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Penicolinate A Sale

(Synonyms: Penicolinate B dimethyl ester) 目录号 : GC41584

A fungal metabolite with diverse biological activities

Penicolinate A Chemical Structure

Cas No.:1418291-68-5

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1mg
¥3,751.00
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5mg
¥15,007.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Penicolinate A is a fungal metabolite produced by Penicillium sp. BCC16054 with diverse biological activities. It exhibits antimalarial and antituberculosis activity (MICs = 3.25 and 12.5 mg/ml for P. falciparum and M. tuberculosis H37Ra, respectively). Penicolinate A is cytotoxic to MCF-7, KB, NCI-H187, and Vero cells (IC50s = 7.49, 18.43, 4.4, and 14.08 μM, respectively).

Chemical Properties

Cas No. 1418291-68-5 SDF
别名 Penicolinate B dimethyl ester
Canonical SMILES O=C(OC)C1=NC=C(CCCCCCCCCC2=CN=C(C(OC)=O)C=C2)C=C1
分子式 C24H32N2O4 分子量 412.5
溶解度 DMF: soluble,DMSO: soluble,Ethanol: soluble,Methanol: soluble 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 2.4242 mL 12.1212 mL 24.2424 mL
5 mM 0.4848 mL 2.4242 mL 4.8485 mL
10 mM 0.2424 mL 1.2121 mL 2.4242 mL
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Research Update

Induction of new metabolites from the endophytic fungus Bionectria sp. through bacterial co-culture

Fitoterapia 2018 Jan;124:132-136.PMID:29106994DOI:10.1016/j.fitote.2017.10.021

A new alkaloid, 1,2-dihydrophenopyrrozin (1), along with five known compounds (2-6) was isolated from an axenic culture of the endophytic fungus, Bionectria sp., obtained from seeds of the tropical plant Raphia taedigera. Co-cultivation of this fungus either with Bacillus subtilis or with Streptomyces lividans resulted in the production of two new o-aminobenzoic acid derivatives, bionectriamines A and B (7 and 8) as well as of two additional known compounds (9 and 10). None of the latter compounds (7-10) were detected in axenic cultures of the fungus or of the bacteria indicating activation of silent biogenetic gene clusters through co-cultivation with bacteria. The structures of the new compounds were unambiguously determined based on detailed NMR and MS spectroscopic analysis and by comparison with the literature. The crystal structure of agathic acid (6) is reported here for the first time. Penicolinate A (4) exhibited potent cytotoxic activity against the human ovarian cancer cell line A2780 with an IC50 value of 4.1μM.