108354-14-9 Usage
Description
Aurachin C is a C-type aurachin, which is a quinolin-4-one derivative with a hydroxy group at position 1, a methyl group at position 2, and a triprenyl group at position 3. It is a naturally occurring compound with potential applications in various fields due to its unique chemical structure and properties.
Uses
Used in Pharmaceutical Industry:
Aurachin C is used as a pharmaceutical compound for its potential therapeutic effects. The expression is: aurachin C is used as a therapeutic agent for its unique chemical structure and properties that may contribute to the development of new drugs and treatments.
Used in Chemical Research:
Aurachin C is used as a research compound in the field of chemical research for understanding its chemical properties, reactivity, and potential applications in the synthesis of other compounds. The expression is: aurachin C is used as a research compound for studying its chemical properties and potential applications in chemical synthesis.
Used in Drug Delivery Systems:
Aurachin C may be used in the development of drug delivery systems due to its unique chemical structure, which could potentially enhance the delivery, bioavailability, and therapeutic outcomes of various drugs. The expression is: aurachin C is used as a component in drug delivery systems for its potential to improve drug efficacy and bioavailability.
Please note that the specific applications and reasons for using aurachin C may vary depending on the context and the ongoing research in the field. The provided uses are based on the general properties of aurachin C and its potential applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 108354-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,5 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108354-14:
(8*1)+(7*0)+(6*8)+(5*3)+(4*5)+(3*4)+(2*1)+(1*4)=109
109 % 10 = 9
So 108354-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C25H33NO2/c1-18(2)10-8-11-19(3)12-9-13-20(4)16-17-22-21(5)26(28)24-15-7-6-14-23(24)25(22)27/h6-7,10,12,14-16,28H,8-9,11,13,17H2,1-5H3/b19-12+,20-16+
108354-14-9Relevant articles and documents
Biosynthesis of aurachins A-L in Stigmatella aurantiaca: A feeding study
Hoefle, Gerhard,Kunze, Brigitte
experimental part, p. 1843 - 1849 (2009/09/28)
The isolation of aurachins A-L (1-11) from Stigmatella aurantiaca strain Sg a15 is described. Their structures and relative configurations were deduced from spectroscopic data, in particular NMR. Three structural types were identified: A-type aurachins (1, 2, 6) are C-3 oxygen-substituted quinolines carrying a farnesyl residue on C-4, C-type aurachins (3, 4, 7-11) are C-4 oxygen-substituted quinolines carrying a farnesyl residue on C-3, and C-type aurachin E (5) has a [1,1a,8,d]imidazoloquinoline structure. Feeding of 13C-labeled precursors showed that the quinoline ring is constructed from anthranihc acid and acetate, and the farnesyl residue from acetate by both the mevalonate and nonmevalonate pathways. Further, feeding of labeled aurachin C (3) indicated the A-type aurachins are derived by a novel intramolecular 3,4-migration of the farnesyl residue that is induced by a 2,3-epoxidation and terminated by a reduction step. 18O-Labeling experiments indicated the new oxygen substituents originate from atomospheric oxygen. On the basis of these results a biosynthetic scheme covering all aurachins is proposed. It is further proposed that quinolones with an unorthodox substitution pattern, such as the 2-geranylquinolones from Pseudonocardia sp. and the 3-heptylquinolones from Pseudomonas sp., are formed by related rearrangement mechanisms.
