NPASS Compound

Natural Product: NPC224430

Natural Product ID	NPC224430
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	INDVLXYUCBVVKW-UHFFFAOYSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	314582
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000258] Steroids and steroid derivatives [CHEMONTID:0003567] Ergostane steroids [CHEMONTID:0001403] Ergosterols and derivatives

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 75 78 0 0 0 0 0 0 0 0999 V2000 6.5395 4.0325 -2.8157 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7297 3.0017 -2.0815 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6153 1.8047 -1.8410 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5074 2.6051 -2.7918 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0585 3.0553 -3.9121 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6591 1.5126 -2.1214 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4679 1.7668 -0.6740 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5629 0.7062 0.0180 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2303 -0.6055 -0.1941 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1727 0.8235 -0.4339 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6298 2.2525 -0.1033 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8732 2.0289 -0.2058 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9371 0.7717 0.5981 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2364 0.1871 0.8887 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2620 0.1784 -0.2222 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5597 -0.1674 0.4296 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5652 -1.1898 1.2738 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8586 -1.5762 1.9611 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9439 -3.0269 2.2210 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6750 -3.6963 2.6284 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.5461 -2.7377 2.8060 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3476 -1.9780 1.5072 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2553 -3.0378 0.4235 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1173 -1.1233 1.5785 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9491 -1.9552 1.1643 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3490 -1.1427 0.9891 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1088 -0.1178 -0.0518 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4033 -0.7044 -1.3641 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.9215 -3.2268 3.2186 O 0 0 0 0 0 0 0 0 0 0 0 0 6.9107 3.7124 -3.7862 H 0 0 0 0 0 0 0 0 0 0 0 0 5.8801 4.9393 -2.9295 H 0 0 0 0 0 0 0 0 0 0 0 0 7.4087 4.3089 -2.1598 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4472 3.4506 -1.0604 H 0 0 0 0 0 0 0 0 0 0 0 0 7.3349 1.6909 -2.6475 H 0 0 0 0 0 0 0 0 0 0 0 0 6.0574 0.8487 -1.7634 H 0 0 0 0 0 0 0 0 0 0 0 0 7.1562 2.0246 -0.8673 H 0 0 0 0 0 0 0 0 0 0 0 0 3.0452 2.5366 -4.2186 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3601 3.7060 -4.6722 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6779 1.5717 -2.6679 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1614 0.5808 -2.3252 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1193 2.7840 -0.4163 H 0 0 0 0 0 0 0 0 0 0 0 0 4.4430 1.6540 -0.1637 H 0 0 0 0 0 0 0 0 0 0 0 0 2.7242 0.9497 1.1041 H 0 0 0 0 0 0 0 0 0 0 0 0 3.3862 -1.1843 0.7453 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2247 -0.5058 -0.6911 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6266 -1.2358 -0.8806 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2476 0.9279 -1.5744 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0106 3.0058 -0.7725 H 0 0 0 0 0 0 0 0 0 0 0 0 0.8414 2.4980 0.9350 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2366 1.9760 -1.2257 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4315 2.8788 0.2962 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4584 1.0405 1.5935 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7008 0.9104 1.6439 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.3434 1.2703 -0.5217 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0212 -0.3740 -1.1056 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.4892 0.3526 0.2683 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.9814 -0.9523 2.8823 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.6645 -1.2796 1.2699 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.3319 -3.5716 1.3060 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.3986 -4.5392 1.9422 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.8193 -4.2023 3.6190 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.8052 -2.0053 3.5834 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6015 -3.2547 3.0720 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6769 -3.8815 0.8372 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.2836 -3.4111 0.2539 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9140 -2.6623 -0.5407 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9719 -0.9156 2.6819 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6913 -2.6112 2.0599 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.1181 -2.6769 0.3712 H 0 0 0 0 0 0 0 0 0 0 0 0 1.1635 -1.8415 0.8587 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4061 -0.6085 1.9929 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9671 -1.6015 -1.3055 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8591 0.1150 -1.9594 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5301 -0.9431 -1.9495 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.5773 -3.9168 2.9661 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 2 4 1 0 4 5 2 0 4 6 1 0 6 7 1 0 7 8 1 0 8 9 1 0 8 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 2 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 22 24 1 0 24 25 1 0 25 26 1 0 26 27 1 0 27 28 1 0 19 29 1 0 27 10 1 0 27 13 1 0 24 14 1 0 22 17 1 0 1 30 1 0 1 31 1 0 1 32 1 0 2 33 1 0 3 34 1 0 3 35 1 0 3 36 1 0 5 37 1 0 5 38 1 0 6 39 1 0 6 40 1 0 7 41 1 0 7 42 1 0 8 43 1 0 9 44 1 0 9 45 1 0 9 46 1 0 10 47 1 0 11 48 1 0 11 49 1 0 12 50 1 0 12 51 1 0 13 52 1 0 14 53 1 0 15 54 1 0 15 55 1 0 16 56 1 0 18 57 1 0 18 58 1 0 19 59 1 0 20 60 1 0 20 61 1 0 21 62 1 0 21 63 1 0 23 64 1 0 23 65 1 0 23 66 1 0 24 67 1 0 25 68 1 0 25 69 1 0 26 70 1 0 26 71 1 0 28 72 1 0 28 73 1 0 28 74 1 0 29 75 1 0 M END

