NPASS Compound

Natural Product: NPC329857

Natural Product ID	NPC329857
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	FGMVUGQMSRSYDL-JDROQCLMSA-N
IUPAC Name	n.a.
Synonyms	12-Epieupalmerone
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL522252
PubChem CID	5472714
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000261] Phenylpropanoids and polyketides [CHEMONTID:0000147] Macrolides and analogues

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 52 54 0 0 0 0 0 0 0 0999 V2000 0.2369 3.8838 -0.6847 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1687 2.3681 -0.6892 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7274 1.9400 0.6732 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2015 2.1935 0.8004 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0281 1.3935 -0.1560 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8860 -0.0847 -0.0068 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4759 -0.8903 -0.9620 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3399 -2.3307 -0.8074 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0604 -2.9756 -1.2208 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1231 -2.5816 -0.4054 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5754 -1.2879 -0.5220 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0112 -1.7273 0.6825 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.0046 -0.8722 -0.4733 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2693 0.2364 0.5499 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2221 1.6162 -0.0564 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1258 1.7917 -1.0031 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3307 1.4072 -2.1690 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.5011 1.6779 -0.7107 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.4360 0.9518 0.0089 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7038 0.9992 -0.1184 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.6919 0.1190 0.9440 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1580 -0.5972 1.9383 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0345 -3.7645 -0.0751 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2595 -0.6974 1.2619 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0875 4.3031 0.2940 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3338 4.3341 -1.5156 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2953 4.1916 -0.8086 H 0 0 0 0 0 0 0 0 0 0 0 0 0.9575 2.0597 -1.4398 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2083 2.5066 1.4866 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5751 0.8699 0.7842 H 0 0 0 0 0 0 0 0 0 0 0 0 2.4867 1.8669 1.8318 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3896 3.2589 0.6355 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9039 1.6577 -1.2231 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1058 1.6624 0.0585 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2675 -0.3955 -1.8653 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2155 -2.7794 -1.3860 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5983 -2.6564 0.2620 H 0 0 0 0 0 0 0 0 0 0 0 0 0.8767 -2.6628 -2.3015 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2445 -4.0803 -1.2078 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0741 -0.5229 -1.0390 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3373 -0.5901 -1.4732 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6158 -1.7682 -0.1648 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5877 0.1344 1.4208 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2424 2.3336 0.7693 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2250 -0.5933 2.1166 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5146 -1.1714 2.5607 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3734 -4.5494 0.3553 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4607 -4.1130 -1.0302 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.7757 -3.4889 0.6816 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3829 -1.1012 1.7982 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7608 0.0573 1.9325 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9921 -1.5321 1.1529 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 3 7 8 1 0 8 9 1 0 9 10 1 0 10 11 1 0 11 12 1 0 11 13 1 0 13 14 1 0 14 15 1 0 15 16 1 0 16 17 2 0 15 18 1 0 18 19 1 0 19 20 2 0 19 21 1 0 21 22 2 0 10 23 1 0 6 24 1 0 16 2 1 0 12 10 1 0 21 14 1 0 1 25 1 0 1 26 1 0 1 27 1 0 2 28 1 0 3 29 1 0 3 30 1 0 4 31 1 0 4 32 1 0 5 33 1 0 5 34 1 0 7 35 1 0 8 36 1 0 8 37 1 0 9 38 1 0 9 39 1 0 11 40 1 0 13 41 1 0 13 42 1 0 14 43 1 0 15 44 1 0 22 45 1 0 22 46 1 0 23 47 1 0 23 48 1 0 23 49 1 0 24 50 1 0 24 51 1 0 24 52 1 0 M END

Standard InCHIKey	FGMVUGQMSRSYDL-JDROQCLMSA-N
Standard InCHI	InChI=1S/C20H28O4/c1-12-7-5-9-13(2)17(21)18-15(14(3)19(22)23-18)11-16-20(4,24-16)10-6-8-12/h8,13,15-16,18H,3,5-7,9-11H2,1-2,4H3/b12-8+/t13-,15+,16-,18-,20-/m1/s1
SMILES	CC1CCCC(=CCCC2(C(O2)CC3C(C1=O)OC(=O)C3=C)C)C

