NPASS Compound

Natural Product: NPC472673

Natural Product ID	NPC472673
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	AOZKPYNHVKLJJH-MLACOVEVSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL3581418
PubChem CID	n.a.
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0001549] Monoterpenoids [CHEMONTID:0000051] Aromatic monoterpenoids

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 91 96 0 0 0 0 0 0 0 0999 V2000 -5.1642 4.7337 -0.9500 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.4058 3.4782 -0.9744 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9008 2.9728 -2.0875 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1288 3.7315 -3.3448 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1534 1.7273 -2.0892 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7013 1.2925 -3.1428 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.9475 1.0426 -0.9617 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.2554 -0.1722 -0.7637 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0961 -1.3247 -0.3535 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2655 -1.5985 1.1279 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9568 -1.7473 1.7885 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6127 -1.0616 3.0233 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3282 -0.4941 2.9210 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2825 -1.0901 1.7928 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8388 -1.2874 0.8556 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0619 0.0239 0.1714 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2106 0.2657 -0.6273 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4540 -1.0331 -1.3672 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2665 -0.7846 -2.6404 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5296 -1.1444 -2.2451 O 0 0 0 0 0 0 0 0 0 0 0 0 3.1380 -0.0778 -1.6990 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5398 -0.6871 -1.4173 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1044 0.3628 -0.5704 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9142 0.6081 0.3930 C 0 0 0 0 0 0 0 0 0 0 0 0 2.7094 0.6627 -0.5455 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4174 0.5630 0.1726 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4877 -0.4232 1.3165 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1178 0.1170 2.4546 O 0 0 0 0 0 0 0 0 0 0 0 0 1.2348 1.9520 0.8273 C 0 0 0 0 0 0 0 0 0 0 0 0 4.3340 1.8736 1.0373 C 0 0 0 0 0 0 0 0 0 0 0 0 6.2880 -0.0744 0.2156 C 0 0 0 0 0 0 0 0 0 0 0 0 6.2952 -1.1681 1.0518 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4813 -1.2486 1.5666 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2703 -0.3060 1.1499 C 0 0 0 0 0 0 0 0 0 0 0 0 7.5427 0.4718 0.2790 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8827 -1.5971 -3.6869 O 0 0 0 0 0 0 0 0 0 0 0 0 0.5224 -0.8487 -4.8130 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5190 1.1392 1.0053 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.7457 -3.2554 2.0403 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9901 -2.8517 1.0988 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.2430 -3.0521 1.5798 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8370 -2.0562 2.1027 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.9622 -4.3544 1.5350 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.2652 4.4867 -0.9159 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.9352 5.2839 -0.0125 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.9188 5.3206 -1.8526 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.2520 2.9382 -0.0323 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5726 4.6983 -3.2702 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.8465 3.1645 -4.2495 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2326 3.9729 -3.3501 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9457 -0.3701 -1.8155 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.0592 -1.2905 -0.8886 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5933 -2.2425 -0.7405 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.0060 -0.9494 1.6204 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3533 -0.3184 3.4236 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5035 -1.7659 3.9091 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5860 -2.1024 2.2005 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7774 -2.1307 0.1752 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0479 1.1005 -1.3479 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3907 -1.5976 -1.7046 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0008 -1.6832 -0.6336 H 0 0 0 0 0 0 0 0 0 0 0 0 1.1969 0.2819 -2.9432 H 0 0 0 0 0 0 0 0 0 0 0 0 3.3899 0.5624 -2.6134 H 0 0 0 0 0 0 0 0 0 0 0 0 4.4162 -1.6199 -0.8109 H 0 0 0 0 0 0 0 0 0 0 0 0 5.0567 -0.9308 -2.3439 H 0 0 0 0 0 0 0 0 0 0 0 0 5.3311 1.2632 -1.1562 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9480 -0.2236 1.0708 H 0 0 0 0 0 0 0 0 0 0 0 0 2.7934 1.7620 -0.8811 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2071 -1.2186 0.9526 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7576 -0.2064 3.2920 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0708 2.6614 0.5148 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2983 1.9289 1.9010 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4186 2.5218 0.3513 H 0 0 0 0 0 0 0 0 0 0 0 0 4.4465 2.7200 0.3022 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4126 1.7153 1.3671 H 0 0 0 0 0 0 0 0 0 0 0 0 3.8622 2.1637 1.9815 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4357 -1.8311 1.2285 H 0 0 0 0 0 0 0 0 0 0 0 0 9.3059 -0.1972 1.4630 H 0 0 0 0 0 0 0 0 0 0 0 0 7.8799 1.3410 -0.2544 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3335 -0.1625 -4.5886 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1771 -1.4983 -5.6407 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3350 -0.2165 -5.1918 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5594 0.8755 1.3780 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8509 1.9687 0.3014 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0260 1.4521 1.8903 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.1236 -3.5133 3.0609 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7299 -3.5867 1.8636 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3828 -3.8411 1.3377 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.0934 -4.8105 2.5163 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.5329 -5.0360 0.7728 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.9993 -4.1199 1.1600 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 3 5 1 0 5 6 2 0 5 7 1 0 7 8 1 0 8 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 15 16 1 0 16 17 1 0 17 18 1 0 18 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 1 0 26 29 1 0 24 30 1 0 23 31 1 0 31 32 2 0 32 33 1 0 33 34 1 0 34 35 2 0 19 36 1 0 36 37 1 0 16 38 1 0 11 39 1 0 10 40 1 0 40 41 1 0 41 42 2 0 41 43 1 0 16 8 1 0 15 11 1 0 27 14 1 0 26 17 1 0 25 21 1 0 35 31 1 0 1 44 1 0 1 45 1 0 1 46 1 0 2 47 1 0 4 48 1 0 4 49 1 0 4 50 1 0 8 51 1 0 9 52 1 0 9 53 1 0 10 54 1 0 12 55 1 0 12 56 1 0 14 57 1 0 15 58 1 0 17 59 1 0 18 60 1 0 18 61 1 0 19 62 1 0 21 63 1 0 22 64 1 0 22 65 1 0 23 66 1 0 24 67 1 0 25 68 1 0 27 69 1 0 28 70 1 0 29 71 1 0 29 72 1 0 29 73 1 0 30 74 1 0 30 75 1 0 30 76 1 0 32 77 1 0 34 78 1 0 35 79 1 0 37 80 1 0 37 81 1 0 37 82 1 0 38 83 1 0 38 84 1 0 38 85 1 0 39 86 1 0 39 87 1 0 39 88 1 0 43 89 1 0 43 90 1 0 43 91 1 0 M END

