MedKoo Cat#: 145507 | Name: Graveolinine

Description:

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

Graveolinine is a quinoline alkaloid.

Chemical Structure

Graveolinine
Graveolinine
CAS#4179-37-7

Theoretical Analysis

MedKoo Cat#: 145507

Name: Graveolinine

CAS#: 4179-37-7

Chemical Formula: C17H13NO3

Exact Mass: 279.0900

Molecular Weight: 279.30

Elemental Analysis: C, 73.11; H, 4.69; N, 5.02; O, 17.19

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
Graveolinine;
IUPAC/Chemical Name
2-(benzo[d][1,3]dioxol-5-yl)-4-methoxyquinoline
InChi Key
QGCORDIPOBZNKC-UHFFFAOYSA-N
InChi Code
1S/C17H13NO3/c1-19-16-9-14(18-13-5-3-2-4-12(13)16)11-6-7-15-17(8-11)21-10-20-15/h2-9H,10H2,1H3
SMILES Code
COC1=CC(=NC2=CC=CC=C12)C3=CC=C4OCOC4=C3
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 279.30 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: Luo W, Lv JW, Wang T, Zhang ZY, Guo HY, Song ZY, Wang CJ, Ma J, Chen YP. Synthesis, in vitro and in vivo biological evaluation of novel graveolinine derivatives as potential anti-Alzheimer agents. Bioorg Med Chem. 2020 Jan 1;28(1):115190. doi: 10.1016/j.bmc.2019.115190. Epub 2019 Nov 9. PMID: 31744779. 2: An ZY, Yan YY, Peng D, Ou TM, Tan JH, Huang SL, An LK, Gu LQ, Huang ZS. Synthesis and evaluation of graveoline and graveolinine derivatives with potent anti-angiogenesis activities. Eur J Med Chem. 2010 Sep;45(9):3895-903. doi: 10.1016/j.ejmech.2010.05.043. Epub 2010 May 26. PMID: 20554355. 3: Singh S, Nerella S, Pabbaraja S, Mehta G. Access to 2-Alkyl/Aryl-4-(1H)-Quinolones via Orthogonal "NH3" Insertion into o-Haloaryl Ynones: Total Synthesis of Bioactive Pseudanes, Graveoline, Graveolinine, and Waltherione F. Org Lett. 2020 Feb 21;22(4):1575-1579. doi: 10.1021/acs.orglett.0c00172. Epub 2020 Feb 4. PMID: 32013447. 4: Wubuli A, Abdulla R, Zang D, Jiang L, Chen L, Aisa HA. Spectrum-effect relationship between UPLC fingerprints and melanogenic effect of Ruta graveolens L. J Chromatogr B Analyt Technol Biomed Life Sci. 2023 Apr 15;1221:123683. doi: 10.1016/j.jchromb.2023.123683. Epub 2023 Mar 20. PMID: 36965451. 5: El Sayed K, Al-Said MS, El-Feraly FS, Ross SA. New quinoline alkaloids from Ruta chalepensis. J Nat Prod. 2000 Jul;63(7):995-7. doi: 10.1021/np000012y. PMID: 10924184. 6: Shahrajabian MH. A Candidate for Health Promotion, Disease Prevention and Treatment, Common Rue (Ruta graveolens L.), an Important Medicinal plant in Traditional Medicine. Curr Rev Clin Exp Pharmacol. 2022 May 10. doi: 10.2174/2772432817666220510143902. Epub ahead of print. PMID: 35538827. 7: Gnyawali KP, Shakenov A, Kirinde Arachchige PT, Yi CS. Benzoquinone Ligand- Enabled Ruthenium-Catalyzed Deaminative Coupling of 2-Aminoaryl Aldehydes and Ketones with Branched Amines for Regioselective Synthesis of Quinoline Derivatives. J Org Chem. 2024 Aug 16;89(16):11119-11135. doi: 10.1021/acs.joc.4c00063. Epub 2024 Jul 26. PMID: 39058560.