Structure

Physi-Chem Properties

Molecular Weight:  252.1
Volume:  249.697
LogP:  1.811
LogD:  1.717
LogS:  -2.693
# Rotatable Bonds:  2
TPSA:  86.99
# H-Bond Aceptor:  5
# H-Bond Donor:  3
# Rings:  2
# Heavy Atoms:  5

MedChem Properties

QED Drug-Likeness Score:  0.549
Synthetic Accessibility Score:  3.718
Fsp3:  0.462
Lipinski Rule-of-5:  Accepted
Pfizer Rule:  Accepted
GSK Rule:  Accepted
BMS Rule:  0
Golden Triangle Rule:  Accepted
Chelating Alert:  1
PAINS Alert:  1

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:  -4.752
MDCK Permeability:  8.771468856139109e-06
Pgp-inhibitor:  0.002
Pgp-substrate:  0.011
Human Intestinal Absorption (HIA):  0.075
20% Bioavailability (F20%):  0.138
30% Bioavailability (F30%):  0.638

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):  0.049
Plasma Protein Binding (PPB):  95.48595428466797%
Volume Distribution (VD):  0.416
Pgp-substrate:  3.892230272293091%

ADMET: Metabolism

CYP1A2-inhibitor:  0.341
CYP1A2-substrate:  0.551
CYP2C19-inhibitor:  0.024
CYP2C19-substrate:  0.125
CYP2C9-inhibitor:  0.085
CYP2C9-substrate:  0.253
CYP2D6-inhibitor:  0.162
CYP2D6-substrate:  0.224
CYP3A4-inhibitor:  0.149
CYP3A4-substrate:  0.287

ADMET: Excretion

Clearance (CL):  14.177
Half-life (T1/2):  0.817

ADMET: Toxicity

hERG Blockers:  0.019
Human Hepatotoxicity (H-HT):  0.124
Drug-inuced Liver Injury (DILI):  0.678
AMES Toxicity:  0.656
Rat Oral Acute Toxicity:  0.203
Maximum Recommended Daily Dose:  0.064
Skin Sensitization:  0.942
Carcinogencity:  0.103
Eye Corrosion:  0.004
Eye Irritation:  0.619
Respiratory Toxicity:  0.655

Download Data

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

  Natural Product: NPC110205

Natural Product ID:  NPC110205
Common Name*:   CALZOMFTGJDTHS-CABZTGNLSA-N
IUPAC Name:   n.a.
Synonyms:  
Standard InCHIKey:  CALZOMFTGJDTHS-CABZTGNLSA-N
Standard InCHI:  InChI=1S/C13H16O5/c1-3-6-10(18-2)4-7-11(13(6)17)8(14)5-9(15)12(7)16/h4,9,12,15-17H,3,5H2,1-2H3/t9-,12-/m0/s1
SMILES:  CCc1c(cc2c(C(=O)C[C@@H]([C@H]2O)O)c1O)OC
Synthetic Gene Cluster:   n.a.
ChEMBL Identifier:   n.a.
PubChem CID:   53360466
Chemical Classification**:  
  • CHEMONTID:0000000 [Organic compounds]
    • [CHEMONTID:0002448] Benzenoids
      • [CHEMONTID:0000048] Tetralins

*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
NPO14117 Diplodia sapinea Species Botryosphaeriaceae Eukaryota n.a. n.a. n.a. PMID[10075753]
NPO20359 Hortaea werneckii Species n.a. Eukaryota n.a. n.a. n.a. PMID[11374967]
NPO24444 Musca domestica Species Muscidae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO21609 Neofuscelia loxodella n.a. n.a. n.a. n.a. n.a. n.a. Database[UNPD]
NPO24174 Zanthoxylum hyemale Species Rutaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO24330 Aconitum firmum Species Ranunculaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO20975 Tiquilia plicata Species Ehretiaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO8045 Xenophyllum dactylophyllum Species Asteraceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO14117 Diplodia sapinea Species Botryosphaeriaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO24285 Dendrodoris nigra Species Dendrodorididae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO24070 Dysphania multifida Species Chenopodiaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO20359 Hortaea werneckii Species n.a. 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

☑ 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 NPC110205 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 NPC110205 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