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

Reactive oxygen species induced oxidative damage to DNA, lipids, and proteins of antibiotic-resistant bacteria by plant-based silver nanoparticles

Ali HM, Karam K, Khan T, Wahab S, Ullah S, Sadiq M

3 Biotech

22-Nov-2023

PMCID:	PMC10665289
doi:	10.1007/s13205-023-03835-1
PMID:	38009163

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

Herbal Arsenal against Skin Ailments: A Review Supported by In Silico Molecular Docking Studies

Singab AN, Mostafa NM, Fawzy IM, Bhatia D, Suryawanshi PT, Kabra A

Molecules

21-Sep-2022

PMCID:	PMC9572213
doi:	10.3390/molecules27196207
PMID:	36234737

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

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 / 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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Salvia moorcroftiana

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Distribution (via POWO/KEW) Top

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