JP2003002820A - Skin care composition - Google Patents

Abstract

PROBLEM TO BE SOLVED: To prepare a cosmetic having elastase-inhibiting activity and which can keep the tension, elasticity and freshness of the skin. SOLUTION: An elastase-inhibiting agent consisting of one or more substances selected from a catechin and/or its glycosides, a flavone and/or its glycosides, a flavonol and/or its glycosides, a flavanone and/or its glycosides, an isoflavone and/or its glycosides, a coumarin and/or its glvcoside, an extract of a mushroom belonging to the genus Fuscopoliae, extracts of plants belonging to the genera Vitis, Oenothera, Bsllis, Gnaphalium, Arctostaphyllos, Centaurea, Lythrum, Hyssopus, thymus, Leontopodium, Centaury, Satoreja, Anthriscus, Raurus, Nymphaea, Syringa, Calendula, Turnera, Scabiosa, Torifolium, Convallaria and so on, and the dried powder of red wine is compounded.

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to an anti-aging cosmetic composition containing a plant extract, and more specifically, it has an elastase inhibitory action, maintains the firmness and elasticity of the skin, and maintains a youthful skin condition. The present invention relates to an anti-aging agent that can be used. INDUSTRIAL APPLICABILITY The anti-aging cosmetic composition of the present invention can be suitably used for basic cosmetics, makeup cosmetics and the like.

[0002]

BACKGROUND OF THE INVENTION Conventionally, the necessity of anti-aging cosmetics has been considered, but since the mechanism and definition of aging have not been clarified, it is generally considered as a moisturizing skin. It has been judged by measuring the moisturizing condition and the elasticity of the skin. However, in recent years, research on aging has been advanced, and as a cause of skin aging, aging is the first important factor, and the effect of ultraviolet rays is mentioned as a direct factor relating to skin aging.
As specific phenomena of skin aging, it is known that collagen and elastin in the skin dermis are reduced, mucopolysaccharides such as hyaluronic acid are reduced, and cell damage due to ultraviolet rays is caused. Of these, elastin forms cross-links with each other and contributes to the elasticity of tissues.However, elastin, which is an elastin-disrupting enzyme, is overexpressed by UV exposure and aging, and elastin is denatured and destroyed. It is believed to lead to reduced skin elasticity.

Therefore, it is important to prevent aging of the skin by suppressing the action of elastase and preventing the degeneration and destruction of elastin which gives elasticity and firmness to the skin. However, many conventional anti-aging cosmetics have a mechanism of activating fibroblasts and increasing the amount of collagen produced, but few have focused on the inhibition of elastase activity.

Therefore, the present invention protects the fiber components of the skin by suppressing the activity of elastase, and prevents the aging of the skin by restoring and maintaining the firmness and elasticity of the skin,
It is an object of the present invention to provide an anti-aging cosmetic which has an effect of maintaining a youthful skin condition.

[0005]

Means for Solving the Problems As a result of extensive studies aimed at solving the above-mentioned problems, the present inventor has found that catechins and / or their glycosides, flavones and / or their glycosides, and flavonols. And / or a glycoside thereof, a flavanone and / or a glycoside thereof, an isoflavone and / or
Or a glycoside thereof, a coumarin and / or a glycoside thereof,
Mushrooms belonging to the genus Fuscoporia, genus Vitis, genus Oenothera, beris
llis genus, Gnaphalium genus, Arctostaphylos genus, Centre
aurea genus, Lythrum genus, Hyssop
us), Thymus, Leontopodium (Le
genus ontopodium, genus Centaurium, genus Saturja, Anthriscus
Genus, genus Laurus, Nymphaea
Genus, Syringa, Calendul
a) genus, Turnera genus, Scurvy
Genus, genus Trifolium, Convalaria (C
onvallaria), Consolida (Consolida), Artemisia (Artemisia), Gardenia (Gardenia),
Camellia, Citrus, Alchemilla
genus emilla, Artemisia, mentor
The present invention has been completed based on the finding that the extract of plants belonging to the genus enth), the plant belonging to the genus Malus, and the dry powder of red wine have elastase inhibitory activity.

