NPASS Compound

Structure

NPC165352 OpenBabel06302215112D 34 39 0 0 1 0 0 0 0 0999 V2000 -0.8215 2.3726 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3834 2.7334 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9769 2.4271 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0399 1.0930 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6333 0.7867 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.0679 0.0464 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -4.0679 -0.9584 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.6987 -1.4674 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9374 -1.9069 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9374 -3.1465 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1760 -1.4674 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4147 -1.9069 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6533 -1.4674 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6533 -0.5883 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4147 -0.1487 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1760 -0.5883 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9374 -0.1487 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.6987 -0.5883 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -5.3382 0.0464 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7483 0.7337 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -4.7283 1.8019 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1295 2.7397 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7483 1.8019 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3396 1.8019 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.3051 0.2051 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3220 -0.0667 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.2319 0.7112 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4896 1.9237 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4108 1.0943 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3576 0.8031 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.2622 1.8766 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 -1.4147 -3.1465 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.3520 3.4005 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 3 2 0 0 0 0 2 34 1 0 0 0 0 3 4 1 0 0 0 0 5 4 1 6 0 0 0 5 25 1 0 0 0 0 5 6 1 0 0 0 0 5 24 1 0 0 0 0 6 7 1 1 0 0 0 6 20 1 0 0 0 0 7 8 2 0 0 0 0 8 18 1 0 0 0 0 8 9 1 0 0 0 0 9 10 2 0 0 0 0 9 11 1 0 0 0 0 11 16 2 0 0 0 0 11 12 1 0 0 0 0 12 13 2 0 0 0 0 12 33 1 0 0 0 0 13 14 1 0 0 0 0 14 32 1 0 0 0 0 14 15 2 0 0 0 0 15 16 1 0 0 0 0 15 27 1 0 0 0 0 16 17 1 0 0 0 0 18 17 1 1 0 0 0 18 19 1 0 0 0 0 18 25 1 0 0 0 0 20 19 1 1 0 0 0 20 21 1 0 0 0 0 21 22 1 0 0 0 0 21 23 1 0 0 0 0 21 24 1 0 0 0 0 25 26 2 0 0 0 0 27 28 1 0 0 0 0 27 29 1 0 0 0 0 27 30 1 0 0 0 0 30 31 1 1 0 0 0 30 32 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	464.22
Volume:	475.791
LogP:	6.322
LogD:	4.213
LogS:	-5.703
# Rotatable Bonds:	2
TPSA:	82.06
# H-Bond Aceptor:	6
# H-Bond Donor:	1
# Rings:	7
# Heavy Atoms:	6

MedChem Properties

QED Drug-Likeness Score:	0.633
Synthetic Accessibility Score:	6.616
Fsp3:	0.571
Lipinski Rule-of-5:	Accepted
Pfizer Rule:	Accepted
GSK Rule:	Rejected
BMS Rule:	0
Golden Triangle Rule:	Accepted
Chelating Alert:	0
PAINS Alert:	0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:	-4.856
MDCK Permeability:	1.8977678337250836e-05
Pgp-inhibitor:	0.983
Pgp-substrate:	0.002
Human Intestinal Absorption (HIA):	0.032
20% Bioavailability (F20%):	0.004
30% Bioavailability (F30%):	0.541

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.23
Plasma Protein Binding (PPB):	97.41654205322266%
Volume Distribution (VD):	1.817
Pgp-substrate:	5.34619140625%

ADMET: Metabolism

CYP1A2-inhibitor:	0.172
CYP1A2-substrate:	0.756
CYP2C19-inhibitor:	0.788
CYP2C19-substrate:	0.862
CYP2C9-inhibitor:	0.894
CYP2C9-substrate:	0.459
CYP2D6-inhibitor:	0.638
CYP2D6-substrate:	0.228
CYP3A4-inhibitor:	0.771
CYP3A4-substrate:	0.914

ADMET: Excretion

Clearance (CL):	9.252
Half-life (T1/2):	0.205

ADMET: Toxicity

hERG Blockers:	0.458
Human Hepatotoxicity (H-HT):	0.912
Drug-inuced Liver Injury (DILI):	0.955
AMES Toxicity:	0.221
Rat Oral Acute Toxicity:	0.911
Maximum Recommended Daily Dose:	0.928
Skin Sensitization:	0.371
Carcinogencity:	0.891
Eye Corrosion:	0.003
Eye Irritation:	0.036
Respiratory Toxicity:	0.833

Download Data

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

Natural Product: NPC165352

Natural Product ID:	NPC165352
*Common Name:**	SSBHLVYWWRGJOH-BGLHXEQJSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	SSBHLVYWWRGJOH-BGLHXEQJSA-N
Standard InCHI:	InChI=1S/C28H32O6/c1-13(2)8-9-27-15-10-16-22(30)20-18(29)11-19-21(25(4,5)14(3)32-19)23(20)33-28(16,24(27)31)12-17(15)26(6,7)34-27/h8,10-11,14-15,17,29H,9,12H2,1-7H3/t14-,15+,17-,27-,28-/m1/s1
SMILES:	CC(=CC[C@@]12[C@H]3C=C4C(=O)c5c(cc6c(c5O[C@@]4(C[C@H]3C(C)(C)O2)C1=O)C(C)(C)[C@@H](C)O6)O)C
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	n.a.
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000002] Organoheterocyclic compounds [CHEMONTID:0000123] Benzopyrans [CHEMONTID:0003410] 1-benzopyrans [CHEMONTID:0002817] Dibenzopyrans [CHEMONTID:0000200] Xanthenes [CHEMONTID:0000204] Xanthones

*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
NPO19764	Tithonia diversifolia	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[11975495]
NPO24016	Cladanthus mixtus	Species	Asteraceae	Eukaryota	Roots	n.a.	n.a.	PMID[14738379]
NPO19764	Tithonia diversifolia	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[19299148]
NPO19764	Tithonia diversifolia	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[23501116]
NPO21003	Cystoseira tamariscifolia	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[25640118]
NPO20116	Ilex cornuta	Species	Aquifoliaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO20116	Ilex cornuta	Species	Aquifoliaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO19764	Tithonia diversifolia	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO20116	Ilex cornuta	Species	Aquifoliaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO20116	Ilex cornuta	Species	Aquifoliaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO21003	Cystoseira tamariscifolia	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO3338	Vatica obscura	Species	Dipterocarpaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO27328	Echinopsis candicans	Species	Cactaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO20927	Scirpophaga incertulas	Species	Crambidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO15534	Parablechnum procerum	Species	Blechnaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO19764	Tithonia diversifolia	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO20116	Ilex cornuta	Species	Aquifoliaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO24016	Cladanthus mixtus	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO16024	Piper sumatranum	Species	Piperaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO13990	Montanoa atriplicifolia	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO19000	Crepis crocea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO825	Stranvaesia davidiana	Species	Rosaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO9019	Asplenium antiquum	Species	Aspleniaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO21675	Persicaria sibirica	Species	Polygonaceae	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 NPC165352 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	420
0.1-0.2	1542
0.2-0.3	2953
0.3-0.4	6413
0.4-0.5	10908
0.5-0.6	6379
0.6-0.7	5788
0.7-0.8	7023
0.8-0.85	1137
0.85-0.9	101
0.9-0.95	25
0.95-1	8

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 NPC165352 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	355
0.1-0.2	907
0.2-0.3	1712
0.3-0.4	2616
0.4-0.5	2018
0.5-0.6	1032
0.6-0.7	355
0.7-0.8	150
0.8-0.85	5
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