NPASS Compound

Natural Product: NPC483859

Natural Product ID	NPC483859
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	WVOVOYUXPWBTPS-YCXRTIKKSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	132525136
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 92 96 0 0 0 0 0 0 0 0999 V2000 -3.1745 2.5903 3.5193 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2951 2.0746 2.1293 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9735 2.6269 1.2297 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.6173 0.9156 1.8090 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.6357 0.3039 0.5243 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.1935 0.4400 0.0114 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.0525 -0.3746 -1.1995 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.1751 -0.2101 -2.1997 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2272 -0.1104 -1.9034 C 0 0 2 0 0 0 0 0 0 0 0 0 0.6033 -1.2293 -2.8770 C 0 0 2 0 0 0 0 0 0 0 0 0 0.4388 -2.5802 -2.2882 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.0787 -2.6755 -1.9623 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.0925 -1.8533 -0.7443 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.0851 -2.1446 0.2964 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.9227 -3.4133 0.0610 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1150 -1.0802 0.5878 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.6340 -1.3105 1.9095 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.9360 -1.6518 2.1822 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7581 -1.7747 1.2353 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.4038 -1.8825 3.5811 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4909 -2.4173 1.5610 O 0 0 0 0 0 0 0 0 0 0 0 0 0.1858 -1.9915 -0.1362 O 0 0 0 0 0 0 0 0 0 0 0 0 0.9694 -2.7877 -0.9109 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4348 -2.5083 -0.7371 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7977 -4.2854 -0.6060 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3850 -4.0208 -1.8816 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1420 -4.6378 -2.8950 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5064 -3.9041 -3.8423 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.4931 -6.0810 -2.8513 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8800 -0.9308 -3.3433 O 0 0 0 0 0 0 0 0 0 0 0 0 1.3620 0.0798 -1.0907 O 0 0 0 0 0 0 0 0 0 0 0 0 2.2431 1.1444 -1.1703 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0298 2.0190 -2.0309 O 0 0 0 0 0 0 0 0 0 0 0 0 3.4047 1.2396 -0.2567 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2201 2.2523 -0.3441 C 0 0 0 0 0 0 0 0 0 0 0 0 5.3923 2.4500 0.5004 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7437 1.5536 1.4887 C 0 0 0 0 0 0 0 0 0 0 0 0 6.8521 1.7237 2.3024 C 0 0 0 0 0 0 0 0 0 0 0 0 7.6633 2.8304 2.1433 C 0 0 0 0 0 0 0 0 0 0 0 0 7.3187 3.7367 1.1529 C 0 0 0 0 0 0 0 0 0 0 0 0 6.2145 3.5534 0.3527 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8539 1.7902 -0.0747 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0042 2.5179 0.7125 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5176 1.8503 1.6154 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2504 3.9454 0.4900 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3729 4.6573 -0.5037 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1237 6.0049 -0.7223 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7796 6.6721 0.0757 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4108 5.9650 1.0768 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1553 4.6046 1.2941 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1466 2.8728 3.7806 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9110 3.4037 3.7295 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4410 1.7107 4.1727 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2958 0.9697 -0.1064 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5873 0.0621 0.8519 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.7863 -0.1909 -3.2373 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9404 -1.0063 -2.1611 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7302 0.7392 -2.0714 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1305 0.7807 -2.5520 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0751 -1.1501 -3.7501 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7265 -3.3292 -3.0300 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5315 -2.2485 -2.8791 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3500 -4.3380 0.1713 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5706 -3.3194 -0.8065 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6478 -3.4572 0.9409 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.0147 -1.2791 -0.0701 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6629 -1.4750 4.2998 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.4283 -2.9927 3.7685 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.3839 -1.4136 3.7502 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5792 -1.6727 2.1692 H 0 0 0 0 0 0 0 0 0 0 0 0 3.0256 -3.4612 -0.5539 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6463 -1.9336 0.2111 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9355 -2.0788 -1.6239 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7597 -4.8632 -1.5606 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7263 -4.6898 -0.0963 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0078 -4.4852 0.0948 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.1269 -6.5804 -1.9550 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0211 -6.5789 -3.7238 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6088 -6.1991 -2.9909 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9895 -1.4430 -4.1877 H 0 0 0 0 0 0 0 0 0 0 0 0 3.5666 0.4741 0.4681 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9842 2.9980 -1.1184 H 0 0 0 0 0 0 0 0 0 0 0 0 5.1611 0.6595 1.6785 H 0 0 0 0 0 0 0 0 0 0 0 0 7.1285 1.0154 3.0823 H 0 0 0 0 0 0 0 0 0 0 0 0 8.5307 2.9872 2.7642 H 0 0 0 0 0 0 0 0 0 0 0 0 7.9653 4.5985 1.0410 H 0 0 0 0 0 0 0 0 0 0 0 0 5.9698 4.2734 -0.4096 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0829 4.1057 -1.1197 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6414 6.5481 -1.5298 H 0 0 0 0 0 0 0 0 0 0 0 0 0.9613 7.7301 -0.1116 H 0 0 0 0 0 0 0 0 0 0 0 0 2.1181 6.5031 1.6927 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6667 4.0674 2.0913 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 2 0 2 4 1 0 4 5 1 0 5 6 1 0 6 7 1 0 7 8 1 6 7 9 1 0 9 10 1 0 10 11 1 0 11 12 1 0 12 13 1 0 13 14 1 0 14 15 1 0 14 16 1 0 16 17 1 0 17 18 1 0 18 19 2 0 18 20 1 0 14 21 1 1 13 22 1 1 22 23 1 0 23 24 1 0 23 25 1 0 12 26 1 0 26 27 1 0 27 28 2 0 27 29 1 0 10 30 1 0 9 31 1 0 31 32 1 0 32 33 2 0 32 34 1 0 34 35 2 0 35 36 1 0 36 37 2 0 37 38 1 0 38 39 2 0 39 40 1 0 40 41 2 0 6 42 1 0 42 43 1 0 43 44 2 0 43 45 1 0 45 46 2 0 46 47 1 0 47 48 2 0 48 49 1 0 49 50 2 0 16 5 1 0 41 36 1 0 50 45 1 0 13 7 1 0 23 11 1 0 1 51 1 0 1 52 1 0 1 53 1 0 5 54 1 6 6 55 1 1 8 56 1 0 8 57 1 0 8 58 1 0 9 59 1 6 10 60 1 6 11 61 1 6 12 62 1 6 15 63 1 0 15 64 1 0 15 65 1 0 16 66 1 6 20 67 1 0 20 68 1 0 20 69 1 0 21 70 1 0 24 71 1 0 24 72 1 0 24 73 1 0 25 74 1 0 25 75 1 0 25 76 1 0 29 77 1 0 29 78 1 0 29 79 1 0 30 80 1 0 34 81 1 0 35 82 1 0 37 83 1 0 38 84 1 0 39 85 1 0 40 86 1 0 41 87 1 0 46 88 1 0 47 89 1 0 48 90 1 0 49 91 1 0 50 92 1 0 M END

