NPASS Compound

Natural Product: NPC474114

Natural Product ID	NPC474114
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	(2Z,6E,10E,14E)-16-(2,5-Dihydroxy-3-Methylphenyl)-1,12-Dihydroxy-2,6,10,14-Tetramethylhexadeca-2,6,10,14-Tetraen-4-One
IUPAC Name	(2Z,6E,10E,14E)-16-(2,5-dihydroxy-3-methylphenyl)-1,12-dihydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,14-tetraen-4-one
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL462112
PubChem CID	44559658
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0001551] Diterpenoids

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 70 70 0 0 0 0 0 0 0 0999 V2000 -7.0526 1.9926 -1.5624 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.2557 0.5705 -1.4592 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.9525 -0.0658 -2.7132 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.0748 -0.9678 -2.9846 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1567 -1.5869 -2.1099 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3883 -2.4732 -2.7364 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.9021 -1.4427 -0.7061 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7424 -0.5531 -0.3639 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7089 -0.9820 0.3316 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5177 -0.1864 0.7205 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4698 -0.1810 2.2357 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3114 0.5663 2.7870 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5779 1.1469 1.9980 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7488 1.9013 2.4771 C 0 0 0 0 0 0 0 0 0 0 0 0 2.7816 1.1530 3.2213 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4662 0.0491 2.5102 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2094 -0.2384 1.2650 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8946 -1.3433 0.5537 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5214 -0.8953 -0.6944 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8752 -1.1800 -1.9003 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4339 -0.7713 -3.0839 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7471 -1.0810 -4.2606 O 0 0 0 0 0 0 0 0 0 0 0 0 5.6177 -0.0880 -3.0904 C 0 0 0 0 0 0 0 0 0 0 0 0 6.2420 0.1849 -1.8989 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7084 -0.2122 -0.6714 C 0 0 0 0 0 0 0 0 0 0 0 0 6.4075 0.1074 0.4824 O 0 0 0 0 0 0 0 0 0 0 0 0 7.5478 0.9311 -1.8773 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4749 -0.8011 3.2421 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3525 3.0742 3.1565 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.2014 0.6518 4.2570 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7341 0.8529 -0.8328 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.7903 0.4012 -3.8995 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.4375 2.4118 -0.7421 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.9283 0.2082 -0.5222 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.4145 0.5568 -1.3658 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.0153 -1.3253 -4.0668 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.5704 -2.5291 -0.3719 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.6883 -1.2681 0.0147 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7441 -2.0344 0.6502 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5843 -0.7146 0.3775 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5659 0.8380 0.3096 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5298 -1.2247 2.5751 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4097 0.3072 2.6052 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3437 1.0247 0.9176 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2575 2.3131 1.5512 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6351 1.8543 3.5246 H 0 0 0 0 0 0 0 0 0 0 0 0 2.4230 0.6843 4.1880 H 0 0 0 0 0 0 0 0 0 0 0 0 2.4902 0.3203 0.6704 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1602 -2.1450 0.3552 H 0 0 0 0 0 0 0 0 0 0 0 0 4.7274 -1.7436 1.1949 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9340 -1.7217 -1.9125 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0635 -1.8487 -4.8178 H 0 0 0 0 0 0 0 0 0 0 0 0 6.0430 0.2267 -4.0352 H 0 0 0 0 0 0 0 0 0 0 0 0 6.6297 1.0984 0.6488 H 0 0 0 0 0 0 0 0 0 0 0 0 7.3692 2.0102 -1.9328 H 0 0 0 0 0 0 0 0 0 0 0 0 8.1390 0.6420 -0.9799 H 0 0 0 0 0 0 0 0 0 0 0 0 8.1608 0.6369 -2.7532 H 0 0 0 0 0 0 0 0 0 0 0 0 4.4172 -0.5895 4.3426 H 0 0 0 0 0 0 0 0 0 0 0 0 5.5054 -0.6146 2.9133 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1834 -1.8599 3.1332 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7715 3.5862 2.5482 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2825 1.5468 4.6366 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2365 0.5560 4.7277 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3124 -0.2711 4.6167 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4484 0.9438 -1.6846 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7328 1.1344 -1.2693 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.0461 1.5256 -0.0125 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.9248 -0.4599 -4.5528 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.7370 0.7538 -3.4898 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.1834 1.1754 -4.3849 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 3 4 2 0 4 5 1 0 5 6 2 0 5 7 1 0 7 8 1 0 8 9 2 0 9 10 1 0 10 11 1 0 11 12 1 0 12 13 2 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 2 0 20 21 1 0 21 22 1 0 21 23 2 0 23 24 1 0 24 25 2 0 25 26 1 0 24 27 1 0 16 28 1 0 14 29 1 0 12 30 1 0 8 31 1 0 3 32 1 0 25 19 1 0 1 33 1 0 2 34 1 0 2 35 1 0 4 36 1 0 7 37 1 0 7 38 1 0 9 39 1 0 10 40 1 0 10 41 1 0 11 42 1 0 11 43 1 0 13 44 1 0 14 45 1 0 15 46 1 0 15 47 1 0 17 48 1 0 18 49 1 0 18 50 1 0 20 51 1 0 22 52 1 0 23 53 1 0 26 54 1 0 27 55 1 0 27 56 1 0 27 57 1 0 28 58 1 0 28 59 1 0 28 60 1 0 29 61 1 0 30 62 1 0 30 63 1 0 30 64 1 0 31 65 1 0 31 66 1 0 31 67 1 0 32 68 1 0 32 69 1 0 32 70 1 0 M END

