Cyclo(prolyltyrosyl); (3S,8aS)-form, 3',5'-Dichloro
AlkaPlorer ID: AK293790
Synonym: 3-(3,5-Dichloro-4-hydroxybenzyl)hexahydropyrrolo[1,2-a]pyrazine-1,4-dione, Cyclo(13',15'-dichloroprolyltyrosyl), 3',5'-Dichloromaculosin 1
IUPAC Name: 3-[(3,5-dichloro-4-hydroxyphenyl)methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione
Structure
SMILES: O=C1C(CC2=CC(Cl)=C(O)C(Cl)=C2)N=C(O)C2CCCN12
InChI: InChI=1S/C14H14Cl2N2O3/c15-8-4-7(5-9(16)12(8)19)6-10-14(21)18-3-1-2-11(18)13(20)17-10/h4-5,10-11,19H,1-3,6H2,(H,17,20)
InChIKey: QLJFYTMVYIVQDQ-UHFFFAOYSA-N
Reference
An Inhibitor of CCL2-Induced Chemotaxis from the Fungus <i>Leptoxyphium</i> sp.
PubChem CID: 74975801
LOTUS: LTS0132978
COCONUT: CNP0304483.1
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Leptoxyphium sp. | Leptoxyphium | Capnodiaceae | Capnodiales | Dothideomycetes | Ascomycota | Fungi | Eukaryota |
Properties Information
Molecule Weight: 329.18300000000016
TPSA？: 73.13
MolLogP？: 2.571200000000001
Number of H-Donors: 2
Number of H-Acceptors: 3
RingCount: 3
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|