Standard InCHIKey	WVOVOYUXPWBTPS-YCXRTIKKSA-N
Standard InCHI	InChI=1S/C37H42O13/c1-20(38)45-28-31(49-33(43)24-16-12-9-13-17-24)35(6)30(48-25(41)19-18-23-14-10-8-11-15-23)27(42)26-29(46-21(2)39)37(35,50-34(26,4)5)36(7,44)32(28)47-22(3)40/h8-19,26-32,42,44H,1-7H3/b19-18+/t26-,27+,28+,29-,30+,31+,32+,35-,36+,37-/m1/s1
SMILES	CC(=O)O[C@H]1[C@@H]([C@@]2(C)[C@H]([C@H]([C@@H]3[C@H]([C@@]2([C@](C)([C@H]1OC(=O)C)O)OC3(C)C)OC(=O)C)O)OC(=O)/C=C/c1ccccc1)OC(=O)c1ccccc1

Calculated Properties

Physi-Chem Properties

Molecular Weight:	694.26	Volume:	688.361 ? Van der Waals volume.
Dense:	1.009	LogP:	3.133 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	2.926 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-5.062 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	13.0	Rigid Bonds:	32.0
TPSA:	181.19 ? Topological Polar Surface Area.	H-Bond Acceptor:	13.0
H-Bond Donor:	2.0	Rings:	5.0
Heavy Atoms:	13.0

MedChem Properties

QED Drug-Likeness Score:	0.234	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	6.172	Fsp³:	0.486
MCE-18:	180.4 ? 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:	0.841	Fluc inhibitor:	0.547 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.022 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.357 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.104	Promiscuous compounds:	0.105