Standard InCHIKey	GPMAKHULTRCGTA-PNDALFHPSA-N
Standard InCHI	InChI=1S/C27H38O5/c1-18(7-6-8-19(2)12-25(30)14-21(4)17-28)11-24(29)13-20(3)9-10-23-16-26(31)15-22(5)27(23)32/h8-9,11,14-16,24,28-29,31-32H,6-7,10,12-13,17H2,1-5H3/b18-11+,19-8+,20-9+,21-14-
SMILES	OC/C(=CC(=O)C/C(=C/CC/C(=C/C(C/C(=C/Cc1cc(O)cc(c1O)C)/C)O)/C)/C)/C

Calculated Properties

Physi-Chem Properties

Molecular Weight:	442.27	Volume:	489.851 ? Van der Waals volume.
Dense:	0.903	LogP:	4.299 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	3.416 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-4.264 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	12.0	Rigid Bonds:	11.0
TPSA:	97.99 ? Topological Polar Surface Area.	H-Bond Acceptor:	5.0
H-Bond Donor:	4.0	Rings:	1.0
Heavy Atoms:	5.0

MedChem Properties

QED Drug-Likeness Score:	0.202	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	3.995	Fsp³:	0.444
MCE-18:	26.0 ? 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:	1
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.873	Fluc inhibitor:	0.157 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.004 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.201 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.504	Promiscuous compounds:	0.006

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.381	MDCK Permeability:	-4.983
Pgp-inhibitor:	0.113	Pgp-substrate:	0.0
PAMPA:	0.105 ? 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):	0.001
20% Bioavailability (F20%):	0.117	30% Bioavailability (F30%):	0.351
50% Bioavailability (F50%):	0.96

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.0	MRP1:	0.908
Plasma Protein Binding (PPB):	82.942%	Volume Distribution (VD):	0.13
Fu:	20.235% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	1.0
OATP1B3 inhibitor:	1.0	BCRP inhibitor:	0.0
BSEP inhibitor:	0.518

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	0.002
CYP2C19-inhibitor:	0.751	CYP2C19-substrate:	0.024
CYP2C9-inhibitor:	0.004	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.102	CYP2D6-substrate:	0.0
CYP3A4-inhibitor:	0.108	CYP3A4-substrate:	0.307
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.769
HLM stability:	0.447 ? 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):

9.054

Half-life (T1/2):