Calculated Properties

Physi-Chem Properties

Molecular Weight:	332.2	Volume:	353.422 ? Van der Waals volume.
Dense:	0.94	LogP:	2.757 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	2.914 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-3.692 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	0.0	Rigid Bonds:	23.0
TPSA:	55.9 ? Topological Polar Surface Area.	H-Bond Acceptor:	4.0
H-Bond Donor:	0.0	Rings:	3.0
Heavy Atoms:	4.0

MedChem Properties

QED Drug-Likeness Score:	0.293	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	4.978	Fsp³:	0.7
MCE-18:	52.941 ? 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:	0.078	Fluc inhibitor:	0.001 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.012 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.379 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.454	Promiscuous compounds:	0.001

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-4.588	MDCK Permeability:	-4.674
Pgp-inhibitor:	0.853	Pgp-substrate:	0.0
PAMPA:	0.047 ? 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):	0.002
20% Bioavailability (F20%):	0.001	30% Bioavailability (F30%):	0.007
50% Bioavailability (F50%):	0.023

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.01	MRP1:	0.936
Plasma Protein Binding (PPB):	90.724%	Volume Distribution (VD):	0.217
Fu:	6.743% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.437
OATP1B3 inhibitor:	0.997	BCRP inhibitor:	0.0
BSEP inhibitor:	1.0

ADMET: Metabolism

CYP1A2-inhibitor:	0.731	CYP1A2-substrate:	0.048
CYP2C19-inhibitor:	0.999	CYP2C19-substrate:	0.003
CYP2C9-inhibitor:	0.886	CYP2C9-substrate:	0.002
CYP2D6-inhibitor:	0.29	CYP2D6-substrate:	0.253
CYP3A4-inhibitor:	0.209	CYP3A4-substrate:	0.008
CYP2B6-substrate:	0.989	CYP2C8-inhibitor:	0.065
HLM stability:	0.892 ? 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):

9.357

Half-life (T1/2):

0.976

ADMET: Toxicity

hERG Blockers:	0.024	hERG Blockers (10um):	0.378
Human Hepatotoxicity (H-HT):	0.556	Drug-induced Liver Injury (DILI):	0.576
AMES Toxicity:	0.08	Rat Oral Acute Toxicity:	0.218
Maximum Recommended Daily Dose:	0.689	Skin Sensitization:	0.882
Carcinogencity:	0.637	Eye Corrosion:	0.031
Eye Irritation:	0.376	Respiratory Toxicity:	0.138
Drug-induced Neurotoxicity:	0.542	Ototoxicity:	0.746
Hematotoxicity:	0.296	Drug-induced Nephrotoxicity:	0.171
Genotoxicity:	0.059	RPMI-8226 Immunitoxicity:	0.09
A549 Cytotoxicity:	0.15	Hek293 Cytotoxicity:	0.207
BCF:	1.023 ? 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:	3.633 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.328 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.687 ? 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
NPO24786	Eunicea pinta	Species	Plexauridae	Eukaryota	n.a.	n.a.	n.a.	PMID[12350138]
NPO24786	Eunicea pinta	Species	Plexauridae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO24786	Eunicea pinta	Species	Plexauridae	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

Activity Type	# Activity
IC50	2
GI50	52

Activity Type	# Activity
Cell line	54

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
NPT388	Cell line	NCI-H322M	Homo sapiens	IC50	=	0.9	ug.mL-1	PMID[24582402]
NPT384	Cell line	TK-10	Homo sapiens	IC50	=	0.13	ug.mL-1	PMID[24582402]
NPT368	Cell line	SN12C	Homo sapiens	GI50	n.a.	5533.5	nM	PMID[11170670]
NPT367	Cell line	MDA-N	Homo sapiens	GI50	n.a.	2735.27	nM	PMID[17363259]
NPT370	Cell line	NCI-H23	Homo sapiens	GI50	n.a.	13995.87	nM	PMID[24180210]
NPT369	Cell line	ACHN	Homo sapiens	GI50	n.a.	1336.6	nM	PMID[20850971]
NPT371	Cell line	UO-31	Homo sapiens	GI50	n.a.	1618.08	nM	PMID[22037378]
NPT372	Cell line	HOP-92	Homo sapiens	GI50	n.a.	1002.31	nM	PMID[9599259]
NPT90	Cell line	DU-145	Homo sapiens	GI50	n.a.	2558.59	nM	PMID[17323939]
NPT116	Cell line	HL-60	Homo sapiens	GI50	n.a.	2716.44	nM	DrugMatrix in vitro pharmacology data
NPT374	Cell line	SF-539	Homo sapiens	GI50	n.a.	2393.32	nM	DrugMatrix in vitro pharmacology data
NPT373	Cell line	SK-MEL-5	Homo sapiens	GI50	n.a.	7585.78	nM	PMID[22304344]
NPT376	Cell line	A498	Homo sapiens	GI50	n.a.	18365.38	nM	PMID[20402524]
NPT111	Cell line	K562	Homo sapiens	GI50	n.a.	2070.14	nM	DOI[10.6019/CHEMBL1201861]
NPT377	Cell line	OVCAR-3	Homo sapiens	GI50	n.a.	1737.8	nM	PMID[21982797]
NPT112	Cell line	MOLT-4	Homo sapiens	GI50	n.a.	1610.65	nM	PMID[19449879]
NPT378	Cell line	NCI/ADR-RES	Homo sapiens	GI50	n.a.	13995.87	nM	PMID[17844995]
NPT379	Cell line	HOP-62	Homo sapiens	GI50	n.a.	11641.26	nM	PMID[22537363]
NPT380	Cell line	U-251	Homo sapiens	GI50	n.a.	2673.01	nM	PMID[25924111]
NPT381	Cell line	OVCAR-8	Homo sapiens	GI50	n.a.	1686.55	nM	PMID[20961671]
NPT382	Cell line	OVCAR-5	Homo sapiens	GI50	n.a.	5597.58	nM	PMID[16933872]
NPT82	Cell line	MDA-MB-231	Homo sapiens	GI50	n.a.	10690.55	nM	PubChem BioAssay data set
NPT383	Cell line	SNB-19	Homo sapiens	GI50	n.a.	11428.78	nM	PMID[17190456]
NPT385	Cell line	SR	Homo sapiens	GI50	n.a.	2454.71	nM	PMID[12444692]
NPT384	Cell line	TK-10	Homo sapiens	GI50	n.a.	135.21	nM	DrugMatrix in vitro pharmacology data
NPT323	Cell line	SW-620	Homo sapiens	GI50	n.a.	1563.15	nM	PMID[12542351]
NPT386	Cell line	KM12	Homo sapiens	GI50	n.a.	4295.36	nM	Patent: US9115116 B2
NPT455	Cell line	NCI-H522	Homo sapiens	GI50	n.a.	1667.25	nM	PMID[12880316]
NPT387	Cell line	M14	Homo sapiens	GI50	n.a.	1674.94	nM	PMID[17242147]
NPT388	Cell line	NCI-H322M	Homo sapiens	GI50	n.a.	901.57	nM	PMID[25760525]
NPT389	Cell line	RPMI-8226	Homo sapiens	GI50	n.a.	2249.05	nM	PMID[12027740]
NPT390	Cell line	LOX IMVI	Homo sapiens	GI50	n.a.	1485.94	nM	PMID[19715321]
NPT147	Cell line	SK-MEL-2	Homo sapiens	GI50	n.a.	5260.17	nM	PMID[24359277]
NPT81	Cell line	A549	Homo sapiens	GI50	n.a.	5821.03	nM	PMID[19228038]
NPT148	Cell line	HCT-15	Homo sapiens	GI50	n.a.	1555.97	nM	PMID[22313254]
NPT393	Cell line	HCT-116	Homo sapiens	GI50	n.a.	1047.13	nM	PMID[12762820]
NPT395	Cell line	SF-268	Homo sapiens	GI50	n.a.	4539.42	nM	PubChem BioAssay data set
NPT306	Cell line	PC-3	Homo sapiens	GI50	n.a.	6760.83	nM	PMID[25052206]
NPT83	Cell line	MCF7	Homo sapiens	GI50	n.a.	3019.95	nM	PMID[23046382]
NPT146	Cell line	SK-OV-3	Homo sapiens	GI50	n.a.	16368.17	nM	PMID[18313805]
NPT396	Cell line	T47D	Homo sapiens	GI50	n.a.	2013.72	nM	PMID[18183025]
NPT397	Cell line	NCI-H460	Homo sapiens	GI50	n.a.	15417.0	nM	PMID[22037378]
NPT308	Cell line	CAKI-1	Homo sapiens	GI50	n.a.	1667.25	nM	PMID[17447750]
NPT398	Cell line	UACC-62	Homo sapiens	GI50	n.a.	5058.25	nM	DOI[10.1039/C5MD00589B]
NPT400	Cell line	MDA-MB-435	Homo sapiens	GI50	n.a.	1981.53	nM	PMID[12398531]
NPT399	Cell line	SF-295	Homo sapiens	GI50	n.a.	14028.14	nM	PMID[25739048]
NPT458	Cell line	IGROV-1	Homo sapiens	GI50	n.a.	2760.58	nM	PubChem BioAssay data set
NPT401	Cell line	786-0	Homo sapiens	GI50	n.a.	1621.81	nM	PMID[12105963]
NPT402	Cell line	Hs-578T	Homo sapiens	GI50	n.a.	6338.7	nM	PMID[8691207]
NPT403	Cell line	UACC-257	Homo sapiens	GI50	n.a.	2985.38	nM	PMID[26927426]
NPT404	Cell line	CCRF-CEM	Homo sapiens	GI50	n.a.	1183.04	nM	PMID[19489596]
NPT405	Cell line	NCI-H226	Homo sapiens	GI50	n.a.	17741.89	nM	PMID[12193011]
NPT139	Cell line	HT-29	Homo sapiens	GI50	n.a.	1896.71	nM	PMID[21419633]
NPT407	Cell line	COLO 205	Homo sapiens	GI50	n.a.	1581.25	nM	PMID[9461661]

