NPASS Compound

Structure

NPC478576 OpenBabel06302215272D 39 41 0 0 1 0 0 0 0 0999 V2000 3.8288 -16.0568 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.8070 -15.8489 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1160 -14.8979 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4468 -14.1547 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.7559 -13.2037 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0867 -12.4605 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.3957 -11.5095 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7266 -10.7663 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0356 -9.8153 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3665 -9.0721 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6755 -8.1211 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0064 -7.3779 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3154 -6.4269 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6463 -5.6837 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9553 -4.7327 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2862 -3.9895 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5952 -3.0385 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9260 -2.2953 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9479 -2.5032 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.6389 -3.4543 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2788 -1.7601 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6994 -1.9680 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.5878 -0.8090 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5388 -0.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4049 -1.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4049 -2.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2709 -2.5000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.1369 -2.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1369 -1.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2709 -0.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2709 0.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4049 1.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4049 2.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.5388 0.5000 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.9456 1.4135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5878 0.8090 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 -1.0000 -0.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.0029 -2.5000 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 3 4 1 0 0 0 0 4 5 1 0 0 0 0 5 6 1 0 0 0 0 6 7 1 0 0 0 0 7 8 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 11 12 1 0 0 0 0 12 13 1 0 0 0 0 13 14 1 0 0 0 0 14 15 1 0 0 0 0 15 16 1 0 0 0 0 16 17 1 0 0 0 0 17 18 1 0 0 0 0 18 19 1 0 0 0 0 19 20 1 6 0 0 0 19 21 1 0 0 0 0 21 22 2 0 0 0 0 21 23 1 0 0 0 0 23 37 1 0 0 0 0 23 24 2 0 0 0 0 24 34 1 0 0 0 0 24 25 1 0 0 0 0 25 30 1 0 0 0 0 25 26 2 0 0 0 0 26 27 1 0 0 0 0 27 28 1 0 0 0 0 28 29 2 0 0 0 0 28 39 1 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 34 1 0 0 0 0 34 35 1 6 0 0 0 34 36 1 0 0 0 0 36 37 1 0 0 0 0 37 38 2 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	538.37
Volume:	596.447
LogP:	9.218
LogD:	4.143
LogS:	-7.231
# Rotatable Bonds:	19
TPSA:	69.67
# H-Bond Aceptor:	5
# H-Bond Donor:	0
# Rings:	3
# Heavy Atoms:	5

MedChem Properties

QED Drug-Likeness Score:	0.093
Synthetic Accessibility Score:	4.131
Fsp3:	0.676
Lipinski Rule-of-5:	Rejected
Pfizer Rule:	Rejected
GSK Rule:	Rejected
BMS Rule:	1
Golden Triangle Rule:	Rejected
Chelating Alert:	0
PAINS Alert:	0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:	-5.184
MDCK Permeability:	8.372578122362029e-06
Pgp-inhibitor:	0.999
Pgp-substrate:	0.136
Human Intestinal Absorption (HIA):	0.011
20% Bioavailability (F20%):	1.0
30% Bioavailability (F30%):	0.999

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.146
Plasma Protein Binding (PPB):	98.75730895996094%
Volume Distribution (VD):	4.207
Pgp-substrate:	1.1544371843338013%

ADMET: Metabolism

CYP1A2-inhibitor:	0.078
CYP1A2-substrate:	0.193
CYP2C19-inhibitor:	0.504
CYP2C19-substrate:	0.084
CYP2C9-inhibitor:	0.253
CYP2C9-substrate:	0.114
CYP2D6-inhibitor:	0.696
CYP2D6-substrate:	0.006
CYP3A4-inhibitor:	0.593
CYP3A4-substrate:	0.297

ADMET: Excretion

Clearance (CL):	2.218
Half-life (T1/2):	0.028

ADMET: Toxicity

hERG Blockers:	0.345
Human Hepatotoxicity (H-HT):	0.845
Drug-inuced Liver Injury (DILI):	0.901
AMES Toxicity:	0.868
Rat Oral Acute Toxicity:	0.098
Maximum Recommended Daily Dose:	0.776
Skin Sensitization:	0.973
Carcinogencity:	0.651
Eye Corrosion:	0.003
Eye Irritation:	0.025
Respiratory Toxicity:	0.899

Download Data

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

Natural Product: NPC478576

Natural Product ID:	NPC478576
*Common Name:**	RPOCDBVFURSTRO-XDCSYDRFSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	RPOCDBVFURSTRO-XDCSYDRFSA-N
Standard InCHI:	InChI=1S/C34H50O5/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25(2)32(36)30-31-28-24-38-26(3)22-27(28)23-29(35)34(31,4)39-33(30)37/h22-25H,5-21H2,1-4H3/t25-,34-/m0/s1
SMILES:	CCCCCCCCCCCCCCCCCC[C@H](C)C(=O)C1=C2C3=COC(=CC3=CC(=O)[C@]2(C)OC1=O)C
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	n.a.
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds]

*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
NPO40080	Colletotrichum sp. BS4	Strain	Glomerellaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[26905687]

☑ 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
MIC	2

Activity Type	# Activity
Organism	2

Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference
NPT4876	Organism	Brevibacillus brevis	Brevibacillus brevis	MIC	=	5.0	ug.mL-1	PMID[26905687]
NPT22	Organism	Bacillus subtilis subsp. spizizenii	Bacillus subtilis subsp. spizizenii	MIC	=	5.0	ug.mL-1	PMID[26905687]

☑ 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 NPC478576 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	232
0.1-0.2	1309
0.2-0.3	5186
0.3-0.4	11442
0.4-0.5	15186
0.5-0.6	6729
0.6-0.7	2296
0.7-0.8	287
0.8-0.85	15
0.85-0.9	7
0.9-0.95	3
0.95-1	5

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 NPC478576 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	209
0.1-0.2	1619
0.2-0.3	3669
0.3-0.4	2449
0.4-0.5	874
0.5-0.6	279
0.6-0.7	49
0.7-0.8	2
0.8-0.85	0
0.85-0.9	0
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