Natural Product: NPC604713

Natural Product IDNPC604713
Common Name
?
The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.
 RNSBFHHWMMKJAM-UHFFFAOYSA-N
IUPAC Name n.a.
Synonyms
Synthetic Gene Cluster n.a.
ChEMBL Identifier CHEMBL4751513
PubChem CID n.a.
Chemical Classification
  • CHEMONTID:0000000 [Organic compounds]

The Chemical Classification was calculated by Classyfire, a software for chemical taxonomy calculation. Reference: DOI:10.1186/s13321-016-0174-y.

  Chemical Representations

Standard InCHIKey RNSBFHHWMMKJAM-UHFFFAOYSA-N
Standard InCHI InChI=1S/C21H16NO5/c1-22-8-14-19(17(23-2)7-18-21(14)27-10-26-18)12-4-3-11-5-15-16(25-9-24-15)6-13(11)20(12)22/h3-8H,9-10H2,1-2H3/q+1
SMILES COc1cc2c(c3c[n+](C)c4c5cc6c(cc5ccc4c13)OCO6)OCO2

  Calculated Properties

Physi-Chem Properties

Molecular Weight:   362.1 Volume:   352.971
?
Van der Waals volume.
Dense:   1.026 LogP:   3.614
?
The logarithm of the n-octanol/water distribution coefficients.
logD7.4:   3.366
?
The logarithm of the n-octanol/water distribution coefficient at pH=7.4.
 LogS:   -5.964
?
The logarithm of aqueous solubility value.
Rotatable Bonds:   1.0 Rigid Bonds:   29.0
TPSA:   50.03
?
Topological Polar Surface Area.
 H-Bond Acceptor:   6.0
H-Bond Donor:   0.0 Rings:   6.0
Heavy Atoms:   6.0

MedChem Properties

QED Drug-Likeness Score:   0.384 GASA:   1.0
?
GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:   3.025 Fsp3:   0.19
MCE-18:   64.8
?
MCE-18 stands for medicinal chemistry evolution.MCE-18≥45 is considered a suitable value.
 Lipinski Rule-of-5:   Rejected
Pfizer Rule:   Accepted GSK Rule:   Rejected
Golden Triangle Rule:   Rejected BMS Rule:   0
Chelating Alert:   0 PAINS Alert:   0
Colloidal aggregators:   0.921 Fluc inhibitor:   0.001
?
The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:   0.884
?
The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1
 Green fluorescence:   0.507
?
The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:   0.036 Promiscuous compounds:   0.49

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:   -4.987 MDCK Permeability:   -4.734
Pgp-inhibitor:   0.0 Pgp-substrate:   0.994
PAMPA:   0.457
?
The experimental data for Peff was logarithmically transformed (logPeff). Molecules with log Peff values below 2.0 were classified as low-permeability (Category 0), while those with log Peff values exceeding 2.5 were classified as high-permeability (Category 1).
 Human Intestinal Absorption (HIA):   0.05
20% Bioavailability (F20%):   0.798 30% Bioavailability (F30%):   0.46
50% Bioavailability (F50%):   0.998

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):   0.035 MRP1:   0.76
Plasma Protein Binding (PPB):   69.352% Volume Distribution (VD):   0.168
Fu: 36.802%
?
The fraction unbound in plasms.
 OATP1B1 inhibitor:   0.003
OATP1B3 inhibitor:   0.01 BCRP inhibitor:   0.051
BSEP inhibitor:   0.712

ADMET: Metabolism

CYP1A2-inhibitor:   1.0 CYP1A2-substrate:   1.0
CYP2C19-inhibitor:   0.996 CYP2C19-substrate:   0.068
CYP2C9-inhibitor:   1.0 CYP2C9-substrate:   1.0
CYP2D6-inhibitor:   1.0 CYP2D6-substrate:   1.0
CYP3A4-inhibitor:   0.025 CYP3A4-substrate:   1.0
CYP2B6-substrate:   0.837 CYP2C8-inhibitor:   0.0
HLM stability:   0.833
?
Human liver microsomal (HLM) stability. Category 0: stable+ (HLM > 30 min); Category 1: unstable- (HLM ≤ 30 min). The output value is the probability of human liver microsomal instability, where a value closer to 1 indicates a higher likelihood of instability.

ADMET: Excretion

Clearance (CL):  3.495 Half-life (T1/2):  0.485

ADMET: Toxicity

hERG Blockers:  0.384 hERG Blockers (10um):  0.562
Human Hepatotoxicity (H-HT):  0.172 Drug-induced Liver Injury (DILI):  0.85
AMES Toxicity:  0.787 Rat Oral Acute Toxicity:  0.797
Maximum Recommended Daily Dose:  0.937 Skin Sensitization:  0.936
Carcinogencity:  0.937 Eye Corrosion:  0.001
Eye Irritation:  0.892 Respiratory Toxicity:  0.907
Drug-induced Neurotoxicity:  0.473 Ototoxicity:  0.153
Hematotoxicity:  0.179 Drug-induced Nephrotoxicity:  0.314
Genotoxicity:  0.997 RPMI-8226 Immunitoxicity:  0.205
A549 Cytotoxicity:  0.016 Hek293 Cytotoxicity:  0.865
BCF:   1.906
?
Bioconcentration factors are used for considering secondary poisoning potential and assessing risks to human health via the food chain. The unit is -log10[(mg/L)/(1000*MW)].
 IGC50:   4.187
?
48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:   5.921
?
48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].
 LC50FM:   5.132
?
96 hour fathead minnow LC50. The unit of LC50FM is -log10[(mg/L)/(1000*MW)].

