MedKoo Cat#: 414468 | Name: Noracronycine
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Description:

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

Noracronycine is an alkaloid originally isolated from G. pentaphylla that has antimalarial activity.

Chemical Structure

Noracronycine
Noracronycine
CAS# 13161-79-0

Theoretical Analysis

MedKoo Cat#: 414468

Name: Noracronycine

CAS#: 13161-79-0

Chemical Formula: C19H17NO3

Exact Mass: 307.1208

Molecular Weight: 307.35

Elemental Analysis: C, 74.25; H, 5.58; N, 4.56; O, 15.62

Price and Availability

Size Price Availability Quantity
1mg USD 349.00 2 Weeks
5mg USD 966.00 2 Weeks
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Related CAS #
No Data
Synonym
Noracronycine; NSC103005; NSC-103005; NSC 103005
IUPAC/Chemical Name
7H-Pyrano(2,3-c)acridin-7-one, 3,12-dihydro-6-hydroxy-3,3,12-trimethyl-
InChi Key
CBXBWBNEFPNSDO-UHFFFAOYSA-N
InChi Code
InChI=1S/C19H17NO3/c1-19(2)9-8-12-15(23-19)10-14(21)16-17(12)20(3)13-7-5-4-6-11(13)18(16)22/h4-10,21H,1-3H3
SMILES Code
O=C1C2=C(C=CC=C2)N(C)C3=C(C=CC(C)(C)O4)C4=CC(O)=C13
Appearance
Solid powder
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 307.35 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: Funayama S, Cordell GA. Chemistry of acronycine. VIII. Selective synthesis of dimers and trimers of noracronycine and related compounds. J Nat Prod. 1985 Jul- Aug;48(4):536-46. doi: 10.1021/np50040a004. PMID: 4045471. 2: Funayama S, Cordell GA. Chemistry of acronycine. IX. Formation of dimers of noracronycine--mechanistic studies. J Nat Prod. 1985 Jul-Aug;48(4):547-54. doi: 10.1021/np50040a005. PMID: 4045472. 3: Funayama S, Cordell GA. Chemistry of acronycine, XII. Further oligomers of noracronycine. J Nat Prod. 1986 Mar-Apr;49(2):210-7. doi: 10.1021/np50044a003. PMID: 3734808. 4: Funayama S, Cordell GA. Chemistry of Acronycine: III. Planta Med. 1983 Aug;48(8):263-7. doi: 10.1055/s-2007-969930. PMID: 17404993. 5: Funayama S, Cordell GA. Chemistry of acronycine IV. Minor constituents of acronine and the phytochemistry of the genus Acronychia. J Nat Prod. 1984 Mar- Apr;47(2):285-91. doi: 10.1021/np50032a009. PMID: 6736969. 6: Funayama S, Cordell GA. Chemistry of Acronycine VI. Proton NMR Spectral Assignments of Acronycine and Derivatives and the Formation of Isonoracronycine. Planta Med. 1984 Apr;50(2):121-3. doi: 10.1055/s-2007-969647. PMID: 17340277.