NPASS Compound

Structure

NPC248549 OpenBabel06302216012D 28 31 0 0 1 0 0 0 0 0999 V2000 -3.2805 3.9911 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3065 3.9914 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.8198 4.8350 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.8193 3.1480 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3061 2.3043 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.8188 1.4610 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8448 1.4613 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.3581 2.3049 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8445 0.4873 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.6876 -0.0005 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6873 -0.9749 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0003 -0.9744 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.8448 -1.4617 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.8451 -2.4366 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6896 -2.9239 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5339 -2.4362 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 3.3779 -2.9234 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2215 -2.4357 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0878 -2.9353 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.2212 -1.4607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3773 -0.9734 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5336 -1.4612 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.5333 -0.4612 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6891 -0.9739 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6888 0.0005 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8443 0.4877 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0000 -0.0000 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.0003 1.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 3 1 0 0 0 0 2 4 1 0 0 0 0 4 5 1 0 0 0 0 5 6 2 0 0 0 0 6 7 1 0 0 0 0 7 8 1 6 0 0 0 9 7 1 6 0 0 0 9 10 1 0 0 0 0 9 27 1 0 0 0 0 10 11 1 0 0 0 0 12 11 1 6 0 0 0 12 13 1 0 0 0 0 12 27 1 0 0 0 0 13 14 1 1 0 0 0 13 24 1 0 0 0 0 14 15 1 0 0 0 0 16 15 1 6 0 0 0 16 17 1 0 0 0 0 16 22 1 0 0 0 0 17 18 1 0 0 0 0 18 19 2 0 0 0 0 18 20 1 0 0 0 0 20 21 1 0 0 0 0 21 22 1 0 0 0 0 22 23 1 6 0 0 0 22 24 1 0 0 0 0 24 25 1 6 0 0 0 25 26 1 0 0 0 0 26 27 1 0 0 0 0 27 28 1 6 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	384.34
Volume:	444.84
LogP:	7.289
LogD:	6.44
LogS:	-6.415
# Rotatable Bonds:	4
TPSA:	17.07
# H-Bond Aceptor:	1
# H-Bond Donor:	0
# Rings:	4
# Heavy Atoms:	1

MedChem Properties

QED Drug-Likeness Score:	0.46
Synthetic Accessibility Score:	4.391
Fsp3:	0.889
Lipinski Rule-of-5:	Accepted
Pfizer Rule:	Rejected
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:	-4.662
MDCK Permeability:	1.3270014278532472e-05
Pgp-inhibitor:	0.983
Pgp-substrate:	0.017
Human Intestinal Absorption (HIA):	0.009
20% Bioavailability (F20%):	0.98
30% Bioavailability (F30%):	0.985

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.464
Plasma Protein Binding (PPB):	94.67638397216797%
Volume Distribution (VD):	1.358
Pgp-substrate:	1.565835952758789%

ADMET: Metabolism

CYP1A2-inhibitor:	0.168
CYP1A2-substrate:	0.281
CYP2C19-inhibitor:	0.208
CYP2C19-substrate:	0.836
CYP2C9-inhibitor:	0.446
CYP2C9-substrate:	0.214
CYP2D6-inhibitor:	0.067
CYP2D6-substrate:	0.423
CYP3A4-inhibitor:	0.618
CYP3A4-substrate:	0.358

ADMET: Excretion

Clearance (CL):	5.654
Half-life (T1/2):	0.23

ADMET: Toxicity

hERG Blockers:	0.962
Human Hepatotoxicity (H-HT):	0.413
Drug-inuced Liver Injury (DILI):	0.798
AMES Toxicity:	0.008
Rat Oral Acute Toxicity:	0.156
Maximum Recommended Daily Dose:	0.843
Skin Sensitization:	0.952
Carcinogencity:	0.243
Eye Corrosion:	0.624
Eye Irritation:	0.643
Respiratory Toxicity:	0.971

Download Data

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

Natural Product: NPC248549

Natural Product ID:	NPC248549
*Common Name:**	UPYVDXJUKQUZDF-XEIIVKPRSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	UPYVDXJUKQUZDF-XEIIVKPRSA-N
Standard InCHI:	InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h6,8,18-20,22-25H,7,9-17H2,1-5H3/b8-6+/t19-,20-,22-,23+,24-,25-,26-,27+/m0/s1
SMILES:	CC(C)C/C=C/[C@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	n.a.
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000258] Steroids and steroid derivatives [CHEMONTID:0003566] Cholestane steroids [CHEMONTID:0001469] Cholesterols and derivatives

*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
NPO9918	Methylococcus capsulatus	Species	Methylococcaceae	Bacteria	n.a.	n.a.	n.a.	PMID[22826256]
NPO10992	Cystobacter fuscus	Species	Archangiaceae	Bacteria	n.a.	n.a.	n.a.	PMID[9589062]
NPO6472	Elsholtzia densa	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO2232	Licania pyrifolia	Species	Chrysobalanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO5488	Herniaria glabra	Species	Caryophyllaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO8959	Lippia helleri	Species	Verbenaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO1636	Glochidion hohenackeri	Species	Phyllanthaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO8765	Lemna paucicostata	Species	Araceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO4310	Garuleum pinnatifidum	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO10992	Cystobacter fuscus	Species	Archangiaceae	Bacteria	n.a.	n.a.	n.a.	Database[UNPD]
NPO9764	Artemisina apollinis	Species	Microcionidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO9568	Teichaxinella morchella	n.a.	n.a.	n.a.	n.a.	n.a.	n.a.	Database[UNPD]
NPO9918	Methylococcus capsulatus	Species	Methylococcaceae	Bacteria	n.a.	n.a.	n.a.	Database[UNPD]
NPO5875	Populus euphratica	Species	Salicaceae	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 NPC248549 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	186
0.1-0.2	2200
0.2-0.3	15089
0.3-0.4	11126
0.4-0.5	6891
0.5-0.6	4979
0.6-0.7	1892
0.7-0.8	271
0.8-0.85	32
0.85-0.9	21
0.9-0.95	9
0.95-1	1

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 NPC248549 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	183
0.1-0.2	2233
0.2-0.3	4686
0.3-0.4	1390
0.4-0.5	325
0.5-0.6	146
0.6-0.7	141
0.7-0.8	39
0.8-0.85	4
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