S-(+)-Methoprene - ≥95% , CAS No.65733-16-6

CAS: 65733-16-6 Cat. No.: S185858 Peso molecular: 310.5 Número EC: 613-834-0 PubChem CID: 1711973

GRADE & PURITY ≥95%

Synonyms

AKOS037643628 | BSPBio_003468 | isopropyl (S,2E,4E)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienoate | UNII-4YIQ0A94UR | AB01563364_01 | Pharorid | Altoside CP 10 | (+)-Methoprene | CHEBI:39255 | DTXSID1035783 | (+)-Methoprene;(7S)-Methoprene;ZR 2458 | Alto

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

AKOS037643628 | BSPBio_003468 | isopropyl (S, 2E, 4E)-11-methoxy-3, 7, 11-trimethyldodeca-2, 4-dienoate | UNII-4YIQ0A94UR | AB01563364_01 | Pharorid | Altoside CP 10 | (+)-Methoprene | CHEBI:39255 | DTXSID1035783 | (+)-Methoprene;(7S)-Methoprene;ZR 2458 | Alto

Especificaciones y pureza

≥95%

Mecanismos bioquímicos y fisiológicos

Insect juvenile hormone analog. Modulates ecdysteroid signaling during insect development. Shows growth regulatory effects in vivo. Orally active.

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 504760614
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504760614
• Sonrisas canónicas: CC(C)OC(=O)C=C(C)C=CCC(C)CCCC(C)(C)OC
• IUPAC Name: propan-2-yl (2E,4E,7S)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienoate
• InChIKey: NFGXHKASABOEEW-GYMWBFJFSA-N
• INCHI: 1S/C19H34O3/c1-15(2)22-18(20)14-17(4)11-8-10-16(3)12-9-13-19(5,6)21-7/h8,11,14-16H,9-10,12-13H2,1-7H3/b11-8+,17-14+/t16-/m1/s1
• Isómeros SMILES: C[C@@H](CCCC(C)(C)OC)C/C=C/C(=C/C(=O)OC(C)C)/C
• PubChem CID: 1711973
• Peso molecular: 310.5

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Prenol lipids
      • Subclass Sesquiterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Prenol lipids
• Subclass: Sesquiterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Sesquiterpenoids
• Alternative Parents: Fatty acid esters Enoate esters Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Sesquiterpenoid - Farsesane sesquiterpenoid - Fatty acid ester - Fatty acyl - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Carboxylic acid derivative - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxide - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.
• External Descriptors: methoprene

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

Objetivos asociados (humanos)

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

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

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

Discover Target: PPARG

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

Objetivos asociados (no humanos)

Bombyx mori (577 Activities)

Explore this target

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

Sitophilus oryzae (115 Activities)

Explore this target

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

Pieris brassicae (110 Activities)

Explore this target

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

Mecanismos de acción

Propiedades químicas y físicas

• Peso molecular: 310.500 g/mol
• XLogP3: 5.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 11
• Exact Mass: 310.251 Da
• Monoisotopic Mass: 310.251 Da
• Topological Polar Surface Area: 35.500 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 378.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 2
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 2
• Covalently-Bonded Unit Count: 1

Referencias

1. Jia Qiangqiang, Yang Liu, Wen Jiamin, Liu Suning, Wen Di, Luo Wei, Wang Weihua, Palli Subba Reddy, Sheng Li.  (2024)  Cyp6g2 is the major P450 epoxidase responsible for juvenile hormone biosynthesis in Drosophila melanogaster.  BMC BIOLOGY,  22  (1): (1-14).  [PMID:38741075] [10.1186/s12915-024-01910-4]