NPASS Compound

Natural Product: NPC485077

Natural Product ID	NPC485077
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	XTHTWHFEWGTQDM-UHFFFAOYSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	n.a.
Chemical Classification	CHEMONTID:0000000 [Organic compounds]

The Chemical Classification was calculated by Classyfire, a software for chemical taxonomy calculation. Reference: DOI:10.1186/s13321-016-0174-y.

Chemical Representations

RDKit 3D 51 51 0 0 0 0 0 0 0 0999 V2000 7.6098 1.4584 -0.8351 C 0 0 0 0 0 0 0 0 0 0 0 0 6.0825 1.4752 -0.6843 C 0 0 0 0 0 0 0 0 0 0 0 0 5.6498 0.0522 -0.5719 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1697 -0.1369 -0.4166 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6516 0.5405 0.8078 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1758 0.3553 0.9683 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7931 -1.1023 1.0825 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3395 -1.2822 1.2439 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4933 -1.1441 0.1586 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.8582 -1.3207 0.3477 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4072 -1.6236 1.5668 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.8502 -1.8300 1.8380 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7429 -1.5542 0.6825 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7454 -0.0815 0.3600 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.6422 0.1008 -0.8441 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7475 1.5185 -1.2893 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.4623 2.1559 -1.6893 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5400 -1.7435 2.5755 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.2575 -1.5885 2.4459 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5381 -1.7114 3.4342 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0147 -0.8339 -1.1065 O 0 0 0 0 0 0 0 0 0 0 0 0 7.9229 0.7319 -1.6150 H 0 0 0 0 0 0 0 0 0 0 0 0 8.0159 1.2230 0.1551 H 0 0 0 0 0 0 0 0 0 0 0 0 7.8970 2.5024 -1.0887 H 0 0 0 0 0 0 0 0 0 0 0 0 5.6926 2.0231 -1.5398 H 0 0 0 0 0 0 0 0 0 0 0 0 5.8907 2.0703 0.2279 H 0 0 0 0 0 0 0 0 0 0 0 0 5.9548 -0.4582 -1.5272 H 0 0 0 0 0 0 0 0 0 0 0 0 6.1776 -0.4170 0.2677 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0222 -1.2438 -0.2720 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6065 0.1171 -1.3266 H 0 0 0 0 0 0 0 0 0 0 0 0 3.8630 1.6204 0.8435 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1401 0.0465 1.6883 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8211 0.8373 1.9192 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6200 0.8717 0.1531 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0598 -1.6103 0.1096 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3884 -1.5520 1.8808 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4987 -1.2511 -0.5399 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.0959 -1.0757 2.6473 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.0126 -2.8691 2.2512 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.7956 -1.7885 0.9973 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4808 -2.1730 -0.2052 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7761 0.3277 0.1836 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2438 0.3910 1.2731 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.6674 -0.2342 -0.5607 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2747 -0.5386 -1.6486 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.4219 1.5562 -2.1881 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.2562 2.1723 -0.5405 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.5502 3.2757 -1.6259 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.2198 1.9644 -2.7760 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5787 1.8781 -1.1194 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4780 -0.1015 -1.6098 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 3 4 1 0 4 5 1 0 5 6 1 0 6 7 1 0 7 8 1 0 8 9 2 0 9 10 1 0 10 11 2 0 11 12 1 0 12 13 1 0 13 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 11 18 1 0 18 19 1 0 19 20 2 0 9 21 1 0 19 8 1 0 1 22 1 0 1 23 1 0 1 24 1 0 2 25 1 0 2 26 1 0 3 27 1 0 3 28 1 0 4 29 1 0 4 30 1 0 5 31 1 0 5 32 1 0 6 33 1 0 6 34 1 0 7 35 1 0 7 36 1 0 10 37 1 0 12 38 1 0 12 39 1 0 13 40 1 0 13 41 1 0 14 42 1 0 14 43 1 0 15 44 1 0 15 45 1 0 16 46 1 0 16 47 1 0 17 48 1 0 17 49 1 0 17 50 1 0 21 51 1 0 M END

