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(1R)-2,3,5,7aβ-テトラヒドロ-1-ヒドロキシ-1H-ピロリザイン-7-メタノール

Retronecine

HCID 10198
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基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
480-85-3
標準SMILES
OCC1=CCN2CC[C@@H](O)[C@@H]12
InChIKey
HJSJELVDQOXCHO-HTQZYQBOSA-N
分子式
C8H13NO2
平均分子量
155.19 g/mol
単同位体質量
155.09462866

概要

Retronecine is a member of pyrrolizines.

名称と識別子

優先名称
Retronecine
IUPAC
(1R,8R)-7-(hydroxymethyl)-2,3,5,8-tetrahydro-1H-pyrrolizin-1-ol
現地名
(1R)-2,3,5,7aβ-テトラヒドロ-1-ヒドロキシ-1H-ピロリザイン-7-メタノール
英語名
retronecine
分子式
C8H13NO2
分子量
155.19

名称と別名

RETRONECINE480-85-3SenecifolineneRetronecin(1R,8R)-7-(hydroxymethyl)-2,3,5,8-tetrahydro-1H-pyrrolizin-1-ol2P5723M6IIDTXSID4010201561H-Pyrrolizine-7-methanol, 2,3,5,7a-beta-tetrahydro-1-alpha-hydroxy-1H-Pyrrolizine-7-methanol, 2,3,5,7a-tetrahydro-1-hydroxy-, (1R-trans)-RefChem:879492DTXCID601478002(+)-Retronecine
名称をさらに表示
(1R)-2,3,5,7aβ-テトラヒドロ-1α-ヒドロキシ-1H-ピロリザイン-7-メタノール(1R)-2,3,5,7aβ-テトラヒドロ-1-ヒドロキシ-1H-ピロリザイン-7-メタノールレトロネシン(1R,7aR)-7-(ヒドロキシメチル)-2,3,5,7a-テトラヒドロ-1H-ピロリジン-1-オールRetronecine-RMRetronecine (Standard)(1R)-2,3,5,7aβ-Tetrahydro-1-hydroxy-1H-pyrrolizine-7-methanol(1R)-2,3,5,7aβ-Tetrahydro-1α-hydroxy-1H-pyrrolizine-7-methanol1H-Pyrrolizine-7-methanol, 2,3,5,7a-tetrahydro-1-hydroxy-, (1R,7aR)-
(1r,7ar)-7-(hydroxymethyl)-2,3,5,7a-tetrahydro-1h-pyrrolizin-1-olCCRIS 5776(1R,7aR)-2,3,5,7a-tetrahydro-1-hydroxy-1H-pyrrolizine-7-methanol( )-RetronecineHSDB 3567UNII-2P5723M6II(1R,7aR)-2,3,5,7a-Tetrahydro-1-hydroxy-1H-pyrrolizine-7-methanol; Retronecine; Retronecin;RETRONECINE [MI]

データベース識別子

CAS
480-85-3
PubChem CID
10198
DTXSID
DTXSID401020156
ChEBI
CHEBI:8821
UNII
2P5723M6II
EC Number
106-825-3
Nikkaji
J12.338B

物性

構造計算による物性

XLogP
-1.3
極性表面積
43.7 Ų
水素結合供与体数
2
水素結合受容体数
3
回転可能結合数
1
重原子数
11
形式電荷
0
複雑度
191

実験および物理化学的性質

LogPlog Kow = -0.56 @ 25 °C /Estimated/
Color/FormCrystals from acetone
Solubility · 2 件

