NPASS Compound

Structure

NPC120414 OpenBabel06302215142D 46 52 0 0 1 0 0 0 0 0999 V2000 4.8835 1.0333 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.8835 0.0333 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 5.7495 -0.4667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7495 -1.4667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.8835 -1.9667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.8835 -2.9667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0174 -3.4667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1514 -2.9667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1514 -1.9667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0174 -1.4667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0174 -0.4667 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 3.7355 0.1740 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2772 0.7032 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6834 1.0737 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0066 1.2528 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3072 1.2244 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6725 0.3943 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5492 0.1623 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6472 0.9912 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0853 0.5737 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3286 0.0092 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2142 0.4737 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2547 1.4729 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.8008 0.6407 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4906 -0.3051 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 -2.2115 -0.9981 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5578 -0.6522 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -0.5817 -1.3518 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3985 -2.0274 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0242 -2.6190 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5078 -3.0739 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1503 -3.3518 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1814 -2.4454 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4921 -1.8560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8462 -3.4280 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5336 -3.2957 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0421 -0.0802 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5017 -0.2910 0.0000 C 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 0.8274 -0.5617 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7275 -0.1260 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4250 -1.2881 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.2501 -1.8531 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2854 -1.4667 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.0174 -4.4667 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.8835 -4.9667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 11 1 0 0 0 0 2 3 1 0 0 0 0 3 4 1 0 0 0 0 4 5 1 0 0 0 0 5 10 2 0 0 0 0 5 6 1 0 0 0 0 6 7 2 0 0 0 0 7 8 1 0 0 0 0 7 45 1 0 0 0 0 8 36 1 0 0 0 0 8 9 2 0 0 0 0 9 10 1 0 0 0 0 9 44 1 0 0 0 0 10 11 1 0 0 0 0 11 12 1 0 0 0 0 12 13 1 0 0 0 0 13 18 2 0 0 0 0 13 14 1 0 0 0 0 14 15 2 0 0 0 0 15 16 1 0 0 0 0 16 17 2 0 0 0 0 16 19 1 0 0 0 0 17 18 1 0 0 0 0 19 20 1 0 0 0 0 20 39 2 0 0 0 0 20 21 1 0 0 0 0 21 27 1 0 0 0 0 21 22 2 0 0 0 0 22 23 1 0 0 0 0 22 37 1 0 0 0 0 23 24 1 0 0 0 0 24 25 1 0 0 0 0 25 26 1 0 0 0 0 25 27 1 0 0 0 0 27 28 1 0 0 0 0 28 29 1 0 0 0 0 29 34 2 0 0 0 0 29 30 1 0 0 0 0 30 31 2 0 0 0 0 31 32 1 0 0 0 0 32 33 2 0 0 0 0 32 35 1 0 0 0 0 33 34 1 0 0 0 0 35 36 1 0 0 0 0 37 38 2 0 0 0 0 38 39 1 0 0 0 0 38 42 1 0 0 0 0 39 40 1 0 0 0 0 40 41 1 0 0 0 0 42 43 1 0 0 0 0 45 46 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	622.3
Volume:	649.006
LogP:	5.327
LogD:	4.083
LogS:	-3.694
# Rotatable Bonds:	3
TPSA:	72.86
# H-Bond Aceptor:	8
# H-Bond Donor:	1
# Rings:	10
# Heavy Atoms:	8

MedChem Properties

QED Drug-Likeness Score:	0.273
Synthetic Accessibility Score:	5.917
Fsp3:	0.368
Lipinski Rule-of-5:	Rejected
Pfizer Rule:	Rejected
GSK Rule:	Rejected
BMS Rule:	0
Golden Triangle Rule:	Rejected
Chelating Alert:	1
PAINS Alert:	1

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:	-5.137
MDCK Permeability:	1.9569821233744733e-05
Pgp-inhibitor:	1.0
Pgp-substrate:	0.175
Human Intestinal Absorption (HIA):	0.005
20% Bioavailability (F20%):	0.005
30% Bioavailability (F30%):	0.865

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.223
Plasma Protein Binding (PPB):	91.08258056640625%
Volume Distribution (VD):	1.02
Pgp-substrate:	7.3614301681518555%

