基本情報
- 標準SMILES
C/C=C/c1cc(OC)c(OC)cc1OC- InChIKey
RKFAZBXYICVSKP-AATRIKPKSA-N- 分子式
- C12H16O3
- 平均分子量
- 208.25 g/mol
- 単同位体質量
- 208.10994437
概要
Alpha-asarone is the trans-isomer of asarone. It has a role as an anticonvulsant and a GABA modulator.
名称と識別子
- 優先名称
- Asarone
- IUPAC
- 1,2,4-trimethoxy-5-[(E)-prop-1-enyl]benzene
- 現地名
- アサロン
- 英語名
- alpha-Asarone
- 分子式
- C12H16O3
- 分子量
- 208.25
名称と別名
名称をさらに表示
データベース識別子
- CAS
2883-98-9、494-40-6- PubChem CID
- 636822
- DTXSID
DTXSID00871878- ChEMBL
CHEMBL333306- ChEBI
CHEBI:78309- UNII
- DQY9PNE5FK
- EC Number
- 220-743-6
- Nikkaji
- J7.927H、J70.975A
物性
構造計算による物性
- XLogP
- 3
- 極性表面積
- 27.7 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 3
- 回転可能結合数
- 4
- 重原子数
- 15
- 形式電荷
- 0
- 複雑度
- 203
実験および物理化学的性質
Color/Form
MONOCLINIC NEEDLES FROM WATER
Needles from light petroleum
Solubility
Yellow to medium brown, moderately viscous liquid with a pleasant, spicy aromatic odor. Acid value: max 4. Ester value: 3-20. Solubility 1 vol in 5 vol of 90% ethanol; solutions may be turbid /cis-asarone/
Practically insol in water; sol in alcohol, ether, glacial acetic acid, carbon tetrachloride, chloroform, petroleum ether
Melting Point
62-63 °C
Crystals. MP: 67 °C. Insoluble in water; soluble in alcohol /isomer not specified/
62 - 63 °C
Refractive Index
INDEX OF REFRACTION: 1.5683 @ 20 °C/D; SADTLER REF NUMBER: 34263 (IR, PRISM)
Index of refraction: 1.5719 at 11 °C/D
Physical Description
Solid; [HSDB] Fine faintly yellow crystals; [MSDSonline]
Solid
Other Experimental Properties
Density: 0.940-0.980 at 25 °C/25 °C. Index of refraction: 1.5010-1.5160 at 20 °C/D. Specific optical rotation: -5 deg to +35 deg. /cis-asarone; European/
Density: 1.060-1.080 at 25 °C/25 °C. Index of refraction: 1.5500-1.55525 at 20 °C/D. Specific optical rotation: -2 deg to +6.5 deg. /cis-asarone; Indian/
物理化学的性質
- 融点
- 57 · 57-61 °C(lit.)
- 沸点
- 296 °C · 296 °C(lit.)
- 比重(密度)
- 1.1227 · 1.1227 (rough estimate)
- 屈折率
- 1.506 · 1.5060 (estimate)
- 貯蔵温度
- 2 · Keep in dark place,Sealed in dry,2-8°C
- 溶解性
- クロロホルム、メタノールに可溶。
- 外見
- Solid
- 色
- ホワイトからオフホワイト
- BRN
- 1910606 · 1910606
- InChI
- InChI=1S/C12H16O3/c1-5-6-9-7-11(14-3)12(15-4)8-10(9)13-2/h5-8H,1-4H3/b6-5+
- InChIKey
- RKFAZBXYICVSKP-AATRIKPKSA-N
- SMILES
- C1(OC)=CC(/C=C/C)=C(OC)C=C1OC
- LogP
- 3.406 · 3.406 (est)
- CAS データベース
- 2883 · 2883-98-9(CAS DataBase Reference)
- NISTの化学物質情報
- Asarone(2883-98-9)
化学的性質
化学的特性Asarone is a colorless tryst. M.P. 66-67℃. B.P. 296℃. Pure Asarone is reported to be virtually odorless and tasteless. However, available samples of the material have in experiments shown perceptible influence upon the odor of compositions containing lower boiling perfume materials. Insoluble in water, soluble in alcohol and oils.
安全と法規制
GHS分類
GHS Classification
Warning
H302 (91.5%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 130 reports by companies from 2 notifications to the ECHA C&L Inventory.
危険有害性情報
安全と保護具
Disposal Methods
SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.