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 NPC329857 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	19598
0.1-0.2	27071
0.2-0.3	2844
0.3-0.4	278
0.4-0.5	46
0.5-0.6	15
0.6-0.7	5
0.7-0.8	0
0.8-0.85	0
0.85-0.9	0
0.9-0.95	0
0.95-1	1

Similarity Score	Similarity Level	Natural Product ID
1.0	High Similarity	NPC469718
0.678	Remote Similarity	NPC482125
0.678	Remote Similarity	NPC482124
0.6207	Remote Similarity	NPC272814
0.619	Remote Similarity	NPC474947
0.6071	Remote Similarity	NPC256273
0.5968	Remote Similarity	NPC474035
0.5968	Remote Similarity	NPC81386
0.5806	Remote Similarity	NPC231889
0.5645	Remote Similarity	NPC476275
0.5469	Remote Similarity	NPC476270
0.5333	Remote Similarity	NPC605615
0.5254	Remote Similarity	NPC38468
0.5254	Remote Similarity	NPC192678
0.5254	Remote Similarity	NPC319795
0.5254	Remote Similarity	NPC50362
0.5254	Remote Similarity	NPC488056
0.5254	Remote Similarity	NPC605079
0.5161	Remote Similarity	NPC489677
0.5077	Remote Similarity	NPC157416
0.5077	Remote Similarity	NPC244841

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC329857 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	6884
0.1-0.2	2209
0.2-0.3	54
0.3-0.4	2
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
0.5254	Remote Similarity	NPD1733	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