NPASS Compound

Structure

NPC220170 OpenBabel06302215592D 50 56 0 0 1 0 0 0 0 0999 V2000 0.0171 -3.9216 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0128 -2.9372 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8586 -2.4440 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8543 -1.4649 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7046 -0.9690 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5592 -1.4575 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7003 0.0153 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5506 0.5112 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4052 0.0227 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2555 0.5186 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1101 0.0302 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1144 -0.9542 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2641 -1.4500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4095 -0.9616 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0043 -0.9791 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8415 -1.4723 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8372 -2.4514 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6875 -2.9473 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.6915 -0.9865 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.6958 -0.0074 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.5525 0.4872 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.5597 1.4714 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4104 1.9556 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4159 2.9386 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2647 2.4419 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2566 1.4612 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.2623 0.4767 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3988 -0.0072 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3984 -1.0021 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2497 -1.4994 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2468 -2.4825 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0954 -1.0120 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1136 -0.0207 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9732 0.4622 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.3441 1.3757 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.5788 -0.3158 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.5553 -0.1803 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.9263 0.7332 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.9029 0.8687 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.2738 1.7822 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.6682 2.5601 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.6916 2.4247 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.3207 1.5112 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9425 -1.5119 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.5378 -1.4809 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8500 0.4858 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3616 1.3404 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3459 1.3361 0.0000 C 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 1.7132 -2.9324 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 17 2 0 0 0 0 2 3 1 0 0 0 0 3 4 2 0 0 0 0 3 50 1 0 0 0 0 4 5 1 0 0 0 0 4 15 1 0 0 0 0 5 6 2 0 0 0 0 5 7 1 0 0 0 0 7 8 2 0 0 0 0 8 9 1 0 0 0 0 9 14 2 0 0 0 0 9 10 1 0 0 0 0 10 11 2 0 0 0 0 11 12 1 0 0 0 0 12 13 2 0 0 0 0 13 14 1 0 0 0 0 15 49 1 0 0 0 0 15 16 2 0 0 0 0 16 17 1 0 0 0 0 17 18 1 0 0 0 0 19 16 1 6 0 0 0 19 20 1 0 0 0 0 19 45 1 0 0 0 0 20 21 1 0 0 0 0 20 46 1 6 0 0 0 21 22 1 1 0 0 0 21 28 1 0 0 0 0 22 23 1 0 0 0 0 23 24 1 0 0 0 0 23 25 1 0 0 0 0 23 26 1 0 0 0 0 26 27 1 0 0 0 0 27 33 2 0 0 0 0 27 28 1 0 0 0 0 28 29 2 0 0 0 0 29 30 1 0 0 0 0 29 45 1 0 0 0 0 30 31 1 0 0 0 0 30 32 2 0 0 0 0 32 33 1 0 0 0 0 32 44 1 0 0 0 0 33 34 1 0 0 0 0 34 35 2 0 0 0 0 34 36 1 0 0 0 0 36 37 2 0 0 0 0 37 38 1 0 0 0 0 38 43 2 0 0 0 0 38 39 1 0 0 0 0 39 40 2 0 0 0 0 40 41 1 0 0 0 0 41 42 2 0 0 0 0 42 43 1 0 0 0 0 46 47 1 0 0 0 0 46 48 1 0 0 0 0 46 49 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	672.27
Volume:	703.231
LogP:	8.926
LogD:	4.276
LogS:	-2.213
# Rotatable Bonds:	6
TPSA:	122.52
# H-Bond Aceptor:	8
# H-Bond Donor:	3
# Rings:	7
# Heavy Atoms:	8

MedChem Properties

QED Drug-Likeness Score:	0.137
Synthetic Accessibility Score:	4.604
Fsp3:	0.286
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:	-5.154
MDCK Permeability:	9.517508260614704e-06
Pgp-inhibitor:	0.998
Pgp-substrate:	0.006
Human Intestinal Absorption (HIA):	0.018
20% Bioavailability (F20%):	0.002
30% Bioavailability (F30%):	0.001

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.0
Plasma Protein Binding (PPB):	111.85157012939453%
Volume Distribution (VD):	0.294
Pgp-substrate:	0.25801074504852295%