The substances and extracts that can be used in the present invention are not particularly limited, but catechins and / or glycosides thereof include catechin, epicatechin, epigallocatechin, epigallocatechin gallate and the like.

Examples of flavones and / or their glycosides include luteolin, flavones and apigenin.

Examples of flavonols and / or their glycosides include quercetin, myricetin, kaempferol, quercitrin, rutin and the like.

Examples of flavanones and / or glycosides thereof include naringenin, flavanone, hesperidin and naringin.

The isoflavones and / or their glycosides include genistein, daidzein genistin and the like.

Coumarins and / or glycosides thereof include esculetin and the like.

Examples of mushrooms belonging to the genus Fuscoporia include white birch mushrooms (Fuscoporia obliqua).

As a plant of the genus Vitis, grapes (V
itis vinifera L.) and the like.

Examples of plants belonging to the genus Oenothera include evening primrose (Oenothera biennis L.) and the like.

Examples of plants of the genus Bellis include Bellis perennis.

Examples of the Gnaphalium genus plant include Everlasting (Gnaphalium uliginosum L.) and the like.

Arctostaphylos
Arctostaphylosuva-ursi (L.) as a genus plant
S _PRENG. ) And the like.

Examples of the plant of the genus Centaurea include cornflower (Centaureacyanus L.) and the like.

Lythrum (Lythrum) plants include Lythrum anceps Makino and grass polly (Lythr).
um salicaria L.) and the like.

Examples of Hyssopus plants include Hyssopus officinalis L. and the like.

Examples of the plant of the genus Thymus include Thymus quinquecostatus Celak. And Wild thyme (Thymus serpyllum L.).

Examples of plants belonging to the genus Leontopodium include Edelweiss (Leontopodium alpinum) and the like.

Examples of the plant of the genus Centaurium include Centaurium erythraea R _AFN .

Examples of the plant of the genus Saturja include savory (Satureja hortensis L.).

Examples of plants belonging to the genus Anthriscus include chervil (Anthriscus cerefolium (L.) H _OFFM .).

Examples of the plant of the genus Rolls include Laurel (Laurus nobilis L.) and the like.

Examples of the plant of the genus Nymphaea include white water lily (Nymphaea alba L.) and the like.

Examples of plants belonging to the genus Syringa include lilac (Syringa vulgaris).

Examples of the plant of the genus Calendula include pot marigold (Calendula officinalis).

[0030] Damner (Turnera diffusa W _{IL LD} .varaphrodisiaca (W _ARD .) U)
_RB .) And the like.

Examples of Scurvy plants include Scurvy grass and the like.

Examples of plants of the genus Trifolium include red clover (Trifolium pratense L.) and the like.

Examples of plants of the genus Convallaria include Lily of the Barry (Convallaria majalis L.) and the like.

Examples of plants belonging to the genus Consolida include cypress (Consolida ambigua) and the like.

Examples of Artemisia plants include tarragon (Artemisia dracunculoildes L.) and the like.

Gardenia jasminoides Ellis f. Grandiflora Mak as a plant of the genus Gardenia
ino) and the like.

As a Camellia plant, camellia (Camellia j
aponica L.) and the like.

Examples of Citrus plants include lemon (Citrus limon B _URM .) And the like.

Examples of Alchemilla genus plants include Alchemilla vulgarisagg.

Examples of Artemisia plants include Artemisia stelleriana Besser and Southern wood (Artemisia abrotanum L.).

As a plant of the genus Menth, water mint (Mentha aquatica L.) and penny royal (Menth)
a pulegium L.) and the like.

As a plant of the genus Malus, apples (Mal
us pumila Mill.), Hana Kaidou (Malus halliana)
Koehne) and the like.

Catechins and / or glycosides thereof, flavones and / or glycosides thereof, flavonols and / or glycosides thereof, flavanones and / or glycosides thereof, isoflavones and As the glycoside, the coumarin and / or the glycoside thereof, commercially available reagents can be used. In addition, various solvents such as water; lower monohydric alcohols such as methyl alcohol and ethyl alcohol, from plants containing a large amount of these compounds;
Liquid polyhydric alcohols such as glycerin, propylene glycol and 1,3-butylene glycol; ketones such as acetone and methyl ethyl ketone; alkyl esters such as ethyl acetate; hydrocarbons such as benzene and hexane; ethers such as diethyl ether; dichloromethane, chloroform It is possible to use by extracting with one or more halogenated alkanes and the like, and extracting and purifying. Moreover,
It is also possible to use a product prepared from the above compound by chemical synthesis.

Furthermore, the use site of mushrooms belonging to the genus Fuscoporia is not particularly limited. Fruiting body,
It may be a spore or a mycelium. These can be extracted raw or dried. Of these, fruiting bodies are preferable because they are easily available.

Vitis genus plant, Oenocera (Oen
othera) plant, Bellis plant, Gnaphalium plant, Arctostaphylos (Ar)
ctostaphylos, Centaurea, Lythrum, Hyssopu
s) genus plant, Thymus genus plant, Leontopodium genus plant, Centauri
um genus plant, Satureja genus plant, Anthriscus genus plant, Laurus genus plant, Nymphaea genus plant, Syringa (Syri)
nga) plants, Calendula plants, Turnera plants, Scurvy plants,
Trifolium genus plant, Convalaria (C
onvallaria plant, Consolida plant, Artemisia plant, Gardenia (G
ardenia plant, Camellia plant, citrus (Citru)
s) plant, Alchemilla plant, Artemisia plant, Menth plant,
The use site of the Malus plant is not particularly limited,
Each leaf, branch, stem, flower, fruit, root, seed, etc., or
The whole grass can be extracted raw or dried. Among them, seeds are preferable for plants of the genus Vitis, plants of the genus Oenothera, and fruit peels are preferable for the plants of the genus Malus.

The preparation of the extract and the dry powder of red wine used in the present invention is not particularly limited, but for example, it is extracted from a low temperature to a high temperature using various suitable organic solvents. Examples of the extraction solvent include water; lower monohydric alcohols such as methyl alcohol and ethyl alcohol; liquid polyhydric alcohols such as glycerin, propylene glycol and 1,3-butylene glycol; ketones such as acetone and methyl ethyl ketone; ethyl acetate and the like. One or more of alkyl esters; hydrocarbons such as benzene and hexane; ethers such as diethyl ether; halogenated alkanes such as dichloromethane and chloroform can be used. Above all, one or a mixture of two or more kinds of water, ethyl alcohol and 1,3-butylene glycol is particularly suitable.

Each extract is, for example, appropriately finely pulverized and dried. For red wine, if wine is evaporated to dryness, the weight ratio is 1 to 1000 times, especially 10 to 100 times. In the case of normal temperature extraction using the above solvent, it is preferable to carry out at 0 ° C. or higher, particularly at 20 ° C. to 40 ° C. for 1 hour or longer, particularly 3 to 7 days. Moreover, you may heat-extract at 60-100 degreeC for 1 hour.

Each of the above extracts obtained under the above conditions may be used as it is as an extracted solution, but if necessary, it may be subjected to a treatment such as filtration, concentrated and pulverized to be used properly. Can be used.

The amount of the extract compounded in the cosmetic of the present invention is preferably 0.00001 to 50.0% by weight in terms of evaporated dry matter, and most preferably 0.01 to 10.0% by weight. is there.

