NPASS Compound

Natural Product: NPC74958

Natural Product ID	NPC74958
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	ZEPPIMJETZCFFQ-UHFFFAOYSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	57381726
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000261] Phenylpropanoids and polyketides [CHEMONTID:0000334] Flavonoids [CHEMONTID:0002585] O-methylated flavonoids [CHEMONTID:0002591] 6-O-methylated flavonoids

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 47 49 0 0 0 0 0 0 0 0999 V2000 6.5746 -0.5446 0.1295 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9202 0.4185 1.2030 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9876 1.0702 1.8479 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5644 0.9388 1.6050 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1655 0.0436 0.6017 O 0 0 0 0 0 0 0 0 0 0 0 0 2.8414 -0.1608 0.2862 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8690 0.5257 0.9660 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5411 0.3230 0.6521 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1601 -0.5690 -0.3465 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1426 -1.2548 -1.0248 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4868 -1.0444 -0.7013 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2615 -0.7533 -0.6470 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.7197 -1.6060 -1.6081 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0983 -1.6879 -1.7941 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.5774 -2.4544 -2.6628 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.9611 -0.9319 -1.0310 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4145 -0.0964 -0.0823 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2805 0.6743 0.6967 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.6482 0.6135 0.5345 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.2023 -0.2243 -0.4172 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.3241 -0.9713 -1.1695 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8494 -1.8210 -2.1320 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.5809 -0.2753 -0.5694 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.3195 0.5373 -1.4296 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.4792 1.3938 1.3263 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1227 -0.0442 0.0652 O 0 0 0 0 0 0 0 0 0 0 0 0 8.3818 0.6171 1.5218 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9576 -1.3488 0.5856 H 0 0 0 0 0 0 0 0 0 0 0 0 7.5047 -0.9850 -0.3286 H 0 0 0 0 0 0 0 0 0 0 0 0 6.0135 -0.0850 -0.7014 H 0 0 0 0 0 0 0 0 0 0 0 0 6.2952 1.7772 2.6397 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1384 1.9659 1.3759 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0073 0.6283 2.5341 H 0 0 0 0 0 0 0 0 0 0 0 0 2.1637 1.2172 1.7402 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.2054 0.8834 1.2103 H 0 0 0 0 0 0 0 0 0 0 0 0 0.9037 -1.9568 -1.8065 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2653 -1.5720 -1.2216 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0354 -2.1951 -2.2020 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.8069 1.3262 1.4401 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.5470 -1.4254 -2.7500 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.3287 0.1542 -2.4498 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.3712 0.6440 -1.0476 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.8924 1.5751 -1.3467 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.0851 2.2657 1.7080 H 0 0 0 0 0 0 0 0 0 0 0 0 8.8603 -0.3727 1.3886 H 0 0 0 0 0 0 0 0 0 0 0 0 8.8598 1.3307 0.8469 H 0 0 0 0 0 0 0 0 0 0 0 0 8.5069 0.9572 2.5644 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 2 3 3 4 1 0 4 5 1 0 5 6 1 0 6 7 2 0 7 8 1 0 8 9 2 0 9 10 1 0 10 11 2 0 9 12 1 0 12 13 2 0 13 14 1 0 14 15 2 0 14 16 1 0 16 17 2 0 17 18 1 0 18 19 2 0 19 20 1 0 20 21 2 0 21 22 1 0 20 23 1 0 23 24 1 0 19 25 1 0 17 26 1 0 2 27 1 0 11 6 1 0 26 12 1 0 21 16 1 0 1 28 1 0 1 29 1 0 1 30 1 0 3 31 1 0 4 32 1 0 4 33 1 0 7 34 1 0 8 35 1 0 10 36 1 0 11 37 1 0 13 38 1 0 18 39 1 0 22 40 1 0 24 41 1 0 24 42 1 0 24 43 1 0 25 44 1 0 27 45 1 0 27 46 1 0 27 47 1 0 M END

Standard InCHIKey	ZEPPIMJETZCFFQ-UHFFFAOYSA-N
Standard InCHI	InChI=1S/C21H20O6/c1-12(2)8-9-26-14-6-4-13(5-7-14)17-10-15(22)19-18(27-17)11-16(23)21(25-3)20(19)24/h4-8,10-11,23-24H,9H2,1-3H3
SMILES	CC(=CCOc1ccc(cc1)c1cc(=O)c2c(cc(c(c2O)OC)O)o1)C

Calculated Properties

Physi-Chem Properties

Molecular Weight:	368.13	Volume:	375.116 ? Van der Waals volume.
Dense:	0.981	LogP:	4.314 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	3.419 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-4.997 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	5.0	Rigid Bonds:	19.0
TPSA:	89.13 ? Topological Polar Surface Area.	H-Bond Acceptor:	6.0
H-Bond Donor:	2.0	Rings:	3.0
Heavy Atoms:	6.0

