Structure

Physi-Chem Properties

Molecular Weight:  282.13
Volume:  302.13
LogP:  4.036
LogD:  3.551
LogS:  -5.003
# Rotatable Bonds:  1
TPSA:  46.53
# H-Bond Aceptor:  3
# H-Bond Donor:  1
# Rings:  3
# Heavy Atoms:  3

MedChem Properties

QED Drug-Likeness Score:  0.866
Synthetic Accessibility Score:  2.848
Fsp3:  0.278
Lipinski Rule-of-5:  Accepted
Pfizer Rule:  Rejected
GSK Rule:  Rejected
BMS Rule:  0
Golden Triangle Rule:  Accepted
Chelating Alert:  0
PAINS Alert:  0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:  -4.974
MDCK Permeability:  2.3003200112725608e-05
Pgp-inhibitor:  0.582
Pgp-substrate:  0.333
Human Intestinal Absorption (HIA):  0.006
20% Bioavailability (F20%):  0.164
30% Bioavailability (F30%):  0.082

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):  0.22
Plasma Protein Binding (PPB):  97.74767303466797%
Volume Distribution (VD):  0.54
Pgp-substrate:  2.0803604125976562%

ADMET: Metabolism

CYP1A2-inhibitor:  0.954
CYP1A2-substrate:  0.953
CYP2C19-inhibitor:  0.622
CYP2C19-substrate:  0.84
CYP2C9-inhibitor:  0.399
CYP2C9-substrate:  0.812
CYP2D6-inhibitor:  0.452
CYP2D6-substrate:  0.8
CYP3A4-inhibitor:  0.32
CYP3A4-substrate:  0.788

ADMET: Excretion

Clearance (CL):  2.954
Half-life (T1/2):  0.236

ADMET: Toxicity

hERG Blockers:  0.304
Human Hepatotoxicity (H-HT):  0.424
Drug-inuced Liver Injury (DILI):  0.864
AMES Toxicity:  0.657
Rat Oral Acute Toxicity:  0.688
Maximum Recommended Daily Dose:  0.923
Skin Sensitization:  0.949
Carcinogencity:  0.761
Eye Corrosion:  0.004
Eye Irritation:  0.825
Respiratory Toxicity:  0.924

Download Data

Data Type Select
General Info & Identifiers & Properties  
Structure MOL file  
Source Organisms  
Biological Activities  
Similar NPs/Drugs  

  Natural Product: NPC58324

Natural Product ID:  NPC58324
Common Name*:   LHHLMRGWOMWQSU-UHFFFAOYSA-N
IUPAC Name:   n.a.
Synonyms:  
Standard InCHIKey:  LHHLMRGWOMWQSU-UHFFFAOYSA-N
Standard InCHI:  InChI=1S/C18H18O3/c1-10-7-13-12(8-16(10)21-4)11-5-6-17(20)18(2,3)14(11)9-15(13)19/h5-9,19H,1-4H3
SMILES:  Cc1cc2c(cc1OC)c1C=CC(=O)C(C)(C)c1cc2O
Synthetic Gene Cluster:   n.a.
ChEMBL Identifier:   n.a.
PubChem CID:   71456927
Chemical Classification**:  
  • CHEMONTID:0000000 [Organic compounds]
    • [CHEMONTID:0002448] Benzenoids
      • [CHEMONTID:0000025] Phenanthrenes and derivatives
        • [CHEMONTID:0003007] Phenanthrols

*Note: the InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.
**Note: the Chemical Classification was calculated by NPClassifier Version 1.5. Reference: PMID:34662515.

  Species Source

Organism ID Organism Name Taxonomy Level Family SuperKingdom Isolation Part Collection Location Collection Time Reference
NPO19424 Trigonostemon howii Species Euphorbiaceae Eukaryota n.a. twig n.a. PMID[21520897]
NPO19424 Trigonostemon howii Species Euphorbiaceae Eukaryota Stems n.a. n.a. PMID[23148674]
NPO19424 Trigonostemon howii Species Euphorbiaceae Eukaryota n.a. n.a. n.a. PMID[23215460]
NPO19424 Trigonostemon howii Species Euphorbiaceae Eukaryota n.a. n.a. n.a. Database[UNPD]