Standard InCHIKey	XTHTWHFEWGTQDM-UHFFFAOYSA-N
Standard InCHI	InChI=1S/C18H30O3/c1-3-5-7-9-11-13-16-17(19)14-15(21-18(16)20)12-10-8-6-4-2/h14,19H,3-13H2,1-2H3
SMILES	CCCCCCCc1c(cc(CCCCCC)oc1=O)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	294.22	Volume:	329.789 ? Van der Waals volume.
Dense:	0.892	LogP:	5.4 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	4.203 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-3.821 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	11.0	Rigid Bonds:	7.0
TPSA:	50.44 ? Topological Polar Surface Area.	H-Bond Acceptor:	3.0
H-Bond Donor:	1.0	Rings:	1.0
Heavy Atoms:	3.0

MedChem Properties

QED Drug-Likeness Score:	0.585	GASA:	0.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	2.344	Fsp³:	0.722
MCE-18:	7.0 ? MCE-18 stands for medicinal chemistry evolution.MCE-18≥45 is considered a suitable value.	Lipinski Rule-of-5:	Rejected
Pfizer Rule:	Accepted	GSK Rule:	Accepted
Golden Triangle Rule:	Rejected	BMS Rule:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.397	Fluc inhibitor:	0.143 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.236 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.279 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.813	Promiscuous compounds:	0.102

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.019	MDCK Permeability:	-4.766
Pgp-inhibitor:	0.268	Pgp-substrate:	0.021
PAMPA:	0.011 ? The experimental data for Peff was logarithmically transformed (logPeff). Molecules with log Peff values below 2.0 were classified as low-permeability (Category 0), while those with log Peff values exceeding 2.5 were classified as high-permeability (Category 1).	Human Intestinal Absorption (HIA):	0.08
20% Bioavailability (F20%):	0.584	30% Bioavailability (F30%):	0.859
50% Bioavailability (F50%):	0.35

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.287	MRP1:	0.975
Plasma Protein Binding (PPB):	98.374%	Volume Distribution (VD):	0.952
Fu:	1.542% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.199
OATP1B3 inhibitor:	0.958	BCRP inhibitor:	0.052
BSEP inhibitor:	0.972

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	1.0
CYP2C19-inhibitor:	0.008	CYP2C19-substrate:	0.822
CYP2C9-inhibitor:	1.0	CYP2C9-substrate:	0.715
CYP2D6-inhibitor:	0.82	CYP2D6-substrate:	0.988
CYP3A4-inhibitor:	0.002	CYP3A4-substrate:	1.0
CYP2B6-substrate:	0.285	CYP2C8-inhibitor:	1.0
HLM stability:	0.991 ? Human liver microsomal (HLM) stability. Category 0: stable+ (HLM > 30 min); Category 1: unstable- (HLM ≤ 30 min). The output value is the probability of human liver microsomal instability, where a value closer to 1 indicates a higher likelihood of instability.

ADMET: Excretion

Clearance (CL):

4.059

Half-life (T1/2):

0.446

ADMET: Toxicity

hERG Blockers:	0.457	hERG Blockers (10um):	0.862
Human Hepatotoxicity (H-HT):	0.47	Drug-induced Liver Injury (DILI):	0.157
AMES Toxicity:	0.109	Rat Oral Acute Toxicity:	0.274
Maximum Recommended Daily Dose:	0.219	Skin Sensitization:	0.929
Carcinogencity:	0.125	Eye Corrosion:	0.995
Eye Irritation:	0.997	Respiratory Toxicity:	0.969
Drug-induced Neurotoxicity:	0.035	Ototoxicity:	0.138
Hematotoxicity:	0.079	Drug-induced Nephrotoxicity:	0.12
Genotoxicity:	0.0	RPMI-8226 Immunitoxicity:	0.069
A549 Cytotoxicity:	0.565	Hek293 Cytotoxicity:	0.444
BCF:	1.573 ? Bioconcentration factors are used for considering secondary poisoning potential and assessing risks to human health via the food chain. The unit is -log10[(mg/L)/(1000*MW)].	IGC50:	4.736 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.632 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	5.231 ? 96 hour fathead minnow LC50. The unit of LC50FM is -log10[(mg/L)/(1000*MW)].

