Natural Product: NPC150534

Natural Product IDNPC150534
Common Name
?
The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.
 (2R,3R)-2,3-Bis(5-Methoxy-3,4-Methylenedioxybenzyl)Butane-1,4-Diol
IUPAC Name (2R,3R)-2,3-bis[(7-methoxy-1,3-benzodioxol-5-yl)methyl]butane-1,4-diol
Synonyms
Synthetic Gene Cluster n.a.
ChEMBL Identifier CHEMBL522274
PubChem CID 11582466
Chemical Classification
  • CHEMONTID:0000000 [Organic compounds]
    • [CHEMONTID:0001392] Lignans, neolignans and related compounds
      • [CHEMONTID:0001969] Dibenzylbutane lignans
        • [CHEMONTID:0001624] Dibenzylbutanediol lignans

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 FPHAWPUGHVPMPC-HOTGVXAUSA-N
Standard InCHI InChI=1S/C22H26O8/c1-25-17-5-13(7-19-21(17)29-11-27-19)3-15(9-23)16(10-24)4-14-6-18(26-2)22-20(8-14)28-12-30-22/h5-8,15-16,23-24H,3-4,9-12H2,1-2H3/t15-,16-/m0/s1
SMILES COc1cc(C[C@@H](CO)[C@@H](Cc2cc(c3c(c2)OCO3)OC)CO)cc2c1OCO2

  Calculated Properties

Physi-Chem Properties

Molecular Weight:   418.16 Volume:   409.345
?
Van der Waals volume.
Dense:   1.022 LogP:   1.952
?
The logarithm of the n-octanol/water distribution coefficients.
logD7.4:   2.239
?
The logarithm of the n-octanol/water distribution coefficient at pH=7.4.
 LogS:   -2.706
?
The logarithm of aqueous solubility value.
Rotatable Bonds:   9.0 Rigid Bonds:   20.0
TPSA:   95.84
?
Topological Polar Surface Area.
 H-Bond Acceptor:   8.0
H-Bond Donor:   2.0 Rings:   4.0
Heavy Atoms:   8.0

MedChem Properties

QED Drug-Likeness Score:   0.64 GASA:   0.0
?
GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:   3.504 Fsp3:   0.455
MCE-18:   68.75
?
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:   Accepted
Golden Triangle Rule:   Rejected BMS Rule:   0
Chelating Alert:   0 PAINS Alert:   0
Colloidal aggregators:   0.307 Fluc inhibitor:   0.111
?
The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:   0.062
?
The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1
 Green fluorescence:   0.353
?
The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:   0.195 Promiscuous compounds:   0.345

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:   -5.028 MDCK Permeability:   -4.803
Pgp-inhibitor:   0.608 Pgp-substrate:   0.022
PAMPA:   0.12
?
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):   0.0
20% Bioavailability (F20%):   0.027 30% Bioavailability (F30%):   0.0
50% Bioavailability (F50%):   0.096

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):   0.487 MRP1:   0.616
Plasma Protein Binding (PPB):   77.191% Volume Distribution (VD):   0.02
Fu: 24.843%
?
The fraction unbound in plasms.
 OATP1B1 inhibitor:   0.986
OATP1B3 inhibitor:   0.655 BCRP inhibitor:   0.013
BSEP inhibitor:   1.0

ADMET: Metabolism

CYP1A2-inhibitor:   0.067 CYP1A2-substrate:   0.614
CYP2C19-inhibitor:   1.0 CYP2C19-substrate:   0.989
CYP2C9-inhibitor:   1.0 CYP2C9-substrate:   0.998
CYP2D6-inhibitor:   0.978 CYP2D6-substrate:   1.0
CYP3A4-inhibitor:   0.219 CYP3A4-substrate:   1.0
CYP2B6-substrate:   0.019 CYP2C8-inhibitor:   0.959
HLM stability:   0.995
?
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):  5.038 Half-life (T1/2):  1.144

ADMET: Toxicity

hERG Blockers:  0.148 hERG Blockers (10um):  0.266
Human Hepatotoxicity (H-HT):  0.828 Drug-induced Liver Injury (DILI):  0.654
AMES Toxicity:  0.626 Rat Oral Acute Toxicity:  0.068
Maximum Recommended Daily Dose:  0.068 Skin Sensitization:  0.964
Carcinogencity:  0.691 Eye Corrosion:  0.001
Eye Irritation:  0.529 Respiratory Toxicity:  0.096
Drug-induced Neurotoxicity:  0.54 Ototoxicity:  0.905
Hematotoxicity:  0.543 Drug-induced Nephrotoxicity:  0.849
Genotoxicity:  0.491 RPMI-8226 Immunitoxicity:  0.13
A549 Cytotoxicity:  0.136 Hek293 Cytotoxicity:  0.193
BCF:   1.511
?
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:   3.689
?
48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:   5.538
?
48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].
 LC50FM:   4.303
?
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
NPO17040 Peperomia duclouxii Species Piperaceae Eukaryota n.a. n.a. n.a. PMID[16499322]
NPO17040 Peperomia duclouxii Species Piperaceae Eukaryota n.a. n.a. n.a. PMID[17358082]
NPO17040 Peperomia duclouxii Species Piperaceae Eukaryota n.a. n.a. n.a. PMID[17547458]
NPO17040 Peperomia duclouxii Species Piperaceae Eukaryota n.a. n.a. n.a. Database[COCONUT]
NPO17040 Peperomia duclouxii Species Piperaceae Eukaryota n.a. n.a. n.a. Database[HerDing]
NPO17040 Peperomia duclouxii Species Piperaceae Eukaryota n.a. n.a. n.a. Database[TCMID]
NPO17040 Peperomia duclouxii Species Piperaceae 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
NPT1475 Cell line WI-38 VA13 Homo sapiens IC50 = 218900.0 nM PMID[15711537]
NPT65 Cell line HepG2 Homo sapiens IC50 = 151400.0 nM PMID[27101894]
NPT2 Others Unspecified n.a. Activity = 97.0 % PMID[16499313]
NPT2 Others Unspecified n.a. Activity = 93.0 % PMID[16499313]
NPT2 Others Unspecified n.a. Activity = 103.0 % PMID[16499313]
NPT2 Others Unspecified n.a. Activity = 107.0 % PMID[16124766]
NPT2 Others Unspecified n.a. Activity = 121.0 % PMID[16124766]
NPT2 Others Unspecified n.a. Activity = 91.0 % PMID[12828470]

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 NPC150534 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
0.7381 Intermediate Similarity NPC196937
0.6341 Remote Similarity NPC40352
0.6341 Remote Similarity NPC213711
0.62 Remote Similarity NPC46591
0.6042 Remote Similarity NPC283949
0.6 Remote Similarity NPC119949
0.587 Remote Similarity NPC11453
0.5625 Remote Similarity NPC474288
0.5577 Remote Similarity NPC226547
0.551 Remote Similarity NPC92693
0.54 Remote Similarity NPC40237
0.5349 Remote Similarity NPC473960
0.5273 Remote Similarity NPC474039

Similar Clinical/Approved Drugs

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

●  The left chart: Distribution of similarity level between NPC150534 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