In addition to the above essential components, the cosmetic of the present invention comprises an aqueous component, an oil component, a plant extract, an animal extract, a powder, a surfactant, an oil agent, an alcohol, a pH adjusting agent, a preservative, an antioxidant, It is prepared by mixing a thickener, a dye, a fragrance and the like as necessary and appropriately blending them. The dosage form of the cosmetic of the present invention is not particularly limited, and various dosage forms such as lotion, emulsion, cream, pack, powder, spray, ointment, dispersion, and cleaning agent can be used.

[0051]

[Examples] Hereinafter, test examples relating to the collagenase inhibitory effect of various extracts according to the present invention will be shown, and examples of application prescriptions to cosmetics using the materials will be described. However, the examples are not limited to the examples described here. Needless to say, it is not done.

(1) Preparation of sample solution As a sample solution, epicatechin, epigallocatechin gallate, luteolin, flavone, flavanone, quercetin, quercitrin, rutin, myricetin, kaempferol, naringenin, naringin, genistein, genistin, esculin As the esculetin, a commercially available reagent was used and dissolved in dimethyl sulfoxide (DMSO) to prepare a sample solution. Grape and evening primrose seeds were dried and finely crushed.Mushroom white birch mushrooms were dried after the fruiting body was finely crushed.Furthermore, daisies, everlasting, ointment, cornflower, miso-hagi, grass polly, hyssop , Ibuki musk, wild thyme, edelweiss, sentry, savory, cherville, laurel, white water lily, lilac, pot marigold, damiana, scabbiegrass, red clover, lily of the barry, japonicum, tarragon, gardenia, camellia, lemon, honeywort, For white wormwood, southern wood, water mint, and penny royal, whole grass is dried and then crushed. Apple and Hana Kaido's pericarp are dried and powdered. It was extracted one week immersed in ℃. The red wine dry powder was obtained by subjecting red wine to vacuum distillation. The extract obtained as described above was dried, and dimethyl sulfoxide (DMSO) was added and dissolved to obtain a sample solution.

(2) N-succynyl-ala-ala-ala-nitride (sigma) 2 as an inhibitory substrate for elastase activity
Dissolve 5 mg in 554 μl DMSO and use 0.2 M Tris-HCl at the time of use.
It was used after being diluted 100-fold with (PH 8.8) buffer (concentration when used 1 mM). The enzyme is elastase (65.8
Unit / ml: sigma company) was used. The reaction is 100 μl of substrate, 20 μl of enzyme (0.1 unit), 50 μl of sample, 0.2M Tris-HCl (PH
8.8) 130 μl of buffer was added to a test tube, the mixture was allowed to stand at 37 ° C. for 30 minutes, and the absorbance at 405 nm was measured. The elastase activity inhibition rate was calculated by the following formula.

[0054]

[Chemical 1]

[0055]

[Table 1] shows the results of the elastase activity measurement of various samples.

As shown in [Table 1], epicatechin, epigallocatechin gallate, luteolin, flavone, flavanone, quercetin, quercitrin, rutin, myricetin, kaempferol, naringenin, naringin, genistein, genistin, esculin, esculetin, and grape , Evening primrose seed, mushroom birch mushroom, plant daisy, everlasting, oak sumac, cornflower, lythrum, grass polly, hyssop, ibuki musk, wild thyme, edelweiss, sentry, savory, chervil, laurel, white water lily, Lilac, pot marigold, damiana, scabigra, red clover, lily of the barry, hien saw, tarragon, gardenia, camellia,
Lemon, pearl worm, southern wood, water mint, penny royal, apple, peony extract and red wine dry powder all showed high inhibitory effect on elastase activity.

[0056]

[Table 1]

Next, examples of formulation of cosmetics containing various components of the present invention will be shown, but the present invention is not limited thereto.

