세파란틴 - 분석 표준, ≥98% , CAS No.481-49-2

Name: 세파란틴 - 분석 표준, ≥98% , CAS No.481-49-2
Brand: Aladdin Scientific
SKU: C102706
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CAS: 481-49-2 Cat. No.: C102706 분자식: C₃₇H₃₈N₂O₆ 분자량: 606.72 EC 번호: 683-114-9

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세파란틴 - 분석 표준, ≥98% CAS No(481-49-2) by Aladdin Scientific

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주문 가능

등급 & 순도 Analytical standard ? ≥98%

Synonyms

(14S,27R)-22,33-dimethoxy-13,28-dimethyl-2,5,7,20-tetraoxa-13,28-diazaoctacyclo[25.6.2.2~16,19~.1~3,10~.1~21,25~.0~4,8~.0~14,39~.0~31,35~]nonatriaconta-1(33),3,8,10(39),16,18,21(36),22,24,31,34,37-dod | NCGC00161621-03 | O-Methylcepharanoline | BSPBio_003

Storage

Room temperature

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보통

사양 이름과 식별자 고급 데이터 Taxonomic Classification 3D 구조 관련 대상(인간) 관련 대상(비인간) 작용 메커니즘 인증서(CoA, COO, BSE/TSE 및 분석 차트) 화학 및 물리적 특성 Citations of This Product 솔루션 계산기 리뷰

사양

동의어

사양 및 순도

분석 표준, ≥98%

생화학 및 생리적 메커니즘

스테파니아 세파란타 하야타 식물에서 추출한 자연 발생 알칼로이드. 항염증, 항알레르기 및 면역 조절 효과를 나타냅니다. NO 생성을 억제할 수 있습니다. 생체 내에서 활성.

보관 조건

Room temperature

배송

보통

등급

분석 표준물질

참고

가능하면 당일에 용액을 준비하여 사용하는 것이 좋습니다. 그러나 미리 원액을 만들어야 하는 경우에는 -20°C에서 단단히 밀봉된 바이알에 소량씩 보관하는 것이 좋습니다. 일반적으로 최대 한 달 동안 사용할 수 있습니다. 사용하기 전에 바이알을 열기 전에 제품을 실온에서 최소 1시간 동안 평형을 이루도록 하는 것이 좋습니다. 용해도, 사용법 및 취급에 대한 추가 정보가 필요하신가요? 자주 묻는 질문(FAQ) 페이지에서 자세한 내용을 확인하세요.

순수함

≥98%

이름과 식별자

Pubchem Sid

508812602

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508812602

정식 스마일

CN1CCC2=CC3=C(C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(C=C8CCN7C)OC)O4)OC)OCO3

IUPAC Name

(14S,27R)-22,33-dimethoxy-13,28-dimethyl-2,5,7,20-tetraoxa-13,28-diazaoctacyclo[25.6.2.216,19.13,10.121,25.04,8.031,35.014,39]nonatriaconta-1(33),3(39),4(8),9,16(38),17,19(37),21,23,25(36),31,34-dodecaene

InChIKey

YVPXVXANRNDGTA-WDYNHAJCSA-N

INCHI

1S/C37H38N2O6/c1-38-13-11-24-18-31(41-4)33-20-27(24)28(38)16-23-7-10-30(40-3)32(17-23)44-26-8-5-22(6-9-26)15-29-35-25(12-14-39(29)2)19-34-36(37(35)45-33)43-21-42-34/h5-10,17-20,28-29H,11-16,21H2,1-4H3/t28-,29+/m1/s1

이성체 SMILES

CN1CCC2=CC3=C(C4=C2[C@@H]1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)C[C@@H]7C8=CC(=C(C=C8CCN7C)OC)O4)OC)OCO3

분자량

606.72

Reaxy-Rn

604585

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=604585&ln=

고급 데이터

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lignans, neolignans and related compounds

Kingdom	Organic compounds
Superclass	Lignans, neolignans and related compounds
분류	Not available
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Lignans, neolignans and related compounds
Alternative Parents	Diarylethers Tetrahydroisoquinolines Benzodioxoles Anisoles Aralkylamines Alkyl aryl ethers Trialkylamines Oxacyclic compounds Azacyclic compounds Acetals Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Oxyneolignan skeleton - Diaryl ether - Tetrahydroisoquinoline - Benzodioxole - Anisole - Alkyl aryl ether - Aralkylamine - Benzenoid - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Oxacycle - Ether - Acetal - Azacycle - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Aromatic heteropolycyclic compound
설명	This compound belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.
External Descriptors	Isoquinoline alkaloids
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D 구조

관련 대상(인간)

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)

Discover Target: GBA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)

Discover Target: GLP1R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A673 (619 Activities)

Lot Number	Certificate Type	날짜	항목
G2228429	Certificate of Analysis	Feb 04, 2026	C102706
G2228431	Certificate of Analysis	Feb 04, 2026	C102706
G2228432	Certificate of Analysis	Feb 04, 2026	C102706
G2228645	Certificate of Analysis	Feb 04, 2026	C102706
G2228678	Certificate of Analysis	Feb 04, 2026	C102706
K2520113	Certificate of Analysis	Nov 28, 2025	C102706
K2125937	Certificate of Analysis	Aug 21, 2023	C102706
K2125783	Certificate of Analysis	Aug 21, 2023	C102706
K1219026	Certificate of Analysis	May 09, 2022	C102706
F2028088	Certificate of Analysis	Apr 27, 2022	C102706

감도	water & moisture & light sensitive
분자량	606.700 g/mol
XLogP3	6.500
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	2
Exact Mass	606.273 Da
Monoisotopic Mass	606.273 Da
Topological Polar Surface Area	61.900 Å²
Heavy Atom Count	45
Formal Charge	0
Complexity	994.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	2
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

세파란틴 - 분석 표준, ≥98% , CAS No.481-49-2

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고급 데이터

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