NPASS Compound

Structure

NPC257783 OpenBabel06302216182D 37 41 0 0 1 0 0 0 0 0999 V2000 -0.8492 -4.3911 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0022 -3.8989 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8542 -4.3902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0017 -2.9155 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8531 -2.4232 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7051 -2.9145 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.8525 -1.4398 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0005 -0.9485 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8206 -1.4233 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6424 -0.9495 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6429 -0.0009 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.4899 -0.4906 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8217 0.4738 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8220 1.4228 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6434 1.8971 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4646 1.4223 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.4652 3.3790 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4644 0.4733 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.2861 -0.0014 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1081 0.4729 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1084 1.4219 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.9304 1.8961 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.5731 1.8957 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.5733 2.8441 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7527 3.3188 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.9307 2.8445 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -4.9310 3.8229 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1089 3.3193 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2869 2.8450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2866 1.8966 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.4395 2.3860 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.2435 1.2248 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.9143 1.8953 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.4887 0.3086 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 0.9835 0.0006 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4912 0.8520 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 5 7 1 0 0 0 0 8 7 1 1 0 0 0 8 9 1 0 0 0 0 8 35 1 0 0 0 0 9 10 1 0 0 0 0 10 11 1 0 0 0 0 11 18 1 0 0 0 0 11 12 1 1 0 0 0 11 13 1 0 0 0 0 13 14 1 0 0 0 0 13 35 1 0 0 0 0 14 15 1 0 0 0 0 15 16 1 0 0 0 0 16 30 1 0 0 0 0 16 17 1 1 0 0 0 16 18 1 0 0 0 0 18 19 1 0 0 0 0 19 20 1 0 0 0 0 21 20 1 6 0 0 0 21 22 1 0 0 0 0 21 30 1 0 0 0 0 22 23 1 0 0 0 0 22 26 1 0 0 0 0 23 24 1 0 0 0 0 23 32 1 0 0 0 0 24 25 1 0 0 0 0 25 26 1 0 0 0 0 26 27 1 0 0 0 0 26 28 1 0 0 0 0 28 29 1 0 0 0 0 29 30 1 0 0 0 0 30 31 1 6 0 0 0 32 33 2 0 0 0 0 32 34 1 0 0 0 0 35 36 1 0 0 0 0 35 37 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	510.44
Volume:	583.441
LogP:	8.37
LogD:	6.832
LogS:	-7.576
# Rotatable Bonds:	5
TPSA:	26.3
# H-Bond Aceptor:	2
# H-Bond Donor:	0
# Rings:	5
# Heavy Atoms:	2

MedChem Properties

QED Drug-Likeness Score:	0.278
Synthetic Accessibility Score:	4.774
Fsp3:	0.914
Lipinski Rule-of-5:	Rejected
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:	-5.127
MDCK Permeability:	4.097017153981142e-05
Pgp-inhibitor:	0.032
Pgp-substrate:	0.0
Human Intestinal Absorption (HIA):	0.003
20% Bioavailability (F20%):	0.003
30% Bioavailability (F30%):	0.612

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.009
Plasma Protein Binding (PPB):	93.73820495605469%
Volume Distribution (VD):	1.252
Pgp-substrate:	1.63338041305542%

ADMET: Metabolism

CYP1A2-inhibitor:	0.024
CYP1A2-substrate:	0.389
CYP2C19-inhibitor:	0.1
CYP2C19-substrate:	0.953
CYP2C9-inhibitor:	0.092
CYP2C9-substrate:	0.71
CYP2D6-inhibitor:	0.014
CYP2D6-substrate:	0.827
CYP3A4-inhibitor:	0.362
CYP3A4-substrate:	0.576

ADMET: Excretion

Clearance (CL):	3.915
Half-life (T1/2):	0.092

ADMET: Toxicity

hERG Blockers:	0.106
Human Hepatotoxicity (H-HT):	0.165
Drug-inuced Liver Injury (DILI):	0.093
AMES Toxicity:	0.001
Rat Oral Acute Toxicity:	0.012
Maximum Recommended Daily Dose:	0.467
Skin Sensitization:	0.761
Carcinogencity:	0.004
Eye Corrosion:	0.988
Eye Irritation:	0.869
Respiratory Toxicity:	0.233

Download Data

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

Natural Product: NPC257783

Natural Product ID:	NPC257783
*Common Name:**	CMAMAVWZYNQUFI-BBMYGQQQSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	CMAMAVWZYNQUFI-BBMYGQQQSA-N
Standard InCHI:	InChI=1S/C35H58O2/c1-22(2)21-29(36)37-28-15-17-33(8)26(31(28,5)6)14-18-35(10)27(33)12-11-25-30-24(23(3)4)13-16-32(30,7)19-20-34(25,35)9/h22,24-28,30H,3,11-21H2,1-2,4-10H3/t24-,25+,26-,27+,28-,30+,32+,33-,34+,35+/m0/s1
SMILES:	CC(C)CC(=O)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC[C@@H]2[C@H]4[C@@H](CC[C@]4(C)CC[C@@]32C)C(=C)C)C1(C)C
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
NPO17048	Jungermannia subulata	Species	Jungermanniaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[11999396]
NPO16027	Niphogeton ternata	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO18366	Papaver commutatum	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO16027	Niphogeton ternata	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO15580	Justicia simplex	Species	Acanthaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO18366	Papaver commutatum	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO15580	Justicia simplex	Species	Acanthaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO18366	Papaver commutatum	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO2066	Streptomyces ipomoeae	Species	Streptomycetaceae	Bacteria	n.a.	n.a.	n.a.	Database[UNPD]
NPO7166	Streptomyces aureus	Species	Streptomycetaceae	Bacteria	n.a.	n.a.	n.a.	Database[UNPD]
NPO15832	Ruscus hypophyllum	Species	Asparagaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO13892	Calea clausseniana	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO16631	Libocedrus yateensis	Species	Cupressaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO15580	Justicia simplex	Species	Acanthaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO426	Camellia reticulata	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO17933	Cylicodaphne sebifera	n.a.	n.a.	n.a.	n.a.	n.a.	n.a.	Database[UNPD]
NPO17488	Rhoiptelea chiliantha	Species	Juglandaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO17048	Jungermannia subulata	Species	Jungermanniaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO18903	Chromodoris willani	Species	Chromodorididae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO17264	Mycena haematopus	Species	Tricholomataceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO18434	Dactylosporangium aurantiacum	Species	Micromonosporaceae	Bacteria	n.a.	n.a.	n.a.	Database[UNPD]
NPO18366	Papaver commutatum	Species	Papaveraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO16942	Asparagus thunbergianus	Species	Asparagaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO17168	Ageratina riparia	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO11999	Piptadenia peregrina	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO18044	Lotus albus	Species	Fabaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO16027	Niphogeton ternata	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO16421	Chalciporus piperatus	Species	Boletaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO5062	Aristolochia tagala	Species	Aristolochiaceae	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 NPC257783 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	208
0.1-0.2	1933
0.2-0.3	9503
0.3-0.4	14585
0.4-0.5	5837
0.5-0.6	4420
0.6-0.7	4919
0.7-0.8	1163
0.8-0.85	96
0.85-0.9	25
0.9-0.95	4
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 NPC257783 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	186
0.1-0.2	2289
0.2-0.3	4436
0.3-0.4	1545
0.4-0.5	292
0.5-0.6	184
0.6-0.7	184
0.7-0.8	32
0.8-0.85	0
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