Natural Product: NPC573338

Natural Product IDNPC573338
Common Name
?
The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.
 (2~{R})-2-(4-hydroxyphenyl)-7,8-dimethoxy-chroman-4-one
IUPAC Name (2~{R})-2-(4-hydroxyphenyl)-7,8-dimethoxy-chroman-4-one
Synonyms
Synthetic Gene Cluster n.a.
ChEMBL Identifier n.a.
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 JICUYFPHCQPXNY-OAHLLOKOSA-N
Standard InCHI InChI=1S/C17H16O5/c1-20-14-8-7-12-13(19)9-15(22-16(12)17(14)21-2)10-3-5-11(18)6-4-10/h3-8,15,18H,9H2,1-2H3/t15-/m1/s1
SMILES COC1=CC=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1OC

  Calculated Properties

Physi-Chem Properties

Molecular Weight:   300.1 Volume:   302.415
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Van der Waals volume.
Dense:   0.992 LogP:   2.54
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The logarithm of the n-octanol/water distribution coefficients.
logD7.4:   2.809
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The logarithm of the n-octanol/water distribution coefficient at pH=7.4.
 LogS:   -4.319
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The logarithm of aqueous solubility value.
Rotatable Bonds:   3.0 Rigid Bonds:   18.0
TPSA:   64.99
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Topological Polar Surface Area.
 H-Bond Acceptor:   5.0
H-Bond Donor:   1.0 Rings:   3.0
Heavy Atoms:   5.0

MedChem Properties

QED Drug-Likeness Score:   0.943 GASA:   0.0
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GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:   2.754 Fsp3:   0.235
MCE-18:   54.238
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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:   1
Chelating Alert:   0 PAINS Alert:   0
Colloidal aggregators:   0.326 Fluc inhibitor:   0.84
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The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:   0.29
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The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1
 Green fluorescence:   0.337
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The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:   0.376 Promiscuous compounds:   0.085

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:   -4.796 MDCK Permeability:   -4.75
Pgp-inhibitor:   0.985 Pgp-substrate:   0.122
PAMPA:   0.319
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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%):   0.001 30% Bioavailability (F30%):   0.268
50% Bioavailability (F50%):   0.957

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):   0.009 MRP1:   0.903
Plasma Protein Binding (PPB):   92.969% Volume Distribution (VD):   0.081
Fu: 8.655%
?
The fraction unbound in plasms.
 OATP1B1 inhibitor:   0.97
OATP1B3 inhibitor:   1.0 BCRP inhibitor:   0.999
BSEP inhibitor:   0.996

ADMET: Metabolism

CYP1A2-inhibitor:   0.043 CYP1A2-substrate:   0.545
CYP2C19-inhibitor:   0.619 CYP2C19-substrate:   0.897
CYP2C9-inhibitor:   0.045 CYP2C9-substrate:   0.0
CYP2D6-inhibitor:   0.116 CYP2D6-substrate:   0.745
CYP3A4-inhibitor:   0.179 CYP3A4-substrate:   0.931
CYP2B6-substrate:   0.0 CYP2C8-inhibitor:   0.852
HLM stability:   0.808
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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):  3.871 Half-life (T1/2):  1.43

ADMET: Toxicity

hERG Blockers:  0.214 hERG Blockers (10um):  0.515
Human Hepatotoxicity (H-HT):  0.717 Drug-induced Liver Injury (DILI):  0.376
AMES Toxicity:  0.675 Rat Oral Acute Toxicity:  0.461
Maximum Recommended Daily Dose:  0.577 Skin Sensitization:  0.558
Carcinogencity:  0.744 Eye Corrosion:  0.043
Eye Irritation:  0.983 Respiratory Toxicity:  0.14
Drug-induced Neurotoxicity:  0.935 Ototoxicity:  0.368
Hematotoxicity:  0.251 Drug-induced Nephrotoxicity:  0.618
Genotoxicity:  0.762 RPMI-8226 Immunitoxicity:  0.119
A549 Cytotoxicity:  0.213 Hek293 Cytotoxicity:  0.52
BCF:   1.114
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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:   3.773
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48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:   4.94
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48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].
 LC50FM:   4.379
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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
NPO51172 Helianthus annuus L cv.Peredovick. Genus Asteraceae Eukaryota n.a. n.a. n.a. Database[COCONUT]

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 NPC573338 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
0.6327 Remote Similarity NPC329225
0.6327 Remote Similarity NPC147686
0.6226 Remote Similarity NPC210084
0.6078 Remote Similarity NPC225153
0.6078 Remote Similarity NPC479876
0.5926 Remote Similarity NPC475267
0.5741 Remote Similarity NPC329203
0.5741 Remote Similarity NPC222342
0.5741 Remote Similarity NPC610021
0.569 Remote Similarity NPC169591
0.569 Remote Similarity NPC298223
0.569 Remote Similarity NPC604412
0.5636 Remote Similarity NPC606248
0.5556 Remote Similarity NPC37392
0.5472 Remote Similarity NPC476480
0.5472 Remote Similarity NPC84585
0.537 Remote Similarity NPC32441
0.537 Remote Similarity NPC79943
0.5357 Remote Similarity NPC485881
0.5273 Remote Similarity NPC1612
0.5273 Remote Similarity NPC183959
0.5263 Remote Similarity NPC474208
0.5179 Remote Similarity NPC300668
0.5179 Remote Similarity NPC324386
0.5091 Remote Similarity NPC264083
0.5091 Remote Similarity NPC603284
0.5088 Remote Similarity NPC469764
0.5088 Remote Similarity NPC486095
0.5082 Remote Similarity NPC39329
0.5082 Remote Similarity NPC472580
0.5082 Remote Similarity NPC51032

Similar Clinical/Approved Drugs

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

●  The left chart: Distribution of similarity level between NPC573338 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
0.6327 Remote Similarity NPD1549 Phase 2
0.537 Remote Similarity NPD1552 Clinical (unspecified phase)

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