MMP-9-IN-1 - 10mM in DMSO , CAS No.502887-71-0

CAS: 502887-71-0 Cat. No.: M424329 Summenformel: C16H17F2N3O3S Molekulargewicht: 369.39
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GRADE & PURITY 10mM in DMSO
Synonyms
OUN87710Acetamide,N-​[4-​(difluoromethoxy)​phenyl]​-​2-​[(1,​6-​dihydro-​6-​oxo-​4-​propyl-​2-​pyrimidinyl)​thio]​-
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Deutschland (EU)
USA*
Price
Qty
1ml
M424329-1ml
—
2 Auf Lager

120,53€

141,35€
Speichern 20,83 € (14.73%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Information

MMP-9-IN-1 MMP-9-IN-1 (OUN87710) is a specific inhibitor of matrix metalloproteinase-9 (MMP-9) . MMP-9-IN-1 selectively targets the hemopexin (PEX) domain of MMP-9 with Kd of 2.1 μM.

Targets

MMP-9 (Cell-free assay) 2.1 μM(Kd)

Specifications

Synonyme
OUN87710Acetamide,N-​[4-​(difluoromethoxy)​phenyl]​-​2-​[(1,​6-​dihydro-​6-​oxo-​4-​propyl-​2-​pyrimidinyl)​thio]​-
Spezifikationen & Reinheit
10mM in DMSO
Biochemische und physiologische Mechanismen
MMP-9-IN-1 (OUN87710) is a specific inhibitor of matrix metalloproteinase-9 (MMP-9). MMP-9-IN-1 selectively targets the hemopexin (PEX) domain of MMP-9 with Kd of 2.1 μM.
Storage
Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
INHIBITOR
Produkteigenschaften
ALogP
3.389
hba_count
4
HBD-Zahl
2
Rotationsfähige Bindung
8
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
CCCC1=CC(=O)NC(=N1)SCC(=O)NC2=CC=C(C=C2)OC(F)F
IUPAC Name
N-[4-(difluoromethoxy)phenyl]-2-[(6-oxo-4-propyl-1H-pyrimidin-2-yl)sulfanyl]acetamide
InChIKey
OLTRRVUORWPRGF-UHFFFAOYSA-N
INCHI
1S/C16H17F2N3O3S/c1-2-3-11-8-13(22)21-16(20-11)25-9-14(23)19-10-4-6-12(7-5-10)24-15(17)18/h4-8,15H,2-3,9H2,1H3,(H,19,23)(H,20,21,22)
Isomere SMILES
CCCC1=CC(=O)NC(=N1)SCC(=O)NC2=CC=C(C=C2)OC(F)F
Molekulargewicht
369.39
Reaxy-Rn
60093174
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=60093174&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
KlasseBenzene and substituted derivatives
SubclassAnilides
Intermediate Tree Nodes Not available
Direct ParentAnilides
Alternative Parents N-arylamides  Phenoxy compounds  Phenol ethers  Alkylarylthioethers  Pyrimidones  Hydropyrimidines  Vinylogous amides  Heteroaromatic compounds  Secondary carboxylic acid amides  Sulfenyl compounds  Azacyclic compounds  Organic oxides  Hydrocarbon derivatives  Alkyl fluorides  Carbonyl compounds  Organofluorides  Organopnictogen compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Anilide - Phenoxy compound - Aryl thioether - Phenol ether - N-arylamide - Pyrimidone - Alkylarylthioether - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Thioether - Sulfenyl compound - Organoheterocyclic compound - Organic oxide - Organopnictogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Alkyl fluoride - Hydrocarbon derivative - Alkyl halide - Carbonyl group - Organic nitrogen compound - Aromatic heteromonocyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

1 results found

Lot NumberCertificate TypeDatumArtikel
H2408010Certificate of AnalysisJun 05, 2026 M424329
Chemische und physikalische Eigenschaften
DMSO (mg/ml) Maximale Löslichkeit74
DMSO (mM) Maximale Löslichkeit200.330274235902
Wasser (mg/ml) Maximale Löslichkeit<1
Molekulargewicht369.400 g/mol
XLogP33.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count8
Exact Mass369.096 Da
Monoisotopic Mass369.096 Da
Topological Polar Surface Area105.000 Ų
Heavy Atom Count25
Formal Charge0
Complexity547.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Lösungsrechner
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