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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Marmesin - 10mM in DMSO , CAS No.13849-08-6
GRADE & PURITY 10mM in DMSO
Synonyms
KBio2_007132 | Spectrum_001516 | UNII-H5D33D6K5D | Marmesin ((+)-Marmesin) | Marmesin | (+)-Marmesin | 7H-Furo[3, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (S)- | DTXSID001030448 | NSC 340840 | Spectrum5_000402 | (2S)-2-(2-HYDROXYPROPAN-2-YL)-2H,3H,7H-FUR
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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.
Vue d’ensemble Information
Marmesin (S-(+)-Marmesin, (+)-Marmesin, (S)-Marmesin) is a natural coumarin withCOX-2and5-LOXdual inhibitory activity.
Targets
COX-2 ; 5-LOX
Specifications Synonymes
KBio2_007132 | Spectrum_001516 | UNII-H5D33D6K5D | Marmesin ((+)-Marmesin) | Marmesin | (+)-Marmesin | 7H-Furo[3, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (S)- | DTXSID001030448 | NSC 340840 | Spectrum5_000402 | (2S)-2-(2-HYDROXYPROPAN-2-YL)-2H,3H,7H-FUR
Spécifications et pureté
10mM in DMSO
Mécanismes biochimiques et physiologiques
Marmesin (S-(+)-Marmesin, (+)-Marmesin, (S)-Marmesin) is a natural coumarin with COX-2 and 5-LOX dual inhibitory activity.
Conditions de stockage de stockage
Store at -80°C
Expédié en
Dry ice packs + Cold packs
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants Sourires canoniques
CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O
IUPAC Name
(2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one
InChIKey
FWYSBEAFFPBAQU-LBPRGKRZSA-N
INCHI
1S/C14H14O4/c1-14(2,16)12-6-9-5-8-3-4-13(15)18-10(8)7-11(9)17-12/h3-5,7,12,16H,6H2,1-2H3/t12-/m0/s1
Isomères SMILES
CC(C)([C@@H]1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=85846&ln=
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 Phenylpropanoids and polyketides Classe Coumarins and derivatives Subclass Furanocoumarins Intermediate Tree Nodes Linear furanocoumarins Direct Parent Psoralens Alternative Parents 1-benzopyrans Coumarans Pyranones and derivatives Alkyl aryl ethers Benzenoids Tertiary alcohols Heteroaromatic compounds Lactones Oxacyclic compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Psoralen - Benzopyran - 1-benzopyran - Coumaran - Alkyl aryl ether - Pyranone - Pyran - Benzenoid - Heteroaromatic compound - Tertiary alcohol - Lactone - Oxacycle - Ether - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as psoralens. These are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one. External Descriptors Furanocoumarins 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Poids moléculaire 246.260 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 246.089 Da Monoisotopic Mass 246.089 Da Topological Polar Surface Area 55.800 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 387.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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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