NPASS Compound

Structure

NPC275315 OpenBabel06302215182D 33 38 0 0 1 0 0 0 0 0999 V2000 1.5068 -0.8699 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5023 -0.8699 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.0000 -1.7399 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0045 -1.7399 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5068 -0.8699 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.0760 -1.6533 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.7655 -2.6087 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9969 -1.3541 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.9969 -0.3858 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.8356 0.0991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6753 -1.3534 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -5.5151 -1.8376 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -6.3542 -1.3525 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.1940 -1.8367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.1946 -2.8060 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -8.0341 -3.2897 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.0344 -4.2586 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -7.1952 -4.7437 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -6.3557 -4.2600 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -6.3554 -3.2912 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -5.4897 -3.7917 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.5157 -2.8070 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -4.6770 -3.2919 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.8372 -2.8077 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.8367 -1.8383 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.9709 -2.3388 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4900 -4.7605 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.1959 -5.7437 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.9006 -4.7582 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.0603 -2.3055 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.0760 -0.0865 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0045 0.0000 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 1 2 1 0 0 0 0 2 3 1 0 0 0 0 2 33 1 0 0 0 0 3 4 1 0 0 0 0 5 4 1 6 0 0 0 5 31 1 0 0 0 0 5 6 1 0 0 0 0 5 32 1 0 0 0 0 6 7 1 0 0 0 0 6 8 1 0 0 0 0 8 9 1 0 0 0 0 8 25 1 0 0 0 0 9 10 1 0 0 0 0 9 31 1 0 0 0 0 10 11 1 0 0 0 0 11 12 1 0 0 0 0 11 25 1 0 0 0 0 12 13 1 0 0 0 0 12 22 1 0 0 0 0 13 14 1 0 0 0 0 14 15 1 0 0 0 0 15 20 1 0 0 0 0 15 16 1 0 0 0 0 15 30 1 6 0 0 0 16 17 1 0 0 0 0 17 18 1 0 0 0 0 17 29 1 1 0 0 0 18 19 1 0 0 0 0 18 28 1 6 0 0 0 19 20 1 0 0 0 0 19 27 1 6 0 0 0 20 21 1 6 0 0 0 20 22 1 0 0 0 0 22 23 1 6 0 0 0 23 24 1 0 0 0 0 24 25 1 0 0 0 0 25 26 1 0 0 0 0 32 33 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	464.31
Volume:	476.951
LogP:	3.332
LogD:	3.752
LogS:	-4.035
# Rotatable Bonds:	0
TPSA:	99.38
# H-Bond Aceptor:	6
# H-Bond Donor:	4
# Rings:	6
# Heavy Atoms:	6

MedChem Properties

QED Drug-Likeness Score:	0.44
Synthetic Accessibility Score:	5.765
Fsp3:	1.0
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:	-4.935
MDCK Permeability:	1.613416498003062e-05
Pgp-inhibitor:	0.978
Pgp-substrate:	0.996
Human Intestinal Absorption (HIA):	0.045
20% Bioavailability (F20%):	0.012
30% Bioavailability (F30%):	0.071

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.349
Plasma Protein Binding (PPB):	63.72615051269531%
Volume Distribution (VD):	0.685
Pgp-substrate:	17.508012771606445%

ADMET: Metabolism

CYP1A2-inhibitor:	0.015
CYP1A2-substrate:	0.791
CYP2C19-inhibitor:	0.008
CYP2C19-substrate:	0.771
CYP2C9-inhibitor:	0.013
CYP2C9-substrate:	0.028
CYP2D6-inhibitor:	0.002
CYP2D6-substrate:	0.077
CYP3A4-inhibitor:	0.372
CYP3A4-substrate:	0.143

ADMET: Excretion

Clearance (CL):	10.819
Half-life (T1/2):	0.197

ADMET: Toxicity

hERG Blockers:	0.624
Human Hepatotoxicity (H-HT):	0.285
Drug-inuced Liver Injury (DILI):	0.045
AMES Toxicity:	0.03
Rat Oral Acute Toxicity:	0.444
Maximum Recommended Daily Dose:	0.652
Skin Sensitization:	0.923
Carcinogencity:	0.777
Eye Corrosion:	0.118
Eye Irritation:	0.062
Respiratory Toxicity:	0.987

Download Data

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

Natural Product: NPC275315

Natural Product ID:	NPC275315
*Common Name:**	OJOIREGWGDMNGQ-HYZHCZHOSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	OJOIREGWGDMNGQ-HYZHCZHOSA-N
Standard InCHI:	InChI=1S/C27H44O6/c1-14-5-10-27(32-13-14)15(2)21-20(33-27)11-18-16-6-9-26(31)12-19(28)22(29)23(30)25(26,4)17(16)7-8-24(18,21)3/h14-23,28-31H,5-13H2,1-4H3/t14-,15-,16+,17-,18-,19-,20-,21-,22+,23+,24+,25-,26-,27+/m0/s1
SMILES:	C[C@H]1CC[C@@]2([C@@H](C)[C@H]3[C@H](C[C@H]4[C@@H]5CC[C@@]6(C[C@@H]([C@H]([C@H]([C@]6(C)[C@H]5CC[C@@]34C)O)O)O)O)O2)OC1
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:0000259] Prenol lipids [CHEMONTID:0001553] Triterpenoids

*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
NPO22018	Hydrangea chinensis	Species	Hydrangeaceae	Eukaryota	Roots	n.a.	n.a.	PMID[11473431]
NPO20244	Melicope semecarpifolia	Species	Rutaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[11575945]
NPO20244	Melicope semecarpifolia	Species	Rutaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[18163582]
NPO26918	Taricha granulosa	Species	Salamandridae	Eukaryota	n.a.	n.a.	n.a.	PMID[32896120]
NPO20244	Melicope semecarpifolia	Species	Rutaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO22018	Hydrangea chinensis	Species	Hydrangeaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO20244	Melicope semecarpifolia	Species	Rutaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO22018	Hydrangea chinensis	Species	Hydrangeaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO22836	Alpinia mutica	Species	Zingiberaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO23001	Halimium umbellatum	Species	Cistaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO18364	Genista lusitanica	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO12967	Reseda suffruticosa	Species	Resedaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO17338	Solanum asperum	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO19482	Tapinoma nigerrimum	Species	Formicidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO20402	Ageratina gilbertii	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO14627	Caloscypha fulgens	Species	Caloscyphaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26918	Taricha granulosa	Species	Salamandridae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO14902	Pteris marginata	Species	Pteridaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO23067	Shorea maranti	Species	Dipterocarpaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO16398	Nicotiana alata	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO1463	Corethrodendron scoparium	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO22402	Lupinus mutabilis	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO20565	Aplysina fulva	Species	Aplysinidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO22018	Hydrangea chinensis	Species	Hydrangeaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO20244	Melicope semecarpifolia	Species	Rutaceae	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 NPC275315 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	513
0.1-0.2	4777
0.2-0.3	13050
0.3-0.4	11389
0.4-0.5	5282
0.5-0.6	4195
0.6-0.7	2356
0.7-0.8	850
0.8-0.85	118
0.85-0.9	147
0.9-0.95	18
0.95-1	2

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 NPC275315 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	500
0.1-0.2	4515
0.2-0.3	2920
0.3-0.4	647
0.4-0.5	293
0.5-0.6	208
0.6-0.7	59
0.7-0.8	6
0.8-0.85	0
0.85-0.9	1
0.9-0.95	1
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