Structure

Physi-Chem Properties

Molecular Weight:  232.15
Volume:  251.998
LogP:  2.15
LogD:  1.505
LogS:  -2.541
# Rotatable Bonds:  0
TPSA:  34.14
# H-Bond Aceptor:  2
# H-Bond Donor:  0
# Rings:  4
# Heavy Atoms:  2

MedChem Properties

QED Drug-Likeness Score:  0.602
Synthetic Accessibility Score:  5.731
Fsp3:  0.733
Lipinski Rule-of-5:  Accepted
Pfizer Rule:  Accepted
GSK Rule:  Accepted
BMS Rule:  0
Golden Triangle Rule:  Accepted
Chelating Alert:  0
PAINS Alert:  0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:  -4.593
MDCK Permeability:  2.2132735466584563e-05
Pgp-inhibitor:  0.005
Pgp-substrate:  0.002
Human Intestinal Absorption (HIA):  0.005
20% Bioavailability (F20%):  0.077
30% Bioavailability (F30%):  0.011

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):  0.873
Plasma Protein Binding (PPB):  83.38452911376953%
Volume Distribution (VD):  1.081
Pgp-substrate:  14.428947448730469%

ADMET: Metabolism

CYP1A2-inhibitor:  0.028
CYP1A2-substrate:  0.51
CYP2C19-inhibitor:  0.078
CYP2C19-substrate:  0.935
CYP2C9-inhibitor:  0.027
CYP2C9-substrate:  0.399
CYP2D6-inhibitor:  0.003
CYP2D6-substrate:  0.219
CYP3A4-inhibitor:  0.152
CYP3A4-substrate:  0.611

ADMET: Excretion

Clearance (CL):  19.411
Half-life (T1/2):  0.402

ADMET: Toxicity

hERG Blockers:  0.004
Human Hepatotoxicity (H-HT):  0.237
Drug-inuced Liver Injury (DILI):  0.086
AMES Toxicity:  0.01
Rat Oral Acute Toxicity:  0.523
Maximum Recommended Daily Dose:  0.137
Skin Sensitization:  0.041
Carcinogencity:  0.872
Eye Corrosion:  0.122
Eye Irritation:  0.163
Respiratory Toxicity:  0.878

Download Data

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

  Natural Product: NPC488195

Natural Product ID:  NPC488195
Common Name*:   CXBDANPQORZFRE-SIPIVGMWSA-N
IUPAC Name:   n.a.
Synonyms:  
Standard InCHIKey:  CXBDANPQORZFRE-SIPIVGMWSA-N
Standard InCHI:  InChI=1S/C15H20O2/c1-8-4-5-15-9(2)6-13(16)11(7-12(8)15)10(3)14(15)17/h6,8,11-12,14,17H,3-5,7H2,1-2H3/t8-,11?,12-,14+,15-/m0/s1
SMILES:  C[C@H]1CC[C@]23C(=CC(=O)C(C[C@@H]12)C(=C)[C@H]3O)C
Synthetic Gene Cluster:   n.a.
ChEMBL Identifier:   n.a.
PubChem CID:   n.a.
Chemical Classification**:  
  • CHEMONTID:0000000 [Organic compounds]

*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
NPO1692 Aquilaria malaccensis Species Thymelaeaceae Eukaryota Seeds n.a. n.a. PMID[28445049]
NPO1692 Aquilaria malaccensis Species Thymelaeaceae Eukaryota Agarwood n.a. n.a. PMID[29083898]
NPO1692 Aquilaria malaccensis Species Thymelaeaceae Eukaryota n.a. n.a. n.a. PMID[30672698]
NPO1692 Aquilaria malaccensis Species Thymelaeaceae Eukaryota n.a. n.a. n.a. PMID[7320738]
NPO1692 Aquilaria malaccensis Species Thymelaeaceae 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
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 430000.0 nM PMID[29083898]
NPT175 Organism Enterococcus faecalis Enterococcus faecalis MIC = 430000.0 nM PMID[29083898]
NPT1531 Organism Enterococcus faecium Enterococcus faecium MIC = 430000.0 nM PMID[29083898]
NPT566 Organism Salmonella typhimurium Salmonella enterica subsp. enterica serovar Typhimurium MIC = 430000.0 nM PMID[29083898]
NPT173 Organism Klebsiella pneumoniae Klebsiella pneumoniae MIC = 430000.0 nM PMID[29083898]
NPT19 Organism Escherichia coli Escherichia coli MIC = 430000.0 nM PMID[29083898]
NPT87 Organism Aspergillus fumigatus Aspergillus fumigatus MIC = 430000.0 nM PMID[29083898]
NPT329 Organism Trichophyton rubrum Trichophyton rubrum MIC = 430000.0 nM PMID[29083898]
NPT330 Organism Trichophyton mentagrophytes Trichophyton mentagrophytes MIC = 430000.0 nM PMID[29083898]
NPT20 Organism Candida albicans Candida albicans MIC = 430000.0 nM PMID[29083898]

☑ 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 NPC488195 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 NPC488195 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