Structure

Physi-Chem Properties

Molecular Weight:  314.04
Volume:  288.342
LogP:  0.383
LogD:  0.399
LogS:  -3.872
# Rotatable Bonds:  1
TPSA:  97.63
# H-Bond Aceptor:  6
# H-Bond Donor:  2
# Rings:  4
# Heavy Atoms:  7

MedChem Properties

QED Drug-Likeness Score:  0.515
Synthetic Accessibility Score:  4.285
Fsp3:  0.067
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:  -5.017
MDCK Permeability:  3.181739202773315e-06
Pgp-inhibitor:  0.011
Pgp-substrate:  0.999
Human Intestinal Absorption (HIA):  0.069
20% Bioavailability (F20%):  0.007
30% Bioavailability (F30%):  0.042

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):  0.061
Plasma Protein Binding (PPB):  86.32703399658203%
Volume Distribution (VD):  0.611
Pgp-substrate:  10.311713218688965%

ADMET: Metabolism

CYP1A2-inhibitor:  0.975
CYP1A2-substrate:  0.749
CYP2C19-inhibitor:  0.096
CYP2C19-substrate:  0.101
CYP2C9-inhibitor:  0.258
CYP2C9-substrate:  0.912
CYP2D6-inhibitor:  0.028
CYP2D6-substrate:  0.241
CYP3A4-inhibitor:  0.128
CYP3A4-substrate:  0.275

ADMET: Excretion

Clearance (CL):  5.107
Half-life (T1/2):  0.879

ADMET: Toxicity

hERG Blockers:  0.004
Human Hepatotoxicity (H-HT):  0.22
Drug-inuced Liver Injury (DILI):  0.854
AMES Toxicity:  0.964
Rat Oral Acute Toxicity:  0.398
Maximum Recommended Daily Dose:  0.982
Skin Sensitization:  0.599
Carcinogencity:  0.978
Eye Corrosion:  0.005
Eye Irritation:  0.453
Respiratory Toxicity:  0.894

Download Data

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

  Natural Product: NPC94798

Natural Product ID:  NPC94798
Common Name*:   CLXJXUMJTHVKDG-QFIPXVFZSA-N
IUPAC Name:   n.a.
Synonyms:  
Standard InCHIKey:  CLXJXUMJTHVKDG-QFIPXVFZSA-N
Standard InCHI:  InChI=1S/C15H10N2O4S/c1-22(21)11-5-12(20)17-9-4-7(18)2-3-8(9)13-10(19)6-16-14(11)15(13)17/h2-6,18-19H,1H3/t22-/m0/s1
SMILES:  C[S@](=O)c1cc(=O)n2c3cc(ccc3c3c(cnc1c23)O)O
Synthetic Gene Cluster:   n.a.
ChEMBL Identifier:   n.a.
PubChem CID:   n.a.
Chemical Classification**:  
  • CHEMONTID:0000000 [Organic compounds]
    • [CHEMONTID:0000279] Alkaloids and derivatives
      • [CHEMONTID:0003805] Indolonaphthyridine alkaloids

*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
NPO22840 Casearia arguta Species Salicaceae Eukaryota n.a. leaf n.a. PMID[21067210]
NPO22840 Casearia arguta Species Salicaceae Eukaryota n.a. n.a. n.a. PMID[21067210]
NPO21012 Mikania sessilifolia Species Asteraceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO20992 Tarenna graveolens Species Rubiaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO18753 Sideritis serrata Species Lamiaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO21697 Irpex pachyodon Species Irpicaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO19973 Cupania glabra Species Sapindaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO21885 Furcraea elegans Species Asparagaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO22840 Casearia arguta Species Salicaceae 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 NPC94798 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 NPC94798 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