NPASS Compound

Structure

NPC251551 OpenBabel06302215322D 86 95 0 0 1 0 0 0 0 0999 V2000 3.4280 2.9688 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5710 2.4740 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.5710 1.4844 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.7140 0.9896 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8570 1.4844 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8570 2.4740 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.7140 2.9688 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0000 2.9688 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0000 3.9583 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.8570 4.4531 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.8570 5.4427 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.0000 5.9375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8570 5.4427 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.8570 4.4531 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.7140 3.9583 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5710 4.4531 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.5710 5.4427 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4280 5.9375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2850 5.4427 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 4.2850 6.4323 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2850 4.4531 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 5.1420 3.9583 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9990 4.4531 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9990 5.4427 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 7.7130 4.4531 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1420 5.9375 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 5.1420 6.9271 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9990 7.4219 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.8560 6.9271 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.7130 7.4219 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 7.7130 8.4115 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.5700 8.9063 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.0648 9.7633 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.0753 9.7633 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.4270 8.4115 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.4270 7.4219 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.5700 6.9271 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 8.5700 5.9375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.7130 5.4427 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.8560 5.9375 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 6.8560 4.9479 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.4270 6.4323 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.4270 5.4427 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.2841 6.9271 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 11.1411 6.4323 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 11.9981 6.9271 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 12.8551 6.4323 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 12.8551 5.4427 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 11.9981 4.9479 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 11.9981 3.9583 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.8551 3.4635 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.8551 2.4740 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 13.7121 1.9792 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 13.7121 0.9896 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 12.8551 0.4948 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 11.9981 0.9896 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 11.1411 0.4948 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.1411 -0.4948 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 11.9981 1.9792 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.8551 -0.4948 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 14.5691 0.4948 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 14.5691 2.4740 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 11.1411 5.4427 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 13.7121 4.9479 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 13.7121 6.9271 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 11.9981 7.9167 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.4280 3.9583 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.9332 3.1013 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9228 3.1013 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9124 3.1013 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7140 5.9375 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7140 3.9583 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0000 0.9896 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7140 0.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.8570 -0.4948 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.8570 -1.4844 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.0000 -1.9792 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.8570 -1.4844 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8570 -0.4948 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.7140 -0.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.7140 0.9896 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 -1.7140 -1.9792 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0000 -2.9688 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7140 -1.9792 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.4280 0.9896 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 7 1 0 0 0 0 3 4 1 0 0 0 0 3 86 1 6 0 0 0 4 5 1 0 0 0 0 4 74 1 1 0 0 0 5 6 1 0 0 0 0 5 73 1 1 0 0 0 6 7 1 0 0 0 0 6 8 1 6 0 0 0 9 8 1 6 0 0 0 9 10 1 0 0 0 0 9 14 1 0 0 0 0 10 11 1 0 0 0 0 10 72 1 1 0 0 0 11 12 1 0 0 0 0 11 71 1 1 0 0 0 12 13 1 0 0 0 0 13 14 1 0 0 0 0 14 15 1 1 0 0 0 16 15 1 1 0 0 0 16 17 1 0 0 0 0 16 67 1 0 0 0 0 17 18 1 0 0 0 0 18 19 1 0 0 0 0 19 26 1 0 0 0 0 19 20 1 1 0 0 0 19 21 1 0 0 0 0 21 22 1 1 0 0 0 21 67 1 0 0 0 0 22 23 1 0 0 0 0 23 24 1 0 0 0 0 24 40 1 0 0 0 0 24 25 1 1 0 0 0 24 26 1 0 0 0 0 26 27 1 1 0 0 0 27 28 1 0 0 0 0 28 29 2 0 0 0 0 29 40 1 0 0 0 0 29 30 1 0 0 0 0 30 31 1 6 0 0 0 30 37 1 0 0 0 0 31 32 1 0 0 0 0 32 33 1 0 0 0 0 32 34 1 0 0 0 0 32 35 1 0 0 0 0 35 36 1 0 0 0 0 36 37 1 0 0 0 0 37 38 1 0 0 0 0 37 42 1 1 0 0 0 38 39 1 0 0 0 0 39 40 1 0 0 0 0 40 41 1 6 0 0 0 42 43 2 0 0 0 0 42 44 1 0 0 0 0 44 45 1 0 0 0 0 45 63 1 0 0 0 0 45 46 1 0 0 0 0 46 47 1 0 0 0 0 46 66 1 6 0 0 0 47 48 1 0 0 0 0 47 65 1 1 0 0 0 48 49 1 0 0 0 0 48 64 1 6 0 0 0 49 50 1 1 0 0 0 49 63 1 0 0 0 0 50 51 1 0 0 0 0 52 51 1 1 0 0 0 52 53 1 0 0 0 0 52 59 1 0 0 0 0 53 54 1 0 0 0 0 53 62 1 6 0 0 0 54 55 1 0 0 0 0 54 61 1 1 0 0 0 55 56 1 0 0 0 0 55 60 1 6 0 0 0 56 57 1 1 0 0 0 56 59 1 0 0 0 0 57 58 1 0 0 0 0 67 68 1 1 0 0 0 67 69 1 0 0 0 0 69 70 1 0 0 0 0 75 74 1 1 0 0 0 75 76 1 0 0 0 0 75 82 1 0 0 0 0 76 77 1 0 0 0 0 76 85 1 6 0 0 0 77 78 1 0 0 0 0 77 84 1 1 0 0 0 78 79 1 0 0 0 0 78 83 1 6 0 0 0 79 80 1 1 0 0 0 79 82 1 0 0 0 0 80 81 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	1236.61
Volume:	1175.518
LogP:	1.227
LogD:	1.138
LogS:	-2.899
# Rotatable Bonds:	15
TPSA:	433.05
# H-Bond Aceptor:	27
# H-Bond Donor:	16
# Rings:	10
# Heavy Atoms:	27