毒性情報
Interactions
The action of asarone and beta-asarone, alone or in combination with either reserpine or chloropromazine, on conditioned avoidance behavior in rats, fighting behavior in mice, and electroshock convulsions in rats was determined. ... Asarone potentiated the action of reserpine and chlorpromazine on conditioned avoidance behavior and fighting behavior; beta-asarone did not. ... Asarone potentiated the lethal effect of chlorpromazine during electroshock convulsions; beta-asarone did not. Pretreatment with Acorus oil, asarone, or beta-asarone did not increase the concentration of 5-hydroxytryptamine in rat brain. /Asarones/
Non-Human Toxicity Excerpts
/LABORATORY ANIMALS: Acute Exposure/ beta-Asarone doubled sleeping time with sodium pentobarbital in mice at a dose of 50 mg/kg bw i.p. and doubled the sleeping time with ethanol at a dose of 75 mg/kg. /beta-Asarone/
/LABORATORY ANIMALS: Acute Exposure/ ... a study was conducted of the biological properties of alpha-asarone (1-propenyl-2,4,5- methoxybenzol)--etherophenol, isolated by the authors from the roots of Asarum europaeum. It was determined that the LD50 of asarone for mice in enteral administration was 417.6 mg/kg, in intra-abdominal 310 mg/kg ...
/LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ ... The drug alpha-asarone (3, 6 and 9 mg/kg bw, ip, for 30 days) ... was administered intraperitoneally 1/2 hr before the animals were exposed to noise-stress (100 dB for 4 hr/day, for 30 days) . ... All the three doses of alpha-asarone had an effectively protective role, by normalizing the increased superoxide dismutase and lipid peroxidation, decreased catalase, glutathione peroxidase, levels of reduced glutathione, Vitamins C and E and protein thiols due to noise exposure. Thus, action of alpha-asarone against noise-stress may be due its antioxidant property ...
/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ Groups of 25 male and 25 female rats were fed diets containing 0, 400, 800, or 2000 ppm (0, 0.04, 0.08, or 0.2%) beta-asarone for two years. A positive control group of the same size received 2500 ppm (0.25%) Jammu oil of calamus (JOC; /approx. 75% beta-asarone/). None of the group receiving 2000 ppm (0.2%) beta-asarone or 2500 ppm (0.25%) JOC survived more than 84 weeks; mortality was also increased on the 800 ppm (0.08%) dose. Median survival time in the females was less than in the males in these groups. The gross pathological changes observed were serous fluid in the abdominal and pleural cavities, liver and kidney changes, and tumourous masses in the intestinal tract. The tumors were identified as leiomyosarcomas of the small intestine and were found in one rat on 400 ppm (0.04%), six on 800 ppm (0.08%), nine on 2000 ppm (0.2%) and one on 2500 ppm (0.25%) JOC. All the test rats with leiomyosarcomas were males. The earliest tumor was observed in a rat 52 weeks old on the 2000 ppm (0.2%) dose. Two leiomyosarcomas were also noted in control females but the location differed from that of the tumors in the treated animals. Atrophy of cardiac muscle cells occurred in controls and all test groups but was most prominent in the 2000 ppm (0.2%) beta-asarone and 2500 ppm (0.25%) JOC groups. Cardiac fibrosis generally paralleled the incidence of cardiac atrophy. Fatty degeneration and fatty infiltration were also in the heart more severe in the treated groups. Thrombosis within the chambers of the heart was observed in the 800 and 2000 ppm (0.08 and 0.27%) beta-asarone and 2500 ppm (0.25%) JOC treated groups. Passive hyperemia of the lung, kidneys and liver was more prominent in the test than control animals indicating faulty cardiac function in the test animals. Incidence of hepatic angiectasis and hepatic coagulative necrosis also tended to increase with increasing beta-asarone dose. Both sexes on 800 and 2000 ppm (0.08 and 0.2%) beta-asarone and 2500 ppm (0.25%) JOC had slightly depressed body weights throughout the study; the males on 400 ppm (0.04%) ß-asarone also had depressed body weights at termination but the number of survivors was small. Hemoglobin, hematocrit, and red and white cell counts were normal except that when the test animals became sick they became anemic with lowered hemoglobin, hematocrit, and red cell count. /beta-Asarone/
For more Non-Human Toxicity Excerpts (Complete) data for TRANS-ASARONE (14 total), please visit the HSDB record page.
Non-Human Toxicity Values
LD50 Rat oral 1010 mg/kg bw /beta-Asarone/
LD50 Mouse oral 184.2 mg/kg bw /beta-asarone/
LD50 Mouse oral 418 mg/kg
LD50 Mouse ip 310 mg/kg
安全データ
- wgk
- 3
- rtecs
- DC2975000
- 毒性
- bird - wild,LD50,oral,750mg/kg (750mg/kg),Archives of Environmental Contamination and Toxicology. Vol. 12, Pg. 355, 1983.
- hs_code
- 29093090
- risk_code
- 22
- hazard_code
- Xn
- safety_code
- 22-24/25
- Hazard Classifications
- Acute Tox. 4 Oral
- ストレージクラス
- 13 - Non Combustible Solids
- 有毒物質データの
- 2883-98-9(Hazardous Substances Data)
化学と産業
薬理情報
Mechanism of Action
Docking experiments using a number of published crystal structures of HMG-CoA reductase with the potent hypocholesterolemic agent alpha-asarone are described. The results indicate that alpha-asarone binds in the enzyme's active site. The methoxy groups play a key role in the binding and probably also in its biological activity, as shown by extensive SAR studies reported for analogues of alpha-asarone. The docking results will be valuable for the structure-based design of novel hypolipidemic agents.
