NPASS Compound

Natural Product: NPC25209

Natural Product ID	NPC25209
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	CYCDWLJKDQJNEU-HOMHNTCQSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	21579206
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0004603] Organic oxygen compounds [CHEMONTID:0000323] Organooxygen compounds [CHEMONTID:0000011] Carbohydrates and carbohydrate conjugates [CHEMONTID:0002105] Glycosyl compounds [CHEMONTID:0004165] Phenolic glycosides

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 79 82 0 0 0 0 0 0 0 0999 V2000 11.3252 -2.9788 -1.3264 C 0 0 0 0 0 0 0 0 0 0 0 0 11.2403 -2.0470 -0.2579 O 0 0 0 0 0 0 0 0 0 0 0 0 10.1494 -1.1652 -0.2286 C 0 0 0 0 0 0 0 0 0 0 0 0 10.0083 -0.2349 0.7840 C 0 0 0 0 0 0 0 0 0 0 0 0 8.9349 0.6510 0.8346 C 0 0 0 0 0 0 0 0 0 0 0 0 7.9831 0.6105 -0.1416 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1164 -0.3124 -1.1526 C 0 0 0 0 0 0 0 0 0 0 0 0 9.1776 -1.1928 -1.2081 C 0 0 0 0 0 0 0 0 0 0 0 0 6.8591 1.5470 -0.0812 C 0 0 0 0 0 0 0 0 0 0 0 0 6.7865 2.3649 0.8690 O 0 0 0 0 0 0 0 0 0 0 0 0 5.8667 1.5802 -1.0210 O 0 0 0 0 0 0 0 0 0 0 0 0 4.7439 2.3920 -1.1038 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8063 2.1480 0.0293 C 0 0 1 0 0 0 0 0 0 0 0 0 2.5597 3.0485 -0.1059 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5828 2.3935 0.6349 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7690 1.0310 0.3884 C 0 0 2 0 0 0 0 0 0 0 0 0 3.1375 0.7818 -0.0704 C 0 0 2 0 0 0 0 0 0 0 0 0 3.8178 -0.1532 0.7363 O 0 0 0 0 0 0 0 0 0 0 0 0 0.7497 0.6368 -0.4328 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.1858 -0.2104 0.1169 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2646 -0.5852 -0.8894 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.9081 0.6545 -1.4633 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.8115 0.1614 -2.6004 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.4243 -1.1692 -2.2443 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.4737 -1.2986 -0.7285 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.1798 -0.2861 -0.1238 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.3204 -0.4362 0.6234 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9286 0.7087 1.1717 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.0689 0.6645 1.9313 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.6897 -0.5355 2.2013 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.0993 -1.6665 1.6668 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9509 -1.6297 0.9007 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.7511 -2.8816 1.9561 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.1842 -4.0530 1.4308 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.8420 -0.6310 2.9625 O 0 0 0 0 0 0 0 0 0 0 0 0 -10.1016 -0.5466 2.2781 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.6313 1.8269 2.4504 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.1097 3.1120 2.2572 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1572 -1.4198 -0.2710 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.6466 -2.2191 -2.7256 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.7445 1.1252 -2.9389 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.9472 