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푸에라린

7-Hydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

HCID 5281807
노트반응

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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
3681-99-0
표준 SMILES
O=c1c(-c2ccc(O)cc2)coc2c([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(O)ccc12
InChIKey
HKEAFJYKMMKDOR-VPRICQMDSA-N
분자식
C21H20O9
평균 분자량
416.382 g/mol
단동위원소 질량
416.11073222

이름 및 식별자

우선 이름
7-Hydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
IUPAC
(1S)-1,5-Anhydro-1-[7-hydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-8-yl]-D-glucitol
현지명
푸에라린
영어명
Puerarin
분자식
C21H20O9
분자량
416.38

이름 및 동의어

푸에라린PSYCHOSINEDAIDZEIN-8-C-GLUCOSIDEPurerarinDaidzeinePuerarinePUERARIN EXTRACTPueraria Root Flavone8-β-D-Glucopyranosyl-3-(4-hydroxyphenyl)-7-hydroxy-4H-1-benzopyran-4-one7-HYDROXY-3-[4-HYDROXYPHENYL]-1-BENZOPYRAN-4-ONE 8-[BETA-D-GLUCOPYRANOSIDEPuerain

데이터베이스 식별자

CAS
3681-99-0
PubChem CID
5281807
DTXSID
DTXSID30958020
ChEMBL
CHEMBL486386
ChEBI
CHEBI:8633
UNII
Z9W8997416
EC Number
609-296-1
Nikkaji
J16.365A

물성

물리화학적 성질

녹는점
187 · 187-189°C
끓는 점
688 · 688.0±55.0 °C(Predicted)
밀도
1.614 · 1.614±0.06 g/cm3(Predicted)
저장 조건
2 · 2-8°C
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)
6.46 · 6.46±0.20(Predicted)
물리적 상태
가루
색상
흰색에서 황백색까지
수용성
DMSO 또는 DMF에 용해됩니다. 물이나 에탄올에 약간 용해됨
BRN
64198 · 64198
화장품 원료 기능
항산화제
InChIKey
HKEAFJYKMMKDOR-NCHCSYJDSA-N
SMILES
OC1=CC=C2C(C(C3C=CC(O)=CC=3)=COC2=C1[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)=O |&1:18,19,20,22,24,r|
LogP
0.408 · 0.408 (est)

화학적 성질

White powder

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

안전 데이터

wgk
3
rtecs
UO5216000
HS 번호
29389090
risk_code
11-34
hazard_code
F,C
safety_code
22-24/25-45-36/37/39-26-16
F 고인화성물질
10
스토리지 클래스
11 - Combustible Solids

화학 및 산업

응용 분야 · 3건

개요Puerarin, also known as pueraria flavonoids, is a kind of flavonoid glycoside extracted from the roots of Pueraria alba or Pueraria thomsonii and is also one of the main effective ingredients of Pueraria lobata. That Pueraria lobate was used to treat diseases has already been recorded in China’s ancient medical books such as Shen Nong’s Materia Medica, Treatise on Miscellaneous Diseases and Medical Dictionary. Kanzu root is widely distributed in our country and of rich resources. It has been reported that puerarin could be extracted from Pueraria lobata (Wild.) Ohwi, Radix Pueraria thomsonii, Pueraria omeiensiswanget Tang, Pueraria edulis Pamp and Pueraria phaseoloides, but the content of puerarin differs. Pueraria has a great value for nutrition and medicine and was considered the south ginseng of China. Puerarin has been widespread concerned over our country for its use of food and medicine in recent years.

역사In 1959, Japanese chemist Shibata Shoji first studied the chemical production of pueraria root, indicating that isoflavones are the main active ingredients of pueraria root, including puerarin, daidzin and daidzein . Then in 2003, David Lee first total synthesized analogical puerarin . And it was in 1974 that puerarin was first extracted by Fang Qicheng and other chemists in China . Due to its strong activity of anti-cardiovascular and anti-cerebrovascular ischemia and hypoxia, expanding the coronary artery and cerebrovascular, reducing myocardial oxygen consumption, and improving myocardial systolic and microcirculation function, puerarin was approved for clinical use by the Ministry of Health in 1993. In recent years, researchers have synthesized a series of puerarin derivatives, and active research showed that the part of the puerarin derivatives has a good biological activity and bioavailability. In a new dosage form research, researchers have developed several types of dosage forms such as quickrelease solid dispersions, solid from microemulsion preparation, etc., which greatly increase the solubility of puerarin, thus improving bioavailability. In recent years,the research on crystal drug has opened up new ways for the application of puerarin.

용도Puerarin is a naturally occuring isoflavonoid derived from Chinese medical herb kudzu root and has been used for the treatment of various cardiovascular diseases. Recent sutdies have shown the potenti al of puerarin treatment as a novel approach to lowering the risk of or improving function in ischemia-reperfusion brain injury-related disorders.

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이 페이지에서기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트

상류 원료

7-methoxy-3-(4-methoxyphenyl)-8-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

공급사100 곳

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추가 설명

정의ChEBI: A hydroxyisoflavone that is isoflavone substituted by hydroxy groups at positions 7 and 4' and a beta-D-glucopyranosyl residue at position 8 via a C-glycosidic linkage.