Structure

Physi-Chem Properties

Molecular Weight:  210.07
Volume:  215.799
LogP:  1.345
LogD:  0.389
LogS:  -2.492
# Rotatable Bonds:  2
TPSA:  34.14
# H-Bond Aceptor:  2
# H-Bond Donor:  0
# Rings:  1
# Heavy Atoms:  3

MedChem Properties

QED Drug-Likeness Score:  0.518
Synthetic Accessibility Score:  4.559
Fsp3:  0.455
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:  -4.496
MDCK Permeability:  3.318105882499367e-05
Pgp-inhibitor:  0.0
Pgp-substrate:  0.005
Human Intestinal Absorption (HIA):  0.007
20% Bioavailability (F20%):  0.003
30% Bioavailability (F30%):  0.001

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):  0.909
Plasma Protein Binding (PPB):  85.26561737060547%
Volume Distribution (VD):  1.403
Pgp-substrate:  14.935697555541992%

ADMET: Metabolism

CYP1A2-inhibitor:  0.039
CYP1A2-substrate:  0.666
CYP2C19-inhibitor:  0.113
CYP2C19-substrate:  0.838
CYP2C9-inhibitor:  0.049
CYP2C9-substrate:  0.221
CYP2D6-inhibitor:  0.01
CYP2D6-substrate:  0.099
CYP3A4-inhibitor:  0.738
CYP3A4-substrate:  0.855

ADMET: Excretion

Clearance (CL):  7.696
Half-life (T1/2):  0.892

ADMET: Toxicity

hERG Blockers:  0.025
Human Hepatotoxicity (H-HT):  0.095
Drug-inuced Liver Injury (DILI):  0.518
AMES Toxicity:  0.088
Rat Oral Acute Toxicity:  0.605
Maximum Recommended Daily Dose:  0.112
Skin Sensitization:  0.713
Carcinogencity:  0.666
Eye Corrosion:  0.99
Eye Irritation:  0.967
Respiratory Toxicity:  0.831

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

  Natural Product: NPC233950

Natural Product ID:  NPC233950
Common Name*:   SYQNUQSGEWNWKV-XUIVZRPNSA-N
IUPAC Name:   n.a.
Synonyms:  
Standard InCHIKey:  SYQNUQSGEWNWKV-XUIVZRPNSA-N
Standard InCHI:  InChI=1S/C11H14O2S/c1-5-7(2)6-11(4)9(12)8(3)10(13)14-11/h5-6,12H,1H2,2-4H3/b7-6+/t11-/m1/s1
SMILES:  C=C/C(=C/[C@]1(C)C(=C(C)C(=O)S1)O)/C
Synthetic Gene Cluster:   n.a.
ChEMBL Identifier:   n.a.
PubChem CID:   n.a.
Chemical Classification**:  
  • CHEMONTID:0000000 [Organic compounds]
    • [CHEMONTID:0000002] Organoheterocyclic compounds
      • [CHEMONTID:0002091] Dihydrothiophenes

*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
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. DOI[10.1016/j.scib.2021.03.002]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. DOI[10.1039/C8GC04066D]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[18485776]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[22938570]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[24603359]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[25769286]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[25981946]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[26032089]
NPO40894 0cardia spp. Species 0cardiaceae Bacteria n.a. n.a. n.a. PMID[27187871]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[28634125]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[28707470]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[29386648]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[29771352]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[30837474]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[31690080]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[32004707]
NPO41883 A new engineered strain of Saccharomyces cerevisiae [n.a.] Strain Saccharomycetaceae Eukaryota n.a. n.a. n.a. PMID[32006629]