1.4668 -2.0594 O 0 0 0 0 0 0 0 0 0 0 0 0 4.3059 2.3854 1.2802 O 0 0 0 0 0 0 0 0 0 0 0 0 10.4784 -3.7081 -1.2865 H 0 0 0 0 0 0 0 0 0 0 0 0 12.2983 -3.4760 -1.3730 H 0 0 0 0 0 0 0 0 0 0 0 0 11.1941 -2.4432 -2.3021 H 0 0 0 0 0 0 0 0 0 0 0 0 10.7620 -0.2034 1.5569 H 0 0 0 0 0 0 0 0 0 0 0 0 8.8800 1.3687 1.6684 H 0 0 0 0 0 0 0 0 0 0 0 0 7.3483 -0.3361 -1.9281 H 0 0 0 0 0 0 0 0 0 0 0 0 9.2408 -1.9020 -2.0224 H 0 0 0 0 0 0 0 0 0 0 0 0 5.0381 3.4880 -1.0212 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1940 2.2714 -2.0643 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2778 3.1675 -1.1690 H 0 0 0 0 0 0 0 0 0 0 0 0 2.8192 4.0034 0.3491 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6132 0.5430 1.3794 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2531 0.4659 -1.1223 H 0 0 0 0 0 0 0 0 0 0 0 0 3.8196 -1.0571 0.3041 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2301 -1.1079 0.5893 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7077 0.3565 0.9180 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8255 -1.1303 -1.7595 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4561 1.2477 -0.7324 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.1463 0.0168 -3.4762 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4347 -1.2840 -2.6974 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9404 -2.2771 -0.5354 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.4333 1.6681 0.9565 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.5613 -2.5517 0.5271 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.1919 -4.0745 0.3213 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.1313 -4.1001 1.8017 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.7005 -4.9552 1.7977 H 0 0 0 0 0 0 0 0 0 0 0 0 -10.5755 0.4315 2.4024 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.9696 -0.7620 1.1868 H 0 0 0 0 0 0 0 0 0 0 0 0 -10.7081 -1.3959 2.6758 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.2713 3.2770 2.9550 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.6898 3.2501 1.2276 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.8939 3.8566 2.4994 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9500 -2.4742 -3.6305 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.3502 2.0071 -2.7326 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7476 2.2790 -1.5358 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7389 1.9027 1.9434 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 6 7 1 0 7 8 2 0 6 9 1 0 9 10 2 0 9 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 1 0 17 18 1 0 16 19 1 0 19 20 1 0 20 21 1 0 21 22 1 0 22 23 1 0 23 24 1 0 24 25 1 0 25 26 1 0 26 27 1 0 27 28 2 0 28 29 1 0 29 30 2 0 30 31 1 0 31 32 2 0 31 33 1 0 33 34 1 0 30 35 1 0 35 36 1 0 29 37 1 0 37 38 1 0 25 39 1 0 24 40 1 0 23 41 1 0 22 42 1 0 13 43 1 1 8 3 1 0 17 13 1 0 39 21 1 0 32 27 1 0 1 44 1 0 1 45 1 0 1 46 1 0 4 47 1 0 5 48 1 0 7 49 1 0 8 50 1 0 12 51 1 0 12 52 1 0 14 53 1 0 14 54 1 0 16 55 1 1 17 56 1 6 18 57 1 0 20 58 1 0 20 59 1 0 21 60 1 6 22 61 1 1 23 62 1 6 24 63 1 6 25 64 1 6 28 65 1 0 32 66 1 0 34 67 1 0 34 68 1 0 34 69 1 0 36 70 1 0 36 71 1 0 36 72 1 0 38 73 1 0 38 74 1 0 38 75 1 0 40 76 1 0 41 77 1 0 42 78 1 0 43 79 1 0 M END