ADMET: Metabolism

CYP1A2-inhibitor:	0.039
CYP1A2-substrate:	0.967
CYP2C19-inhibitor:	0.059
CYP2C19-substrate:	0.977
CYP2C9-inhibitor:	0.041
CYP2C9-substrate:	0.45
CYP2D6-inhibitor:	0.019
CYP2D6-substrate:	0.946
CYP3A4-inhibitor:	0.062
CYP3A4-substrate:	0.959

ADMET: Excretion

Clearance (CL):	9.081
Half-life (T1/2):	0.226

ADMET: Toxicity

hERG Blockers:	0.964
Human Hepatotoxicity (H-HT):	0.09
Drug-inuced Liver Injury (DILI):	0.05
AMES Toxicity:	0.088
Rat Oral Acute Toxicity:	0.143
Maximum Recommended Daily Dose:	0.949
Skin Sensitization:	0.751
Carcinogencity:	0.028
Eye Corrosion:	0.003
Eye Irritation:	0.003
Respiratory Toxicity:	0.362

Download Data

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

Natural Product: NPC120414

Natural Product ID:	NPC120414
*Common Name:**	BPJPWJSSKSLGNM-UHFFFAOYSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	BPJPWJSSKSLGNM-UHFFFAOYSA-N
Standard InCHI:	InChI=1S/C38H42N2O6/c1-39-16-14-26-20-31(42-3)36-35(41)33(26)29(39)18-24-10-12-28(13-11-24)46-38-34-27(21-32(43-4)37(38)44-5)15-17-40(2)30(34)19-23-6-8-25(9-7-23)22-45-36/h6-13,20-21,29-30,41H,14-19,22H2,1-5H3
SMILES:	CN1CCc2cc(c3c(c2C1Cc1ccc(cc1)Oc1c2c(CCN(C)C2Cc2ccc(cc2)CO3)cc(c1OC)OC)O)OC
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	159552
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0004603] Organic oxygen compounds [CHEMONTID:0000323] Organooxygen compounds [CHEMONTID:0000254] Ethers [CHEMONTID:0002463] Diarylethers

*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
NPO12773	Stephania tetrandra	Species	Menispermaceae	Eukaryota	n.a.	root	n.a.	PMID[20030508]
NPO11351	Stephania japonica	Species	Menispermaceae	Eukaryota	Aerial parts	n.a.	n.a.	PMID[20426456]
NPO18410	Cyclea racemosa	Species	Menispermaceae	Eukaryota	roots	n.a.	n.a.	PMID[20593839]
NPO12773	Stephania tetrandra	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[3728032]
NPO11351	Stephania japonica	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[9392886]
NPO12773	Stephania tetrandra	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[Article]
NPO18410	Cyclea racemosa	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO11351	Stephania japonica	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO12773	Stephania tetrandra	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO8034	Aristolochia kaempferi	Species	Aristolochiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO8034	Aristolochia kaempferi	Species	Aristolochiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO11351	Stephania japonica	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO12773	Stephania tetrandra	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO18410	Cyclea racemosa	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO12773	Stephania tetrandra	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO18410	Cyclea racemosa	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO11351	Stephania japonica	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO12773	Stephania tetrandra	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO12773	Stephania tetrandra	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO18410	Cyclea racemosa	Species	Menispermaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO8034	Aristolochia kaempferi	Species	Aristolochiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO11351	Stephania japonica	Species	Menispermaceae	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 NPC120414 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	368
0.1-0.2	1731
0.2-0.3	8443
0.3-0.4	10016
0.4-0.5	5391
0.5-0.6	8743
0.6-0.7	6489
0.7-0.8	1238
0.8-0.85	129
0.85-0.9	55
0.9-0.95	50
0.95-1	44

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 NPC120414 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	211
0.1-0.2	785
0.2-0.3	1184
0.3-0.4	2248
0.4-0.5	2416
0.5-0.6	1527
0.6-0.7	639
0.7-0.8	130
0.8-0.85	4
0.85-0.9	0
0.9-0.95	4
0.95-1	2

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