☑ Note for Reference:
In addition to directly collecting NP source organism data from primary literature (where reference will provided as NCBI PMID or DOI links), NPASS also integrated them from below databases:
UNPD: Universal Natural Products Database [PMID: 23638153].
StreptomeDB: a database of streptomycetes natural products [PMID: 33051671].
TM-MC: a database of medicinal materials and chemical compounds in Northeast Asian traditional medicine [PMID: 26156871].
TCM@Taiwan: a Traditional Chinese Medicine database [PMID: 21253603].
TCMID: a Traditional Chinese Medicine database [PMID: 29106634].
TCMSP: The traditional Chinese medicine systems pharmacology database and analysis platform [PMID: 24735618].
HerDing: a herb recommendation system to treat diseases using genes and chemicals [PMID: 26980517].
MetaboLights: a metabolomics database [PMID: 27010336].
FooDB: a database of constituents, chemistry and biology of food species [www.foodb.ca].

  NP Quantity Composition/Concentration

Organism ID NP ID Organism Material Preparation Organism Part NP Quantity (Standard) NP Quantity (Minimum) NP Quantity (Maximum) Quantity Unit Reference

☑ Note for Reference:
In addition to directly collecting NP quantitative data from primary literature (where reference will provided as NCBI PMID or DOI links), NPASS also integrated NP quantitative records for specific NP domains (e.g., NPS from foods or herbs) from domain-specific databases. These databases include:
DUKE: Dr. Duke's Phytochemical and Ethnobotanical Databases.
PHENOL EXPLORER: is the first comprehensive database on polyphenol content in foods [PMID: 24103452], its homepage can be accessed at here.
FooDB: a database of constituents, chemistry and biology of food species [www.foodb.ca].

  Biological Activity

Target ID Target Type Target Name Target Organism Activity Type Activity Relation Value Unit Reference
NPT660 Cell Line SW480 Homo sapiens IC50 > 40000.0 nM PMID[23148674]
NPT83 Cell Line MCF7 Homo sapiens IC50 > 40000.0 nM PMID[23148674]
NPT81 Cell Line A549 Homo sapiens IC50 = 35630.0 nM PMID[23148674]
NPT659 Cell Line SMMC-7721 Homo sapiens IC50 > 40000.0 nM PMID[23148674]
NPT116 Cell Line HL-60 Homo sapiens IC50 = 24840.0 nM PMID[23148674]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 25.0 ug.mL-1 PMID[23148674]
NPT18 Organism Pseudomonas aeruginosa Pseudomonas aeruginosa MIC = 25.0 ug.mL-1 PMID[23148674]

☑ Note for Activity Records:
☉ The quantitative biological activities were primarily integrated from ChEMBL (Version-30) database and were also directly collected from PubMed literature. PubMed PMID was provided as the reference link for each activity record.

  Chemically structural similarity: I. Similar Active Natural Products in NPASS

Top-200 similar NPs were calculated against the active-NP-set (includes 4,3285 NPs with experimentally-derived bioactivity available in NPASS)

Similarity level is defined by Tanimoto coefficient (Tc) between two molecules. Tc lies between [0, 1] where '1' indicates the highest similarity. What is Tanimoto coefficient

●  The left chart: Distribution of similarity level between NPC58324 and all remaining natural products in the NPASS database.
●  The right table: Most similar natural products (Tc>=0.56 or Top200).

Similarity Score Similarity Level Natural Product ID

  Chemically structural similarity: II. Similar Clinical/Approved Drugs

Similarity level is defined by Tanimoto coefficient (Tc) between two molecules.

●  The left chart: Distribution of similarity level between NPC58324 and all drugs/candidates.
●  The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

Similarity Score Similarity Level Drug ID Developmental Stage

  Bioactivity similarity: Similar Natural Products in NPASS

Bioactivity similarity was calculated based on bioactivity descriptors of compounds. The bioactivity descriptors were calculated by a recently developed AI algorithm Chemical Checker (CC) [Nature Biotechnology, 38:1087–1096, 2020; Nature Communications, 12:3932, 2021], which evaluated bioactivity similarities at five levels:
A: chemistry similarity;
B: biological targets similarity;
C: networks similarity;
D: cell-based bioactivity similarity;
E: similarity based on clinical data.

Those 5 categories of CC bioactivity descriptors were calculated and then subjected to manifold projection using UMAP algorithm, to project all NPs on a 2-Dimensional space. The current NP was highlighted with a small circle in the 2-D map. Below figures: left-to-right, A-to-E.

A: chemistry similarity
B: biological targets similarity
C: networks similarity
D: cell-based bioactivity similarity
E: similarity based on clinical data