(C6CC5)(C)C)O)C(=O)C2(OC3(C)C)O)C=C 482.60 unknown https://doi.org/10.1021/JO990024S
19-Ethenyl-9,13-dihydroxy-5,5,15,15-tetramethyl-22-propan-2-yl-14-oxahexacyclo[11.7.2.01,11.04,9.011,17.016,22]docos-18-ene-12,21-dione 162982003 Click to see CC(C)C12C3C4C=C(CC5(C1=O)C4(CC6(CCCC(C6CC5)(C)C)O)C(=O)C2(OC3(C)C)O)C=C 482.60 unknown https://doi.org/10.1021/JO990024S
> 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/10.3797/SCIPHARM.AUT-00-39
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-39

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