NPASS Compound

Structure

NPC134542 OpenBabel06302216172D 44 49 0 0 1 0 0 0 0 0999 V2000 4.2435 0.4900 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2435 1.4700 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0922 1.9600 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9409 1.4700 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9409 0.4900 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0922 -0.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0922 -0.9800 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.7896 -0.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.7896 1.9600 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.3948 1.9600 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 2.5461 1.4700 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6974 1.9600 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 1.6974 2.9400 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8487 3.4300 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8487 4.4100 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6974 4.9000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5461 4.4100 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5461 3.4300 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3948 2.9400 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.6974 5.8800 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0000 2.9400 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0000 0.9800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8487 1.4700 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6974 0.9800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6974 0.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8487 -0.4900 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8487 -1.4700 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0000 -1.9600 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8487 -1.4700 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6974 -1.9600 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6974 -2.9400 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5461 -3.4300 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3948 -2.9400 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3948 -1.9600 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5461 -1.4700 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5461 -0.4900 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.2435 -3.4300 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5461 -4.4100 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.8487 -0.4900 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 -0.0000 -2.9400 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.5461 -0.4900 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8487 2.4500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5461 0.4900 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1 6 2 0 0 0 0 1 2 1 0 0 0 0 2 3 2 0 0 0 0 3 4 1 0 0 0 0 4 5 2 0 0 0 0 4 9 1 0 0 0 0 5 6 1 0 0 0 0 5 8 1 0 0 0 0 6 7 1 0 0 0 0 10 2 1 6 0 0 0 10 11 1 0 0 0 0 10 19 1 0 0 0 0 11 12 1 0 0 0 0 11 44 1 6 0 0 0 12 13 1 0 0 0 0 12 22 1 1 0 0 0 13 18 2 0 0 0 0 13 14 1 0 0 0 0 14 15 2 0 0 0 0 14 21 1 0 0 0 0 15 16 1 0 0 0 0 16 17 2 0 0 0 0 16 20 1 0 0 0 0 17 18 1 0 0 0 0 18 19 1 0 0 0 0 22 40 2 0 0 0 0 22 23 1 0 0 0 0 23 24 2 0 0 0 0 23 43 1 0 0 0 0 24 25 1 0 0 0 0 25 26 2 0 0 0 0 25 42 1 0 0 0 0 26 40 1 0 0 0 0 26 27 1 0 0 0 0 27 28 1 0 0 0 0 28 29 1 0 0 0 0 28 41 1 6 0 0 0 29 30 1 6 0 0 0 29 39 1 0 0 0 0 30 35 2 0 0 0 0 30 31 1 0 0 0 0 31 32 2 0 0 0 0 32 33 1 0 0 0 0 32 38 1 0 0 0 0 33 34 2 0 0 0 0 33 37 1 0 0 0 0 34 35 1 0 0 0 0 35 36 1 0 0 0 0 39 40 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	1137.49
Volume:	1117.154
LogP:	1.264
LogD:	1.344
LogS:	-1.262
# Rotatable Bonds:	22
TPSA:	349.43
# H-Bond Aceptor:	24
# H-Bond Donor:	9
# Rings:	5
# Heavy Atoms:	25

MedChem Properties

QED Drug-Likeness Score:	0.058
Synthetic Accessibility Score:	7.357
Fsp3:	0.527
Lipinski Rule-of-5:	Rejected
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:	-6.473
MDCK Permeability:	8.108050678856671e-06
Pgp-inhibitor:	0.426
Pgp-substrate:	0.998
Human Intestinal Absorption (HIA):	0.99
20% Bioavailability (F20%):	0.998
30% Bioavailability (F30%):	1.0

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.021
Plasma Protein Binding (PPB):	88.4955062866211%
Volume Distribution (VD):	0.547
Pgp-substrate:	1.7643709182739258%

ADMET: Metabolism

CYP1A2-inhibitor:	0.0
CYP1A2-substrate:	0.005
CYP2C19-inhibitor:	0.042
CYP2C19-substrate:	0.033
CYP2C9-inhibitor:	0.095
CYP2C9-substrate:	0.241
CYP2D6-inhibitor:	0.036
CYP2D6-substrate:	0.09
CYP3A4-inhibitor:	0.093
CYP3A4-substrate:	0.008

ADMET: Excretion

Clearance (CL):	1.692
Half-life (T1/2):	0.378

ADMET: Toxicity

hERG Blockers:	0.164
Human Hepatotoxicity (H-HT):	0.986
Drug-inuced Liver Injury (DILI):	0.966
AMES Toxicity:	0.01
Rat Oral Acute Toxicity:	0.554
Maximum Recommended Daily Dose:	0.977
Skin Sensitization:	0.291
Carcinogencity:	0.157
Eye Corrosion:	0.003
Eye Irritation:	0.004
Respiratory Toxicity:	0.841