MeSH Pharmacological Classification
Substances that increase the risk of NEOPLASMS in humans or animals. Both genotoxic chemicals, which affect DNA directly, and nongenotoxic chemicals, which induce neoplasms by other mechanism, are included.
Fibrinolysin or agents that convert plasminogen to FIBRINOLYSIN.
用途と製造
Uses
Found in calamus oil from roots of Acorus calamus L.; Used as a grain fumigant and insect chemosterilant; Calamus oil is used in perfumes and alcoholic beverages, but use is limited by potential toxicity of beta-asarone; [HSDB] Asarones occur in nature as a mixture of two isomers alpha (trans) and beta (cis); [Merck Index]
Farming (Pesticides) [Category: Industry]
Grain fumigant, insect chemisterilant /isomer not specified/
Essential oil ... Calamus oil is used in perfumery for spicy-herbaceous notes: small quantities are also employed in the alcoholic beverage industry. However, use is legally restricted because of the potential toxicity of beta-asarone. /cis-asarone/
Tranquilizer ... chemisterilant for insects /asarone, i.e. 2,4,5-trimethoxy-1-propenylbenzene)/
IFRA Fragrance Standards
cis-and trans-Asarone
494-40-6:; Benzene, 1,2,4-trimethoxy-5-(1-propen-1-yl)- (unspecified isomer); (E)-and (Z)-2,4,5-Trimethoxypropen-1-yl benzene); 2883-98-9:; α-Asarone; trans-Asarone; Benzene, 1,2,4-trimethoxy-5-(1-propenyl)-, (E)-; trans-Isoasarone; 5273-86-9:; Ã-Asarone; cis-Ã-Asarone; Benzene, 1,2,4-trimethoxy-5-(1-propenyl)-, (Z)-; cis-Isoasarone
IFRA_STD_110.pdf
40
IFRA 51st Amendment - Guidance for the use of IFRA Standards
Prohibition: This material should not be used as a fragrance ingredient_Restriction: This material should be used only in the limited quantity as stated in the Standard
Methods of Manufacturing
SESHADRI, THIRUVENGADAM, PROC INDIAN ACAD SCI 32A, 110 (1950); SHARMA, DANDIYA, INDIAN J APPL CHEM 32, 236 (1969).
Either extracted from calamus oil or synthesized (Wittig reaction).
Calamus oil is obtained by steam distillation of fresh or unpeeled, dried roots of Acorus calamus L. (Araceae) ... The plant occurs in polyploid varieties and the corresponding essential oils differ predominantly in their content of beta-asarone (cis-isoasarone, 5273-86-9) /cis-asarone/
General Manufacturing Information
UV irridiation of trans-isoasarone formed cis-isoasarone & asaronaldehyde. The isomerization rate decreased the concentration from 0.5 to 0.1% in methanol. Solvent affected the reaction, with the concentrations of cis-asarone & asaronaldehyde after 5 hr being: hexane 58.5 & 3.6, ethanol 55.4 & 2.5, methanol 40.0 & 2.7, acetone 50.9 & 7.3 & benzene 5.0 & nil. The tincture contains chlorogenic acid which retarded isomerization in vitro. No isomerization was found in irradiated tinctures (brown glass bottles) or tablets of the root.
Indian Acorus calamus from the Jammu area is tetraploid and yields an oil containing approximately 75% beta-asarone; Acorus calamus from Kashmir is hexaploid and yields an oil containing approximately 5% beta-asarone (Vashist & Handa, 1964). /cis-asarone/
応用分野
解説1-(2,4,5-trimethoxyphenyl)-1-propene.C12H16O3(208.25).(E)-体のα-アサロンと(Z)-体のβ-アサロンが知られている.α-アサロンはAsarum europenumの根,セキショウの精油から得られる."無色の結晶.融点62~63 ℃,沸点296 ℃.d30301.112.n20D 1.5683.エタノール,エーテル,クロロホルムに可溶,水に不溶.果実エッセンスとして用いられる.LD50 418 mg/kg(ネズミ,経口).β-アサロンもAcorusの精油から得られる油状物質.d2441.073.n20D 1.561.十二指腸に悪性腫瘍を起こすことが知られている.森北出版「化学辞典(第2版)
用途日本薬局方収載「ソヨウ(紫蘇葉、蘇葉)」の定量法用
一般的な説明Asarones are toxic morphogenetic agents. It is also known for its chemosterlant and oviposition stimulant properties. Naturally it can be extracted from Acorus calamus. α-Asarone is considered as growth inhibitor. This isomer acts as antifeedant with less toxicity.
上流・下流製品情報
上流原料
サプライヤー50 社
補足説明
定義ChEBI: The trans-isomer of asarone.
関連反応
関連ノート
読み込み中…