paraherquamide (Q27287870)

Paraherquamide (English)

(1'S,6'R,7'R,8R,9'R)-6'-Hydroxy-4,4,6',10',10',13'-hexamethylspiro[10H-[1,4]dioxepino[2,3-g]indole-8,11'-3,13-diazatetracyclo[5.5.2.01,9.03,7]tetradecane]-9,14'-dione

14 October 2016

stereoisomer of

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₈H₃₅N₃O₅

1 reference

Paraherquamide (English)

14 October 2016

canonical SMILES

CC1(C=COC2=C(O1)C=CC3=C2NC(=O)C34CC56CN7CCC(C7(CC5C4(C)C)C(=O)N6C)(C)O)C

1 reference

Paraherquamide (English)

14 October 2016

isomeric SMILES

C[C@]1(CCN2[C@]13C[C@@H]4[C@](C2)(C[C@@]5(C4(C)C)C6=C(C7=C(C=C6)OC(C=CO7)(C)C)NC5=O)N(C3=O)C)O

1 reference

Paraherquamide (English)

14 October 2016

found in taxon

Penicillium paraherquei

2 references

Paraherquonin, a new meroterpenoid from penicillium paraherquei

The structure of paraherquamide, a toxic metabolite from

Penicillium simplicissimum

2 references

Paraherquonin, a new meroterpenoid from penicillium paraherquei

The structure of paraherquamide, a toxic metabolite from

Penicillium charlesii

1 reference

Novel antinematodal and antiparasitic agents from Penicillium charlesii. I. Fermentation, isolation and biological activity

Penicillium dierckxii

4 references

Novel antinematodal and antiparasitic agents from Penicillium charlesii. I. Fermentation, isolation and biological activity

Studies on the Biosynthesis of Paraherquamide A. Origin of the β-Methylproline Ring

Detection of VM55599 and preparaherquamide from Aspergillus japonicus and Penicillium fellutanum: biosynthetic implications

Detection of VM55599 and preparaherquamide from Aspergillus japonicus and Penicillium fellutanum: biosynthetic implications

Aspergillus japonicus

2 references

Detection of VM55599 and preparaherquamide from Aspergillus japonicus and Penicillium fellutanum: biosynthetic implications

Detection of VM55599 and preparaherquamide from Aspergillus japonicus and Penicillium fellutanum: biosynthetic implications

Penicillium

2 references

Further novel metabolites of the paraherquamide family

New paraherquamide antibiotics with anthelmintic activity

Penicillium cluniae

1 reference

Insecticidal activity of Paraherquamides, including paraherquamide H and paraherquamide I, two new alkaloids isolated from Penicillium cluniae.

Penicillium brasilianum

2 references

Paraherquonin, a new meroterpenoid from penicillium paraherquei

The structure of paraherquamide, a toxic metabolite from

Identifiers

InChI

InChI=1S/C28H35N3O5/c1-23(2)10-12-35-20-17(36-23)8-7-16-19(20)29-21(32)27(16)14-26-15-31-11-9-25(5,34)28(31,22(33)30(26)6)13-18(26)24(27,3)4/h7-8,10,12,18,34H,9,11,13-15H2,1-6H3,(H,29,32)/t18-,25+,26+,27+,28-/m0/s1

1 reference

Paraherquamide (English)

14 October 2016

1 reference

Global Substance Registration System

Paraherquamide (English)

14 October 2016

1 reference

UNII

R72VB4E4KC

paraherquamide (English)

14 October 2016

1 reference

(-)-Paraherquamide A (English)

14 October 2016

2 references

Paraherquamide (English)

14 October 2016

ChEBI ID

200643

mapping relation type

exact match

1 reference

International Chemical Identifier

InChI

InChI=1S/C28H35N3O5/c1-23(2)10-12-35-20-17(36-23)8-7-16-19(20)29-21(32)27(16)14-26-15-31-11-9-25(5,34)28(31,22(33)30(26)6)13-18(26)24(27,3)4/h7-8,10,12,18,34H,9,11,13-15H2,1-6H3,(H,29,32)/t18-,25+,26+,27+,28-/m0/s1

1 reference

1 reference

DSSTOX compound identifier

0 references

2 references

Global Substance Registration System

UNII

R72VB4E4KC

paraherquamide (English)

14 October 2016

Natural Product Atlas ID

NPA003590

2 references

based on heuristic

inferred from InChIKey