(Q105035322)

English

(1R,20R,28S)-28-hydroxy-3,11,19,21-tetrazaheptacyclo[17.10.0.02,11.04,9.012,17.020,28.022,27]nonacosa-2,4,6,8,12,14,16,22,24,26-decaene-10,18-dione

chemical compound

In more languages

Statements

type of chemical entity

0 references

28-Hydroxy-3,11,19,21-tetrazaheptacyclo[17.10.0.02,11.04,9.012,17.020,28.022,27]nonacosa-2,4,6,8,12,14,16,22,24,26-decaene-10,18-dione

1 reference

based on heuristic

inferred from SMILES

422.137890436 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₅H₁₈N₄O₃

0 references

canonical SMILES

O=C1C=2C=CC=CC2N=C3N1C=4C=CC=CC4C(=O)N5C3CC6(O)C=7C=CC=CC7NC56

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isomeric SMILES

O=C1c2ccccc2-n2c(nc3ccccc3c2=O)[C@H]2C[C@]3(O)c4ccccc4N[C@@H]3N12

0 references

Aspergillus alliaceus

2 references

Novel cholecystokinin antagonists from Aspergillus alliaceus. I. Fermentation, isolation, and biological properties

Novel cholecystokinin antagonists from Aspergillus alliaceus. II. Structure determination of asperlicins B, C, D, and E

Identifiers

InChI=1S/C25H18N4O3/c30-22-14-7-1-4-10-17(14)26-21-20-13-25(32)16-9-3-5-11-18(16)27-24(25)29(20)23(31)15-8-2-6-12-19(15)28(21)22/h1-12,20,24,27,32H,13H2/t20-,24-,25+/m1/s1

0 references

HYHLSEUXMRFVND-ZPZUNKDASA-N

0 references

1 reference

17 September 2022

based on heuristic

inferred from InChIKey

UniChem compound ID

1 reference

Natural Product Atlas ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

HYHLSEUXMRFVND-ZPZUNKDASA-N

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