Standard InCHIKey	CYCDWLJKDQJNEU-HOMHNTCQSA-N
Standard InCHI	InChI=1S/C28H36O15/c1-35-15-7-5-14(6-8-15)25(33)40-12-28(34)13-41-27(24(28)32)39-11-19-20(29)21(30)22(31)26(43-19)42-16-9-17(36-2)23(38-4)18(10-16)37-3/h5-10,19-22,24,26-27,29-32,34H,11-13H2,1-4H3/t19-,20-,21+,22-,24+,26-,27-,28-/m1/s1
SMILES	COc1ccc(cc1)C(=O)OC[C@]1(CO[C@H]([C@@H]1O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@H](Oc2cc(c(c(c2)OC)OC)OC)O1)O)O)O)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	612.21	Volume:	572.016 ? Van der Waals volume.
Dense:	1.07	LogP:	1.164 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	1.537 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-2.591 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	13.0	Rigid Bonds:	24.0
TPSA:	201.29 ? Topological Polar Surface Area.	H-Bond Acceptor:	15.0
H-Bond Donor:	5.0	Rings:	4.0
Heavy Atoms:	15.0

MedChem Properties

QED Drug-Likeness Score:	0.187	GASA:	0.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	4.42	Fsp³:	0.536
MCE-18:	99.14 ? MCE-18 stands for medicinal chemistry evolution.MCE-18≥45 is considered a suitable value.	Lipinski Rule-of-5:	Accepted
Pfizer Rule:	Rejected	GSK Rule:	Accepted
Golden Triangle Rule:	Accepted	BMS Rule:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.367	Fluc inhibitor:	0.178 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.066 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.295 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.076	Promiscuous compounds:	0.026

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-6.015	MDCK Permeability:	-5.073
Pgp-inhibitor:	0.0	Pgp-substrate:	0.466
PAMPA:	0.881 ? 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):	0.472
20% Bioavailability (F20%):	0.16	30% Bioavailability (F30%):	0.53
50% Bioavailability (F50%):	0.963

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.038	MRP1:	0.236
Plasma Protein Binding (PPB):	76.605%	Volume Distribution (VD):	-0.259
Fu:	23.799% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	1.0
OATP1B3 inhibitor:	1.0	BCRP inhibitor:	0.412
BSEP inhibitor:	0.396

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.0	CYP2C19-substrate:	0.003
CYP2C9-inhibitor:	0.0	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.693
CYP3A4-inhibitor:	0.078	CYP3A4-substrate:	0.997
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.99
HLM stability:	0.997 ? 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):

1.688

Half-life (T1/2):

2.527

ADMET: Toxicity

hERG Blockers:	0.07	hERG Blockers (10um):	0.366
Human Hepatotoxicity (H-HT):	0.362	Drug-induced Liver Injury (DILI):	0.971
AMES Toxicity:	0.68	Rat Oral Acute Toxicity:	0.013
Maximum Recommended Daily Dose:	0.058	Skin Sensitization:	0.942
Carcinogencity:	0.19	Eye Corrosion:	0.0
Eye Irritation:	0.402	Respiratory Toxicity:	0.011
Drug-induced Neurotoxicity:	0.106	Ototoxicity:	0.797
Hematotoxicity:	0.179	Drug-induced Nephrotoxicity:	0.929
Genotoxicity:	0.059	RPMI-8226 Immunitoxicity:	0.32
A549 Cytotoxicity:	0.225	Hek293 Cytotoxicity:	0.147
BCF:	0.452 ? 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:	3.269 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	4.842 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	3.99 ? 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
NPO487	Tabebuia avellanedae	Species	Bignoniaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[17950604]
NPO487	Tabebuia avellanedae	Species	Bignoniaceae	Eukaryota	n.a.	bark	n.a.	PMID[17950604]
NPO487	Tabebuia avellanedae	Species	Bignoniaceae	Eukaryota	n.a.	Brazilian	n.a.	PMID[19674905]
NPO487	Tabebuia avellanedae	Species	Bignoniaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[32044231]
NPO3751	Orthantha lutea	n.a.	n.a.	n.a.	n.a.	n.a.	n.a.	Database[COCONUT]
NPO487	Tabebuia avellanedae	Species	Bignoniaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO12083	Hydnellum zonatum	Species	Thelephoraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO487	Tabebuia avellanedae	Species	Bignoniaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO3751	Orthantha lutea	n.a.	n.a.	n.a.	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 NPC25209 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	18282
0.1-0.2	28363
0.2-0.3	2637
0.3-0.4	492
0.4-0.5	69
0.5-0.6	12
0.6-0.7	1
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
0.8169	Intermediate Similarity	NPC602634
0.6765	Remote Similarity	NPC171533
0.5946	Remote Similarity	NPC166277
0.5769	Remote Similarity	NPC23253
0.5641	Remote Similarity	NPC242756
0.5584	Remote Similarity	NPC227980
0.5532	Remote Similarity	NPC169645
0.5513	Remote Similarity	NPC25821
0.5325	Remote Similarity	NPC287429
0.5233	Remote Similarity	NPC212748
0.519	Remote Similarity	NPC213723
0.5122	Remote Similarity	NPC34965
0.5063	Remote Similarity	NPC111785
0.5063	Remote Similarity	NPC472859

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC25209 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4867
0.1-0.2	4198
0.2-0.3	79
0.3-0.4	5
0.4-0.5	1
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