NPASS Compound

Natural Product: NPC555407

Natural Product ID	NPC555407
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	(E)-Eruciflorine
IUPAC Name	(4~{E},6~{S},7~{S},17~{S})-7-hydroxy-4-(2-hydroxyethylidene)-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0^{14,17}]heptadec-11-ene-3,8-dione
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 50 52 0 0 0 0 0 0 0 0999 V2000 -4.0501 -0.0562 1.0997 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7293 0.1792 0.2220 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.2279 1.4559 0.7701 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0942 2.1443 0.1851 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2864 3.3255 -0.4540 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6163 3.9010 -0.5589 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5947 5.1519 0.0724 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2814 1.7277 0.2431 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1643 2.4362 -0.3539 O 0 0 0 0 0 0 0 0 0 0 0 0 0.7304 0.5746 0.9297 O 0 0 0 0 0 0 0 0 0 0 0 0 2.0707 0.3409 0.8476 C 0 0 0 0 0 0 0 0 0 0 0 0 2.7639 -0.5223 1.8191 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1613 -0.5771 1.1615 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9800 -0.0528 -0.1969 N 0 0 0 0 0 0 0 0 0 0 0 0 4.5777 -1.0267 -1.0883 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6873 -2.1956 -0.9271 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4695 -1.7314 -0.5437 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3401 -2.6526 -0.2908 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1596 -2.2073 0.1268 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8308 -1.4064 -0.4140 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5868 -0.9891 -1.5716 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.0557 -1.0944 0.3308 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.0813 -2.1560 -0.2093 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9311 -1.4745 1.6803 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5258 -0.2873 -0.4529 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.7558 -0.5857 2.0191 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.7436 -0.6683 0.5344 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4986 0.9122 1.3219 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2319 0.3350 -0.7958 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0686 2.1454 1.0991 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8565 1.1467 1.8445 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4692 3.8678 -0.8988 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7212 4.1903 -1.6687 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4794 3.2925 -0.3594 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9207 5.6863 -0.4220 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6036 1.3427 0.8864 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3589 -1.5501 1.9036 H 0 0 0 0 0 0 0 0 0 0 0 0 2.8283 -0.0257 2.7910 H 0 0 0 0 0 0 0 0 0 0 0 0 4.8062 0.1251 1.7193 H 0 0 0 0 0 0 0 0 0 0 0 0 4.5650 -1.5874 1.1714 H 0 0 0 0 0 0 0 0 0 0 0 0 5.5859 -1.3062 -0.7219 H 0 0 0 0 0 0 0 0 0 0 0 0 4.6031 -0.6773 -2.1183 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0214 -3.2097 -1.1028 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2276 -3.3716 -1.1862 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7273 -3.3988 0.4937 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6155 -1.7685 -1.0714 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5360 -3.0704 -0.5118 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7748 -2.4522 0.5890 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.7123 -2.4553 1.7279 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2294 0.2757 -1.3457 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 2 0 5 6 1 0 6 7 1 0 4 8 1 0 8 9 2 0 8 10 1 0 10 11 1 0 11 12 1 0 12 13 1 0 13 14 1 0 14 15 1 0 15 16 1 0 16 17 2 0 17 18 1 0 18 19 1 0 19 20 1 0 20 21 2 0 20 22 1 0 22 23 1 0 22 24 1 1 17 25 1 0 22 2 1 0 25 11 1 0 25 14 1 0 1 26 1 0 1 27 1 0 1 28 1 0 2 29 1 6 3 30 1 0 3 31 1 0 5 32 1 0 6 33 1 0 6 34 1 0 7 35 1 0 11 36 1 0 12 37 1 0 12 38 1 0 13 39 1 0 13 40 1 0 15 41 1 0 15 42 1 0 16 43 1 0 18 44 1 0 18 45 1 0 23 46 1 0 23 47 1 0 23 48 1 0 24 49 1 0 25 50 1 6 M END

Standard InCHIKey	NSKVSAYYBLAAGQ-JEJIEOHYSA-N
Standard InCHI	InChI=1S/C18H25NO6/c1-11-9-12(5-8-20)16(21)25-14-4-7-19-6-3-13(15(14)19)10-24-17(22)18(11,2)23/h3,5,11,14-15,20,23H,4,6-10H2,1-2H3/b12-5+/t11-,14?,15-,18-/m0/s1
SMILES	C[C@H]1C/C(=CCO)C(=O)OC2CCN3CC=C(COC(=O)[C@@]1(C)O)[C@@H]23

