NPs Basic Information

Name
chaetoglobosin R
Molecular Formula C32H38N2O6
IUPAC Name*
(1R,3E,6R,7E,9S,11E,13R,14S,15S,16S,17R,18S)-6,14,15-trihydroxy-18-(1H-indol-3-ylmethyl)-7,9,15,16-tetramethyl-19-azatricyclo[11.7.0.01,17]icosa-3,7,11-triene-2,5,20-trione
SMILES
C[C@H]\1C/C=C/[C@H]2[C@@H]([C@@]([C@H]([C@@H]3[C@@]2(C(=O)/C=C/C(=O)[C@@H](/C(=C1)/C)O)C(=O)N[C@H]3CC4=CNC5=CC=CC=C54)C)(C)O)O
InChI
InChI=1S/C32H38N2O6/c1-17-8-7-10-22-29(38)31(4,40)19(3)27-24(15-20-16-33-23-11-6-5-9-21(20)23)34-30(39)32(22,27)26(36)13-12-25(35)28(37)18(2)14-17/h5-7,9-14,16-17,19,22,24,27-29,33,37-38,40H,8,15H2,1-4H3,(H,34,39)/b10-7+,13-12+,18-14+/t17-,19-,22-,24-,27-,28+,29-,31-,32+/m0/s1
InChIKey
GXXPQGPTEVHUTJ-NOQRJRBPSA-N
Synonyms
chaetoglobosin R; CHEBI:68737; Q27137156; (1R,3E,6R,7E,9S,11E,13R,14S,15S,16S,17R,18S)-6,14,15-trihydroxy-18-(1H-indol-3-ylmethyl)-7,9,15,16-tetramethyl-19-azatricyclo[11.7.0.01,17]icosa-3,7,11-triene-2,5,20-trione; (3S,3aR,4S,5S,6S,6aR,7E,10S,11E,13R,15E,17aR)-5,6,13-trihydroxy-3-(1H-indol-3-ylmethyl)-4,5,10,12-tetramethyl-2,3,3a,4,5,6,6a,9,10,13-decahydro-1H-cyclotrideca[d]isoindole-1,14,17-trione
CAS NA
PubChem CID 11192029
ChEMBL ID NA
*Note: the IUPAC Name was collected from PubChem.
Chemical Classification:
  • Kingdom: Organic compounds
    • Superclass: Organoheterocyclic compou
      • Class: Isoindoles and derivative
        • Subclass: Isoindolines
          • Direct Parent: Isoindolones

ClassyFire Version 1.0
PMID:27867422

NPs Species Source

Endophyte ID Endophyte Name Family Genus Taxonomy ID GenBank ID Closest GenBank ID Reference
Endophyte ID Endophyte Name Family Genus Taxonomy ID GenBank ID Closest GenBank ID Reference

NPs Content

*Note: The vaules in Content Percentage are calculated by dividing the content value by the maximum content value in NP Content.
**Note: The units with different NP content, due to their incomparable values, are separated into different tables.

NPs Biological Activity

Bioactivity Name Target ID Target Name Target Type Target Organism Target Organism ID Potency of Bioactivity Activity Type Value Unit Endophyte ID Endophyte Name
Bioactivity Name Target ID Target Name Target Type Target Organism Target Organism ID Potency of Bioactivity Activity Type Value Unit Endophyte ID Endophyte Name

NPs Physi-Chem Properties

Molecular Weight: 546.7 ALogp: 2.7
HBD: 5 HBA: 6
Rotatable Bonds: 2 Lipinski's rule of five: Rejected
Polar Surface Area: 140.0 Aromatic Rings: 5
Heavy Atoms: 40 QED Weighted: 0.288

NPs ADMET Properties*

ADMET: Absorption

Caco-2 Permeability: -5.007 MDCK Permeability: 0.00001260
Pgp-inhibitor: 0.97 Pgp-substrate: 0.937
Human Intestinal Absorption (HIA): 0.171 20% Bioavailability (F20%): 0.097
30% Bioavailability (F30%): 0.008

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB): 0.287 Plasma Protein Binding (PPB): 94.87%
Volume Distribution (VD): 0.271 Fu: 3.12%

ADMET: Metabolism

CYP1A2-inhibitor: 0.03 CYP1A2-substrate: 0.218
CYP2C19-inhibitor: 0.164 CYP2C19-substrate: 0.422
CYP2C9-inhibitor: 0.205 CYP2C9-substrate: 0.43
CYP2D6-inhibitor: 0.024 CYP2D6-substrate: 0.114
CYP3A4-inhibitor: 0.892 CYP3A4-substrate: 0.259

ADMET: Excretion

Clearance (CL): 4.978 Half-life (T1/2): 0.634

ADMET: Toxicity

hERG Blockers: 0.047 Human Hepatotoxicity (H-HT): 0.456
Drug-inuced Liver Injury (DILI): 0.223 AMES Toxicity: 0.041
Rat Oral Acute Toxicity: 0.712 Maximum Recommended Daily Dose: 0.932
Skin Sensitization: 0.156 Carcinogencity: 0.107
Eye Corrosion: 0.003 Eye Irritation: 0.007
Respiratory Toxicity: 0.936
*Note: the ADMET properties was calculated by ADMETlab 2.0. Reference: PMID: 33893803.

Similar Compounds*

Compounds similar to EMNPD with top10 similarity:

Similar NPs Similar Drugs
NPs ID NPs 2D Structure Similarity Score TTD ID Drug 2D Structure Similarity Score
ENC004473 0.840 D01TSI 0.266
ENC002440 0.802 D0V3ZA 0.259
ENC003226 0.744 D0SP3D 0.259
ENC006149 0.698 D09NNH 0.253
ENC002953 0.677 D0W7WC 0.245
ENC003586 0.672 D02DMQ 0.245
ENC002679 0.649 D0BV3J 0.244
ENC002681 0.639 D05EJG 0.236
ENC002955 0.639 D02XIY 0.231
ENC004470 0.622 D0R5OS 0.223
*Note: the compound similarity was calculated by RDKIT.