NPASS Compound

Natural Product: NPC167739

Natural Product ID	NPC167739
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	NWSWVIKHALGAER-KVLFNOHQSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	442171
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0001283] Terpene lactones [CHEMONTID:0001543] Sesquiterpene lactones

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 40 43 0 0 0 0 0 0 0 0999 V2000 -0.2079 -2.4659 -1.6714 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2096 -1.2326 -0.8564 C 0 0 2 0 0 0 0 0 0 0 0 0 1.3845 -1.6717 -0.0595 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7672 -0.8597 1.1039 C 0 0 2 0 0 0 0 0 0 0 0 0 1.5901 0.6186 1.0236 C 0 0 1 0 0 0 0 0 0 0 0 0 2.4287 0.9224 -0.1495 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3454 1.8125 -1.1091 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5019 -0.0646 -0.0412 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5187 -0.2208 -0.7983 O 0 0 0 0 0 0 0 0 0 0 0 0 3.2194 -0.8593 1.0947 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2748 1.2010 1.1103 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8638 0.6696 0.3689 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.1631 1.5302 -0.8667 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8699 -0.7799 0.0594 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.2658 -0.9619 -0.5148 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.1127 0.0361 0.2619 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.1619 0.7572 1.1954 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.5296 2.0769 1.4039 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.2596 -1.3334 0.3533 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0957 1.2628 2.4806 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.4592 -3.2769 -0.9326 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0905 -2.2908 -2.2738 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6448 -2.8338 -2.2459 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5111 -0.4447 -1.5757 H 0 0 0 0 0 0 0 0 0 0 0 0 1.1479 -2.7130 0.3166 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2176 -1.8613 -0.7998 H 0 0 0 0 0 0 0 0 0 0 0 0 1.4247 -1.2866 2.0715 H 0 0 0 0 0 0 0 0 0 0 0 0 2.1943 1.0245 1.9010 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5388 2.5370 -1.1696 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1032 1.8389 -1.8792 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3743 2.2973 0.8363 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2280 1.4847 -1.1422 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9763 2.5851 -0.5305 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4743 1.3372 -1.6866 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8298 -1.3501 0.9886 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4222 -0.9006 -1.5993 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.8741 0.6310 -0.2844 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0408 0.1854 2.1298 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4585 2.2596 1.0954 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0134 0.3395 2.8233 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 2 0 6 8 1 0 8 9 2 0 8 10 1 0 5 11 1 0 11 12 1 0 12 13 1 6 12 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 17 18 1 0 16 19 1 0 11 20 1 0 14 2 1 0 19 15 1 0 10 4 1 0 17 12 1 0 1 21 1 0 1 22 1 0 1 23 1 0 2 24 1 6 3 25 1 0 3 26 1 0 4 27 1 1 5 28 1 1 7 29 1 0 7 30 1 0 11 31 1 6 13 32 1 0 13 33 1 0 13 34 1 0 14 35 1 1 15 36 1 6 16 37 1 6 17 38 1 1 18 39 1 0 20 40 1 0 M END

Standard InCHIKey	NWSWVIKHALGAER-KVLFNOHQSA-N
Standard InCHI	InChI=1S/C15H20O5/c1-5-4-7-8(6(2)14(18)19-7)12(16)15(3)9(5)10-11(20-10)13(15)17/h5,7-13,16-17H,2,4H2,1,3H3/t5-,7-,8-,9-,10-,11-,12+,13+,15-/m1/s1
SMILES	C[C@@H]1C[C@@H]2[C@@H](C(=C)C(=O)O2)[C@@H]([C@@]2(C)[C@H]1[C@@H]1[C@H]([C@@H]2O)O1)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	280.13	Volume:	272.449 ? Van der Waals volume.
Dense:	1.028	LogP:	0.688 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	0.942 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-1.795 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	0.0	Rigid Bonds:	19.0
TPSA:	79.29 ? Topological Polar Surface Area.	H-Bond Acceptor:	5.0
H-Bond Donor:	2.0	Rings:	4.0
Heavy Atoms:	5.0