Standard InCHIKey	INDVLXYUCBVVKW-UHFFFAOYSA-N
Standard InCHI	InChI=1S/C28H46O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h9,18,20,22-26,29H,3,7-8,10-17H2,1-2,4-6H3
SMILES	CC(C)C(=C)CCC(C)C1CCC2C3CC=C4CC(CCC4(C)C3CCC12C)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	398.35	Volume:	462.136 ? Van der Waals volume.
Dense:	0.862	LogP:	6.743 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	4.809 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-6.944 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	5.0	Rigid Bonds:	21.0
TPSA:	20.23 ? Topological Polar Surface Area.	H-Bond Acceptor:	1.0
H-Bond Donor:	1.0	Rings:	4.0
Heavy Atoms:	1.0

MedChem Properties

QED Drug-Likeness Score:	0.474	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	4.378	Fsp³:	0.857
MCE-18:	69.577 ? MCE-18 stands for medicinal chemistry evolution.MCE-18≥45 is considered a suitable value.	Lipinski Rule-of-5:	Rejected
Pfizer Rule:	Accepted	GSK Rule:	Accepted
Golden Triangle Rule:	Rejected	BMS Rule:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.809	Fluc inhibitor:	0.0 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.003 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.008 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.541	Promiscuous compounds:	0.012

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-4.827	MDCK Permeability:	-4.822
Pgp-inhibitor:	0.505	Pgp-substrate:	0.001
PAMPA:	0.001 ? 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):	0.0
20% Bioavailability (F20%):	0.029	30% Bioavailability (F30%):	0.61
50% Bioavailability (F50%):	1.0

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.766	MRP1:	1.0
Plasma Protein Binding (PPB):	91.604%	Volume Distribution (VD):	0.171
Fu:	11.559% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.006
OATP1B3 inhibitor:	0.985	BCRP inhibitor:	0.492
BSEP inhibitor:	0.999

ADMET: Metabolism

CYP1A2-inhibitor:	0.025	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.956	CYP2C19-substrate:	0.091
CYP2C9-inhibitor:	0.457	CYP2C9-substrate:	0.001
CYP2D6-inhibitor:	0.002	CYP2D6-substrate:	0.0
CYP3A4-inhibitor:	1.0	CYP3A4-substrate:	1.0
CYP2B6-substrate:	1.0	CYP2C8-inhibitor:	1.0
HLM stability:	0.899 ? 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):

14.427

Half-life (T1/2):

0.562

ADMET: Toxicity

hERG Blockers:	0.258	hERG Blockers (10um):	0.68
Human Hepatotoxicity (H-HT):	0.66	Drug-induced Liver Injury (DILI):	0.066
AMES Toxicity:	0.075	Rat Oral Acute Toxicity:	0.129
Maximum Recommended Daily Dose:	0.824	Skin Sensitization:	0.112
Carcinogencity:	0.346	Eye Corrosion:	0.007
Eye Irritation:	0.359	Respiratory Toxicity:	0.747
Drug-induced Neurotoxicity:	0.237	Ototoxicity:	0.862
Hematotoxicity:	0.158	Drug-induced Nephrotoxicity:	0.098
Genotoxicity:	0.001	RPMI-8226 Immunitoxicity:	0.036
A549 Cytotoxicity:	0.175	Hek293 Cytotoxicity:	0.313
BCF:	2.762 ? 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:	5.2 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	6.364 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	6.443 ? 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
NPO25840	Sargassum fusiforme	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO12354	Sargassum pallidum	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO25840	Sargassum fusiforme	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO25840	Sargassum fusiforme	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO4145	Hijikia fusiforme	n.a.	n.a.	n.a.	n.a.	n.a.	n.a.	Database[TM-MC]
NPO12354	Sargassum pallidum	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO25840	Sargassum fusiforme	Species	Sargassaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO12354	Sargassum pallidum	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

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 NPC224430 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	24020
0.1-0.2	21719
0.2-0.3	3647
0.3-0.4	298
0.4-0.5	85
0.5-0.6	38
0.6-0.7	20
0.7-0.8	2
0.8-0.85	6
0.85-0.9	0
0.9-0.95	0
0.95-1	1

