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Dihydropergillin

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

Category Bioactive by-products
Catalog number BBF-01410
CAS
Molecular Weight 262.30
Molecular Formula C15H18O4

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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

Dihydropergillin is produced by the strain of Aspergillus ustus. It can inhibit the growth of plants.

  • Specification
  • Properties
  • Reference Reading
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IUPAC Name (7R)-7-hydroxy-7-methyl-2-propan-2-yl-6,9-dihydrofuro[3,2-h]isochromen-3-one
Canonical SMILES CC(C)C1C(=O)C2=C(O1)C3=C(CC(OC3)(C)O)C=C2
InChI InChI=1S/C15H18O4/c1-8(2)13-12(16)10-5-4-9-6-15(3,17)18-7-11(9)14(10)19-13/h4-5,8,13,17H,6-7H2,1-3H3/t13?,15-/m1/s1
InChI Key CYPMCDMSUWADNK-AWKYBWMHSA-N
Appearance Crystalline
Melting Point 122-126°C
1. Synthesis and structural characterization of natural benzofuranoids
Kouji Kuramochi, Kazunori Tsubaki J Nat Prod. 2015 May 22;78(5):1056-66. doi: 10.1021/np5010483. Epub 2015 Apr 23.
The synthesis of ustusoranes A, B, and E, pergillin, dihydropergillin, (±)-penicisochroman A, and (-)-brassicadiol, starting from optically active (R)-benzolactone, is described. The synthesis of ustusoranes A and E established the absolute configurations of these natural products. The synthesis of pergillin and (±)-penicisochroman A led to the structural revision of aspergiones E and F. This study clearly indicates that (R)-benzolactone is a potential intermediate in the synthesis of natural benzofuranoids.

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Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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