Mavatrep - ≥99% , Vanilloid receptor antagonist, CAS No.956274-94-5, Vanilloid receptor antagonist

CAS: 956274-94-5 Cat. No.: M647100 Summenformel: C25H21F3N2O Molekulargewicht: 422.44 PubChem CID: 17751090
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QUALITÄT & REINHEIT ≥99%
Synonyms
F197218T99 | Mavatrep (USAN) | Mavatrep(JNJ-39439335) | Mavatrep [USAN] | Mavatrep | (E)-2-(2-(2-(4-(trifluoromethyl)styryl)-1H-benzo[d]imidazol-6-yl)phenyl)propan-2-ol|2-[2-[2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-3H-benzimidazol-5-yl
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Preis
Menge
1mg
M647100-1mg
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3 Auf Lager
49,37€
5mg
M647100-5mg
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3 Auf Lager
121,40€
25mg
M647100-25mg
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2 Auf Lager
394,73€
100mg
M647100-100mg
Auf Bestellung · 8–12 Wochen
1.014,30€
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Warum diese Qualität

≥99% für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Protected from light,Store at -20°C Versand Ice chest + Ice pads. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Literaturbeleg

In 0 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

Mavatrep (JNJ-39439335) is an orally active, selective and potent TRPV1 antagonist with high affinity for hTRPV1 channels ( K i =6.5 nM). Mavatrep antagonizes capsaicin-induced Ca 2+ influx with an IC 50 value of 4.6 nM. Mavatrep can be used in some studies of neuropathic pain.

In Vitro

Mavatrep (series of decreasing concentrations from 1 μM; 25 min) inhibits capsaicin-induced Ca 2+ influx in HEK293 cells expressing TRPV1 channels. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: HEK293 cells (stably expressing TRPV1 channels) Concentration: Series of decreasing concentrations from 1 μM Incubation Time: 25 min Result: Inhibited capsaicin-induced Ca 2+ influx with an IC 50 value of 4.6 nM.

In Vivo

Mavatrep (1, 3, 10, 30 mg/kg; p.o.; single) shows complete reversal of thermal hypersensitivity both in CFA model of inflammatory of pain and (0.1, 0.3, 1, 3, 10 mg/kg) carrageenan model of inflammatory pain . Mavatrep (10 mg/kg; p.o.; single) exhibits substantial bioavailability in the rat (51%) . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male Sprague-Dawley rats (195-350 g; CFA model of inflammatory of pain) . Dosage: 10 mg/kg Administration: Oral administration, single. Result: Significantly reversed CFA-induced thermal hypersensitivity, beginning 30 min after administration and lasting for at least 3 h. Animal Model: Male Sprague-Dawley rats (195-350 g; CFA model of inflammatory of pain) . Dosage: 1, 3, 10, 30 mg/kg Administration: Oral administration, single. Result: Exhibited complete reversal of thermal hypersensitivity, with ED 50 and ED 80 values of 1.8 and 7.8 mg/kg, and the corresponding plasma levels were 41.9 and 270.8 ng/mL, respectively. Animal Model: Male Sprague-Dawley rats (195-350 g; carrageenan model of inflammatory pain) . Dosage: 0.1, 0.3, 1, 3, 10 mg/kg Administration: Oral administration, single. Result: Completely reversed carrageenan-induced thermal hypersensitivity, with ED 50 and ED 80 values of 0.18 and 0.48 mg/kg, and the corresponding plasma levels were 3.8 and 9.2 ng/mL, respectively. Animal Model: Male Sprague-Dawley rats (195-350 g) . Dosage: 2 mg/kg (for i.v.); 10 mg/kg (for p.o.). (Dissolved in 20% HPβCD) Administration: Oral administration, single. Result: 1.19 Pharmacokinetic Parameters of Mavatrep in male Sprague-Dawley rats . IV (2 mg/kg) PO (10 mg/kg) CL (mL/min/kg) V ss (L/kg) T 1/2 (h) C max (ng/mL) AUC max (ng•h/mL) T 1/2 (h) F (%) 33 10 3.4 421 4203 3.8 51

