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· · COA & SDS 모든 제품에 대한 사용 가능 · 주식 상품에 대한 같은 날 배송 홈 목표 / 경로 / 질병에 따라 신호 전달 경로를 통해 자가포식 자가포식 PF 750 - 몰리간드™, ≥98%(HPLC) , Inhibitor of epoxide hydrolase 2;Inhibitor of Fatty acid amide hydrolase, CAS No.959151-50-9, Inhibitor of epoxide hydrolase 2;Inhibitor of Fatty acid amide hydrolase PF 750 - 몰리간드™, ≥98%(HPLC) , Inhibitor of epoxide hydrolase 2;Inhibitor of Fatty acid amide hydrolase, CAS No.959151-50-9, Inhibitor of epoxide hydrolase 2;Inhibitor of Fatty acid amide hydrolase
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%(HPLC) Synonyms
NCGC00370873-01 | Q27088336 | N-phenyl-4-(quinolin-3-ylmethyl)piperidine-1-carboxamide | BDBM26740 | BRD-K83213911-001-01-0 | DTXSID00648906 | PF750 | PF-750 | N-Phenyl-4-(3-quinolinylmethyl)-1-piperidinecarboxamide | PF 750 | GTPL5244 | PF-750, >=98% (HP
Shipped In
아이스 박스 + 아이스 패드
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Why this grade 몰리간드™, ≥98%(HPLC) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping 20°C에서 보관 Ships 아이스 박스 + 아이스 패드 Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
개요 제품 설명:
PF 750은 선택적 공유 지방산 아미드 가수 분해 효소 억제제로, 다양한 사전 배양 시간에서 16.2~595 nM의 IC50을 보여줍니다.
Specifications 동의어
NCGC00370873-01 | Q27088336 | N-phenyl-4-(quinolin-3-ylmethyl)piperidine-1-carboxamide | BDBM26740 | BRD-K83213911-001-01-0 | DTXSID00648906 | PF750 | PF-750 | N-Phenyl-4-(3-quinolinylmethyl)-1-piperidinecarboxamide | PF 750 | GTPL5244 | PF-750, >=98% (HP
생화학 및 생리적 메커니즘
비가역적 지방산 아미드 가수분해효소(FAAH) 억제제(IC50= 16.2 nM)로 다른 세린 가수분해효소에는 활성을 나타내지 않습니다. 중추 신경계 내에서 FAAH를 선택적으로 억제합니다. 경구 활성.
작동 메커니즘
Inhibitor of epoxide hydrolase 2;Inhibitor of Fatty acid amide hydrolase
이름과 식별자 Pubchem Sid 528766587 정식 스마일 C1CN(CCC1CC2=CC3=CC=CC=C3N=C2)C(=O)NC4=CC=CC=C4 IUPAC Name N-phenyl-4-(quinolin-3-ylmethyl)piperidine-1-carboxamide InChIKey BIODYGOZWZNCAG-UHFFFAOYSA-N INCHI 1S/C22H23N3O/c26-22(24-20-7-2-1-3-8-20)25-12-10-17(11-13-25)14-18-15-19-6-4-5-9-21(19)23-16-18/h1-9,15-17H,10-14H2,(H,24,26) 이성체 SMILES C1CN(CCC1CC2=CC3=CC=CC=C3N=C2)C(=O)NC4=CC=CC=C4 WGK 독일 3 PubChem CID 25154868 분자량 345.44
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds 분류 Quinolines and derivatives Subclass Not available Intermediate Tree Nodes Not available Direct Parent Quinolines and derivatives Alternative Parents N-phenylureas Piperidinecarboxamides Pyridines and derivatives Heteroaromatic compounds Ureas Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents N-phenylurea - Quinoline - 1-piperidinecarboxamide - Piperidinecarboxamide - Monocyclic benzene moiety - Piperidine - Pyridine - Benzenoid - Heteroaromatic compound - Carbonic acid derivative - Urea - Azacycle - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Aromatic heteropolycyclic compound 설명 This compound belongs to the class of organic compounds known as quinolines and derivatives. These are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene. External Descriptors Not available Data sources 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.
3D 구조 관련 대상(인간) 관련 대상(비인간) 작용 메커니즘 인증서(CoA, COO, BSE/TSE 및 분석 차트) 화학 및 물리적 특성 용해성 Solvent:DMSO, Max Conc. mg/mL: 34.54, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 34.54, Max Conc. mM: 100 분자량 345.400 g/mol XLogP3 4.100 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 3 Exact Mass 345.184 Da Monoisotopic Mass 345.184 Da Topological Polar Surface Area 45.200 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 454.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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
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