Similarity Score	Similarity Level	Natural Product ID
1.0	High Similarity	NPC134847
0.8163	Intermediate Similarity	NPC162742
0.8163	Intermediate Similarity	NPC304309
0.8163	Intermediate Similarity	NPC470228
0.8	Intermediate Similarity	NPC22105
0.8	Intermediate Similarity	NPC34019
0.8	Intermediate Similarity	NPC107059
0.7843	Intermediate Similarity	NPC136188
0.7843	Intermediate Similarity	NPC28657
0.7843	Intermediate Similarity	NPC474216
0.7778	Intermediate Similarity	NPC477522
0.7736	Intermediate Similarity	NPC87604
0.7692	Intermediate Similarity	NPC230301
0.7692	Intermediate Similarity	NPC198968
0.7692	Intermediate Similarity	NPC285893
0.7547	Intermediate Similarity	NPC241290
0.7547	Intermediate Similarity	NPC164840
0.7547	Intermediate Similarity	NPC484739
0.7547	Intermediate Similarity	NPC209944
0.7547	Intermediate Similarity	NPC155986
0.7407	Intermediate Similarity	NPC321381
0.7273	Intermediate Similarity	NPC472265
0.7273	Intermediate Similarity	NPC59453
0.7222	Intermediate Similarity	NPC264245
0.7143	Intermediate Similarity	NPC603646
0.7018	Intermediate Similarity	NPC473943
0.6981	Remote Similarity	NPC600590
0.6897	Remote Similarity	NPC488870
0.6852	Remote Similarity	NPC154330
0.6727	Remote Similarity	NPC84694
0.6727	Remote Similarity	NPC113733
0.6727	Remote Similarity	NPC143182
0.6724	Remote Similarity	NPC155011
0.6667	Remote Similarity	NPC221758
0.661	Remote Similarity	NPC47761
0.6379	Remote Similarity	NPC33913
0.6333	Remote Similarity	NPC474164
0.6316	Remote Similarity	NPC51014
0.6271	Remote Similarity	NPC26117
0.6271	Remote Similarity	NPC19607
0.6207	Remote Similarity	NPC328714
0.6167	Remote Similarity	NPC243985
0.6167	Remote Similarity	NPC280710
0.6167	Remote Similarity	NPC240650
0.6102	Remote Similarity	NPC318495
0.6038	Remote Similarity	NPC96319
0.5965	Remote Similarity	NPC328313
0.5932	Remote Similarity	NPC600056
0.5781	Remote Similarity	NPC234335
0.5781	Remote Similarity	NPC601043
0.5781	Remote Similarity	NPC605412
0.5667	Remote Similarity	NPC209620
0.5645	Remote Similarity	NPC186688
0.5606	Remote Similarity	NPC489072
0.5593	Remote Similarity	NPC209430
0.5574	Remote Similarity	NPC1272
0.5574	Remote Similarity	NPC470614
0.5556	Remote Similarity	NPC278648
0.5517	Remote Similarity	NPC151519
0.55	Remote Similarity	NPC603214
0.5455	Remote Similarity	NPC218186
0.5424	Remote Similarity	NPC20688
0.537	Remote Similarity	NPC111234
0.5345	Remote Similarity	NPC81306
0.5333	Remote Similarity	NPC76879
0.5303	Remote Similarity	NPC176012
0.5238	Remote Similarity	NPC474752
0.5238	Remote Similarity	NPC474683
0.5217	Remote Similarity	NPC235126
0.5217	Remote Similarity	NPC242419
0.5167	Remote Similarity	NPC109546
0.5167	Remote Similarity	NPC317458
0.5167	Remote Similarity	NPC47982
0.5161	Remote Similarity	NPC31564
0.5161	Remote Similarity	NPC145879
0.5161	Remote Similarity	NPC85095
0.5152	Remote Similarity	NPC13385
0.5147	Remote Similarity	NPC91604
0.5143	Remote Similarity	NPC147835
0.5143	Remote Similarity	NPC253645
0.5143	Remote Similarity	NPC85001
0.5143	Remote Similarity	NPC95920
0.5082	Remote Similarity	NPC28862
0.507	Remote Similarity	NPC486119

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC224430 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	7671
0.1-0.2	1305
0.2-0.3	130
0.3-0.4	37
0.4-0.5	2
0.5-0.6	1
0.6-0.7	2
0.7-0.8	2
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
0.7843	Intermediate Similarity	NPD6942	Phase 4
0.7692	Intermediate Similarity	NPD7339	Approved
0.6667	Remote Similarity	NPD4786	Phase 1
0.6038	Remote Similarity	NPD3701	Pre-clinical
0.5517	Remote Similarity	NPD3667	Phase 4

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