Salvia moorcroftiana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Salvia moorcroftiana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Internal ID UUID643febcf3c9cd420142934
Scientific name Salvia moorcroftiana
Authority Wall. ex Benth.
First published in Pl. Asiat. Rar. 1: 67 (1830)

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No known synonyms.

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000301647
Tropicos 17600597
KEW urn:lsid:ipni.org:names:456738-1
The Plant List kew-183244
Open Tree Of Life 5801007
NCBI Taxonomy 1585254
IPNI 456738-1
iNaturalist 1159291
GBIF 3895412
Freebase /m/05h3zjh
EOL 2879213
USDA GRIN 32948
Wikipedia Salvia_moorcroftiana

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
Biogenic Salvia species synthesized silver nanoparticles with catalytic, sensing, antimicrobial, and antioxidant properties Ihsan S, Gul H, Jamila N, Khan N, Ullah R, Bari A, Nee TW, Hwang JH, Masood R Heliyon 06-Feb-2024
PMCID:PMC10875438
doi:10.1016/j.heliyon.2024.e25814
PMID:38375246
Solvent based fractional biosynthesis, phytochemical analysis, and biological activity of silver nanoparticles obtained from the extract of Salvia moorcroftiana Khan M, Khan T, Wahab S, Aasim M, Sherazi TA, Zahoor M, Yun SI PLoS One 26-Oct-2023
PMCID:PMC10602276
doi:10.1371/journal.pone.0287080
PMID:37883497
Vegetation diversity pattern during spring season in relation to topographic and edaphic variables in sub-tropical zone Ali H, Muhammad Z, Majeed M, Aziz R, Khan A, Mangrio WM, Abdo HG, Almohamad H, Al Dughairi AA Bot Stud 16-Sep-2023
PMCID:PMC10505133
doi:10.1186/s40529-023-00398-5
PMID:37716923
Spatial distribution of the four invasive plants and their impact on natural communities’ dynamics across the arid and semi-arid environments in northwest Pakistan Khan N, Ullah R, Okla MK, Abdel-Maksoud MA, Saleh IA, Abu-Harirah HA, AlRamadneh TN, AbdElgawad H Front Plant Sci 25-Aug-2023
PMCID:PMC10485558
doi:10.3389/fpls.2023.1207222
PMID:37692447
Allelopathy: an alternative tool for sustainable agriculture Ain Q, Mushtaq W, Shadab M, Siddiqui MB Physiol Mol Biol Plants 24-Apr-2023
PMCID:PMC10172429
doi:10.1007/s12298-023-01305-9
PMID:37187777
Traditional foraging for ecological transition? Wild food ethnobotany among three ethnic groups in the highlands of the eastern Hindukush, North Pakistan Khan AH, Adil M, Aziz MA, Sõukand R, Pieroni A J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064566
doi:10.1186/s13002-023-00581-9
PMID:37004043
Prolonged Repellent Activity of Plant Essential Oils against Dengue Vector, Aedes aegypti Haris A, Azeem M, Abbas MG, Mumtaz M, Mozūratis R, Binyameen M Molecules 31-Jan-2023
PMCID:PMC9919174
doi:10.3390/molecules28031351
PMID:36771017
Amelioration of Scopolamine-Induced Cognitive Dysfunction in Experimental Mice Using the Medicinal Plant Salvia moorcroftiana Wahid F, Jan T, Al-Joufi FA, Ali Shah SW, Nisar M, Zahoor M Brain Sci 07-Jul-2022
PMCID:PMC9320495
doi:10.3390/brainsci12070894
PMID:35884701
Processing of Distillery Stillage to Recover Phenolic Compounds with Ultrasound-Assisted and Microwave-Assisted Extractions Mikucka W, Zielinska M, Bulkowska K, Witonska I Int J Environ Res Public Health 25-Feb-2022
PMCID:PMC8910419
doi:10.3390/ijerph19052709
PMID:35270409
Classification and Characterization of the Manoor Valley’s (Lesser Himalaya) Vegetation from the Subtropical-Temperate Ecotonal Forests to the Alpine Pastures along Ecological Variables Rahman IU, Afzal A, Iqbal Z, Alzain MN, Al-Arjani AB, Alqarawi AA, Abd_Allah EF, Ali N, Sakhi S, Khan MA, Khan U, Ijaz F, Mumtaz S, Calixto ES Plants (Basel) 28-Dec-2021
PMCID:PMC8747448
doi:10.3390/plants11010087
PMID:35009089
Exploration of ethnomedicinal plants and their practices in human and livestock healthcare in Haripur District, Khyber Pakhtunkhwa, Pakistan Siddique Z, Shad N, Shah GM, Naeem A, Yali L, Hasnain M, Mahmood A, Sajid M, Idrees M, Khan I J Ethnobiol Ethnomed 08-Sep-2021
PMCID:PMC8424965
doi:10.1186/s13002-021-00480-x
PMID:34496911
Gathered Wild Food Plants among Diverse Religious Groups in Jhelum District, Punjab, Pakistan Majeed M, Bhatti KH, Pieroni A, Sõukand R, Bussmann RW, Khan AM, Chaudhari SK, Aziz MA, Amjad MS Foods 11-Mar-2021
PMCID:PMC7999103
doi:10.3390/foods10030594
PMID:33799901
A high-throughput method for dereplication and assessment of metabolite distribution in Salvia species using LC-MS/MS Ul Haq F, Ali A, Akhtar N, Aziz N, Khan MN, Ahmad M, Musharraf SG J Adv Res 03-Feb-2020
PMCID:PMC7082496
doi:10.1016/j.jare.2020.02.001
PMID:32211205
Herbal Teas and Drinks: Folk Medicine of the Manoor Valley, Lesser Himalaya, Pakistan Rahman IU, Afzal A, Iqbal Z, Hart R, Abd_Allah EF, Hashem A, Alsayed MF, Ijaz F, Ali N, Shah M, Bussmann RW, Calixto ES Plants (Basel) 07-Dec-2019
PMCID:PMC6963793
doi:10.3390/plants8120581
PMID:31817913
An ethnobotanical study of medicinal plants used to treat skin diseases in northern Pakistan Malik K, Ahmad M, Zafar M, Ullah R, Mahmood HM, Parveen B, Rashid N, Sultana S, Shah SN, Lubna BMC Complement Altern Med 13-Aug-2019
PMCID:PMC6693210
doi:10.1186/s12906-019-2605-6
PMID:31409400