Prescription example of cosmetics (1) Cosmetic cream (% by weight) a) Beeswax ... 2.0 b) Stearyl alcohol ... 5.0 c) Stearic acid ... 8.0 d) Squalane ... 10.0 e) Self-emulsifying glyceryl monostearate ... 3.0 f) Polyoxyethylene cetyl ether (20E.O.) ... 1.0 g) Laurel (leaf) 50% ethanol aqueous solution extract ... 2.0 h) 1,3-Butylene glycol ... 5.0 i) Potassium hydroxide ... 0.3 j) Preservative Agents / antioxidants ... Appropriate amount k) Purified water ... Remaining manufacturing methods a) to f) are dissolved by heating and kept at 80 ° C. g) to k) are melted by heating, kept at 80 ° C, added to a) to f) and emulsified.
Cool to 0 ° C with stirring.

(2) Cosmetic cream (% by weight) a) Beeswax ... 2.0 b) Stearyl alcohol ... 5.0 c) Stearic acid ... 8.0 d) Squalane ... 10.0 e) Self-emulsifying glyceryl monostearate ... 3.0 f) Polyoxy Ethylene cetyl ether (20 E.O.)… 1.0 g) Esculetin… 1.0 h) 1,3-butylene glycol… 5.0 i) Potassium hydroxide… 0.3 j) Preservatives / antioxidants… Appropriate amount k) Purified water… Remainder manufacturing method Dissolve a) to g) by heating and keep at 80 ° C. h) to k) are melted by heating, kept at 80 ° C, added to a) to g) and emulsified,
Cool to 40 ° C with stirring.

(3) Emulsion (% by weight) a) Beeswax ... 0.5 b) Vaseline ... 2.0 c) Squalane ... 8.0 d) Sorbitan sesquioleate ... 0.8 e) Polyoxyethylene oleyl ether (20 E.O.) ... 1.2 f ) Grape (leaf) 50% ethanol aqueous solution extract… 2.0 g) Red wine dry powder… 2.0 h) 1,3-butylene glycol… 7.0 i) Carboxyvinyl polymer… 0.2 j) Potassium hydroxide… 0.1 k) Purified water… The balance l) Preservatives / antioxidants ... Appropriate amount m) Ethanol ... 7.0 Dissolve by heating process a) to e) and keep at 80 ° C. f) to l) are melted by heating, kept at 80 ° C, added to a) to e) and emulsified to 50
Cool to 0 ° C with stirring. M) at 50 ℃, add 40 ℃
Cool down.

(4) Emulsion (% by weight) a) Beeswax ... 0.5 b) Vaseline ... 2.0 c) Squalane ... 8.0 d) Sorbitan sesquioleate ... 0.8 e) Polyoxyethylene oleyl ether (20 E.O.) ... 1.2 f ) Wild time (flower) 50% ethanol aqueous solution extract ...
2.0 g) 1,3-butylene glycol ... 7.0 h) Carboxyvinyl polymer ... 0.2 i) Potassium hydroxide ... 0.1 j) Purified water ... Balance k) Preservatives / antioxidants ... Appropriate amount l) Ethanol ... 7.0 Manufacturing method a) ~ Heat up to e) and keep at 80 ℃. f) to k) are melted by heating, kept at 80 ° C, added to a) to e) and emulsified.
Cool to 0 ° C with stirring. L) at 50 ℃, add 40 ℃
Cool down.

(5) Lotion (% by weight) a) Damiana (stem) 50% ethanol aqueous solution extract ... 1.0 b) Hyssop (root) 50% 1,3-butylene glycol aqueous solution extract ... 1.
0 c) Glycerin ... 5.0 d) Polyoxyethylene sorbitan monolaurate (20E.
O.)… 1.0 e) Ethanol… 6.0 f) Perfume… Appropriate amount g) Preservative / antioxidant… Appropriate amount h) Purified water… The rest of the manufacturing methods a) to h) are mixed and uniformly dissolved.