Calculated Properties

Physi-Chem Properties

Molecular Weight:	351.17	Volume:	347.407 ? Van der Waals volume.
Dense:	1.011	LogP:	-0.05 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	0.635 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-1.789 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	1.0	Rigid Bonds:	22.0
TPSA:	96.3 ? Topological Polar Surface Area.	H-Bond Acceptor:	7.0
H-Bond Donor:	2.0	Rings:	3.0
Heavy Atoms:	7.0

MedChem Properties

QED Drug-Likeness Score:	0.395	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	5.119	Fsp³:	0.667
MCE-18:	52.0 ? 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:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.012	Fluc inhibitor:	0.001 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.015 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.085 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.006	Promiscuous compounds:	0.493

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.039	MDCK Permeability:	-4.837
Pgp-inhibitor:	0.004	Pgp-substrate:	0.218
PAMPA:	0.993 ? 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):	0.005
20% Bioavailability (F20%):	0.04	30% Bioavailability (F30%):	0.579
50% Bioavailability (F50%):	0.946

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.0	MRP1:	0.741
Plasma Protein Binding (PPB):	23.446%	Volume Distribution (VD):	-0.118
Fu:	79.062% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.999
OATP1B3 inhibitor:	1.0	BCRP inhibitor:	0.073
BSEP inhibitor:	0.39

ADMET: Metabolism

CYP1A2-inhibitor:	0.635	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.284	CYP2C19-substrate:	0.0
CYP2C9-inhibitor:	0.024	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.04
CYP3A4-inhibitor:	0.724	CYP3A4-substrate:	0.0
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.019
HLM stability:	0.167 ? 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):

4.6

Half-life (T1/2):

2.298

ADMET: Toxicity

hERG Blockers:	0.022	hERG Blockers (10um):	0.101
Human Hepatotoxicity (H-HT):	0.87	Drug-induced Liver Injury (DILI):	0.613
AMES Toxicity:	0.448	Rat Oral Acute Toxicity:	0.198
Maximum Recommended Daily Dose:	0.898	Skin Sensitization:	1.0
Carcinogencity:	0.886	Eye Corrosion:	0.001
Eye Irritation:	0.166	Respiratory Toxicity:	0.229
Drug-induced Neurotoxicity:	0.267	Ototoxicity:	0.677
Hematotoxicity:	0.669	Drug-induced Nephrotoxicity:	0.958
Genotoxicity:	0.992	RPMI-8226 Immunitoxicity:	0.215
A549 Cytotoxicity:	0.034	Hek293 Cytotoxicity:	0.178
BCF:	0.353 ? 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:	3.059 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	4.627 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	3.788 ? 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
NPO59489	Solanecio angulatus	Species	Asteraceae	Eukaryota	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

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 NPC555407 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	18659
0.1-0.2	29897
0.2-0.3	1266
0.3-0.4	7
0.4-0.5	9
0.5-0.6	2
0.6-0.7	7
0.7-0.8	0
0.8-0.85	0
0.85-0.9	2
0.9-0.95	0
0.95-1	0

Similarity Score	Similarity Level	Natural Product ID
0.875	High Similarity	NPC130124
0.875	High Similarity	NPC193471
0.7705	Intermediate Similarity	NPC201889
0.7705	Intermediate Similarity	NPC106791
0.7705	Intermediate Similarity	NPC607716
0.7258	Intermediate Similarity	NPC47857
0.7258	Intermediate Similarity	NPC181510
0.7258	Intermediate Similarity	NPC168758
0.7258	Intermediate Similarity	NPC602310
0.7213	Intermediate Similarity	NPC608663
0.7143	Intermediate Similarity	NPC23963
0.6562	Remote Similarity	NPC608751
0.6508	Remote Similarity	NPC30911
0.6462	Remote Similarity	NPC609037
0.625	Remote Similarity	NPC608092
0.6119	Remote Similarity	NPC316984
0.6119	Remote Similarity	NPC608959
0.6087	Remote Similarity	NPC600980
0.5714	Remote Similarity	NPC474497
0.5286	Remote Similarity	NPC235625

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC555407 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	5560
0.1-0.2	3557
0.2-0.3	32
0.3-0.4	0
0.4-0.5	0
0.5-0.6	0
0.6-0.7	1
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
0.6508	Remote Similarity	NPD2204	Approved

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