Download Data

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

Natural Product: NPC134542

Natural Product ID:	NPC134542
*Common Name:**	LJEHGUMLAXBRJI-GYPOYYOSSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	LJEHGUMLAXBRJI-GYPOYYOSSA-N
Standard InCHI:	InChI=1S/C30H26O14/c31-10-3-17(36)23-22(4-10)43-28(9-1-19(38)26(41)20(39)2-9)27(42)25(23)24-18(37)8-14(33)12-6-21(40)29(44-30(12)24)11-5-15(34)16(35)7-13(11)32/h1-5,7-8,21,25,27-29,31-42H,6H2/t21-,25-,27-,28-,29-/m1/s1
SMILES:	c1c(cc(c(c1O)O)O)[C@@H]1[C@@H]([C@H](c2c(cc(cc2O1)O)O)c1c(cc(c2C[C@H]([C@@H](c3cc(c(cc3O)O)O)Oc12)O)O)O)O
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	n.a.
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000261] Phenylpropanoids and polyketides [CHEMONTID:0000334] Flavonoids [CHEMONTID:0001586] Biflavonoids and polyflavonoids

*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
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	Leaves	n.a.	n.a.	PMID[12088434]
NPO22423	Microtropis fokienensis	Species	Celastraceae	Eukaryota	stem	n.a.	n.a.	PMID[16643054]
NPO22423	Microtropis fokienensis	Species	Celastraceae	Eukaryota	leaves	n.a.	n.a.	PMID[17125218]
NPO22423	Microtropis fokienensis	Species	Celastraceae	Eukaryota	n.a.	root	n.a.	PMID[17315960]
NPO22423	Microtropis fokienensis	Species	Celastraceae	Eukaryota	roots	n.a.	n.a.	PMID[17315960]
NPO22423	Microtropis fokienensis	Species	Celastraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[18590313]
NPO22791	Astraeus pteridis	Species	Astraeaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[19067555]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[21707257]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	Plant	n.a.	n.a.	Database[FooDB]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	Shoot	n.a.	n.a.	Database[FooDB]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota		n.a.	n.a.	Database[FooDB]
NPO4594	Vitellaria paradoxa	Species	Sapotaceae	Eukaryota		n.a.	n.a.	Database[FooDB]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	n.a.	n.a.		Database[FooDB]
NPO4594	Vitellaria paradoxa	Species	Sapotaceae	Eukaryota	n.a.	n.a.		Database[FooDB]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	Essential Oil	n.a.	n.a.	Database[FooDB]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	Leaf	n.a.	n.a.	Database[FooDB]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO5054	Limonium gmelinii	Species	Plumbaginaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	n.a.	n.a.		Database[Phenol-Explorer]
NPO5054	Limonium gmelinii	Species	Plumbaginaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO5054	Limonium gmelinii	Species	Plumbaginaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO19472	Thymus vulgaris	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO4594	Vitellaria paradoxa	Species	Sapotaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO23879	Serratula inermis	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO23954	Tridachia crispata	n.a.	n.a.	n.a.	n.a.	n.a.	n.a.	Database[UNPD]
NPO24327	Machilus macrantha	Species	Lauraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO21956	Alyxia reinwardtii	Species	Apocynaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO22791	Astraeus pteridis	Species	Astraeaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO23494	Centaurea linifolia	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO5054	Limonium gmelinii	Species	Plumbaginaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO25848	Oscillochloris trichoides	Species	Oscillochloridaceae	Bacteria	n.a.	n.a.	n.a.	Database[UNPD]
NPO22423	Microtropis fokienensis	Species	Celastraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO20604	Cneoridium dumosum	Species	Rutaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO19472	Thymus vulgaris	Species	Lamiaceae	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 NPC134542 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	548
0.1-0.2	1856
0.2-0.3	5101
0.3-0.4	11716
0.4-0.5	6164
0.5-0.6	4411
0.6-0.7	6528
0.7-0.8	5105
0.8-0.85	820
0.85-0.9	357
0.9-0.95	67
0.95-1	24

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 NPC134542 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	450
0.1-0.2	924
0.2-0.3	2112
0.3-0.4	2724
0.4-0.5	1478
0.5-0.6	863
0.6-0.7	506
0.7-0.8	83
0.8-0.85	7
0.85-0.9	3
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