MedChem Properties

QED Drug-Likeness Score:	0.655	GASA:	0.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	2.572	Fsp³:	0.19
MCE-18:	19.0 ? 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:	Accepted
Golden Triangle Rule:	Rejected	BMS Rule:	0
Chelating Alert:	1	PAINS Alert:	0
Colloidal aggregators:	0.811	Fluc inhibitor:	0.898 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.974 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.781 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.234	Promiscuous compounds:	0.178

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-4.894	MDCK Permeability:	-4.657
Pgp-inhibitor:	0.566	Pgp-substrate:	0.405
PAMPA:	0.149 ? 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):	0.025
20% Bioavailability (F20%):	0.219	30% Bioavailability (F30%):	0.583
50% Bioavailability (F50%):	0.868

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.089	MRP1:	0.888
Plasma Protein Binding (PPB):	97.73%	Volume Distribution (VD):	-0.47
Fu:	1.892% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.651
OATP1B3 inhibitor:	0.942	BCRP inhibitor:	0.901
BSEP inhibitor:	0.762

ADMET: Metabolism

CYP1A2-inhibitor:	0.975	CYP1A2-substrate:	0.791
CYP2C19-inhibitor:	0.12	CYP2C19-substrate:	0.004
CYP2C9-inhibitor:	0.994	CYP2C9-substrate:	0.012
CYP2D6-inhibitor:	1.0	CYP2D6-substrate:	0.999
CYP3A4-inhibitor:	0.002	CYP3A4-substrate:	0.159
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	1.0
HLM stability:	0.954 ? 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):

5.255

Half-life (T1/2):

1.0

ADMET: Toxicity

hERG Blockers:	0.16	hERG Blockers (10um):	0.57
Human Hepatotoxicity (H-HT):	0.476	Drug-induced Liver Injury (DILI):	0.77
AMES Toxicity:	0.58	Rat Oral Acute Toxicity:	0.341
Maximum Recommended Daily Dose:	0.59	Skin Sensitization:	0.72
Carcinogencity:	0.706	Eye Corrosion:	0.118
Eye Irritation:	0.971	Respiratory Toxicity:	0.817
Drug-induced Neurotoxicity:	0.097	Ototoxicity:	0.184
Hematotoxicity:	0.229	Drug-induced Nephrotoxicity:	0.123
Genotoxicity:	0.651	RPMI-8226 Immunitoxicity:	0.071
A549 Cytotoxicity:	0.277	Hek293 Cytotoxicity:	0.505
BCF:	1.647 ? 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:	4.341 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.392 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	5.044 ? 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
NPO1170	Amyris madrensis	Species	Rutaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[22260294]
NPO1170	Amyris madrensis	Species	Rutaceae	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 NPC74958 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	21889
0.1-0.2	24471
0.2-0.3	2632
0.3-0.4	664
0.4-0.5	175
0.5-0.6	16
0.6-0.7	6
0.7-0.8	0
0.8-0.85	1
0.85-0.9	0
0.9-0.95	0
0.95-1	0

Similarity Score	Similarity Level	Natural Product ID
0.8065	Intermediate Similarity	NPC213622
0.7903	Intermediate Similarity	NPC470402
0.7857	Intermediate Similarity	NPC156222
0.7	Intermediate Similarity	NPC256283
0.678	Remote Similarity	NPC293183
0.6667	Remote Similarity	NPC241498
0.6613	Remote Similarity	NPC255350
0.6557	Remote Similarity	NPC100887
0.6129	Remote Similarity	NPC284552
0.6094	Remote Similarity	NPC83508
0.5873	Remote Similarity	NPC44079
0.5781	Remote Similarity	NPC184136
0.5781	Remote Similarity	NPC231772
0.5781	Remote Similarity	NPC145379
0.5625	Remote Similarity	NPC203891
0.5385	Remote Similarity	NPC274327
0.5385	Remote Similarity	NPC29353
0.5303	Remote Similarity	NPC57030
0.5294	Remote Similarity	NPC160951
0.5294	Remote Similarity	NPC52005
0.5224	Remote Similarity	NPC603662
0.5152	Remote Similarity	NPC600177
0.5075	Remote Similarity	NPC176775
0.5075	Remote Similarity	NPC266597
0.5075	Remote Similarity	NPC604462
0.5072	Remote Similarity	NPC223579

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC74958 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4178
0.1-0.2	4836
0.2-0.3	127
0.3-0.4	6
0.4-0.5	2
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
0.6613	Remote Similarity	NPD2801	Pre-clinical

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