NPASS Compound

Structure

NPC130997 OpenBabel06302215572D 26 29 0 0 1 0 0 0 0 0999 V2000 0.4067 -3.5316 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9945 -2.7226 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 1.9456 -3.0316 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8966 -2.7226 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 3.4844 -1.9135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4355 -2.2226 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.4844 -0.9135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4626 -1.1215 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1536 -0.1704 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8966 -0.1045 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9456 0.2045 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9945 -0.1045 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.4067 -0.9135 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.4067 -1.9135 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.4593 -2.4135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3253 -1.9135 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.1913 -2.4135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2959 -3.4081 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2740 -3.6160 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7740 -2.7500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.1049 -2.0068 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3253 -0.9135 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.4593 -0.4135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4593 0.5865 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0000 -0.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.4844 -3.5316 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2 1 1 1 0 0 0 2 3 1 0 0 0 0 2 14 1 0 0 0 0 3 4 1 0 0 0 0 4 5 1 0 0 0 0 4 26 1 1 0 0 0 5 6 2 0 0 0 0 5 7 1 0 0 0 0 7 8 1 0 0 0 0 7 9 1 0 0 0 0 7 10 1 0 0 0 0 10 11 1 0 0 0 0 12 11 1 1 0 0 0 12 13 1 0 0 0 0 12 25 1 0 0 0 0 13 23 1 1 0 0 0 13 14 1 0 0 0 0 13 25 1 0 0 0 0 14 15 1 6 0 0 0 15 16 1 0 0 0 0 16 17 1 6 0 0 0 16 22 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 1 0 0 0 0 23 24 2 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	618.25
Volume:	621.478
LogP:	4.64
LogD:	3.426
LogS:	-4.664
# Rotatable Bonds:	10
TPSA:	130.87
# H-Bond Aceptor:	10
# H-Bond Donor:	0
# Rings:	6
# Heavy Atoms:	10

MedChem Properties

QED Drug-Likeness Score:	0.132
Synthetic Accessibility Score:	5.808
Fsp3:	0.486
Lipinski Rule-of-5:	Accepted
Pfizer Rule:	Accepted
GSK Rule:	Rejected
BMS Rule:	0
Golden Triangle Rule:	Rejected
Chelating Alert:	0
PAINS Alert:	0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:	-5.308
MDCK Permeability:	3.153256329824217e-05
Pgp-inhibitor:	0.986
Pgp-substrate:	0.001
Human Intestinal Absorption (HIA):	0.103
20% Bioavailability (F20%):	0.974
30% Bioavailability (F30%):	0.782

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.058
Plasma Protein Binding (PPB):	89.7499771118164%
Volume Distribution (VD):	2.024
Pgp-substrate:	8.484663963317871%

ADMET: Metabolism

CYP1A2-inhibitor:	0.049
CYP1A2-substrate:	0.071
CYP2C19-inhibitor:	0.829
CYP2C19-substrate:	0.091
CYP2C9-inhibitor:	0.932
CYP2C9-substrate:	0.017
CYP2D6-inhibitor:	0.861
CYP2D6-substrate:	0.053
CYP3A4-inhibitor:	0.947
CYP3A4-substrate:	0.636

ADMET: Excretion

Clearance (CL):	8.496
Half-life (T1/2):	0.644

ADMET: Toxicity

hERG Blockers:	0.355
Human Hepatotoxicity (H-HT):	0.901
Drug-inuced Liver Injury (DILI):	0.911
AMES Toxicity:	0.007
Rat Oral Acute Toxicity:	0.959
Maximum Recommended Daily Dose:	0.99
Skin Sensitization:	0.114
Carcinogencity:	0.048
Eye Corrosion:	0.003
Eye Irritation:	0.039
Respiratory Toxicity:	0.969

Download Data

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

Natural Product: NPC130997

Natural Product ID:	NPC130997
*Common Name:**	LPDOLIVBSRFDNT-OYGONXEOSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	LPDOLIVBSRFDNT-OYGONXEOSA-N
Standard InCHI:	InChI=1S/C20H26O6/c1-11-8-14(21)17(22)19(2,3)6-4-16-20(26-16)13(11)9-15(25-18(20)23)12-5-7-24-10-12/h5,7,10-11,13-16,21H,4,6,8-9H2,1-3H3/t11-,13+,14+,15-,16+,20+/m1/s1
SMILES:	C[C@@H]1C[C@@H](C(=O)C(C)(C)CC[C@H]2[C@]3([C@H]1C[C@H](c1ccoc1)OC3=O)O2)O
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	n.a.
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000002] Organoheterocyclic compounds [CHEMONTID:0000050] Lactones [CHEMONTID:0001244] Delta valerolactones

*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
NPO12285	Cassipourea guianensis	Species	Rhizophoraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[6387055]
NPO1153	Crotalaria madurensis	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO5747	Streptomyces rugosporus	Species	Streptomycetaceae	Bacteria	n.a.	n.a.	n.a.	Database[UNPD]
NPO15108	Angiopteris evecta	Species	Marattiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO1153	Crotalaria madurensis	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO12285	Cassipourea guianensis	Species	Rhizophoraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO11224	Byrsonima microphylla	Species	Malpighiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO9010	Lomatia silaifolia	Species	Proteaceae	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 NPC130997 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	319
0.1-0.2	1278
0.2-0.3	3251
0.3-0.4	6957
0.4-0.5	11778
0.5-0.6	9127
0.6-0.7	8580
0.7-0.8	1240
0.8-0.85	141
0.85-0.9	25
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 NPC130997 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	271
0.1-0.2	1025
0.2-0.3	2261
0.3-0.4	2655
0.4-0.5	1893
0.5-0.6	798
0.6-0.7	231
0.7-0.8	16
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