NPASS Compound

Natural Product: NPC112318

Natural Product ID	NPC112318
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	CKESVQPODPXKGQ-UHFFFAOYSA-M
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	24848106
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000002] Organoheterocyclic compounds [CHEMONTID:0001797] Imidazopyrimidines [CHEMONTID:0000245] Purines and purine derivatives [CHEMONTID:0000247] Xanthines

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 63 60 0 0 0 0 0 0 0 0999 V2000 4.4262 1.6935 1.1810 C 0 0 0 0 0 3 0 0 0 0 0 0 3.6031 0.6867 0.3810 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1666 1.0378 0.5575 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2694 0.0772 -0.0364 N 0 0 0 0 0 0 0 0 0 0 0 0 -0.0100 0.2934 0.0540 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9759 -0.6299 -0.5198 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4984 -1.7497 -1.1674 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3510 -2.6703 -1.7363 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7039 -2.4229 -1.6297 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1944 -1.3056 -0.9839 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3242 -0.3793 -0.4111 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8095 0.7474 0.2403 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.1876 0.9459 0.3173 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5877 2.1603 1.0231 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.8044 2.4351 1.1498 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.6708 3.0412 1.5704 O 0 0 0 0 0 1 0 0 0 0 0 0 -0.4960 1.4188 0.7047 O 0 0 0 0 0 0 0 0 0 0 0 0 3.8236 -0.5657 0.9927 O 0 0 0 0 0 0 0 0 0 0 0 0 4.4148 -1.4196 0.0708 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3787 2.0108 0.1128 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5201 0.8374 0.0446 N 0 0 0 0 0 0 0 0 0 0 0 0 -1.0726 -0.3852 -0.0511 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2518 -1.4804 -0.1144 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1117 -1.2769 -0.0769 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8701 -2.2773 -0.1347 O 0 0 0 0 0 0 0 0 0 0 0 0 1.6469 -0.0423 0.0193 N 0 0 0 0 0 0 0 0 0 0 0 0 3.0802 0.1815 0.0594 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8192 1.0168 0.0800 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3324 2.1625 0.1696 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0637 -2.5563 -0.2042 N 0 0 0 0 0 0 0 0 0 0 0 0 -2.3503 -2.1439 -0.1969 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3640 -0.8037 -0.1025 N 0 0 0 0 0 0 0 0 0 0 0 0 0.0000 0.0000 0.0000 Hg 0 0 0 0 0 15 0 0 0 0 0 0 0.0000 0.0000 0.0000 Na 0 0 0 0 0 15 0 0 0 0 0 0 -0.0002 0.3840 -0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0063 0.3808 -0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.8836 1.9533 2.1278 H 0 0 0 0 0 0 0 0 0 0 0 0 4.5047 2.6614 0.6269 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9425 0.6937 -0.6570 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9695 2.0299 0.1060 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9406 1.0492 1.6506 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5807 -1.9250 -1.2394 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9966 -3.5610 -2.2521 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4314 -3.1054 -2.0542 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.2393 -1.1020 -0.8942 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.5841 0.9066 -0.7356 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6357 0.0547 0.8347 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1859 2.0144 1.1722 H 0 0 0 0 0 0 0 0 0 0 0 0 5.3957 -1.0091 -0.2843 H 0 0 0 0 0 0 0 0 0 0 0 0 4.6469 -2.3654 0.6055 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7471 -1.6897 -0.7648 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.3764 1.7953 -0.2878 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9340 2.8200 -0.5292 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4412 2.3527 1.1610 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6361 -0.5212 -0.5992 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2959 1.2358 -0.1412 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4215 -0.0056 1.1185 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2512 -2.7307 -0.2536 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2100 -0.1892 -0.0735 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7961 -0.1919 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7959 -0.1921 -0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8096 -0.1926 -0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 0.8158 -0.1882 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 3 4 1 0 4 5 2 3 5 6 1 0 6 7 2 0 7 8 1 0 8 9 2 0 9 10 1 0 10 11 2 0 11 12 1 0 12 13 1 0 13 14 1 0 14 15 2 0 14 16 1 0 5 17 1 0 2 18 1 0 18 19 1 0 20 21 1 0 21 22 1 0 22 23 2 0 23 24 1 0 24 25 2 0 24 26 1 0 26 27 1 0 26 28 1 0 28 29 2 0 23 30 1 0 30 31 2 0 31 32 1 0 11 6 1 0 28 21 1 0 32 22 1 0 1 37 1 0 1 38 1 0 2 39 1 0 3 40 1 0 3 41 1 0 7 42 1 0 8 43 1 0 9 44 1 0 10 45 1 0 13 46 1 0 13 47 1 0 17 48 1 0 19 49 1 0 19 50 1 0 19 51 1 0 20 52 1 0 20 53 1 0 20 54 1 0 27 55 1 0 27 56 1 0 27 57 1 0 31 58 1 0 32 59 1 0 35 60 1 0 35 61 1 0 36 62 1 0 36 63 1 0 M CHG 2 16 -1 34 1 M RAD 1 1 2 M END

