Get A Quote

Neohydroxyaspergillic acid

* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

Neohydroxyaspergillic acid
Category Antibiotics
Catalog number BBF-04494
CAS 72598-34-6
Molecular Weight 240.30
Molecular Formula C12H20N2O3
Purity ≥95%

Online Inquiry

Capabilities & Facilities

Fermentation Lab

4 R&D and scale-up labs

2 Preparative purification labs

Fermentation Plant

Semi pilot, pilot and industrial plant 4 Manufacturing sites 7 Production lines at pilot scale 100+ Reactors of 30-4000 L; 170+ reactors of 20 KL-30 KL; 24+ reactors of >100 KL 2 Hydrogenation reactors (200 L, 4Mpa and 1000L, 4Mpa)

Product Description

Neohydroxyaspergillic acid is an antibiotic produced by Aspergillus sckrotiorum, which is active against some bacteriophages and fungus.

  • Specification
  • Properties
  • Reference Reading
  • Price Product List
Synonyms NSC 613947; 2(1H)-Pyrazinone, 1-hydroxy-6-[(1S)-1-hydroxy-2-methylpropyl]-3-(2-methylpropyl)-
Storage Store at -20°C
IUPAC Name 1-hydroxy-6-[(1S)-1-hydroxy-2-methylpropyl]-3-(2-methylpropyl)pyrazin-2-one
Canonical SMILES CC(C)CC1=NC=C(N(C1=O)O)C(C(C)C)O
InChI InChI=1S/C12H20N2O3/c1-7(2)5-9-12(16)14(17)10(6-13-9)11(15)8(3)4/h6-8,11,15,17H,5H2,1-4H3/t11-/m0/s1
InChI Key QTTAJMQGQJRLDK-NSHDSACASA-N
Appearance Light Yellow Needles
Antibiotic Activity Spectrum Fungi; Bacterial
Boiling Point 391.0±34.0°C (Predicted)
Melting Point 164-166°C
Density 1.19±0.1 g/cm3 (Predicted)
Solubility Soluble in Methanol, Ethanol
1. Bioactive Metabolites from the Endophytic Fungus Aspergillus sp. SPH2
Elena Trujillo, Viridiana Morales-Sánchez, Carmen E Díaz, Rubén Muñoz, Sonia A Olmeda, María Fe Andrés, Azucena González-Coloma, Felix Valcarcel J Fungi (Basel) . 2021 Feb 2;7(2):109. doi: 10.3390/jof7020109.
In the current study, an ethyl acetate extract from the endophytic fungusAspergillussp. SPH2 isolated from the stem parts of the endemic plantBethencourtia palmensiswas screened for its biocontrol properties against plant pathogens (Fusarium moniliforme,Alternaria alternata,andBotrytis cinerea), insect pests (Spodoptera littoralis,Myzus persicae,Rhopalosiphum padi), plant parasites (Meloidogyne javanica), and ticks (Hyalomma lusitanicum). SPH2 gave extracts with strong fungicidal and ixodicidal effects at different fermentation times. The bioguided isolation of these extracts gave compounds1-3. Mellein (1) showed strong ixodicidal effects and was also fungicidal. This is the first report on the ixodicidal effects of1. Neoaspergillic acid (2) showed potent antifungal effects. Compound2appeared during the exponential phase of the fungal growth while neohydroxyaspergillic acid (3) appeared during the stationary phase, suggesting that2is the biosynthetic precursor of3. The mycotoxin ochratoxin A was not detected under the fermentation conditions used in this work. Therefore, SPH2 could be a potential biotechnological tool for the production of ixodicidal extracts rich in mellein.

Bio Calculators

Stock concentration: *
Desired final volume: *
Desired concentration: *

L

* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
g/mol
g

Recently viewed products

Online Inquiry

Copyright © 2025 BOC Sciences. All rights reserved.

cartIcon
Inquiry Basket