(6) Lotion (% by weight) a) White water lily (whole grass) aqueous solution extract ... 1.0 b) Glycerin ... 5.0 c) Polyoxyethylene sorbitan monolaurate (20E.
O.) ... 1.0 d) Ethanol ... 6.0 e) Perfume ... Appropriate amount f) Preservative / antioxidant ... Appropriate amount g) Purified water ... Remaining manufacturing method a) to g) are mixed and uniformly dissolved.

(7) Packing agent (% by weight) a) Gardenia (leaf) 50% ethanol aqueous solution extract 1.0 b) Ladies mantle (root) 50% ethanol aqueous solution extract 2.0 c) Vinyl acetate resin emulsion 15.0 d ) Polyvinyl alcohol… 10.0 e) Olive oil… 3.0 f) Glycerin… 5.0 g) Titanium oxide… 8.0 h) Kaolin… 7.0 i) Ethanol… 8.0 j) Perfume… Appropriate amount k) Preservatives / antioxidants… Appropriate amount l) Purified water … The rest of the production methods a) to l) are mixed and well stirred and dispersed to homogenize.

(8) Packing agent (% by weight) a) Water mint (whole grass) 50% ethanol aqueous solution extract ... 1.0 b) Vinyl acetate resin emulsion ... 15.0 c) Polyvinyl alcohol ... 10.0 d) Olive oil ... 3.0 e) Glycerin … 5.0 f) Titanium oxide… 8.0 g) Kaolin… 7.0 h) Ethanol… 8.0 i) Perfume… Appropriate amount j) Preservatives / antioxidants… Appropriate amount k) Purified water… The balance a) to k) are mixed, Stir well and disperse well to make uniform.

[0066]

[Effect confirmation test] (1) Effect confirmation test in human by application As test subjects, 15 women aged 20 to 50 years twice a day (morning, night) for 3 consecutive months, each of the invention product and the comparative product The state of the application site was compared before and after the test, and the improvement effect was investigated. For this test,

In the comparative example, the cosmetics shown in

The cosmetics obtained by removing the laurel extract from the cosmetics shown in (4) were prepared, and the effect of the application was investigated. While applying the cosmetic containing the active ingredient of the present invention every day, the state of wrinkles on the skin was collected by questionnaires before the start of application and after application for 3 months to confirm the effect. Result is

It shows in [Table 2].

<Judgment Criteria> Remarkable effect: Wrinkles on the skin were remarkably improved as compared with before the start of application. Effective: Wrinkles on the skin were improved compared to before application. Slightly effective: Wrinkles on the skin were slightly improved compared with before application. Ineffective: There was no change compared to before application.

[0068]

As is clear from [Table 2], higher effects were observed in all cases as compared with the control product.

[0069]

[Table 2]

[0070]

As described in detail above, the cosmetic composition of the present invention has an excellent elastase activity suppressing effect and is effective in preventing wrinkles on the skin.

Continued front page    F-term (reference) 4C083 AA082 AA111 AA112 AA122                       AB032 AB242 AC022 AC072                       AC102 AC122 AC182 AC242                       AC422 AC442 AC841 AC842                       AD092 AD112 AD391 BB01                       BB13 BB21 BB41 BB44 BB47                       BB48 CC04 CC05 CC07 DD08                       DD17 DD22 DD31 EE12

Claims (4)