Standard InCHIKey	CKESVQPODPXKGQ-UHFFFAOYSA-M
Standard InCHI	InChI=1S/C13H16NO5.C7H8N4O2.Hg.Na.2H2O/c1-9(18-2)7-14-13(17)10-5-3-4-6-11(10)19-8-12(15)16;1-10-5-4(8-3-9-5)6(12)11(2)7(10)13;;;;/h3-6,9H,1,7-8H2,2H3,(H,14,17)(H,15,16);3H,1-2H3,(H,8,9);;;2*1H2/q;;;+1;;/p-1
SMILES	[CH2]C(CN=C(c1ccccc1OCC(=O)[O-])O)OC.Cn1c2c(c(=O)n(C)c1=O)nc[nH]2.[Hg].[Na+].O.O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	265.1	Volume:	263.977 ? Van der Waals volume.
Dense:	1.004	LogP:	-0.445 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	-0.404 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-1.567 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	7.0	Rigid Bonds:	8.0
TPSA:	91.18 ? Topological Polar Surface Area.	H-Bond Acceptor:	6.0
H-Bond Donor:	1.0	Rings:	1.0
Heavy Atoms:	6.0

MedChem Properties

QED Drug-Likeness Score:	0.552	GASA:	0.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	3.813	Fsp³:	0.308
MCE-18:	16.0 ? 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:	Rejected
Golden Triangle Rule:	Rejected	BMS Rule:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.031	Fluc inhibitor:	0.003 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.035 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.293 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.024	Promiscuous compounds:	0.02

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-4.716	MDCK Permeability:	-4.422
Pgp-inhibitor:	0.0	Pgp-substrate:	0.021
PAMPA:	0.991 ? 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):	0.01
20% Bioavailability (F20%):	0.077	30% Bioavailability (F30%):	0.011
50% Bioavailability (F50%):	0.218

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.064	MRP1:	0.721
Plasma Protein Binding (PPB):	67.578%	Volume Distribution (VD):	-0.238
Fu:	34.845% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.903
OATP1B3 inhibitor:	0.991	BCRP inhibitor:	0.0
BSEP inhibitor:	0.029

ADMET: Metabolism

CYP1A2-inhibitor:	0.003	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.925	CYP2C19-substrate:	0.13
CYP2C9-inhibitor:	0.992	CYP2C9-substrate:	0.002
CYP2D6-inhibitor:	0.084	CYP2D6-substrate:	0.0
CYP3A4-inhibitor:	0.958	CYP3A4-substrate:	0.002
CYP2B6-substrate:	0.002	CYP2C8-inhibitor:	0.001
HLM stability:	0.008 ? 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):

2.518

Half-life (T1/2):

1.952

ADMET: Toxicity

hERG Blockers:	0.074	hERG Blockers (10um):	0.127
Human Hepatotoxicity (H-HT):	0.842	Drug-induced Liver Injury (DILI):	0.739
AMES Toxicity:	0.638	Rat Oral Acute Toxicity:	0.577
Maximum Recommended Daily Dose:	0.106	Skin Sensitization:	0.963
Carcinogencity:	0.727	Eye Corrosion:	0.0
Eye Irritation:	0.515	Respiratory Toxicity:	0.475
Drug-induced Neurotoxicity:	0.539	Ototoxicity:	0.631
Hematotoxicity:	0.406	Drug-induced Nephrotoxicity:	0.508
Genotoxicity:	0.951	RPMI-8226 Immunitoxicity:	0.008
A549 Cytotoxicity:	0.004	Hek293 Cytotoxicity:	0.036
BCF:	0.232 ? 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:	2.839 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	3.908 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	3.296 ? 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
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[ 16712885]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	DOI[10.1016/j.foodchem.2013.08.121]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	DOI[10.1016/S0031-9422(00)00169-2]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	fruit	n.a.	PMID[15128023]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Flowers	n.a.	n.a.	PMID[16180814]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	seeds	Shizuoka prefecture, Japan	n.a.	PMID[16499314]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[18068204]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[18068204]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[21434603]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	flower	n.a.	PMID[21922925]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	flower buds	n.a.	n.a.	PMID[21925888]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	leaves	n.a.	n.a.	PMID[22377672]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	leaf	n.a.	PMID[23265489]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Leaves	Bandung, West Java, Indonesia		PMID[23621359]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[37255739]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO26505	Cola acuminata	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO21254	Paullinia cupana	Species	Sapindaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Cotyledon	n.a.	n.a.	Database[FooDB]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	Seed	n.a.	n.a.	Database[FooDB]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	Root	n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Plant	n.a.	n.a.	Database[FooDB]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	Plant	n.a.	n.a.	Database[FooDB]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	Petiole	n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Leaf Essent. Oil	n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Leaf	n.a.	n.a.	Database[FooDB]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	Fruit	n.a.	n.a.	Database[FooDB]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota		n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota		n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Seed	n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Seed Oil	n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Shoot	n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	Stem	n.a.	n.a.	Database[FooDB]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	Testa	n.a.	n.a.	Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.		Database[FooDB]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO26505	Cola acuminata	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO21254	Paullinia cupana	Species	Sapindaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	n.a.		Database[Phenol-Explorer]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO26505	Cola acuminata	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO21254	Paullinia cupana	Species	Sapindaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO15401	Theobroma cacao	Species	Malvaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO21254	Paullinia cupana	Species	Sapindaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO8258	Camellia sinensis	Species	Theaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26505	Cola acuminata	Species	Malvaceae	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 NPC112318 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	24791
0.1-0.2	24969
0.2-0.3	96
0.3-0.4	1
0.4-0.5	2
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	Natural Product ID
		NPC

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC112318 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	2270
0.1-0.2	6669
0.2-0.3	202
0.3-0.4	4
0.4-0.5	4
0.5-0.6	0
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	Drug ID	Developmental Stage
0.6164	Remote Similarity	NPD1048	Approved

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