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.474	MDCK Permeability:	-4.893
Pgp-inhibitor:	1.0	Pgp-substrate:	0.098
PAMPA:	0.27 ? 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%):	0.12	30% Bioavailability (F30%):	0.982
50% Bioavailability (F50%):	0.987

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.001	MRP1:	0.992
Plasma Protein Binding (PPB):	83.516%	Volume Distribution (VD):	-0.345
Fu:	15.967% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	1.0
OATP1B3 inhibitor:	0.997	BCRP inhibitor:	0.005
BSEP inhibitor:	1.0

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	0.237
CYP2C19-inhibitor:	0.0	CYP2C19-substrate:	0.01
CYP2C9-inhibitor:	0.0	CYP2C9-substrate:	0.637
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.0
CYP3A4-inhibitor:	0.0	CYP3A4-substrate:	1.0
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	1.0
HLM stability:	0.465 ? 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):

6.06

Half-life (T1/2):

0.883

ADMET: Toxicity

hERG Blockers:	0.015	hERG Blockers (10um):	0.167
Human Hepatotoxicity (H-HT):	0.238	Drug-induced Liver Injury (DILI):	0.601
AMES Toxicity:	0.419	Rat Oral Acute Toxicity:	0.215
Maximum Recommended Daily Dose:	0.47	Skin Sensitization:	0.997
Carcinogencity:	0.192	Eye Corrosion:	0.003
Eye Irritation:	0.355	Respiratory Toxicity:	0.111
Drug-induced Neurotoxicity:	0.075	Ototoxicity:	0.31
Hematotoxicity:	0.053	Drug-induced Nephrotoxicity:	0.873
Genotoxicity:	0.838	RPMI-8226 Immunitoxicity:	0.054
A549 Cytotoxicity:	0.024	Hek293 Cytotoxicity:	0.102
BCF:	0.626 ? 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:	3.551 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.33 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.748 ? 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
NPO26437	Maytenus jelskii	Species	Celastraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[20146433]
NPO26437	Maytenus jelskii	Species	Celastraceae	Eukaryota	fruits	n.a.	n.a.	PMID[21856049]
NPO26437	Maytenus jelskii	Species	Celastraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[27541714]
NPO26437	Maytenus jelskii	Species	Celastraceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO26437	Maytenus jelskii	Species	Celastraceae	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	2

Activity Type	# Activity
Others	2

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
NPT2	Others	Unspecified	n.a.	Activity	=	88.6	%	PMID[27541714]
NPT2	Others	Unspecified	n.a.	Activity	>	60.0	%	PMID[27541714]

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 NPC483859 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	13137
0.1-0.2	33871
0.2-0.3	2216
0.3-0.4	536
0.4-0.5	66
0.5-0.6	21
0.6-0.7	4
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
0.7284	Intermediate Similarity	NPC188865
0.716	Intermediate Similarity	NPC483861
0.716	Intermediate Similarity	NPC483860
0.6279	Remote Similarity	NPC171525
0.6235	Remote Similarity	NPC25768
0.6	Remote Similarity	NPC483880
0.6	Remote Similarity	NPC156941
0.593	Remote Similarity	NPC483867
0.5862	Remote Similarity	NPC605086
0.5747	Remote Similarity	NPC472571
0.5732	Remote Similarity	NPC471101
0.573	Remote Similarity	NPC488916
0.5568	Remote Similarity	NPC470159
0.5556	Remote Similarity	NPC184817
0.5506	Remote Similarity	NPC70403
0.5506	Remote Similarity	NPC177940
0.5444	Remote Similarity	NPC125106
0.5444	Remote Similarity	NPC472573
0.5444	Remote Similarity	NPC483865
0.5422	Remote Similarity	NPC291599
0.5393	Remote Similarity	NPC476971
0.5312	Remote Similarity	NPC476975
0.5281	Remote Similarity	NPC29704
0.5281	Remote Similarity	NPC470157
0.5275	Remote Similarity	NPC469349
0.5227	Remote Similarity	NPC51602
0.5222	Remote Similarity	NPC603877
0.5055	Remote Similarity	NPC475122

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC483859 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4811
0.1-0.2	4259
0.2-0.3	80
0.3-0.4	0
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