Form:Solid

Spezifikationen

Synonyme
F197218T99 | Mavatrep (USAN) | Mavatrep(JNJ-39439335) | Mavatrep [USAN] | Mavatrep | (E)-2-(2-(2-(4-(trifluoromethyl)styryl)-1H-benzo[d]imidazol-6-yl)phenyl)propan-2-ol | 2-[2-[2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-3H-benzimidazol-5-yl
Spezifikationen & Reinheit
≥99%
Biochemische und physiologische Mechanismen
Mavatrep (JNJ-39439335) is an orally active, selective and potent TRPV1 antagonist with high affinity for hTRPV1 channels ( K i =6.5 nM). Mavatrep antagonizes capsaicin-induced Ca 2+ influx with an IC 50 value of 4.6 nM. Mavatrep can be used in some studi
Storage
Protected from light,Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
ANTAGONIST
Mechanismus der Wirkung
Vanilloid receptor antagonist
Reinheit
≥99%
Produkteigenschaften
ALogP
6
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
CC(C)(C1=CC=CC=C1C2=CC3=C(C=C2)N=C(N3)C=CC4=CC=C(C=C4)C(F)(F)F)O
IUPAC Name
2-[2-[2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-3H-benzimidazol-5-yl]phenyl]propan-2-ol
InChIKey
ORDHXXHTBUZRCN-NTEUORMPSA-N
INCHI
1S/C25H21F3N2O/c1-24(2,31)20-6-4-3-5-19(20)17-10-13-21-22(15-17)30-23(29-21)14-9-16-7-11-18(12-8-16)25(26,27)28/h3-15,31H,1-2H3,(H,29,30)/b14-9+
Isomere SMILES
CC(C)(C1=CC=CC=C1C2=CC3=C(C=C2)N=C(N3)/C=C/C4=CC=C(C=C4)C(F)(F)F)O
Alternative CAS-Nummer
956274-94-5
PubChem CID
17751090
MeSH-Eintrag
2-(2-(2-(2-(4-trifluoromethylphenyl)vinyl)-1H-benzimidazol-5-yl)phenyl)propan-2-ol;mavatrep
Molekulargewicht
422.44

Dokumentation

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
KlasseBenzene and substituted derivatives
SubclassTrifluoromethylbenzenes
Intermediate Tree Nodes Not available
Direct ParentTrifluoromethylbenzenes
Alternative Parents Phenylpropanes  Benzimidazoles  Styrenes  Tertiary alcohols  Imidazoles  Heteroaromatic compounds  Azacyclic compounds  Organonitrogen compounds  Organofluorides  Hydrocarbon derivatives  Aromatic alcohols  Alkyl fluorides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Trifluoromethylbenzene - Benzimidazole - Phenylpropane - Styrene - Azole - Imidazole - Tertiary alcohol - Heteroaromatic compound - Organoheterocyclic compound - Azacycle - Alkyl halide - Hydrocarbon derivative - Alkyl fluoride - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic nitrogen compound - Alcohol - Organic oxygen compound - Aromatic alcohol - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as trifluoromethylbenzenes. These are organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
TRPV1 Tclin Transient receptor potential cation channel subfamily V member 1 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TRPV1 Tclin Vanilloid receptor (8273 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Trpv2 Transient receptor potential cation channel subfamily V member 2 (148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cavia porcellus (23802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rhesus monkey (3147 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpm8 Transient receptor potential cation channel subfamily M member 8 (889 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:

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4 results found

Lot NumberCertificate TypeDatumArtikel
H2518420H2518420Certificate of AnalysisApr 16, 2025 M647100
H2518425H2518425Certificate of AnalysisApr 16, 2025 M647100
H2518426H2518426Certificate of AnalysisApr 16, 2025 M647100
H2518427H2518427Certificate of AnalysisApr 16, 2025 M647100
Chemische und physikalische Eigenschaften
LöslichkeitDMSO : 16.67 mg/mL (39.46 mM; ultrasonic and warming and heat to 60°C)
EmpfindlichkeitLight sensitive;Heat sensitive
Molekulargewicht422.400 g/mol
XLogP36.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass422.161 Da
Monoisotopic Mass422.161 Da
Topological Polar Surface Area48.900 Ų
Heavy Atom Count31
Formal Charge0
Complexity627.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Lösungsrechner
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