[Claims] 1. Catechins and / or glycosides thereof, flavones and / or glycosides thereof, flavonols and / or glycosides thereof, flavanones and / or glycosides thereof, isoflavones and / or A cosmetic comprising an elastase inhibitor comprising one or more of glycosides, coumarins and / or glycosides thereof. [Claim 2] Mushrooms belonging to the genus Fuscoporia, genus Vitis, Oenothera
Genus, genus Bellis, Gnaphaliu
m) genus, Arctostaphylos genus,
Genus Centaurea, genus Lythrum,
Hyssopus, Thymus, Leontopodium, Centory
aurium genus, Satureja genus, Anthriscus genus, Laurus genus, Nymphaea genus, Syringa genus, Calendula genus, Tornera genus, Snorvy Genus, Trifolium genus,
The genus Convallaria, Consolida
genus da), genus Artemisia, gardenia (G
ardenia, Camellia, Citrus
genus rus, genus Alchemilla, genus Artemisia, genus Menth, Malus
s) A cosmetic comprising an extract of a plant belonging to the genus and an elastase inhibitor consisting of one or more of red wine dry powder. 3. Catechins and / or glycosides thereof are catechin, epicatechin, epigallocatechin, epigallocatechin gallate, flavones are luteolin, flavones, apigenin and / or glycosides thereof, and flavonols are quercetin, Myricetin, kaempferol and / or its glycosides, flavanones are naringenin, flavanones, hesperidin and / or its glycosides, isoflavones are genistein, daidzein and / or their glycosides, coumarins are esculetins and / or their The cosmetic according to claim 1, which is a glycoside. [Claim 4] Mushrooms belonging to the genus Fuscoporia are white birch mushrooms (Fuscoporia obliqua) and Viti
s) plants are grapes (Vitis vinifera L.) and Oenothera plants are Oenothera bie.
nnis L.), plants belonging to the genus Bellis are daisies (Bellis perennis), and gnafalium (Gnaphaliu).
m) plants belonging to the genus Everlasting (Gnaphaliumu
liginosum L.), Arctostaphyl
The plant belonging to the os genus is Arctostaphylos uva
-ursi (L.) S _PRENG. ), a plant belonging to the genus Centaurea is cornflower (Centaurea cyanus L.),
A plant belonging to the genus Lythrum is Lythr.
um anceps Makino), grass polly (Lythrum salica)
ria L.), plants belonging to the genus Hyssopus are Hyssopus officinalis L., Thymus
The plant belonging to the genus is Thymus quinqu
ecostatus Celak.), Wild Time (Thymus serpyl
lum L.), plants belonging to the genus Leontopodium are Edelweiss (Leontopodiumalpinum), plants belonging to the genus Centaurium (Centaurium erythraeaR _AFN. ), and Saturja (Satur) _.
A plant belonging to the genus eja) is a savory (Satureja hortensis
L.), a plant belonging to the genus Anthriscus (Anthriscus cerefolium (L.) H _OFFM .), And a plant belonging to the genus Rolls (Laurus) are laurel (Laurus n
obilis L.), a plant belonging to the genus Nymphaea (Nymphaea) is white water lily (Nymphaea albaL.),
Plants belonging to the genus Syringa are lilacs (Syringa)
inga vulgaris) and plants belonging to the genus Calendula (Calendula) are pot marigolds (Calendula officinali).
s), plants belonging to the genus Turnera (Turnera diffusa W _ILLD .varaphrodisiaca (W _ARD .)
U _RB .), Plants belonging to the genus Scurvy are Scurvy grass, Trifolium
Plants belonging to the genus Red clover (Trifolium praten
se L.), plants belonging to the genus Convallaria are Lily of the Barry (Convallaria majalis L.), plants belonging to the genus Consolida
onsolida ambigua), the plant belonging to the genus Artemisia (Artemisia) is taragon (Artemisia dracunculoildes)
L.), a plant belonging to the genus Gardenia is gardenia jasminoides Ellis f. Grandiflora Maki
no), Camellia jap is a plant belonging to the genus Camellia.
onicaL.), plants belonging to the genus Citrus are lemons (Citrus limon B _URM .), Alchemilla.
The plants belonging to the genus are Alchemilla vulgarisa
gg.), plants belonging to the genus Artemisia are Artemisia stelleriana Besser, southern wood (Artemisia abrotanum L.), and plants belonging to the genus Menth are water mint (Mentha aquatica).
L.), Penny Royal (Mentha pulegium L.), Malus (Malus) plants belonging to the genus Apple (Maluspumila Mil
l.), and Hana Kaido (Malus halliana Koehne).