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Ginsenoside F2

HCID 9918692
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
62025-49-4
표준 SMILES
CC(C)=CCC[C@](C)(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H]1CC[C@]2(C)[C@@H]1[C@H](O)C[C@@H]1[C@@]3(C)CC[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(C)(C)[C@@H]3CC[C@]12C
InChIKey
SWIROVJVGRGSPO-JBVRGBGGSA-N
분자식
C42H72O13
평균 분자량
785 g/mol
단동위원소 질량
784.49729235

개요

Ginsenoside F2 is a ginsenoside found in Panax species that is dammarane which is substituted by hydroxy groups at the 3beta, 12beta and 20 pro-S positions, in which the hydroxy groups at positions 3 and 20 have been converted to the corresponding beta-D-glucopyranosides, and in which a double bond has been introduced at the 24-25 position. It has a role as an antineoplastic agent, an apoptosis inducer and a plant metabolite. It is a beta-D-glucoside, a tetracyclic triterpenoid, a 12beta-hydroxy steroid and a ginsenoside. It derives from a hydride of a dammarane.

이름 및 식별자

우선 이름
Ginsenoside F2
IUPAC
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-6-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol
영어명
GINSENOSIDE F2
분자식
C42H72O13
분자량
785.01

이름 및 동의어

ginsenoside F262025-49-4ginsenoside-F2CHEBI:77145DTXSID20432763(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(((3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-((2S)-6-methyl-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxyhept-5-en-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta(a)phenanthren-3-yl)oxy)oxane-3,4,5-triol(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-6-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triolRefChem:143211DTXCID9038359120(S)-Ginsenoside F2MFCD06410948(20S)-ginsenoside F2
이름 더 보기
Ginsenoside F2(AS)20(S)-Ginsenoside-F2Ginsenoside F2, >=98%-D-glucopyranosidederiv.20(S)-Ginsenoside F2 ,98%Ginsenoside F2 (Standard)

물성

구조 계산 물성

XLogP
4
극성 표면적
219 Ų
수소 결합 공여자 수
9
수소 결합 수용자 수
13
회전 가능 결합 수
10
무거운 원자 수
55
형식 전하
0
복잡도
1,370

물리화학적 성질

녹는점
195 · 195-200°C
끓는 점
871.5 · 871.5±65.0 °C(Predicted)
밀도
1.3 · 1.30±0.1 g/cm3(Predicted)
저장 조건
-20 °C · Hygroscopic, -20°C Freezer, Under inert atmosphere
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)
12.91 · 12.91±0.70(Predicted)
물리적 상태
고체
색상
흰색에서 황백색까지
안정성
흡습성
InChIKey
SWIROVJVGRGSPO-IGNDSYMUNA-N

안전 및 규제

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

안전 데이터

신호 어
Warning
유해·위험 문구
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드 H302

화학 및 산업

응용 분야 · 2건

개요Ginsenoside F2 is a ginsenoside that has been found in P. ginseng and has diverse biological activities. It increases the proliferation of human hair dermal papilla cells (HHDPCs) and HaCaT human keratinocytes when used at concentrations of 0.01, 0.1, and 1 μM. Ginsenoside F2 (0.5 and 2.5 mg/kg) induces hair growth and increases hair density following depilation in mice. It is cytotoxic to U373MG glioblastoma cells in vitro (IC50 = 50 μg/ml) and reduces tumor growth in a U373MG mouse xenograft model when administered at a dose of 35 mg/kg every other day. Ginsenoside F2 (1 mg/ear) reduces ear edema induced by phorbol 12-myristate 13-acetate (TPA; ) in mice. It is a human intestinal bacterial metabolite of ginsenoside Rb1 via the intermediate ginsenoside Rd .

용도Ginsenoside F2 is a bioactive metabolite of the ginsenoside component of Panax ginseng with the ability to regulate element-binding protein cleavage activating protein and transforming growth factor-β pathways. This control over apoptosis can lead to a control over hair growth and hair loss in mammals.

상·하류 제품 정보

상류 원료

진세노사이드알디제일인산나트륨 수화물

공급사100 곳

北京华美互利生物化工010-56205725 · [email protected]
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南京普怡生物科技有限公司13814510036 · [email protected]
合肥翰刚医药科技有限公司

관련 반응

1건
반응 기록 만들기
HRID 1484199 반응식
HRID 1484199생성물로uspto-grants-2016_08

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
Ginsenoside F2, 10 mM in DMSO
Ginsenoside F2, 98%, from Panax ginseng C. A. Mey.
(20S)-3β,20-Bis(β-D-glucopyranosyloxy)-5α-dammar-24-ene-12β-ol
CHEMBL109500720-(S)-Ginsenoside F2(2R,3R,4S,5S,6R)-2-(((3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-((S)-6-methyl-2-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hept-5-en-2-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol3beta,20-bis(beta-D-glucopyranosyloxy)dammar-24-en-12beta-ol(3ss,12ss)-12-Hydroxydammar-24-ene-3,20-diyl bis-ss-D-glucopyranosideGinsenosideF2(20S)-3|?-(|?-D-Glucopyranosyloxy)-20-(|?-D-glucopyranosyloxy)dammar-24-ene-12|?-olorb1221949

데이터베이스 식별자

CAS
62025-49-4
PubChem CID
9918692
DTXSID
DTXSID20432763
ChEMBL
CHEMBL1095007
ChEBI
CHEBI:77145
Nikkaji
J38.857B
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추가 설명 · 1건

정의ChEBI: A ginsenoside found in Panax species that is dammarane which is substituted by hydroxy groups at the 3beta, 12beta and 20 pro-S positions, in which the hydroxy groups at positions 3 and 20 have been converted to the corresponding beta-D-glucopyranosides, and in which a double bond has been introduced at the 24-25 position.