MedChem Properties

QED Drug-Likeness Score:	0.378	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	5.11	Fsp³:	0.8
MCE-18:	68.519 ? MCE-18 stands for medicinal chemistry evolution.MCE-18≥45 is considered a suitable value.	Lipinski Rule-of-5:	Rejected
Pfizer Rule:	Rejected	GSK Rule:	Rejected
Golden Triangle Rule:	Rejected	BMS Rule:	1
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.471	Fluc inhibitor:	0.004 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.03 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.0 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.352	Promiscuous compounds:	0.485

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.705	MDCK Permeability:	-5.164
Pgp-inhibitor:	0.023	Pgp-substrate:	0.391
PAMPA:	0.97 ? 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):	0.215
20% Bioavailability (F20%):	0.887	30% Bioavailability (F30%):	0.845
50% Bioavailability (F50%):	0.952

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.023	MRP1:	0.496
Plasma Protein Binding (PPB):	43.823%	Volume Distribution (VD):	-0.157
Fu:	60.952% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.964
OATP1B3 inhibitor:	0.969	BCRP inhibitor:	0.007
BSEP inhibitor:	0.448

ADMET: Metabolism

CYP1A2-inhibitor:	0.005	CYP1A2-substrate:	0.011
CYP2C19-inhibitor:	0.507	CYP2C19-substrate:	0.001
CYP2C9-inhibitor:	0.025	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.009
CYP3A4-inhibitor:	0.091	CYP3A4-substrate:	0.393
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.227
HLM stability:	0.247 ? 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):

4.65

Half-life (T1/2):

2.375

ADMET: Toxicity

hERG Blockers:	0.013	hERG Blockers (10um):	0.202
Human Hepatotoxicity (H-HT):	0.707	Drug-induced Liver Injury (DILI):	0.873
AMES Toxicity:	0.881	Rat Oral Acute Toxicity:	0.431
Maximum Recommended Daily Dose:	0.556	Skin Sensitization:	0.997
Carcinogencity:	0.581	Eye Corrosion:	0.087
Eye Irritation:	0.859	Respiratory Toxicity:	0.688
Drug-induced Neurotoxicity:	0.309	Ototoxicity:	0.789
Hematotoxicity:	0.83	Drug-induced Nephrotoxicity:	0.933
Genotoxicity:	0.834	RPMI-8226 Immunitoxicity:	0.241
A549 Cytotoxicity:	0.322	Hek293 Cytotoxicity:	0.208
BCF:	0.487 ? 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:	3.148 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	4.672 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	3.792 ? 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
NPO26233	Helenium autumnale	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO26233	Helenium autumnale	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO26233.1	Helenium autumnale var. montanum	Varieties	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO26233	Helenium autumnale	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO26233.1	Helenium autumnale var. montanum	Varieties	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO26233	Helenium autumnale	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO26233	Helenium autumnale	Species	Asteraceae	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	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

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

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 NPC167739 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	18423
0.1-0.2	27483
0.2-0.3	3672
0.3-0.4	247
0.4-0.5	19
0.5-0.6	13
0.6-0.7	2
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	Natural Product ID
0.6275	Remote Similarity	NPC483168
0.6275	Remote Similarity	NPC35959
0.5882	Remote Similarity	NPC606717
0.5769	Remote Similarity	NPC155935
0.5556	Remote Similarity	NPC29821
0.5556	Remote Similarity	NPC142529
0.5556	Remote Similarity	NPC43777
0.5357	Remote Similarity	NPC91771
0.5283	Remote Similarity	NPC212340
0.5273	Remote Similarity	NPC54065
0.5263	Remote Similarity	NPC63193
0.5091	Remote Similarity	NPC193645
0.5091	Remote Similarity	NPC48803
0.5091	Remote Similarity	NPC168679
0.5091	Remote Similarity	NPC275960

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC167739 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	6592
0.1-0.2	2526
0.2-0.3	31
0.3-0.4	0
0.4-0.5	0
0.5-0.6	1
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
0.5091	Remote Similarity	NPD1698	Clinical (unspecified phase)

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