NPASS Compound

Natural Product: NPC234304

Natural Product ID	NPC234304
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	Genameside C
IUPAC Name	methyl (1S,4aS,7aS)-1-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate
Synonyms	Genameside C
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL2311862
PubChem CID	11692460
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0002049] Terpene glycosides [CHEMONTID:0004081] Iridoid O-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 72 75 0 0 0 0 0 0 0 0999 V2000 -6.8423 4.0697 -1.4137 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.0720 3.0373 -0.8297 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.6239 1.9652 -1.5975 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9496 1.9866 -2.8200 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.8294 0.8808 -1.0416 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.4537 -0.0897 -1.8576 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7006 -1.1197 -1.3362 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.9660 -0.9920 -0.1241 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.7520 -0.2385 0.9205 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.8269 -1.0994 1.5025 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9481 -0.4127 1.6542 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7705 0.9684 1.2024 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5005 0.9404 0.3893 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.6836 -2.5446 1.8732 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8700 -3.0509 2.3879 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7000 -0.4571 -0.3267 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.6757 -1.3312 -0.0017 C 0 0 1 0 0 0 0 0 0 0 0 0 0.1478 -1.7511 -1.2079 C 0 0 1 0 0 0 0 0 0 0 0 0 1.5822 -1.9235 -0.7540 C 0 0 2 0 0 0 0 0 0 0 0 0 2.0591 -0.5458 -0.3284 C 0 0 1 0 0 0 0 0 0 0 0 0 1.0993 0.0089 0.6655 C 0 0 1 0 0 0 0 0 0 0 0 0 0.4909 1.2793 0.1137 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3040 1.8217 1.1430 O 0 0 0 0 0 0 0 0 0 0 0 0 0.1208 -0.9077 1.0445 O 0 0 0 0 0 0 0 0 0 0 0 0 3.3709 -0.5430 0.0814 O 0 0 0 0 0 0 0 0 0 0 0 0 4.2645 0.1571 -0.6722 C 0 0 1 0 0 0 0 0 0 0 0 0 4.8028 1.2876 0.1733 C 0 0 1 0 0 0 0 0 0 0 0 0 6.2554 1.5904 -0.1183 C 0 0 2 0 0 0 0 0 0 0 0 0 7.0316 0.3140 0.1260 C 0 0 1 0 0 0 0 0 0 0 0 0 6.3169 -0.8938 -0.3700 C 0 0 1 0 0 0 0 0 0 0 0 0 5.9039 -1.7510 0.7900 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9911 -2.0058 1.6244 O 0 0 0 0 0 0 0 0 0 0 0 0 5.2715 -0.6108 -1.2318 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2556 0.4628 -0.5234 O 0 0 0 0 0 0 0 0 0 0 0 0 6.6732 2.6397 0.6627 O 0 0 0 0 0 0 0 0 0 0 0 0 4.0407 2.4275 -0.0748 O 0 0 0 0 0 0 0 0 0 0 0 0 2.3367 -2.4337 -1.7970 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.3599 -2.9069 -1.7933 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.6046 5.0286 -0.8879 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.9183 3.8306 -1.3680 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.5485 4.1460 -2.4781 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.7318 -0.0658 -2.8906 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8292 -2.0235 0.2614 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0883 0.0927 1.7258 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.8910 -0.8144 2.0628 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.6535 1.3122 0.6291 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.6618 1.6237 2.1097 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9788 1.9104 0.6006 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9121 -2.6103 2.6414 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4131 -3.1372 0.9575 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.7988 -3.1451 3.3879 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.1731 -2.2812 0.3546 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0624 -0.9485 -1.9638 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5606 -2.5646 0.1392 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0032 0.0702 -1.2487 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5913 0.3148 1.6246 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3336 2.0086 -0.0153 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0731 1.1453 -0.8109 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4618 1.1660 1.8698 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6963 0.6192 -1.5205 H 0 0 0 0 0 0 0 0 0 0 0 0 4.6418 1.0533 1.2535 H 0 0 0 0 0 0 0 0 0 0 0 0 6.3206 1.8851 -1.1856 H 0 0 0 0 0 0 0 0 0 0 0 0 7.1825 0.2235 1.2189 H 0 0 0 0 0 0 0 0 0 0 0 0 7.0432 -1.5054 -0.9656 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4961 -2.7345 0.4717 H 0 0 0 0 0 0 0 0 0 0 0 0 5.1254 -1.2889 1.4312 H 0 0 0 0 0 0 0 0 0 0 0 0 6.9472 -1.4897 2.4636 H 0 0 0 0 0 0 0 0 0 0 0 0 8.4434 -0.3756 -1.0266 H 0 0 0 0 0 0 0 0 0 0 0 0 5.9112 3.1096 1.0636 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3004 2.8415 -0.9523 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7262 -2.9118 -2.4279 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8332 -2.7133 -2.6595 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 3 5 1 0 5 6 2 0 6 7 1 0 7 8 1 0 8 9 1 0 9 10 1 0 10 11 2 0 11 12 1 0 12 13 1 0 10 14 1 0 14 15 1 0 8 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 21 24 1 0 20 25 1 0 25 26 1 0 26 27 1 0 27 28 1 0 28 29 1 0 29 30 1 0 30 31 1 0 31 32 1 0 30 33 1 0 29 34 1 0 28 35 1 0 27 36 1 0 19 37 1 0 18 38 1 0 13 5 1 0 24 17 1 0 33 26 1 0 13 9 1 0 1 39 1 0 1 40 1 0 1 41 1 0 6 42 1 0 8 43 1 1 9 44 1 1 11 45 1 0 12 46 1 0 12 47 1 0 13 48 1 6 14 49 1 0 14 50 1 0 15 51 1 0 17 52 1 1 18 53 1 6 19 54 1 1 20 55 1 6 21 56 1 1 22 57 1 0 22 58 1 0 23 59 1 0 26 60 1 6 27 61 1 1 28 62 1 6 29 63 1 1 30 64 1 6 31 65 1 0 31 66 1 0 32 67 1 0 34 68 1 0 35 69 1 0 36 70 1 0 37 71 1 0 38 72 1 0 M END

