Molecule

Chrysosporazine H

AlkaPlorer ID: AK124638

Synonym: None

IUPAC Name: (3S,7Z,8S,8aS)-2-acetyl-7-benzylidene-8-(7-methoxy-1,3-benzodioxol-5-yl)-3-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3,4,8,8a-tetrahydro-1H-pyrrolo[1,2-a]pyrazin-6-one

Structure

SMILES: COC1=CC(C[C@H]2CN3C(=O)/C(=C\C4=CC=CC=C4)[C@H](C4=CC(OC)=C5OCOC5=C4)[C@H]3CN2C(C)=O)=CC2=C1OCO2

InChI: InChI=1S/C33H32N2O8/c1-19(36)34-16-25-30(22-13-27(39-3)32-29(14-22)41-18-43-32)24(10-20-7-5-4-6-8-20)33(37)35(25)15-23(34)9-21-11-26(38-2)31-28(12-21)40-17-42-31/h4-8,10-14,23,25,30H,9,15-18H2,1-3H3/b24-10-/t23-,25+,30-/m0/s1

InChIKey: LHSUMYDJXGUUCA-CLUGHXIFSA-N

Reference

Chrysosporazines F–M: P-Glycoprotein Inhibitory Phenylpropanoid Piperazines from an Australian Marine Fish Derived Fungus, <i>Chrysosporium</i> sp. CMB-F294

PubChem CID: 146684650

LOTUS: LTS0129773

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NPAtlas: NPA028571

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Chrysosporium sp.	Chrysosporium	Onygenaceae	Onygenales	Eurotiomycetes	Ascomycota	Fungi	Eukaryota

Properties Information

Molecule Weight: 584.6250000000003

TPSA？: 96.0

MolLogP？: 4.012600000000003

Number of H-Donors: 0

Number of H-Acceptors: 8

RingCount: 7

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi