Natural Product: NPC111494

Natural Product IDNPC111494
Common Name
?
The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.
 VFXXNAVZODKBIW-FONPPYIRSA-N
IUPAC Name n.a.
Synonyms
Synthetic Gene Cluster n.a.
ChEMBL Identifier n.a.
PubChem CID 10108263
Chemical Classification
  • CHEMONTID:0000000 [Organic compounds]
    • [CHEMONTID:0000012] Lipids and lipid-like molecules
      • [CHEMONTID:0000259] Prenol lipids
        • [CHEMONTID:0001283] Terpene lactones

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 VFXXNAVZODKBIW-FONPPYIRSA-N
Standard InCHI InChI=1S/C15H14O6/c1-3-7-11-15(21-13(7)17)5-4-8-9(12(16)18-2)6-19-14(20-11)10(8)15/h3-6,8,10-11,14H,1-2H3/b7-3-/t8-,10-,11?,14-,15+/m1/s1
SMILES C/C=C1/C2[C@@]3(C=C[C@@H]4C(=CO[C@@H]([C@H]34)O2)C(=O)OC)OC1=O

  Calculated Properties

Physi-Chem Properties

Molecular Weight:   290.08 Volume:   273.329
?
Van der Waals volume.
Dense:   1.061 LogP:   1.887
?
The logarithm of the n-octanol/water distribution coefficients.
logD7.4:   2.005
?
The logarithm of the n-octanol/water distribution coefficient at pH=7.4.
 LogS:   -3.05
?
The logarithm of aqueous solubility value.
Rotatable Bonds:   2.0 Rigid Bonds:   20.0
TPSA:   71.06
?
Topological Polar Surface Area.
 H-Bond Acceptor:   6.0
H-Bond Donor:   0.0 Rings:   4.0
Heavy Atoms:   6.0

MedChem Properties

QED Drug-Likeness Score:   0.405 GASA:   1.0
?
GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:   5.608 Fsp3:   0.467
MCE-18:   79.455
?
MCE-18 stands for medicinal chemistry evolution.MCE-18≥45 is considered a suitable value.
 Lipinski Rule-of-5:   Rejected
Pfizer Rule:   Rejected GSK Rule:   Rejected
Golden Triangle Rule:   Rejected BMS Rule:   0
Chelating Alert:   0 PAINS Alert:   0
Colloidal aggregators:   0.127 Fluc inhibitor:   0.001
?
The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:   0.067
?
The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1
 Green fluorescence:   0.002
?
The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:   0.656 Promiscuous compounds:   0.091

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:   -4.987 MDCK Permeability:   -4.655
Pgp-inhibitor:   0.061 Pgp-substrate:   0.072
PAMPA:   0.127
?
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):   0.086
20% Bioavailability (F20%):   0.691 30% Bioavailability (F30%):   0.929
50% Bioavailability (F50%):   0.672

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):   0.603 MRP1:   0.969
Plasma Protein Binding (PPB):   88.771% Volume Distribution (VD):   0.14
Fu: 12.837%
?
The fraction unbound in plasms.
 OATP1B1 inhibitor:   0.281
OATP1B3 inhibitor:   0.663 BCRP inhibitor:   0.002
BSEP inhibitor:   0.951

ADMET: Metabolism

CYP1A2-inhibitor:   0.384 CYP1A2-substrate:   0.646
CYP2C19-inhibitor:   0.155 CYP2C19-substrate:   0.499
CYP2C9-inhibitor:   0.408 CYP2C9-substrate:   0.17
CYP2D6-inhibitor:   0.28 CYP2D6-substrate:   0.461
CYP3A4-inhibitor:   0.235 CYP3A4-substrate:   0.829
CYP2B6-substrate:   0.021 CYP2C8-inhibitor:   0.925
HLM stability:   0.808
?
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):  8.786 Half-life (T1/2):  1.684

ADMET: Toxicity

hERG Blockers:  0.026 hERG Blockers (10um):  0.23
Human Hepatotoxicity (H-HT):  0.563 Drug-induced Liver Injury (DILI):  0.905
AMES Toxicity:  0.967 Rat Oral Acute Toxicity:  0.825
Maximum Recommended Daily Dose:  0.82 Skin Sensitization:  0.999
Carcinogencity:  0.899 Eye Corrosion:  0.005
Eye Irritation:  0.595 Respiratory Toxicity:  0.358
Drug-induced Neurotoxicity:  0.826 Ototoxicity:  0.555
Hematotoxicity:  0.856 Drug-induced Nephrotoxicity:  0.918
Genotoxicity:  0.996 RPMI-8226 Immunitoxicity:  0.183
A549 Cytotoxicity:  0.671 Hek293 Cytotoxicity:  0.479
BCF:   0.838
?
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:   3.57
?
48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:   4.828
?
48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].
 LC50FM:   4.461
?
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
NPO16662 Plumbago indica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. DOI[10.1007/s10529-015-1969-z]
NPO16662 Plumbago indica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. DOI[10.1016/j.jbiosc.2011.02.003]
NPO25454 Plumbago europaea Species Plumbaginaceae Eukaryota n.a. root n.a. DOI[10.2225/vol5-issue3-fulltext-4]
NPO13608 Plumbago zeylanica Species Plumbaginaceae Eukaryota n.a. root n.a. PMID[16078700]
NPO13608 Plumbago zeylanica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. PMID[23848163]
NPO5188 Allamanda cathartica Species Apocynaceae Eukaryota n.a. n.a. n.a. PMID[25832441]
NPO25454 Plumbago europaea Species Plumbaginaceae Eukaryota n.a. n.a. n.a. PMID[37800169]
NPO5188 Allamanda cathartica Species Apocynaceae Eukaryota n.a. n.a. n.a. PMID[9428163]
NPO5188 Allamanda cathartica Species Apocynaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO14370 Ceratostigma willmottianum Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO2551 Plumbagella micrantha Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO13608 Plumbago zeylanica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO25454 Plumbago europaea Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO16662 Plumbago indica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO3770 Drosera rotundifolia Species Droseraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO18595 Ceratostigma plumbaginoides Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO29820 Allemanda cathartica n.a. n.a. n.a. n.a. n.a. n.a. Database[COCONUT]
NPO22736.1 Drosera peltata var. lunata Varieties Droseraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO26780 Dionaea muscipula Species Droseraceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO29820 Allemanda cathartica n.a. n.a. n.a. n.a. n.a. n.a. Database[HerDing]
NPO18595 Ceratostigma plumbaginoides Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO25454 Plumbago europaea Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO16662 Plumbago indica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO3770 Drosera rotundifolia Species Droseraceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO14370 Ceratostigma willmottianum Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO13608 Plumbago zeylanica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO2551 Plumbagella micrantha Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO22736.1 Drosera peltata var. lunata Varieties Droseraceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO16662 Plumbago indica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO13608 Plumbago zeylanica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO22736.1 Drosera peltata var. lunata Varieties Droseraceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO26780 Dionaea muscipula Species Droseraceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO25454 Plumbago europaea Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO18595 Ceratostigma plumbaginoides Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO2551 Plumbagella micrantha Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO5188 Allamanda cathartica Species Apocynaceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO14370 Ceratostigma willmottianum Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO3770 Drosera rotundifolia Species Droseraceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO29820 Allemanda cathartica n.a. n.a. n.a. n.a. n.a. n.a. Database[TCM_Taiwan]
NPO5188 Allamanda cathartica Species Apocynaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO14370 Ceratostigma willmottianum Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO18595 Ceratostigma plumbaginoides Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO26780 Dionaea muscipula Species Droseraceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO13608 Plumbago zeylanica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO25454 Plumbago europaea Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO16662 Plumbago indica Species Plumbaginaceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO3770 Drosera rotundifolia Species Droseraceae Eukaryota n.a. n.a. n.a. Database[UNPD]
NPO2551 Plumbagella micrantha Species Plumbaginaceae 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

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 NPC111494 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
1.0 High Similarity NPC305157
1.0 High Similarity NPC307846
0.6032 Remote Similarity NPC210330
0.6 Remote Similarity NPC473428
0.5507 Remote Similarity NPC76211
0.5167 Remote Similarity NPC475960

Similar Clinical/Approved Drugs

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

●  The left chart: Distribution of similarity level between NPC111494 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
NPD

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