Get A Quote

Strobilurin G

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

Strobilurin G
Category Antibiotics
Catalog number BBF-03490
CAS 129145-64-8
Molecular Weight 442.54
Molecular Formula C26H34O6

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

Strobilurin G is an antibiotic produced by Bolina lutea Sacc. It has strong anti-fungal activity, and its in vitro anti-tumor proliferation IC50 is 0.01 µmol/L.

  • Specification
  • Properties
  • Reference Reading
  • Price Product List
Related CAS 132056-04-3
Synonyms 6-(3,4-DIHYDRO-4,4-DIMETHYL-3-((3-METHYL-2-BUTENYL)OXY)-2H-1,5-BENZODIOXEPIN-7-YL)-2-(METHOXYMETHYLENE)-3-METHYL-, 3,5-HEXADIENOIC ACID METHYL ESTER; STROBILURIN G; 6-(3,4-dihydro-4,4-dimethyl-3-((3-methyl-2-butenyl)oxy)-2H-1,5-benzodioxepin-7-yl)-2-(metho
IUPAC Name methyl (2E,3Z,5E)-6-[4,4-dimethyl-3-(3-methylbut-2-enoxy)-2,3-dihydro-1,5-benzodioxepin-7-yl]-2-(methoxymethylidene)-3-methylhexa-3,5-dienoate
Canonical SMILES CC(=CCOC1COC2=C(C=C(C=C2)C=CC=C(C)C(=COC)C(=O)OC)OC1(C)C)C
InChI InChI=1S/C26H34O6/c1-18(2)13-14-30-24-17-31-22-12-11-20(15-23(22)32-26(24,4)5)10-8-9-19(3)21(16-28-6)25(27)29-7/h8-13,15-16,24H,14,17H2,1-7H3/b10-8+,19-9-,21-16+
InChI Key CGBAOGDKJZIWTF-QILZHMQOSA-N
Appearance Yellow Oil
Antibiotic Activity Spectrum fungi; neoplastics (Tumor)
Boiling Point 573.6°C at 760 mmHg
Density 1.11 g/cm3
1. Monochlorinated calocerins A-D and 9-oxostrobilurin derivatives from the basidiomycete Favolaschia calocera
Clara Chepkirui, Christian Richter, Josphat Clement Matasyoh, Marc Stadler Phytochemistry. 2016 Dec;132:95-101. doi: 10.1016/j.phytochem.2016.10.001. Epub 2016 Oct 13.
Eight previously undescribed compounds were isolated and characterised from the supernatant and mycelium of a culture of the basidiomycete Favolaschia calocera originating from Kakamega equatorial rainforest in Kenya. These were: 9- oxostrobilurins A, G, K and I and the four monochlorinated calocerins A, B, C and D. The calocerins extend our knowledge of halogenated compounds obtained from natural sources. Four further known compounds were also identified: strobilurin G, favolon, pterulinic acid and 2,3 -dihydro-1-benzoxepin derivative. The four oxostrobilurins exhibited prominent antifungal and cytotoxic activities while the four calocerins only showed cytotoxic activity.
2. Investigations into the biosynthesis of the antifungal strobilurins
Zafar Iqbal, Li-Chen Han, Anna M Soares-Sello, Risa Nofiani, Gerald Thormann, Axel Zeeck, Russell J Cox, Christine L Willis, Thomas J Simpson Org Biomol Chem. 2018 Aug 1;16(30):5524-5532. doi: 10.1039/c8ob00608c.
The strobilurins are important antifungal metabolites isolated from a number of basidiomycetes and have been valuable leads for the development of commercially important fungicides. Isotopic labelling studies with early and advanced intermediates confirm for the first time that they are produced via a linear tetraketide, primed with the rare benzoate starter unit, itself derived from phenylalanine via cinnamate. Isolation of a novel biphenyl metabolite, pseudostrobilurin B, provides evidence for the involvement of an epoxide in the key rearrangement to form the β-methoxyacrylate moiety essential for biological activity. Formation of two bolineol related metabolites, strobilurins Y and Z, also probably involves epoxide intermediates. Time course studies indicate a likely biosynthetic pathway from strobilurin A, with the simplest non-subsubstituted benzoate ring, to strobilurin G with a complex dioxepin terpenoid-derived substituent. Precursor-directed biosynthetic studies allow production of a number of novel ring-halogenated analogues as well as a new pyridyl strobilurin. These studies also provide evidence for a non-linear biosynthetic relationship between strobilurin A and strobilurin B.
3. Biologically active metabolites from fungi 14 3-chloro-4-hydroxy-5-(3,7,11-trimethyldodeca-2,6,10-trienyl)-benzamide, a new antibacterial agent from a soil fungus
K Krohn, M John, H J Aust, S Draeger, B Schulz Nat Prod Lett. 2001;15(1):9-12. doi: 10.1080/10575630108041251.
The antibacterial 3-chloro-4-hydroxy-5-(3,7,11-trimethyldodeca-2,6,10-trienyl)-benzamide, and the antifungal strobilurins B and D were isolated from an unidentified South African soil fungus.
BBF-03868 Honokiol Inquiry
BBF-00969 Hygromycin A Inquiry
BBF-03937 Pirarubicin Inquiry
BBF-03753 Baicalin Inquiry
BBF-04061 Allocholic acid Inquiry
BBF-03988 Gamithromycin Inquiry

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