NPASS Compound

Structure

NPC202918 OpenBabel06302216132D 27 32 0 0 1 0 0 0 0 0999 V2000 -2.5142 -2.4511 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3801 -1.9509 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.5349 -1.4632 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6906 -1.9510 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8454 -1.4634 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8451 -0.4876 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6895 0.0002 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5346 -0.4875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3795 0.0006 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2246 -0.4870 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 -5.0905 0.0132 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2249 -1.4628 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -5.0698 -1.9499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9144 -1.4623 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.7589 -1.9499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.7589 -2.9251 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9144 -3.4128 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0698 -2.9251 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2249 -3.4132 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3801 -2.9261 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.5142 -3.4264 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.6864 -3.2265 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.2597 -2.4375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.6864 -1.6485 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8446 1.4625 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0003 0.9747 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 2 1 1 6 0 0 0 2 20 1 0 0 0 0 2 3 1 0 0 0 0 2 12 1 0 0 0 0 3 8 2 0 0 0 0 3 4 1 0 0 0 0 4 5 2 0 0 0 0 5 6 1 0 0 0 0 6 27 1 0 0 0 0 6 7 2 0 0 0 0 7 8 1 0 0 0 0 7 25 1 0 0 0 0 8 9 1 0 0 0 0 9 10 1 0 0 0 0 10 11 1 0 0 0 0 10 12 1 0 0 0 0 12 13 1 1 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 24 1 0 0 0 0 15 16 1 0 0 0 0 16 17 2 0 0 0 0 16 22 1 0 0 0 0 17 18 1 0 0 0 0 18 19 1 0 0 0 0 19 20 1 0 0 0 0 20 21 1 1 0 0 0 22 23 1 0 0 0 0 23 24 1 0 0 0 0 25 26 1 0 0 0 0 26 27 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	367.14
Volume:	359.563
LogP:	2.838
LogD:	2.608
LogS:	-4.054
# Rotatable Bonds:	0
TPSA:	60.39
# H-Bond Aceptor:	6
# H-Bond Donor:	1
# Rings:	6
# Heavy Atoms:	6

MedChem Properties

QED Drug-Likeness Score:	0.772
Synthetic Accessibility Score:	4.034
Fsp3:	0.429
Lipinski Rule-of-5:	Accepted
Pfizer Rule:	Accepted
GSK Rule:	Accepted
BMS Rule:	0
Golden Triangle Rule:	Accepted
Chelating Alert:	0
PAINS Alert:	0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:	-5.034
MDCK Permeability:	3.0515462640323676e-05
Pgp-inhibitor:	0.045
Pgp-substrate:	0.717
Human Intestinal Absorption (HIA):	0.001
20% Bioavailability (F20%):	0.029
30% Bioavailability (F30%):	0.033

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.975
Plasma Protein Binding (PPB):	93.70111846923828%
Volume Distribution (VD):	1.853
Pgp-substrate:	7.312365531921387%

ADMET: Metabolism

CYP1A2-inhibitor:	0.936
CYP1A2-substrate:	0.269
CYP2C19-inhibitor:	0.942
CYP2C19-substrate:	0.894
CYP2C9-inhibitor:	0.073
CYP2C9-substrate:	0.788
CYP2D6-inhibitor:	0.978
CYP2D6-substrate:	0.913
CYP3A4-inhibitor:	0.961
CYP3A4-substrate:	0.88

ADMET: Excretion

Clearance (CL):	15.651
Half-life (T1/2):	0.298

ADMET: Toxicity

hERG Blockers:	0.266
Human Hepatotoxicity (H-HT):	0.081
Drug-inuced Liver Injury (DILI):	0.379
AMES Toxicity:	0.078
Rat Oral Acute Toxicity:	0.724
Maximum Recommended Daily Dose:	0.993
Skin Sensitization:	0.401
Carcinogencity:	0.778
Eye Corrosion:	0.003
Eye Irritation:	0.061
Respiratory Toxicity:	0.948

Download Data

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

Natural Product: NPC202918

Natural Product ID:	NPC202918
*Common Name:**	IQUGPRHKZNCHGC-TYPHKJRUSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	IQUGPRHKZNCHGC-TYPHKJRUSA-N
Standard InCHI:	InChI=1S/C21H21NO5/c1-21-14-3-4-15-19(27-10-24-15)13(14)8-22(2)20(21)12-7-17-16(25-9-26-17)5-11(12)6-18(21)23/h3-5,7,18,20,23H,6,8-10H2,1-2H3/t18-,20+,21-/m0/s1
SMILES:	C[C@]12c3ccc4c(c3CN(C)[C@@H]2c2cc3c(cc2C[C@@H]1O)OCO3)OCO4
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	177014
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000279] Alkaloids and derivatives [CHEMONTID:0002665] Benzophenanthridine alkaloids [CHEMONTID:0002666] Hexahydrobenzophenanthridine alkaloids

*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
NPO6328	Corydalis incisa	Species	Papaveraceae	Eukaryota	n.a.	aerial part	n.a.	PMID[17366734]
NPO24584	Corydalis bungeana	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO6328	Corydalis incisa	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO6328	Corydalis incisa	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO24584	Corydalis bungeana	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO6328	Corydalis incisa	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO24584	Corydalis bungeana	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO24584	Corydalis bungeana	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO6328	Corydalis incisa	Species	Papaveraceae	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

Activity Type	# Activity
IC50	3
Others	2

Activity Type	# Activity
Cell Line	1
Individual Protein	4

Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference
NPT113	Cell Line	RAW264.7	Mus musculus	IC50	=	2510.0	nM	PMID[530547]
NPT582	Individual Protein	Monoamine oxidase B	Homo sapiens	IC50	>	20000.0	nM	PMID[530548]
NPT261	Individual Protein	Monoamine oxidase A	Homo sapiens	IC50	>	20000.0	nM	PMID[530548]
NPT582	Individual Protein	Monoamine oxidase B	Homo sapiens	Activity	=	87.6	%	PMID[530548]
NPT261	Individual Protein	Monoamine oxidase A	Homo sapiens	Activity	=	87.9	%	PMID[530548]

☑ 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 NPC202918 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	304
0.1-0.2	1380
0.2-0.3	4873
0.3-0.4	11885
0.4-0.5	6487
0.5-0.6	12667
0.6-0.7	4151
0.7-0.8	587
0.8-0.85	236
0.85-0.9	112
0.9-0.95	11
0.95-1	4

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 NPC202918 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	195
0.1-0.2	680
0.2-0.3	966
0.3-0.4	2223
0.4-0.5	2607
0.5-0.6	1682
0.6-0.7	644
0.7-0.8	133
0.8-0.85	18
0.85-0.9	2
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