Very sol in water, alc; sol in acetone; slightly sol in ether

In water, 8X10+5 mg/L @ 25 °C /Estimated/

Boiling Point80 °C @ 0.01 mm Hg
Melting Point119-120 °C
Vapor Pressure1.5X10-5 mm Hg @ 25 °C /Estimated/
Optical RotationSpecific optical rotation: +27.4 deg (water)/D, +50.2 deg (alcohol) @ 26 °C/D
Henry's Law ConstantHenry's Law constant = 4.1X10-11 atm-cu m/mol @ 25 °C /Estimated/
Stability/Shelf LifeStable at room temperature in closed containers; for long periods the substance is best stored under nitrogen at 15 °C.
Dissociation ConstantspKa = 7.75 /Estimated/
Other Experimental PropertiesHydroxyl radical reaction rate constant = 1.2X10-10 cu cm/molec-sec /Estimated/

物理化学的性質

融点
119 · 119-120°
比旋光度
20 D · 20D +4.95° (c = 0.58 in alc)
沸点
80 °C · 80 °C(Press: 0.01 Torr)
比重(密度)
1.29 · 1.29±0.1 g/cm3(Predicted)
貯蔵温度
2 · 2-8°C
溶解性
エタノール(微量)、メタノール(微量)
酸解離定数(Pka)
14.48 · 14.48±0.40(Predicted)
色
オフホワイトからライトブラウン

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 4 件

Danger

H300+H310+H330 (100%): Fatal if swallowed, in contact with skin or if inhaled [Danger Acute toxicity, oral; acute toxicity, dermal; acute toxicity, inhalation]

P260, P262, P264, P270, P271, P280, P284, P301+P316, P302+P352, P304+P340, P316, P320, P321, P330, P361+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

危険有害性情報

Hazard Classes and CategoriesAcute Tox. 2 (100%)
Hazardous Reactivities and IncompatibilitiesReadily hydrolysed with alkali, reacts with oxidizing agents (slowly with atmospheric oxygen) to form dihydropyrrolizine and other derivatives.

毒性情報

Toxicity Summary · 1 件

Retronecine is classified as a pyrrolizidine alkaloid (PA). Unsaturated pyrrolizidine alkaloids are hepatotoxic, that is, damaging to the liver. PAs also cause hepatic veno-occlusive disease and liver cancer. PAs are tumorigenic. Disease associated with consumption of PAs is known as pyrrolizidine alkaloidosis. (Wikipedia)

Natural Pollution SourcesMOST OF SENECIO SPECIES CONTAIN ALKALOIDS...KNOWN AS PYRROLIZIDINE ALKALOIDS...RETRORSINE /CONTAINS/ (RETRONECINE + ISATINECIC ACID). SENECIO JACOBAEA CONTAINS JACOBINE (RETRONECINE + JACOBINECIC ACID)... /SENECIO/
Human Toxicity Excerpts · 2 件

/HUMAN EXPOSURE STUDIES/ The two main sources of pyrrolizidine alkaloid poisoning reported in human beings are the consumption of cereal grain contaminated by weeds containing the alkaloids and the use of alkaloid-containing herbs for medicinal and dietary purposes. ...Three of the largest outbreaks of the disease have been reported from South Asia, two from the same site in central India and one from North-West Afghanistan. The first Indian outbreak... occurred in a group of 5 tribal villages in central India in 1972-73. ...Out of a total population of 2,060 in these villages, 71 households with 366 members were investigated. Among these, 39 cases had developed and 19 had died before commencement of the investigations. The incidence rate was 1.1% and the case fatality rate was 50%. All cases occurred among 20 households. In many households, several members were affected. In one household, 4 out of 5 cases died. ...The etiological factor of this outbreak was not established, though dietary contamination with pyrrolizidine alkaloids was considered. A second outbreak occurred at the same site in 1975... . A total population of 486 was affected, 67 cases were reported, of whom 28 (46%) had died. There was a strong family history... . In a later survey, 108 patients were studied and the mortality rate was estimated to be 63%. This time the etiological factor was identified as the plant Crotalaria nana Burm, which had been growing in the fields of millet (Panicum miliare), their staple food crop. The seeds of this plant became mixed with the cereal grain during harvesting. The toxic seeds contained pyrrolizidine alkaloids that were identified as a macrocyclic ester closely similar to monocrotaline. The total alkaloid content was estimated to be 5.3 g/kg of seed, expressed as monocrotaline. The levels of contamination of the millet with seeds were reported to be 0-3.4 g/kg in the unaffected and 0-19 g/kg in the affected households... . /Pyrrolizidine alkaloids/