Standard InCHIKey	JRYVBZDSFXDJAN-NWTASXAMSA-N
Standard InCHI	InChI=1S/C23H34O15/c1-33-20(32)10-7-34-21(13-8(4-24)2-3-9(10)13)38-23-18(31)16(29)19(12(6-26)36-23)37-22-17(30)15(28)14(27)11(5-25)35-22/h2,7,9,11-19,21-31H,3-6H2,1H3/t9-,11-,12-,13-,14-,15+,16-,17-,18-,19-,21+,22+,23+/m1/s1
SMILES	COC(=O)C1=CO[C@H]([C@@H]2C(=CC[C@H]12)CO)O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)O)O)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	550.19	Volume:	496.082 ? Van der Waals volume.
Dense:	1.109	LogP:	-1.836 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	-1.216 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-0.888 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	9.0	Rigid Bonds:	23.0
TPSA:	234.29 ? Topological Polar Surface Area.	H-Bond Acceptor:	15.0
H-Bond Donor:	8.0	Rings:	4.0
Heavy Atoms:	15.0

MedChem Properties

QED Drug-Likeness Score:	0.105	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	5.15	Fsp³:	0.783
MCE-18:	75.122 ? 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:	1
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.446	Fluc inhibitor:	0.001 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.021 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.007 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.364	Promiscuous compounds:	0.069

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-6.009	MDCK Permeability:	-5.117
Pgp-inhibitor:	0.0	Pgp-substrate:	0.583
PAMPA:	0.997 ? 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):	0.993
20% Bioavailability (F20%):	0.392	30% Bioavailability (F30%):	0.999
50% Bioavailability (F50%):	0.941

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.022	MRP1:	0.473
Plasma Protein Binding (PPB):	26.874%	Volume Distribution (VD):	-0.564
Fu:	72.494% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.997
OATP1B3 inhibitor:	1.0	BCRP inhibitor:	0.004
BSEP inhibitor:	0.0

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.0	CYP2C19-substrate:	0.0
CYP2C9-inhibitor:	0.0	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.002
CYP3A4-inhibitor:	0.0	CYP3A4-substrate:	0.0
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.502
HLM stability:	0.009 ? 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):

0.913

Half-life (T1/2):