☑ 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
NPT83 Cell Line MCF7 Homo sapiens IC50 = 38.4 ug.mL-1 PMID[15715465]
NPT83 Cell Line MCF7 Homo sapiens IC50 > 80.0 ug.mL-1 PMID[15715465]
NPT83 Cell Line MCF7 Homo sapiens IC50 = 41.8 ug.mL-1 PMID[15715465]
NPT2919 Individual Protein 3-oxoacyl-[acyl-carrier-protein] synthase 3 Escherichia coli K-12 Kd = 121000.0 nM PMID[19185501]
NPT886 Cell Line NIH3T3 Mus musculus Activity = 85.0 % PMID[22104972]
NPT49 Individual Protein DNA-(apurinic or apyrimidinic site) lyase Homo sapiens IC50 = 1000.0 nM PMID[28161249]
NPT2 Others Unspecified IC50 = 74900.0 nM PMID[14698162]
NPT88 Organism Mycobacterium tuberculosis Mycobacterium tuberculosis MIC = 25.0 ug.mL-1 PMID[10966749]
NPT865 Individual Protein Fatty acid synthase Homo sapiens IC50 = 21.1 ug.mL-1 PMID[15715465]
NPT865 Individual Protein Fatty acid synthase Homo sapiens IC50 = 30.0 ug.mL-1 PMID[15715465]
NPT19 Organism Escherichia coli Escherichia coli MIC = 6000.0 nM PMID[16392800]
NPT865 Individual Protein Fatty acid synthase Homo sapiens IC50 = 100000.0 nM PMID[16392800]
NPT15045 SINGLE PROTEIN 3-oxoacyl-[acyl-carrier-protein] synthase III Mycobacterium tuberculosis IC50 = 87000.0 nM PMID[16392800]
NPT15046 SINGLE PROTEIN 3-oxoacyl-[acyl-carrier-protein] synthase 2 Mycobacterium tuberculosis IC50 = 6000.0 nM PMID[16392800]
NPT15045 SINGLE PROTEIN 3-oxoacyl-[acyl-carrier-protein] synthase III Mycobacterium tuberculosis IC50 = 4000.0 nM PMID[16392800]
NPT88 Organism Mycobacterium tuberculosis Mycobacterium tuberculosis MIC = 62500.0 nM PMID[16392800]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 128.0 ug.mL-1 PMID[17507223]
NPT1121 Organism Moraxella catarrhalis Moraxella catarrhalis MIC = 0.25 ug.mL-1 PMID[17507223]
NPT1122 Organism Haemophilus influenzae Haemophilus influenzae MIC = 2.0 ug.mL-1 PMID[17507223]
NPT1092 Organism Bacteroides fragilis Bacteroides fragilis MIC = 1.0 ug.mL-1 PMID[17507223]
NPT2 Others Unspecified IC50 > 80.0 ug.mL-1 PMID[17507223]
NPT15045 SINGLE PROTEIN 3-oxoacyl-[acyl-carrier-protein] synthase III Mycobacterium tuberculosis IC50 = 75000.0 nM PMID[17766110]
NPT2 Others Unspecified IC50 > 330000.0 nM PMID[19191586]
NPT6 Organism Plasmodium falciparum Plasmodium falciparum IC50 = 50000.0 nM PMID[19191586]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 128.0 ug.mL-1 PMID[18805004]
NPT1121 Organism Moraxella catarrhalis Moraxella catarrhalis MIC = 0.25 ug.mL-1 PMID[18805004]
NPT1122 Organism Haemophilus influenzae Haemophilus influenzae MIC = 2.0 ug.mL-1 PMID[18805004]
NPT2 Others Unspecified IC50 > 0.08 ug.mL-1 PMID[18805004]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 64.0 ug.mL-1 PMID[16562839]
NPT175 Organism Enterococcus faecalis Enterococcus faecalis MIC > 250.0 ug.mL-1 PMID[16562839]
NPT1531 Organism Enterococcus faecium Enterococcus faecium MIC > 250.0 ug.mL-1 PMID[16562839]
NPT19 Organism Escherichia coli Escherichia coli MIC > 250.0 ug.mL-1 PMID[16562839]
NPT19 Organism Escherichia coli Escherichia coli MIC = 128.0 ug.mL-1 PMID[19185501]
