Structure

Physi-Chem Properties

Molecular Weight:  226.16
Volume:  240.026
LogP:  1.49
LogD:  0.533
LogS:  -3.091
# Rotatable Bonds:  2
TPSA:  52.99
# H-Bond Aceptor:  3
# H-Bond Donor:  2
# Rings:  2
# Heavy Atoms:  3

MedChem Properties

QED Drug-Likeness Score:  0.556
Synthetic Accessibility Score:  4.561
Fsp3:  0.846
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:  -4.793
MDCK Permeability:  2.2790020011598244e-05
Pgp-inhibitor:  0.0
Pgp-substrate:  0.671
Human Intestinal Absorption (HIA):  0.052
20% Bioavailability (F20%):  0.032
30% Bioavailability (F30%):  0.038

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):  0.922
Plasma Protein Binding (PPB):  74.34664916992188%
Volume Distribution (VD):  1.723
Pgp-substrate:  32.943153381347656%

ADMET: Metabolism

CYP1A2-inhibitor:  0.022
CYP1A2-substrate:  0.727
CYP2C19-inhibitor:  0.051
CYP2C19-substrate:  0.882
CYP2C9-inhibitor:  0.034
CYP2C9-substrate:  0.096
CYP2D6-inhibitor:  0.003
CYP2D6-substrate:  0.112
CYP3A4-inhibitor:  0.042
CYP3A4-substrate:  0.825

ADMET: Excretion

Clearance (CL):  6.819
Half-life (T1/2):  0.576

ADMET: Toxicity

hERG Blockers:  0.027
Human Hepatotoxicity (H-HT):  0.478
Drug-inuced Liver Injury (DILI):  0.289
AMES Toxicity:  0.455
Rat Oral Acute Toxicity:  0.818
Maximum Recommended Daily Dose:  0.976
Skin Sensitization:  0.287
Carcinogencity:  0.793
Eye Corrosion:  0.006
Eye Irritation:  0.53
Respiratory Toxicity:  0.957

Download Data

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

  Natural Product: NPC310267

Natural Product ID:  NPC310267
Common Name*:   BVNCCXWAZAZQNM-ASZAWAPASA-N
IUPAC Name:   n.a.
Synonyms:  
Standard InCHIKey:  BVNCCXWAZAZQNM-ASZAWAPASA-N
Standard InCHI:  InChI=1S/C13H22O3/c1-9(14)5-6-13-11(2,3)7-10(15)8-12(13,4)16-13/h5-6,9-10,14-15H,7-8H2,1-4H3/b6-5+/t9-,10-,12-,13+/m1/s1
SMILES:  C[C@H](/C=C/[C@]12C(C)(C)C[C@H](C[C@@]1(C)O2)O)O
Synthetic Gene Cluster:   n.a.
ChEMBL Identifier:   n.a.
PubChem CID:   n.a.
Chemical Classification**:  
  • CHEMONTID:0000000 [Organic compounds]
    • [CHEMONTID:0000002] Organoheterocyclic compounds
      • [CHEMONTID:0001729] Oxepanes

*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
NPO25507 Spongia agaricina Species Spongiidae Eukaryota n.a. n.a. n.a. PMID[9548857]
NPO25446 Acia oblonga n.a. n.a. n.a. n.a. n.a. n.a. Database[UNPD]
NPO25567 Dichilus reflexus Species Fabaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO25332 Polyalthia acuminata Species Annonaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO25507 Spongia agaricina Species Spongiidae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO28244 Trichocereus peruvianus Species Cactaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO25676 Stereospermum acuminatissimum Species Bignoniaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO21053 Oenanthe pimpinelloides Species Apiaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO24945 Hoya carnosa Species Apocynaceae 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 NPC310267 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 NPC310267 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