  Species Source

Organism ID Organism Name Taxonomy Level Family SuperKingdom Isolation Part Collection Location Collection Time Reference
NPO53854 Chelidonium majus L. Genus Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO57382 Eschscholtzia californica n.a. n.a. n.a. n.a. n.a. n.a. Database[COCONUT]
NPO51014 Actaea spicata L. Genus Ranunculaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO4790 Bocconia cordata Species Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO53502 Dicranostigma franchetianum Fedde Genus Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO52072 Dicranostigma lactucoides Species Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO42287 Dicranostigma lactucoides Hook.et Thoms. Genus Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO49232 Dicranostigma leptopodum Fedde Genus Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO42217 Glaucium squamigerum Kar.et Kir. Genus Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO57756 Papaver oreophillum Genus Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO56669 Stylophorum lasiocarpum Species Papaveraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO4790 Bocconia cordata Species Papaveraceae 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 Organism Name 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

Molecular-level activity

Target ID Target Type Target Name Target Organism Activity Type Activity Relation Value Unit Reference

In vitro activity

Target ID Target Type Target Name Target Organism Activity Type Activity Relation Value Unit Reference
NPT28438 Unchecked Unchecked n.a. Activity n.a. n.a. n.a. PMID[33065438]
NPT88 Organism Mycobacterium tuberculosis Mycobacterium tuberculosis MIC = 12.5 ug.mL-1 PMID[35168150]
NPT88 Organism Mycobacterium tuberculosis Mycobacterium tuberculosis MIC = 12.5 ug.mL-1 PMID[28628823]

In vivo activity

Target ID Target Type Target Name Target Organism Activity Type Activity Relation Value Unit Reference





 Experimental ADME

Experiment Model Experiment Tissue ADME Type ADME Relation ADME Value ADME Unit Reference





 Experimental Toxicity

Quantitative toxicity

Experiment Model Experiment Organism Toxicity Type Toxicity Relation Toxicity Value Toxicity Unit Reference

Common Abbreviations:
LC: Lethal Concentration; LD: Lethal Dose; LT:Lethal Time; NOAEL: No-observed-adverse-effect Level; BMDL: Benchmark Dose Lower Confidence Limit; BMD: Benchmark Dose; BMC:Benchmark Concentration; LOAEL: Lowest Observed Adverse Effect Level; RfD:Reference Dose; RfC:Reference Concentration; MRL: Minimal Risk Level; MEG: Maximum Exposure Guideline; PAC: Protective Action Criteria

Categorical toxicity labels

Hepatotoxicity Carcinogenicity Mutagenicity Cardiotoxicity Respiratory Toxicity Eye Irritation Endocrine Disruption
Hepatotoxicity Carcinogenicity Mutagenicity Cardiotoxicity Respiratory Toxicity Eye Irritation Endocrine Disruption

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 toxicity records from domain-specific databases. These databases include:
☉ ToxValDB: a curated database that compiles quantitative toxicity values for chemicals from diverse public sources to support toxicological research and risk assessment.
☉ TOXRIC: a comprehensive, free-to-access, online database providing toxicological/feature data. The toxicity labels are retrieved from this database. [PMID: 36400569]


  Chemically structural similarity

Similar Active Natural Products in NPASS

Top-200 similar NPs were calculated against the active-NP-set (includes approximately 50,000 NPs with experimentally-derived bioactivity available in NPASS)

Similarity is measured using the Tanimoto coefficient (Tc) , which compares the binary fingerprints of two molecules. Tc is calculated as the intersection divided by the union of '1' bits in the fingerprints, ranging from 0 to 1, with 1 indicating highest similarity.

●  The left chart: Distribution of similarity level between NPC604713 and all remaining natural products in the NPASS database.
●  The right table: Most similar natural products (Tc>=0.5 or Top200).

Similarity Score Similarity Level Natural Product ID
0.9038 High Similarity NPC611429
0.7368 Intermediate Similarity NPC128345
0.6724 Remote Similarity NPC46451
0.661 Remote Similarity NPC100079
0.661 Remote Similarity NPC23614
0.65 Remote Similarity NPC602221
0.6207 Remote Similarity NPC271215
0.6102 Remote Similarity NPC149471
0.5692 Remote Similarity NPC604320

Similar Clinical/Approved Drugs

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

●  The left chart: Distribution of similarity level between NPC604713 and all drugs/candidates.
●  The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

Similarity Score Similarity Level Drug ID Developmental Stage
0.6724 Remote Similarity NPD3763 Phase 2

Bioactivity similarity

  Bioactivity similarity

Similar Natural Products in NPASS

Similarity level is defined by 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