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MedKoo Cat#: 145602 | Name: Anigorufone

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Anigorufone is a bioactive phytochemical.

Chemical Structure

Anigorufone
Anigorufone
CAS#56252-32-5

Theoretical Analysis

MedKoo Cat#: 145602

Name: Anigorufone

CAS#: 56252-32-5

Chemical Formula: C19H12O2

Exact Mass: 272.0800

Molecular Weight: 272.30

Elemental Analysis: C, 83.81; H, 4.44; O, 11.75

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Anigorufone;
IUPAC/Chemical Name
2-hydroxy-9-phenyl-1H-phenalen-1-one
InChi Key
ACJJXELQAJQSLK-UHFFFAOYSA-N
InChi Code
1S/C19H12O2/c20-16-11-14-8-4-7-13-9-10-15(12-5-2-1-3-6-12)18(17(13)14)19(16)21/h1-11,20H
SMILES Code
OC1=CC2=C3C(C=CC(C4=CC=CC=C4)=C3C1=O)=CC=C2
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 272.30 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Sethiya NK, Shekh MR, Singh PK. Wild banana [Ensete superbum (Roxb.) Cheesman.]: Ethnomedicinal, phytochemical and pharmacological overview. J Ethnopharmacol. 2019 Apr 6;233:218-233. doi: 10.1016/j.jep.2018.12.048. Epub 2019 Jan 25. PMID: 30686574. 2: Ocampos FMM, de Souza AJB, Antar GM, Wouters FC, Colnago LA. Phytotoxicity of Schiekia timida Seed Extracts, a Mixture of Phenylphenalenones. Molecules. 2021 Jul 10;26(14):4197. doi: 10.3390/molecules26144197. PMID: 34299471; PMCID: PMC8304753. 3: Otálvaro F, Görls H, Hölscher D, Schmitt B, Echeverri F, Quiñones W, Schneider B. Dimeric phenylphenalenones from Musa acuminata and various Haemodoraceae species. Crystal structure of anigorootin. Phytochemistry. 2002 May;60(1):61-6. doi: 10.1016/s0031-9422(02)00066-3. PMID: 11985853. 4: Hölscher D, Dhakshinamoorthy S, Alexandrov T, Becker M, Bretschneider T, Buerkert A, Crecelius AC, De Waele D, Elsen A, Heckel DG, Heklau H, Hertweck C, Kai M, Knop K, Krafft C, Maddula RK, Matthäus C, Popp J, Schneider B, Schubert US, Sikora RA, Svatoš A, Swennen RL. Phenalenone-type phytoalexins mediate resistance of banana plants (Musa spp.) to the burrowing nematode Radopholus similis. Proc Natl Acad Sci U S A. 2014 Jan 7;111(1):105-10. doi: 10.1073/pnas.1314168110. Epub 2013 Dec 9. PMID: 24324151; PMCID: PMC3890884. 5: Mathew NS, Negi PS. Traditional uses, phytochemistry and pharmacology of wild banana (Musa acuminata Colla): A review. J Ethnopharmacol. 2017 Jan 20;196:124-140. doi: 10.1016/j.jep.2016.12.009. Epub 2016 Dec 14. PMID: 27988402. 6: Monakhova Y, Schneider B. The intramolecular Diels-Alder reaction of diarylheptanoids--quantum chemical calculation of structural features favoring the formation of phenylphenalenones. Molecules. 2014 Apr 23;19(4):5231-42. doi: 10.3390/molecules19045231. PMID: 24762963; PMCID: PMC6271999. 7: Munde T, Maddula RK, Svatos A, Schneider B. The biosynthetic origin of oxygen functions in phenylphenalenones of Anigozanthos preissii inferred from NMR- and HRMS-based isotopologue analysis. Phytochemistry. 2011 Jan;72(1):49-58. doi: 10.1016/j.phytochem.2010.10.007. Epub 2010 Nov 1. PMID: 21047660. 8: Luque-Ortega JR, Martínez S, Saugar JM, Izquierdo LR, Abad T, Luis JG, Piñero J, Valladares B, Rivas L. Fungus-elicited metabolites from plants as an enriched source for new leishmanicidal agents: antifungal phenyl-phenalenone phytoalexins from the banana plant (Musa acuminata) target mitochondria of Leishmania donovani promastigotes. Antimicrob Agents Chemother. 2004 May;48(5):1534-40. doi: 10.1128/AAC.48.5.1534-1540.2004. PMID: 15105102; PMCID: PMC400542.

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Phenescaline

Phenescaline