/HUMAN EXPOSURE STUDIES/ The largest outbreak reported to date occurred in the Gulran district of Herat Province in northwest Afghanistan, close to the border of the USSR. ...The outbreak, was estimated to have affected a population of approximately 35,000 in 98 villages. Examination of 7,200 inhabitants of the affected villages showed evidence of disease in 22.6%, which was more serious in 15%. Thus, it was estimated that approximately 8,000 subjects suffered from the disease including 5,000 who were seriously affected. All age groups were affected, but 46% of subjects were below 14 years of age. However, no sign of disease was found in children below 2 years of age. A detailed report concerning the pathological material obtained from 14 liver biopsies and 8 autopsies was made... /although/ the time interval between the onset of symptoms and the biopsy/autopsy was not indicated. Pathological findings were characteristic, ranging from acute disease with characteristic veno-occlusion to non-portal cirrhosis, which was observed in 5 of the above 22 cases. The outbreak was ascribed to massive contamination of wheat, the staple food crop, following 2 years of drought, with the seeds of Heliotropium popovii H. Riedl subsp. gillianum H. Riedl, which had been growing profusely among the wheat crop. The seeds contained pyrrolizidine alkaloids at concentrations reported by 2 laboratories to be 7.2 and 13.2-14.9 g/kg, identified mainly as the N-oxide of heliotrine (74%)..., and one or two other compounds similar in character to lasiocarpine. Samples of wheat from several villages contained an average of 40 seeds/kg, i.e., 0.03% by weight. It was estimated that an adult consumed at least 700 g flour/day, containing approximately 2 mg alkaloid (based on a mean of the seed analyses). /Pyrrolizidine alkaloids/

Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).
Non-Human Toxicity Excerpts · 5 件

/LABORATORY ANIMALS: Acute Exposure/ The acute toxicity of ... retronecine has been determined in mice. ... Intravenous injection of large doses of retronecine is followed by either rapid death or complete recovery. No hepatic injury has resulted.

/LABORATORY ANIMALS: Acute Exposure/ 62 pyrrolizidine alkaloids, including heliotridine, and derivatives have been screened for acute and chronic hepato- and pneumotoxicity in rats by the single dose method. On a molar basis, diesters of heliotridine and retronecine are about 4 times as toxic as the respective mono-esters and heliotridine esters are 2-4 times as toxic as retronecine esters.

/GENOTOXICITY/ ...Retronecine /was/ cultured for 2 hr with cells and an external metabolizing system. ...DNA cross-links which consisted primarily of proteinase-sensitive cross-links (DPC), but also to a smaller extent, DNA interstrand cross-links (ISC) /were induced/.

/ALTERNATIVE IN VITRO TESTS/ Six compd, incl retronecine, related to pyrrolizidine alkaloids were subjected to an in vitro mammalian cell transformation test. Retrorsine and monocrotaline gave positive results.

/OTHER TOXICITY INFORMATION/ /Pyrrolizidine alkaloids/ (PAs) are noted mainly for the poisoning of livestock due to the animals grazing on PA-containing toxic weeds, and large-scale outbreaks have been recorded. /Pyrrolizidine alkaloids/

Antidote and Emergency Treatment · 3 件

Basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if needed. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . Cover skin burns with dry sterile dressings after decontamination ... . /Poison A and B/

Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in respiratory arrest. Positive pressure ventilation techniques with a bag valve mask device may be beneficial. Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start an IV with D5W /SRP: "To keep open", minimal flow rate/. Use lactated Ringer's if signs of hypovolemia are present. Watch for signs of fluid overload. Consider drug therapy for pulmonary edema ... . For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam (Valium) ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Poison A and B/