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/S0367-326X(01)00299-4
https://doi.org/10.1002/HLCA.200390159
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
3-Oxodecyl 4-hydroxybenzoate 90762940 Click to see CCCCCCCC(=O)CCOC(=O)C1=CC=C(C=C1)O 292.40 unknown https://doi.org/10.1016/S0367-326X(01)00299-4
Nonyl 4-hydroxybenzoate 586708 Click to see CCCCCCCCCOC(=O)C1=CC=C(C=C1)O 264.36 unknown https://doi.org/10.1002/HLCA.200390159
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bS)-4-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-phenanthren-3-one 14104679 Click to see CC(C)C1=CC2=CC=C3C(CCCC3(C2=C(C1=O)O)C)(C)C 298.40 unknown https://doi.org/10.1016/0031-9422(86)88043-8
Taxodione 73588 Click to see CC(C)C1=CC2=CC(=O)C3C(CCCC3(C2=C(C1=O)O)C)(C)C 314.40 unknown https://doi.org/10.1016/0031-9422(86)88043-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2S,3R,4S,5R,6S)-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxy-5-methyl-2-propan-2-ylphenoxy)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 11113500 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C(C(=C3)C)O)C(C)C)CO)O)O)O)O)O 474.50 unknown https://doi.org/10.1002/HLCA.200390159
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(4-hydroxy-5-methyl-2-propan-2-ylphenoxy)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 85403568 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C(C(=C3)C)O)C(C)C)CO)O)O)O)O)O 474.50 unknown https://doi.org/10.1002/HLCA.200390159
> 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/10.1016/S0367-326X(01)00299-4
3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,10-diol 72745631 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0367-326X(01)00299-4
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/10.1016/S0367-326X(01)00299-4
Lup-20(29)-ene-2alpha,3beta-diol 15127233 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0367-326X(01)00299-4
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/10.1016/S0367-326X(01)00299-4
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/10.1016/S0367-326X(99)00109-4
https://doi.org/10.1078/094471102321621386
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1078/094471102321621386
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1078/094471102321621386
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/10.1078/094471102321621386
https://doi.org/10.1016/S0367-326X(99)00109-4
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/10.1078/094471102321621386
https://doi.org/10.1016/S0367-326X(99)00109-4
> 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/10.1016/S0367-326X(01)00299-4
> 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/S0367-326X(99)00109-4
https://doi.org/10.1078/094471102321621386
https://doi.org/10.1016/S0008-6215(02)00008-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-[4-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one 11092942 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3=CC(=O)C4=C(C=C(C=C4O3)OC)O)O)OC5C(C(C(CO5)O)O)O)O 562.50 unknown https://doi.org/10.1002/HLCA.200390159
2-[4-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one 11114610 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC=C(C=C3)C4=CC(=O)C5=C(C=C(C=C5O4)OC)O)CO)O)O)O)O)O 592.50 unknown https://doi.org/10.1002/HLCA.200390159
2-[4-[3,5-Dihydroxy-6-methyl-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one 85396290 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3=CC(=O)C4=C(C=C(C=C4O3)OC)O)O)OC5C(C(C(CO5)O)O)O)O 562.50 unknown https://doi.org/10.1002/HLCA.200390159
2-[4-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one 75580666 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC=C(C=C3)C4=CC(=O)C5=C(C=C(C=C5O4)OC)O)CO)O)O)O)O)O 592.50 unknown https://doi.org/10.1002/HLCA.200390159
5-hydroxy-7-methoxy-2-[4-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]chromen-4-one 162964846 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0008-6215(02)00008-3
Luteolin 3'-glucoside 12309350 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1002/HLCA.200390159
https://doi.org/10.1016/S0008-6215(02)00008-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Takakin 44258588 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O 300.26 unknown https://doi.org/10.1016/S0367-326X(01)00299-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/S0367-326X(99)00109-4
https://doi.org/10.1078/094471102321621386
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/S0008-6215(02)00008-3
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1078/094471102321621386

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