Standard InCHIKey	AOZKPYNHVKLJJH-MLACOVEVSA-N
Standard InCHI	InChI=1S/C34H48O9/c1-9-17(2)31(37)43-25-14-24(41-19(4)35)32(5)16-40-28-29(32)33(25,6)23-13-26(38-8)42-22-12-21(20-10-11-39-15-20)18(3)27(22)34(23,7)30(28)36/h9-11,15,18,21-30,36H,12-14,16H2,1-8H3/b17-9+/t18?,21-,22+,23-,24-,25+,26?,27-,28-,29+,30-,32-,33+,34-/m1/s1
SMILES	CC=C(C)C(=O)OC1CC(C2(COC3C2C1(C4CC(OC5CC(C(C5C4(C3O)C)C)C6=COC=C6)OC)C)C)OC(=O)C

Calculated Properties

Physi-Chem Properties

Molecular Weight:	600.33	Volume:	611.211 ? Van der Waals volume.
Dense:	0.982	LogP:	3.31 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	3.434 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-4.243 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	7.0	Rigid Bonds:	32.0
TPSA:	113.66 ? Topological Polar Surface Area.	H-Bond Acceptor:	9.0
H-Bond Donor:	1.0	Rings:	6.0
Heavy Atoms:	9.0

MedChem Properties

QED Drug-Likeness Score:	0.368	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	5.887	Fsp³:	0.765
MCE-18:	151.2 ? 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:	Accepted	BMS Rule:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.215	Fluc inhibitor:	0.0 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.005 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.287 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.028	Promiscuous compounds:	0.002

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.135	MDCK Permeability:	-4.748
Pgp-inhibitor:	0.034	Pgp-substrate:	0.546
PAMPA:	0.574 ? 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):	0.145
20% Bioavailability (F20%):	0.165	30% Bioavailability (F30%):	0.595
50% Bioavailability (F50%):	0.949