Presentation depends on the active toxic agent. In most cases, vomiting, abdominal pain, and diarrhea occur within 60 to 90 minutes of significant ingestion. With some toxins, severe gastroenteritis may result in massive fluid and electrolyte loss. ... Maintain open airway and assist ventilation if necessary. Administer supplemental oxygen. Treat coma, seizures, arrhythmias, and hypotension if they occur. Replace fluid loss caused by gastroenteritis with intravenous crystalloid solutions. ... Administer activated charcoal if available ... Gastric emptying is not necessary if activated charcoal is given promptly. /Plants and Herbal Medicines: Group 1/

Non-Human Toxicity ValuesLD50 Mouse iv 634.0 + or - 26.0 mg/kg

安全データ

wgk
3
rtecs
VH7175000
ridadr
1544
毒性
LD50 i.v. in mice: 634.0 ±26.0 mg/kg (Harris)
hazard_class
6.1(b)
packing_group
III
有毒物質データの
480-85-3(Hazardous Substances Data)

化学と産業

薬理情報

Metabolism/Metabolites · 3 件

Steric hindrance around the ester groups was the major factor inhibiting hydrolysis of pyrrolizidine alkaloids. Enzymic hydrolysis of retronecine di-isovalerate occurred primarily at the allylic 9-ester group. The results supported the view that a factor contributing to the lower hepatotoxicity of semisynthetic retronecine diesters compared with some natural pyrrolizidine alkaloids, is their greater susceptibility to detoxication by hydrolysis.

Levels of pyrrolic metabolites were measured in the livers of rats given some pyrrolizidine alkaloids and semisynthetic derivatives. Structural and chemical features favoring the formation of such metabolites were defined. The most important of these were steric hindrance or chemical properties giving resistance to ester hydrolysis; lipophilic character, allowing access to hepatic microsomal enzymes; a conformation favoring microsomal oxidation of the pyrroline ring in preference to n-oxidation.

Levels of pyrrolic metabolites were measured in the livers of rats given some pyrrolizidine alkaloids and semisynthetic derivatives. ... Heliotridine-based alkaloids gave more pyrrole than similar retronecine esters, heliotridine ditiglate gave less pyrrole than retronecine ditiglate because the former was more open to hydrolytic attack.

Absorption, Distribution and Excretion · 1 件

Lactating rats dosed with (3)H-retronecine excreted within 3 hr approx 0.08% of the applied radioactivity in the milk mainly as yet not identified water soluble retronecine-derived metabolites and approx 0.02% as unchanged pyrrolizidine alkaloids (pas). Highest tissue levels of pas and metabolites, 6 hr after admin were found in liver and lungs.

用途と製造

Uses · 2 件

Some of the Senecio species in which it occurs have been used as medicinal herbs; e.g., S. discolor (S.W.) DC. was used against coughs, colds, fevers and indigestion in Jamaica; S. bupleuroides DC. was reported to be an ingredient in an African remedy for chest troubles; and S. vulgaris was used in Europe for dysmenorrhea and amenorrhea and in the USA as a diaphoretic, diuretic, tonic and emmenagogue.

Retronecine is a pyrrolizidine alkaloid found in a variety of plants in the genera Senecio and Crotalaria, and the family Boraginaceae.

General Manufacturing Information · 2 件

... /Senecio/ isatideus is a high-yielding source suitable for preparative purposes.

The most common base portion of pyrrolizidine alkaloids.

応用分野

使用(+)-Retronecine, is a Pyrrolizidine alkaloid (PA) , which is a hepatotoxic, that is, damaging to the liver. It is also tumorigenic. It can also be used as an intermediate for the synthesis of (+)-Lycopsamine (L487525), and (E325580).

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