NPASS Compound

Structure

NPC242946 OpenBabel06302215212D 26 28 0 0 1 0 0 0 0 0999 V2000 -4.2821 -0.6812 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2821 0.3188 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -5.1482 0.8188 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1482 1.8188 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2821 2.3188 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.4312 3.3076 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7510 4.0407 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7538 3.9659 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1905 3.1397 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4852 2.1841 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4161 1.8188 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.4161 0.8188 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.5466 -0.1727 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4502 1.0776 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.7431 0.3705 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0019 -0.5954 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.7771 0.6293 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4188 1.5629 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5799 1.5106 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8387 0.5446 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0000 -0.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1163 4.9715 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4929 5.7534 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.1052 5.1206 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.4705 6.0515 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2849 2.3935 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2 1 1 6 0 0 0 2 3 1 0 0 0 0 2 12 1 0 0 0 0 3 4 1 0 0 0 0 4 5 1 0 0 0 0 5 11 1 0 0 0 0 5 6 1 0 0 0 0 5 26 1 1 0 0 0 6 7 1 0 0 0 0 7 8 2 0 0 0 0 7 22 1 0 0 0 0 8 9 1 0 0 0 0 9 10 1 0 0 0 0 11 10 1 6 0 0 0 11 12 1 0 0 0 0 12 13 1 6 0 0 0 12 14 1 0 0 0 0 14 15 1 0 0 0 0 15 16 2 0 0 0 0 15 17 1 0 0 0 0 17 21 2 0 0 0 0 17 18 1 0 0 0 0 18 19 2 0 0 0 0 19 20 1 0 0 0 0 20 21 1 0 0 0 0 22 23 2 0 0 0 0 22 24 1 0 0 0 0 24 25 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	360.19
Volume:	376.872
LogP:	3.322
LogD:	2.892
LogS:	-4.305
# Rotatable Bonds:	5
TPSA:	76.74
# H-Bond Aceptor:	5
# H-Bond Donor:	1
# Rings:	3
# Heavy Atoms:	5

MedChem Properties

QED Drug-Likeness Score:	0.65
Synthetic Accessibility Score:	4.384
Fsp3:	0.619
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:	-4.819
MDCK Permeability:	2.3740518372505903e-05
Pgp-inhibitor:	0.811
Pgp-substrate:	0.003
Human Intestinal Absorption (HIA):	0.013
20% Bioavailability (F20%):	0.171
30% Bioavailability (F30%):	0.851

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.323
Plasma Protein Binding (PPB):	89.3022232055664%
Volume Distribution (VD):	0.682
Pgp-substrate:	10.00302791595459%

ADMET: Metabolism

CYP1A2-inhibitor:	0.267
CYP1A2-substrate:	0.554
CYP2C19-inhibitor:	0.689
CYP2C19-substrate:	0.51
CYP2C9-inhibitor:	0.592
CYP2C9-substrate:	0.085
CYP2D6-inhibitor:	0.156
CYP2D6-substrate:	0.183
CYP3A4-inhibitor:	0.884
CYP3A4-substrate:	0.242

ADMET: Excretion

Clearance (CL):	12.099
Half-life (T1/2):	0.515

ADMET: Toxicity

hERG Blockers:	0.035
Human Hepatotoxicity (H-HT):	0.517
Drug-inuced Liver Injury (DILI):	0.109
AMES Toxicity:	0.009
Rat Oral Acute Toxicity:	0.728
Maximum Recommended Daily Dose:	0.757
Skin Sensitization:	0.438
Carcinogencity:	0.835
Eye Corrosion:	0.007
Eye Irritation:	0.042
Respiratory Toxicity:	0.971

Download Data

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

Natural Product: NPC242946

Natural Product ID:	NPC242946
*Common Name:**	GBCUXCIKPZPERP-PZQWHJIPSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	GBCUXCIKPZPERP-PZQWHJIPSA-N
Standard InCHI:	InChI=1S/C21H28O5/c1-14-7-9-21(24)11-15(19(23)25-3)5-4-6-18(21)20(14,2)12-17(22)16-8-10-26-13-16/h5,8,10,13-14,18,24H,4,6-7,9,11-12H2,1-3H3/t14-,18-,20+,21+/m1/s1
SMILES:	C[C@@H]1CC[C@@]2(CC(=CCC[C@@H]2[C@@]1(C)CC(=O)c1ccoc1)C(=O)OC)O
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	n.a.
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0004603] Organic oxygen compounds [CHEMONTID:0000323] Organooxygen compounds [CHEMONTID:0001831] Carbonyl compounds [CHEMONTID:0000118] Ketones [CHEMONTID:0003670] Aryl ketones [CHEMONTID:0003671] Aryl alkyl ketones

*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
NPO17682	Lamellodysidea chlorea	Species	Dysideidae	Eukaryota	n.a.	n.a.	n.a.	PMID[15332844]
NPO11403	Bussea sakalava	Species	Fabaceae	Eukaryota	n.a.	root	n.a.	PMID[20942441]
NPO22782	Lens culinaris	Species	Fabaceae	Eukaryota		n.a.	n.a.	Database[FooDB]
NPO22782	Lens culinaris	Species	Fabaceae	Eukaryota	Seed	n.a.	n.a.	Database[FooDB]
NPO22782	Lens culinaris	Species	Fabaceae	Eukaryota	Sprout Seedling	n.a.	n.a.	Database[FooDB]
NPO22782	Lens culinaris	Species	Fabaceae	Eukaryota	n.a.	n.a.		Database[FooDB]
NPO22782	Lens culinaris	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO22782	Lens culinaris	Species	Fabaceae	Eukaryota	Seeds	n.a.		Database[Phenol-Explorer]
NPO22782	Lens culinaris	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO18072	Coespeletia moritziana	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO11403	Bussea sakalava	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO6383	Lepisanthes tetraphylla	Species	Sapindaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO16922	Xenia viridis	Species	Xeniidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO15912	Cheimonophyllum candidissimum	Species	Tricholomataceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO1712	Tetragonotheca repanda	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO22782	Lens culinaris	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO11670	Stomozoa murrayi	n.a.	n.a.	n.a.	n.a.	n.a.	n.a.	Database[UNPD]
NPO17682	Lamellodysidea chlorea	Species	Dysideidae	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	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

☑ 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 NPC242946 and all remaining natural products in the NPASS database.
● The right table: Most similar natural products (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	289
0.1-0.2	1372
0.2-0.3	2990
0.3-0.4	6478
0.4-0.5	11935
0.5-0.6	8861
0.6-0.7	9005
0.7-0.8	1528
0.8-0.85	218
0.85-0.9	20
0.9-0.95	1
0.95-1	0

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 NPC242946 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	251
0.1-0.2	1032
0.2-0.3	1989
0.3-0.4	2609
0.4-0.5	2044
0.5-0.6	919
0.6-0.7	276
0.7-0.8	30
0.8-0.85	0
0.85-0.9	0
0.9-0.95	0
0.95-1	0

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