1.235

ADMET: Toxicity

hERG Blockers:	0.044	hERG Blockers (10um):	0.439
Human Hepatotoxicity (H-HT):	0.775	Drug-induced Liver Injury (DILI):	0.028
AMES Toxicity:	0.073	Rat Oral Acute Toxicity:	0.225
Maximum Recommended Daily Dose:	0.755	Skin Sensitization:	0.969
Carcinogencity:	0.16	Eye Corrosion:	0.0
Eye Irritation:	0.544	Respiratory Toxicity:	0.973
Drug-induced Neurotoxicity:	0.103	Ototoxicity:	0.832
Hematotoxicity:	0.263	Drug-induced Nephrotoxicity:	0.229
Genotoxicity:	0.249	RPMI-8226 Immunitoxicity:	0.052
A549 Cytotoxicity:	0.189	Hek293 Cytotoxicity:	0.68
BCF:	2.06 ? 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:	4.966 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	6.443 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	5.71 ? 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
NPO8863	Cystoseira crinita	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[12880316]
NPO8863	Cystoseira crinita	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO8863	Cystoseira crinita	Species	Sargassaceae	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
Activity	8
Inhibition	5
GI50	3
TGI	3

Activity Type	# Activity
Cell line	4
Others	8
Non-molecular	7

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
NPT65	Cell line	HepG2	Homo sapiens	GI50	=	1.8	ug.mL-1	PMID[24992075]
NPT65	Cell line	HepG2	Homo sapiens	TGI	=	3.5	ug.mL-1	PMID[23062825]
NPT83	Cell line	MCF7	Homo sapiens	TGI	=	2.5	ug.mL-1	DrugMatrix in vitro pharmacology data
NPT83	Cell line	MCF7	Homo sapiens	GI50	=	1.6	ug.mL-1	DrugMatrix in vitro pharmacology data
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	Inhibition	=	9.0	%	PMID[12880316]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	Inhibition	=	22.3	%	PMID[12880316]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	Inhibition	=	35.3	%	PMID[12880316]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	Inhibition	=	67.5	%	PMID[12880316]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	Inhibition	=	71.1	%	PMID[12880316]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	GI50	=	0.9	ug.mL-1	PMID[12880316]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	TGI	=	2.4	ug.mL-1	PMID[12880316]
NPT1	Others	Radical scavenging activity	n.a.	Activity	=	7.4	%	PMID[8450319]
NPT1	Others	Radical scavenging activity	n.a.	Activity	=	16.2	%	PMID[25871261]
NPT1	Others	Radical scavenging activity	n.a.	Activity	=	30.7	%	PMID[22483590]
NPT1	Others	Radical scavenging activity	n.a.	Activity	=	79.2	%	PMID[16872140]
NPT1	Others	Radical scavenging activity	n.a.	Activity	=	95.6	%	DOI[10.6019/CHEMBL1201861]
NPT1	Others	Radical scavenging activity	n.a.	Activity	=	95.7	%	PMID[17488817]
NPT35	Others	n.a.	n.a.	Activity	=	0.09	mmol/L	PMID[20429578]
NPT2	Others	Unspecified	n.a.	Activity	=	0.72	mmol/L	PMID[25647077]

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 NPC474114 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	10456
0.1-0.2	37093
0.2-0.3	2142
0.3-0.4	144
0.4-0.5	13
0.5-0.6	2
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	0

Similarity Score	Similarity Level	Natural Product ID
0.7812	Intermediate Similarity	NPC474050
0.7344	Intermediate Similarity	NPC28784
0.7344	Intermediate Similarity	NPC296144
0.6984	Remote Similarity	NPC208229
0.6719	Remote Similarity	NPC282855
0.6719	Remote Similarity	NPC26013
0.6667	Remote Similarity	NPC68260
0.6667	Remote Similarity	NPC279887
0.5385	Remote Similarity	NPC278832
0.5385	Remote Similarity	NPC64157

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC474114 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	3598
0.1-0.2	5512
0.2-0.3	39
0.3-0.4	1
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