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.477	MRP1:	0.999
Plasma Protein Binding (PPB):	63.907%	Volume Distribution (VD):	-0.125
Fu:	38.827% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.0
OATP1B3 inhibitor:	0.125	BCRP inhibitor:	0.011
BSEP inhibitor:	0.961

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	0.009
CYP2C19-inhibitor:	1.0	CYP2C19-substrate:	0.007
CYP2C9-inhibitor:	0.983	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.004	CYP2D6-substrate:	0.947
CYP3A4-inhibitor:	0.987	CYP3A4-substrate:	0.0
CYP2B6-substrate:	1.0	CYP2C8-inhibitor:	0.894
HLM stability:	0.936 ? 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):

9.331

Half-life (T1/2):

1.822

ADMET: Toxicity

hERG Blockers:	0.205	hERG Blockers (10um):	0.417
Human Hepatotoxicity (H-HT):	0.54	Drug-induced Liver Injury (DILI):	0.905
AMES Toxicity:	0.492	Rat Oral Acute Toxicity:	0.716
Maximum Recommended Daily Dose:	0.939	Skin Sensitization:	0.253
Carcinogencity:	0.411	Eye Corrosion:	0.0
Eye Irritation:	0.007	Respiratory Toxicity:	0.461
Drug-induced Neurotoxicity:	0.552	Ototoxicity:	0.89
Hematotoxicity:	0.07	Drug-induced Nephrotoxicity:	0.179
Genotoxicity:	0.653	RPMI-8226 Immunitoxicity:	0.162
A549 Cytotoxicity:	0.156	Hek293 Cytotoxicity:	0.361
BCF:	0.826 ? 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:	3.889 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.882 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	5.013 ? 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
NPO9173	Munronia henryi	Species	Meliaceae	Eukaryota	whole plants	Wenshan, Yunnan Province, China	2012-Nov	PMID[25798528]
NPO9173	Munronia henryi	Species	Meliaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO9173	Munronia henryi	Species	Meliaceae	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
Inhibition	4
IC50	5

Activity Type	# Activity
Cell line	5
Organism	4

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
NPT116	Cell line	HL-60	Homo sapiens	IC50	>	10000.0	nM	PMID[18975929]
NPT659	Cell line	SMMC-7721	Homo sapiens	IC50	>	10000.0	nM	PMID[23398362]
NPT81	Cell line	A549	Homo sapiens	IC50	>	10000.0	nM	PMID[15161186]
NPT83	Cell line	MCF7	Homo sapiens	IC50	>	10000.0	nM	PMID[17958396]
NPT660	Cell line	SW480	Homo sapiens	IC50	>	10000.0	nM	PMID[19700225]
NPT786	Organism	Tobacco mosaic virus	Tobacco mosaic virus	Inhibition	=	43.9	%	PMID[12502321]
NPT786	Organism	Tobacco mosaic virus	Tobacco mosaic virus	Inhibition	=	31.5	%	PMID[27301680]
NPT786	Organism	Tobacco mosaic virus	Tobacco mosaic virus	Inhibition	=	50.0	%	DrugMatrix in vivo data: Pathology
NPT786	Organism	Tobacco mosaic virus	Tobacco mosaic virus	Inhibition	=	53.6	%	PMID[18973387]

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 NPC472673 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	12886
0.1-0.2	35059
0.2-0.3	1812
0.3-0.4	63
0.4-0.5	17
0.5-0.6	15
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	Natural Product ID
0.7021	Intermediate Similarity	NPC307781
0.7021	Intermediate Similarity	NPC472670
0.7021	Intermediate Similarity	NPC601577
0.6495	Remote Similarity	NPC264690
0.5979	Remote Similarity	NPC610307
0.5918	Remote Similarity	NPC470792
0.58	Remote Similarity	NPC608851
0.58	Remote Similarity	NPC610301
0.5728	Remote Similarity	NPC608993
0.5619	Remote Similarity	NPC11062
0.549	Remote Similarity	NPC472671
0.5446	Remote Similarity	NPC599832
0.5258	Remote Similarity	NPC601664
0.5204	Remote Similarity	NPC34421
0.5204	Remote Similarity	NPC237259
0.52	Remote Similarity	NPC609027
0.51	Remote Similarity	NPC98206
0.51	Remote Similarity	NPC29695
0.5049	Remote Similarity	NPC308205

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC472673 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4475
0.1-0.2	4656
0.2-0.3	19
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