MedKoo Cat#: 146065 | Name: Pukateine

Description:

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

Pukateine is a naturally occurring alkaloid isolated from certain plant species, known for its potential pharmacological properties, including anti-inflammatory and antimicrobial effects. It works by interacting with specific cellular pathways, including modulating immune responses and inhibiting bacterial growth, making it a candidate for treating infections and inflammatory conditions. The compound’s mechanism involves the inhibition of key enzymes involved in inflammation, as well as disrupting the cellular functions of pathogens.

Chemical Structure

Pukateine
Pukateine
CAS#81-67-4

Theoretical Analysis

MedKoo Cat#: 146065

Name: Pukateine

CAS#: 81-67-4

Chemical Formula: C18H17NO3

Exact Mass: 295.1200

Molecular Weight: 295.34

Elemental Analysis: C, 73.20; H, 5.80; N, 4.74; O, 16.25

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
Pukateine; Pukatein;
IUPAC/Chemical Name
(R)-7-methyl-6,7,7a,8-tetrahydro-5H-[1,3]dioxolo[4',5':4,5]benzo[1,2,3-de]benzo[g]quinolin-12-ol
InChi Key
IKMXUUHNYQWZBC-GFCCVEGCSA-N
InChi Code
1S/C18H17NO3/c1-19-6-5-11-8-14-18(22-9-21-14)17-15(11)12(19)7-10-3-2-4-13(20)16(10)17/h2-4,8,12,20H,5-7,9H2,1H3/t12-/m1/s1
SMILES Code
[H][C@@]12CC3=C(C(O)=CC=C3)C4=C1C(CCN2C)=CC5=C4OCO5
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 295.34 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: Dajas-Bailador FA, Asencio M, Bonilla C, Scorza MC, Echeverry C, Reyes-Parada M, Silveira R, Protais P, Russell G, Cassels BK, Dajas F. Dopaminergic pharmacology and antioxidant properties of pukateine, a natural product lead for the design of agents increasing dopamine neurotransmission. Gen Pharmacol. 1999 Mar;32(3):373-9. doi: 10.1016/s0306-3623(98)00210-9. PMID: 10211594. 2: Valiente M, D'Ocon P, Noguera MA, Cassels BK, Lugnier C, Ivorra MD. Vascular activity of (-)-anonaine, (-)-roemerine and (-)-pukateine, three natural 6a(R)-1,2-methylenedioxyaporphines with different affinities for alpha1-adrenoceptor subtypes. Planta Med. 2004 Jul;70(7):603-9. doi: 10.1055/s-2004-827181. PMID: 15254852. 3: Kametani T, Fukumoto K, Shibuya S, Nemoto H, Nakano T. Studies on the syntheses of heterocyclic compounds. CDLXII. Total photolytic syntheses of aporphine ((plus or minus)-N-methyl-laurotetanine, (plus or minus)-cassythicine, and (plus or minus)-pukateine), proaporphine ((plus or minus)-orientalinone), and morphinandienone ((plus or minus)-pallidine and (plus or minus)-salutaridine) alkaloids. J Chem Soc Perkin 1. 1972;12:1435-41. doi: 10.1039/p19720001435. PMID: 5065332. 4: Quiroz-Carreño S, Pastene-Navarrete E, Espinoza-Pinochet C, Muñoz-Núñez E, Devotto-Moreno L, Céspedes-Acuña CL, Alarcón-Enos J. Assessment of Insecticidal Activity of Benzylisoquinoline Alkaloids from Chilean Rhamnaceae Plants against Fruit-Fly Drosophila melanogaster and the Lepidopteran Crop Pest Cydia pomonella. Molecules. 2020 Nov 3;25(21):5094. doi: 10.3390/molecules25215094. PMID: 33153001; PMCID: PMC7663414. 5: Hsu CC, Dobberstein RH, Cordell GA, Farnsworth NR. Structure elucidation of norlaureline and puterine, new noraporphine alkaloids from Guatteria elata. Lloydia. 1977 Sep-Oct;40(5):505-7. PMID: 927039.