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Huperzine A

HCID 854026
노트반응

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

CAS
102518-79-6
표준 SMILES
C/C=C1\[C@H]2C=C(C)C[C@]1(N)c1ccc(=O)[nH]c1C2
InChIKey
ZRJBHWIHUMBLCN-YQEJDHNASA-N
분자식
C15H18N2O
평균 분자량
242.322 g/mol
단동위원소 질량
242.1419132

이름 및 식별자

우선 이름
Huperzine A
IUPAC
(5R,9R,11E)-5-Amino-11-ethylidene-7-methyl-5,6,9,10-tetrahydro-5,9-methanocycloocta[b]pyridin-2(1H)-one
영어명
(-)-Huperzine A
분자식
C15H18N2O
분자량
242.32

이름 및 동의어

HUPERZINE A 1%Huperizine AHupAHaboyinHupzine AHUPERIZINEKimpukan AIsoselagine(-)-SelagineHUPERZINE A(P)

데이터베이스 식별자

CAS
102518-79-6、120786-18-7
PubChem CID
854026
DTXSID
DTXSID8046038
ChEMBL
CHEMBL395280
ChEBI
CHEBI:78330
UNII
0111871I23
EC Number
600-320-6、634-239-2
Nikkaji
J128.649H

물성

물리화학적 성질

녹는점
211 · 211-216oC
끓는 점
505 · 505.0±50.0 °C(Predicted)
밀도
1.2 · 1.20±0.1 g/cm3(Predicted)
저장 조건
2 · Keep in dark place,Inert atmosphere,2-8°C
용해도
2 O; · insoluble in H2O; ≥12.12 mg/mL in DMSO; ≥23.13 mg/mL in EtOH
산도 계수 (pKa)
12.25 · 12.25±0.60(Predicted)
물리적 상태
Solid
색상
흰색에서 거의 흰색
InChI
InChI=1S/C15H18N2O/c1-3-11-10-6-9(2)8-15(11,16)12-4-5-14(18)17-13(12)7-10/h3-6,10H,7-8,16H2,1-2H3,(H,17,18)/b11-3+/t10-,15+/m0/s1
InChIKey
ZRJBHWIHUMBLCN-YQEJDHNASA-N
SMILES
C12C[C@@]3([H])/C(=C\C)/[C@@](N)(C=1C=CC(=O)N2)CC(C)=C3
LogP
0.833 · 0.833 (est)

화학적 성질

Pale Brown Solid

안전 및 규제

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

안전 데이터

wgk
3
rtecs
PB9185700
ridadr
UN 1544 6.1/PG 2
HS 번호
29339900
risk_code
26/27/28-36/37/38
hazard_code
T+
safety_code
26-36/37/39-45

화학 및 산업

응용 분야 · 2건

개요Huperzine A is obtained from Huperzia serrata, which is the perennial fern. It shows activities in antipyretic, hemostasis, and dehumidification and is used for the treatment in folk of pneumonia, lung abscess, hematemesis, hematochezia, traumatic injury, etc.

용도Huperzine A is a potential therapeutic agent for Alzheimer disease that reversible alkaloid inhibitor of AChE which crosses the blood-brain barrier. It reduces cell death induced by glutamate in primary cultures derived from forebrain, hippocampus, cortex and cere.In China, it is approved for use in the treatment of Alzheimer’s disease (AD). Huperzine A was classified as a dietary supplement by the FDA in 1997. As a nutraceutical, it is available in American health food stores or via the Internet, labeled as a memory aid.

제조 방법 · 1건

(-)-Huperzine A, a Lyco-podium alkaloid isolated in 1986 from the club moss Huperzia serrata, has drawn considerable attention after it was revealed to be a potent, selective, and reversible AChE inhibitor.The total synthesis of Lycopodium alkaloid (-)-huperzine A has been accomplished in 10 steps with 17% overall yield from commercially abundant (R)-pulegone. The synthetic route features an efficient synthesis of 4 via a Buchwald–Hartwig coupling reaction, a dianion-mediated highly stereoselective alkylation of 4, and a rare example of an intramolecular Heck reaction of an enamine-type substrate. The stereoselective β-elimination and the accompanying Wagner–Meerwein rearrangement are of particular interest.[1] RUI DING Guo Q L Bing Feng Sun*. An Efficient Total Synthesis of (-)-Huperzine A [J]. Organic Letters, 2012, 14 17: 4446-4449. DOI:10.1021/ol301951r.[2] RUI DING. Divergent Total Synthesis of the Lycopodium Alkaloids Huperzine A, Huperzine B, and Huperzine U[J]. The Journal of Organic Chemistry, 2013, 79 1: 240-250. DOI:10.1021/jo402419h.[3] TUN M K M, WüSTMANN D J, HERZON S B. A robust and scalable synthesis of the potent neuroprotective agent (-)-huperzine A [J]. Chemical Science, 2011, 11: 2251-2253. DOI:10.1039/C1SC00455G.

상·하류 제품 정보

상류 원료

Huperzine A

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이 페이지에서기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
(-)- HUPPERZINE A
Carbamic acid, N-[(5R,9R,11E)-11-ethylidene-9,10-dihydro-2-methoxy-7-methyl-5,9-methanocycloocta[b]pyridin-5(6H)-yl]-, methyl ester
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추가 설명 · 1건

정의ChEBI: Huperzine A is a sesquiterpene alkaloid isolated from a club moss Huperzia serrata that has been shown to exhibit neuroprotective activity. It is also an effective inhibitor of acetylcholinesterase and has attracted interest as a therapeutic candidate for Alzheimer's disease. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, a neuroprotective agent, a plant metabolite and a nootropic agent. It is a sesquiterpene alkaloid, a pyridone, a primary amino compound and an organic heterotricyclic compound. It is a conjugate base of a huperzine A(1+).