3.124

ADMET: Toxicity

hERG Blockers:	0.005	hERG Blockers (10um):	0.019
Human Hepatotoxicity (H-HT):	0.717	Drug-induced Liver Injury (DILI):	0.982
AMES Toxicity:	0.984	Rat Oral Acute Toxicity:	0.01
Maximum Recommended Daily Dose:	0.003	Skin Sensitization:	1.0
Carcinogencity:	0.222	Eye Corrosion:	0.0
Eye Irritation:	0.012	Respiratory Toxicity:	0.002
Drug-induced Neurotoxicity:	0.006	Ototoxicity:	0.997
Hematotoxicity:	0.789	Drug-induced Nephrotoxicity:	0.92
Genotoxicity:	0.362	RPMI-8226 Immunitoxicity:	0.116
A549 Cytotoxicity:	0.48	Hek293 Cytotoxicity:	0.17
BCF:	0.317 ? 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:	2.593 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	4.263 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	3.435 ? 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
NPO17824	Genipa americana	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[10425120]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	Fruits	n.a.	n.a.	PMID[16309325]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	n.a.	Seoul, Korea	2000-Jun	PMID[16643034]
NPO17824	Genipa americana	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[1667413]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	fruit	n.a.	n.a.	PMID[18505286]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	fruit	n.a.	n.a.	PMID[19650637]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	fruits	n.a.	n.a.	PMID[23305920]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[32141747]
NPO17824	Genipa americana	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO17824	Genipa americana	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO17824	Genipa americana	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO17824	Genipa americana	Species	Rubiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO9518	Gardenia jasminoides	Species	Rubiaceae	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	1

Activity Type	# Activity
Cell line	1

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
NPT113	Cell line	RAW264.7	Mus musculus	IC50	>	100000.0	nM	PMID[23305920]

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 NPC234304 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	22742
0.1-0.2	23662
0.2-0.3	3015
0.3-0.4	314
0.4-0.5	73
0.5-0.6	39
0.6-0.7	6
0.7-0.8	0
0.8-0.85	0
0.85-0.9	3
0.9-0.95	0
0.95-1	0

Similarity Score	Similarity Level	Natural Product ID
0.85	High Similarity	NPC255677
0.85	High Similarity	NPC22149
0.85	High Similarity	NPC306344
0.7391	Intermediate Similarity	NPC197541
0.7391	Intermediate Similarity	NPC118761
0.6812	Remote Similarity	NPC222062
0.6364	Remote Similarity	NPC482656
0.6351	Remote Similarity	NPC267869
0.6351	Remote Similarity	NPC284929
0.6184	Remote Similarity	NPC86095
0.6087	Remote Similarity	NPC298255
0.5942	Remote Similarity	NPC474730
0.5942	Remote Similarity	NPC117596
0.5915	Remote Similarity	NPC37240
0.5857	Remote Similarity	NPC35185
0.5857	Remote Similarity	NPC4899
0.5857	Remote Similarity	NPC177013
0.5769	Remote Similarity	NPC488459
0.5694	Remote Similarity	NPC27687
0.5634	Remote Similarity	NPC250545
0.5616	Remote Similarity	NPC231710
0.5616	Remote Similarity	NPC470573
0.5616	Remote Similarity	NPC120021
0.5616	Remote Similarity	NPC216826
0.5616	Remote Similarity	NPC270908
0.5616	Remote Similarity	NPC65665
0.56	Remote Similarity	NPC41681
0.5479	Remote Similarity	NPC106668
0.5467	Remote Similarity	NPC488472
0.5467	Remote Similarity	NPC257424
0.5417	Remote Similarity	NPC307699
0.5417	Remote Similarity	NPC475928
0.5342	Remote Similarity	NPC148270
0.5294	Remote Similarity	NPC488469
0.5278	Remote Similarity	NPC170432
0.527	Remote Similarity	NPC61201
0.5217	Remote Similarity	NPC220167
0.5205	Remote Similarity	NPC195510
0.5205	Remote Similarity	NPC13171
0.5185	Remote Similarity	NPC488470
0.5132	Remote Similarity	NPC475851
0.5132	Remote Similarity	NPC475924
0.5109	Remote Similarity	NPC69367
0.5109	Remote Similarity	NPC611523
0.5062	Remote Similarity	NPC488456
0.5062	Remote Similarity	NPC488471
0.5062	Remote Similarity	NPC488466
0.5062	Remote Similarity	NPC488465
0.5062	Remote Similarity	NPC488460
0.5062	Remote Similarity	NPC488462

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC234304 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	7415
0.1-0.2	1667
0.2-0.3	52
0.3-0.4	16
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