NPT173 Organism Klebsiella pneumoniae Klebsiella pneumoniae MIC = 256.0 ug.mL-1 PMID[19185501]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 256.0 ug.mL-1 PMID[19185501]
NPT175 Organism Enterococcus faecalis Enterococcus faecalis MIC = 256.0 ug.mL-1 PMID[19185501]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 128.0 ug.mL-1 PMID[19185501]
NPT19 Organism Escherichia coli Escherichia coli MIC = 128000.0 nM PMID[19595597]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 256000.0 nM PMID[19595597]
NPT175 Organism Enterococcus faecalis Enterococcus faecalis MIC = 256000.0 nM PMID[19595597]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC = 128000.0 nM PMID[19595597]
NPT175 Organism Enterococcus faecalis Enterococcus faecalis MIC = 128000.0 nM PMID[19595597]
NPT6 Organism Plasmodium falciparum Plasmodium falciparum IC50 > 100000.0 nM PMID[20206517]
NPT2 Others Unspecified IC50 > 20000.0 nM PMID[20206517]
NPT6 Organism Plasmodium falciparum Plasmodium falciparum IC50 = 49000.0 nM PMID[20185316]
NPT6 Organism Plasmodium falciparum Plasmodium falciparum IC50 > 20000.0 nM PMID[21376591]
NPT2 Others Unspecified IC50 > 100000.0 nM PMID[21376591]
NPT790 Organism Mycobacterium tuberculosis H37Rv Mycobacterium tuberculosis H37Rv Inhibition = -3.8 % PMID[21376591]
NPT790 Organism Mycobacterium tuberculosis H37Rv Mycobacterium tuberculosis H37Rv Inhibition = 58.6 % PMID[21376591]
NPT790 Organism Mycobacterium tuberculosis H37Rv Mycobacterium tuberculosis H37Rv MIC > 128000.0 nM PMID[21376591]
NPT1531 Organism Enterococcus faecium Enterococcus faecium MIC = 128.0 ug.mL-1 PMID[22104972]
NPT2 Others Unspecified Kd = 55400.0 nM PMID[22104972]
NPT865 Individual Protein Fatty acid synthase Homo sapiens IC50 > 380000.0 nM PMID[21726077]
NPT15059 SINGLE PROTEIN Fatty acid synthase Rattus norvegicus IC50 > 951000.0 nM PMID[21726077]
NPT2 Others Unspecified IC50 = 1900.0 nM PMID[21726077]
NPT20529 NON-MOLECULAR NON-PROTEIN TARGET n.a. MIC = 12.5 ug.mL-1 PMID[27894872]
NPT2 Others Unspecified MIC90 = 2.8 ug.mL-1 PMID[27187871]
NPT88 Organism Mycobacterium tuberculosis Mycobacterium tuberculosis MIC90 = 3.1 ug.mL-1 PMID[27187871]
NPT2 Others Unspecified Ki = 175400.0 nM PMID[27187871]
NPT2 Others Unspecified Ki = 226000.0 nM PMID[27187871]
NPT2907 Organism Burkholderia pseudomallei Burkholderia pseudomallei MIC = 8.0 ug.mL-1 PMID[27187871]
NPT25741 SINGLE PROTEIN 3-oxoacyl-[acyl-carrier-protein] synthase 2 Staphylococcus aureus Kd = 88000.0 nM PMID[27187871]
NPT25741 SINGLE PROTEIN 3-oxoacyl-[acyl-carrier-protein] synthase 2 Staphylococcus aureus Kd = 107000.0 nM PMID[27187871]
NPT1206 Organism Yersinia pestis Yersinia pestis MIC90 = 8.0 ug.mL-1 PMID[27187871]
NPT16 Organism Staphylococcus aureus Staphylococcus aureus MIC90 = 75.0 ug.mL-1 PMID[27187871]
NPT88 Organism Mycobacterium tuberculosis Mycobacterium tuberculosis MIC = 25.0 ug.mL-1 PMID[31103404]
NPT27922 SINGLE PROTEIN 3-oxoacyl-[acyl-carrier-protein] synthase 1 Escherichia coli K-12 IC50 = 12000.0 nM PMID[16392800]

☑ 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 NPC233950 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 NPC233950 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