Species Source

Organism ID	Organism Name	Taxonomy Level	Family	SuperKingdom	Isolation Part	Collection Location	Collection Time	Reference
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[11976110]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[12930985]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[16347440]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[2013566]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[22609920]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[25912724]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[28335605]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[28478925]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[8195105]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[9031664]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	PMID[9157190]
NPO30084	Pseudomonas sp.	Species	Pseudomonadaceae	Bacteria	n.a.	n.a.	n.a.	Database[COCONUT]

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	Organism Name	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	4

Activity Type	# Activity
Organism	4

Molecular-level activity

Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference

In vitro activity

Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference
NPT79	Organism	Bacillus subtilis	Bacillus subtilis	IC50	=	0.7	ug.mL-1	PMID[28478925]
NPT16	Organism	Staphylococcus aureus	Staphylococcus aureus	IC50	=	0.04	ug.mL-1	PMID[28478925]
NPT19	Organism	Escherichia coli	Escherichia coli	IC50	>	1000.0	ug.mL-1	PMID[28478925]
NPT18	Organism	Pseudomonas aeruginosa	Pseudomonas aeruginosa	IC50	>	1000.0	ug.mL-1	PMID[28478925]

In vivo activity

Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference

Experimental ADME

Experiment Model	Experiment Tissue	ADME Type	ADME Relation	ADME Value	ADME Unit	Reference

Experimental Toxicity

Quantitative toxicity

Experiment Model	Experiment Organism	Toxicity Type	Toxicity Relation	Toxicity Value	Toxicity Unit	Reference

Common Abbreviations:
LC: Lethal Concentration; LD: Lethal Dose; LT:Lethal Time; NOAEL: No-observed-adverse-effect Level; BMDL: Benchmark Dose Lower Confidence Limit; BMD: Benchmark Dose; BMC:Benchmark Concentration; LOAEL: Lowest Observed Adverse Effect Level; RfD:Reference Dose; RfC:Reference Concentration; MRL: Minimal Risk Level; MEG: Maximum Exposure Guideline; PAC: Protective Action Criteria

Categorical toxicity labels

Hepatotoxicity	Carcinogenicity	Mutagenicity	Cardiotoxicity	Respiratory Toxicity	Eye Irritation	Endocrine Disruption

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 toxicity records from domain-specific databases. These databases include:
☉ ToxValDB: a curated database that compiles quantitative toxicity values for chemicals from diverse public sources to support toxicological research and risk assessment.
☉ TOXRIC: a comprehensive, free-to-access, online database providing toxicological/feature data. The toxicity labels are retrieved from this database. [PMID: 36400569]

Chemically structural similarity

Similar Active Natural Products in NPASS

Top-200 similar NPs were calculated against the active-NP-set (includes approximately 50,000 NPs with experimentally-derived bioactivity available in NPASS)

Similarity is measured using the Tanimoto coefficient (Tc) , which compares the binary fingerprints of two molecules. Tc is calculated as the intersection divided by the union of '1' bits in the fingerprints, ranging from 0 to 1, with 1 indicating highest similarity.

● The left chart: Distribution of similarity level between NPC485077 and all remaining natural products in the NPASS database.
● The right table: Most similar natural products (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	21310
0.1-0.2	26775
0.2-0.3	1593
0.3-0.4	144
0.4-0.5	17
0.5-0.6	7
0.6-0.7	6
0.7-0.8	0
0.8-0.85	1
0.85-0.9	0
0.9-0.95	1
0.95-1	3

Similarity Score	Similarity Level	Natural Product ID
1.0	High Similarity	NPC485078
1.0	High Similarity	NPC294618
1.0	High Similarity	NPC485079
0.9474	High Similarity	NPC265050
0.8462	Intermediate Similarity	NPC485076
0.75	Intermediate Similarity	NPC485075
0.6809	Remote Similarity	NPC485070
0.6809	Remote Similarity	NPC485071
0.6809	Remote Similarity	NPC485072
0.6341	Remote Similarity	NPC485074
0.625	Remote Similarity	NPC485069
0.6087	Remote Similarity	NPC313444
0.5957	Remote Similarity	NPC315597
0.5833	Remote Similarity	NPC316029
0.5833	Remote Similarity	NPC485068
0.5652	Remote Similarity	NPC315115
0.56	Remote Similarity	NPC316324
0.56	Remote Similarity	NPC315394
0.5208	Remote Similarity	NPC485067

Similar Clinical/Approved Drugs

Similarity level is defined by Tanimoto coefficient (Tc) between two molecules.

● The left chart: Distribution of similarity level between NPC485077 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	3804
0.1-0.2	5230
0.2-0.3	109
0.3-0.4	7
0.4-0.5	0
0.5-0.6	0
0.6-0.7	0
0.7-0.8	0
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
		NPD

Bioactivity similarity

Similar Natural Products in NPASS

Similarity level is defined by 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