ADMET: Metabolism

CYP1A2-inhibitor:	0.059
CYP1A2-substrate:	0.137
CYP2C19-inhibitor:	0.798
CYP2C19-substrate:	0.096
CYP2C9-inhibitor:	0.857
CYP2C9-substrate:	0.987
CYP2D6-inhibitor:	0.077
CYP2D6-substrate:	0.146
CYP3A4-inhibitor:	0.153
CYP3A4-substrate:	0.677

ADMET: Excretion

Clearance (CL):	1.074
Half-life (T1/2):	0.012

ADMET: Toxicity

hERG Blockers:	0.019
Human Hepatotoxicity (H-HT):	0.749
Drug-inuced Liver Injury (DILI):	0.938
AMES Toxicity:	0.044
Rat Oral Acute Toxicity:	0.953
Maximum Recommended Daily Dose:	0.826
Skin Sensitization:	0.916
Carcinogencity:	0.449
Eye Corrosion:	0.003
Eye Irritation:	0.756
Respiratory Toxicity:	0.175

Download Data

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

Natural Product: NPC220170

Natural Product ID:	NPC220170
*Common Name:**	RPVZMUGANNMZGT-OZVLZUDLSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	RPVZMUGANNMZGT-OZVLZUDLSA-N
Standard InCHI:	InChI=1S/C42H40O8/c1-22-34(45)30(27(43)19-17-24-13-9-7-10-14-24)39-32(35(22)46)40-33(42(5,6)50-39)26-21-41(3,4)49-38-29(26)37(48-40)23(2)36(47)31(38)28(44)20-18-25-15-11-8-12-16-25/h7-20,26,33,40,45-47H,21H2,1-6H3/b19-17+,20-18+/t26-,33+,40+/m1/s1
SMILES:	Cc1c(c(C(=O)/C=C/c2ccccc2)c2c(c1O)[C@H]1[C@H]([C@@H]3CC(C)(C)Oc4c3c(c(C)c(c4C(=O)/C=C/c3ccccc3)O)O1)C(C)(C)O2)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:0003467] Linear 1,3-diarylpropanoids [CHEMONTID:0001630] Chalcones and dihydrochalcones [CHEMONTID:0003472] 2'-Hydroxychalcones

*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
NPO28717	Miconia myriantha	Species	Melastomataceae	Eukaryota	n.a.	n.a.	n.a.	PMID[11678651]
NPO29365	Baileya multiradiata	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO29331	Pyrrosia sheareri	Species	Polypodiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO28899	Eupatorium hyssopifolium	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO29049	Sinoadina racemosa	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO29331	Pyrrosia sheareri	Species	Polypodiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO29365	Baileya multiradiata	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO28899	Eupatorium hyssopifolium	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO29049	Sinoadina racemosa	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO29331	Pyrrosia sheareri	Species	Polypodiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO29365	Baileya multiradiata	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO29331	Pyrrosia sheareri	Species	Polypodiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO29444	Erigeron linifolius	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO29259	Streptomyces toyocaensis	Species	Streptomycetaceae	Bacteria	n.a.	n.a.	n.a.	Database[UNPD]
NPO27663	Onoseris lopezii	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO29049	Sinoadina racemosa	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO29331	Pyrrosia sheareri	Species	Polypodiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO28806	Populus grandidentata	Species	Salicaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO28717	Miconia myriantha	Species	Melastomataceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO28899	Eupatorium hyssopifolium	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO28884	Cladonia cryptochlorophaea	Species	Cladoniaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO29365	Baileya multiradiata	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO29204	Picea breweriana	Species	Pinaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO29345	Maytenus horrida	Species	Celastraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO29467	Virola elongata	Species	Myristicaceae	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 NPC220170 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	405
0.1-0.2	1469
0.2-0.3	3173
0.3-0.4	8358
0.4-0.5	10712
0.5-0.6	3807
0.6-0.7	6040
0.7-0.8	5548
0.8-0.85	2052
0.85-0.9	814
0.9-0.95	293
0.95-1	26

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 NPC220170 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	349
0.1-0.2	948
0.2-0.3	1496
0.3-0.4	2607
0.4-0.5	2034
0.5-0.6	1110
0.6-0.7	415
0.7-0.8	152
0.8-0.85	24
0.85-0.9	12
0.9-0.95	3
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