MedChem Properties

QED Drug-Likeness Score:	0.045
Synthetic Accessibility Score:	7.28
Fsp3:	0.949
Lipinski Rule-of-5:	Rejected
Pfizer Rule:	Accepted
GSK Rule:	Rejected
BMS Rule:	1
Golden Triangle Rule:	Rejected
Chelating Alert:	0
PAINS Alert:	0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:	-6.376
MDCK Permeability:	0.00017551440396346152
Pgp-inhibitor:	0.488
Pgp-substrate:	0.157
Human Intestinal Absorption (HIA):	1.0
20% Bioavailability (F20%):	0.753
30% Bioavailability (F30%):	1.0

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.119
Plasma Protein Binding (PPB):	53.96519470214844%
Volume Distribution (VD):	-0.186
Pgp-substrate:	17.119443893432617%

ADMET: Metabolism

CYP1A2-inhibitor:	0.0
CYP1A2-substrate:	0.226
CYP2C19-inhibitor:	0.0
CYP2C19-substrate:	0.064
CYP2C9-inhibitor:	0.0
CYP2C9-substrate:	0.001
CYP2D6-inhibitor:	0.0
CYP2D6-substrate:	0.03
CYP3A4-inhibitor:	0.044
CYP3A4-substrate:	0.002

ADMET: Excretion

Clearance (CL):	-0.356
Half-life (T1/2):	0.829

ADMET: Toxicity

hERG Blockers:	0.219
Human Hepatotoxicity (H-HT):	0.121
Drug-inuced Liver Injury (DILI):	0.008
AMES Toxicity:	0.061
Rat Oral Acute Toxicity:	0.053
Maximum Recommended Daily Dose:	0.007
Skin Sensitization:	0.023
Carcinogencity:	0.019
Eye Corrosion:	0.003
Eye Irritation:	0.006
Respiratory Toxicity:	0.063

Download Data

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

Natural Product: NPC251551

Natural Product ID:	NPC251551
*Common Name:**	VUEGHZSQVJADCO-LKMNSLIASA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	VUEGHZSQVJADCO-LKMNSLIASA-N
Standard InCHI:	InChI=1S/C59H96O27/c1-24-34(64)46(84-49-43(73)40(70)37(67)29(20-61)81-49)45(75)51(79-24)85-47-35(65)27(63)21-77-52(47)83-33-11-12-55(4)31(56(33,5)23-62)10-13-58(7)32(55)9-8-25-26-18-54(2,3)14-16-59(26,17-15-57(25,58)6)53(76)86-50-44(74)41(71)38(68)30(82-50)22-78-48-42(72)39(69)36(66)28(19-60)80-48/h8,24,26-52,60-75H,9-23H2,1-7H3/t24-,26-,27-,28+,29+,30+,31+,32+,33-,34-,35-,36+,37+,38+,39-,40-,41-,42+,43+,44+,45+,46+,47+,48+,49-,50?,51-,52-,55-,56-,57+,58+,59-/m0/s1
SMILES:	C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]1[C@H]([C@H](CO[C@H]1O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC=C2[C@@H]4CC(C)(C)CC[C@@]4(CC[C@@]32C)C(=O)OC2[C@@H]([C@H]([C@@H]([C@@H](CO[C@H]3[C@@H]([C@H]([C@@H]([C@@H](CO)O3)O)O)O)O2)O)O)O)[C@]1(C)CO)O)O)O)O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)O)O
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	118705383
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0002049] Terpene glycosides [CHEMONTID:0001580] Triterpene glycosides [CHEMONTID:0002358] Triterpene saponins

*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

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Organism ID	Organism Name	Taxonomy Level	Family	SuperKingdom	Isolation Part	Collection Location	Collection Time	Reference
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	Flower buds	n.a.	n.a.	PMID[24279769]
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	n.a.	leaf	n.a.	PMID[23265495]
NPO17072	Lonicera macranthoides	Species	Caprifoliaceae	Eukaryota	n.a.	flower bud	n.a.	PMID[22822669]
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	flower buds	Henan province, China	2005-MAY	PMID[21942812]
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	n.a.	flower bud	n.a.	PMID[21942812]
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	n.a.	flower	n.a.	PMID[21804227]
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	Flower buds	n.a.	n.a.	PMID[18321056]
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	Flowers	n.a.	n.a.	PMID[17328234]
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	Flowers	n.a.	n.a.	PMID[11077184]
NPO1515	Lonicera japonica	Species	Caprifoliaceae	Eukaryota	Flowers	n.a.	n.a.	DOI[10.1016/j.foodchem.2012.02.124]

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☑ 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

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Organism ID	NP ID	Organism Material Preparation	Organism Part	NP Quantity (Standard)	NP Quantity (Minimum)	NP Quantity (Maximum)	Quantity Unit	Reference
No data available in table

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☑ 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

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Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference
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☑ 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 NPC251551 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	261
0.1-0.2	1737
0.2-0.3	5108
0.3-0.4	11934
0.4-0.5	10269
0.5-0.6	6164
0.6-0.7	3984
0.7-0.8	1930
0.8-0.85	607
0.85-0.9	291
0.9-0.95	169
0.95-1	243

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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 NPC251551 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	241
0.1-0.2	2042
0.2-0.3	3876
0.3-0.4	1952
0.4-0.5	598
0.5-0.6	266
0.6-0.7	142
0.7-0.8	21
0.8-0.85	8
0.85-0.9	3
0.9-0.95	1
0.95-1	0

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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