Pyriproxifen - 10mM in DMSO , CAS No.95737-68-1

CAS: 95737-68-1 Cat. No.: P427120 Summenformel: C₂₀H₁₉NO₃ Molekulargewicht: 321.37 EG-Nummer: 429-800-1

GRADE & PURITY 10mM in DMSO

Synonyms

Pyriproxyfen 100 microg/mL in Acetonitrile | JUVENTOX | P2612 | KS-5363 | NCGC00163945-02 | VECTRA FELIS COMPONENT PYRIPROXYFEN | D08455 | Tox21_300716 | UNII-3Q9VOR705O | 2-(1-(4-phenoxyphenoxy)propan-2-yloxy)pyridine | HY-B2031 | NCGC00163945-04 | PYRIP

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Synonyme

Pyriproxyfen 100 microg/mL in Acetonitrile | JUVENTOX | P2612 | KS-5363 | NCGC00163945-02 | VECTRA FELIS COMPONENT PYRIPROXYFEN | D08455 | Tox21_300716 | UNII-3Q9VOR705O | 2-(1-(4-phenoxyphenoxy)propan-2-yloxy)pyridine | HY-B2031 | NCGC00163945-04 | PYRIP

Spezifikationen & Reinheit

10mM in DMSO

Biochemische und physiologische Mechanismen

Insect juvenile hormone mimetic. Larvicidal agent. Inhibits maturation in a broad spectrum of insect species and sterilizes adult females. Orally active.

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Namen und Kennungen

• Pubchem Sid: 528770728
• Kanonisches Lächeln: CC(COC1=CC=C(C=C1)OC2=CC=CC=C2)OC3=CC=CC=N3
• IUPAC Name: 2-[1-(4-phenoxyphenoxy)propan-2-yloxy]pyridine
• InChIKey: NHDHVHZZCFYRSB-UHFFFAOYSA-N
• INCHI: 1S/C20H19NO3/c1-16(23-20-9-5-6-14-21-20)15-22-17-10-12-19(13-11-17)24-18-7-3-2-4-8-18/h2-14,16H,15H2,1H3
• Isomere SMILES: CC(COC1=CC=C(C=C1)OC2=CC=CC=C2)OC3=CC=CC=N3
• WGK Deutschland: 2
• RTECS: UT5804000
• UN-Nummer: 3077
• Molekulargewicht: 321.37
• Reaxy-Rn: 6932868
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6932868&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Benzene and substituted derivatives
      • Subclass Diphenylethers

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Benzene and substituted derivatives
• Subclass: Diphenylethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Diphenylethers
• Alternative Parents: Diarylethers Phenoxy compounds Phenol ethers Alkyl aryl ethers Pyridines and derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Diphenylether - Diaryl ether - Phenoxy compound - Phenol ether - Alkyl aryl ether - Pyridine - Heteroaromatic compound - Ether - Organoheterocyclic compound - Azacycle - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group.
• External Descriptors: Pesticides

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.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

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

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

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

AHR Tclin Aryl hydrocarbon receptor (1071 Activities)

Discover Target: AHR

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

Zugehörige Ziele (nicht menschlich)

Bemisia tabaci (599 Activities)

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Spodoptera litura (1708 Activities)

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

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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

Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)

Discover Target: Nr1i2

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

Diaphorina citri (62 Activities)

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

Trialeurodes vaporariorum (2 Activities)

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Schmelzpunkt (°C): 45-47°C
• Molekulargewicht: 321.400 g/mol
• XLogP3: 4.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 7
• Exact Mass: 321.136 Da
• Monoisotopic Mass: 321.136 Da
• Topological Polar Surface Area: 40.600 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 338.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referenzen

1. Cong Zhang, Bin Wan, Meng-Ru Jin, Xi Wang, Yu-Jing Wei, Ling Zhong, Bin Xia.  (2023)  Inhibition of ecdysone receptor (DcEcR) and ultraspiracle (DcUSP) expression in Diaphorina citri increased susceptibility to pesticides.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:37532332] [10.1016/j.pestbp.2023.105518]