NPASS Compound

Natural Product: NPC60666

Natural Product ID	NPC60666
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	HRUAQJXBUYEBPK-FMPMANLDSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	101131177
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000258] Steroids and steroid derivatives [CHEMONTID:0001671] Physalins 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 2D 67 74 0 0 0 0 0 0 0 0999 V2000 2.1328 3.1443 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7062 2.6807 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4086 3.6844 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.8351 3.2209 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1470 1.7537 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3605 2.6354 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0323 0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3943 1.2135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2760 0.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0494 0.1929 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.3943 -1.2135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4150 -3.0731 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6975 -3.8511 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6651 -5.3507 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3501 -6.0724 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3177 -7.5721 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0028 -8.2938 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2798 -7.5159 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2473 -6.0163 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6151 -5.4005 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0676 -5.2945 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2149 -4.5166 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1000 -3.7949 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3401 -3.3754 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0619 -2.0605 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6424 -0.6203 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1342 -0.4635 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2663 -1.4476 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.4460 1.0037 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8924 -1.9194 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.8787 -0.9975 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.6353 0.2976 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0944 1.6967 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8650 3.1791 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9107 4.2545 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.4665 3.7215 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0323 -0.7500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.6052 3.4304 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8466 4.6167 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9277 1.8722 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.1128 5.0089 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6521 4.7451 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8192 4.3530 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.5741 3.5171 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.5096 1.6713 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6334 3.9473 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8192 2.0952 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.7362 -2.3629 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1688 -4.1434 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4073 -2.5296 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9476 -6.1286 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6002 -8.3500 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0297 -9.7935 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7510 -7.2236 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8231 -8.9140 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5827 -3.9009 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4008 -5.4351 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9484 -3.0405 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0933 -2.2949 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7971 -3.7322 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.7345 -4.8227 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4296 -1.4447 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2636 -2.9582 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5630 -2.2823 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7296 -0.7282 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 3.8790 1.1363 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1203 2.7911 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2 1 1 1 2 3 1 0 3 4 1 0 4 5 1 0 5 6 1 6 5 7 1 0 7 8 1 0 8 9 1 0 9 10 2 0 9 11 1 0 11 12 1 0 12 13 1 0 13 14 1 0 14 15 2 0 15 16 1 0 16 17 2 0 17 18 1 0 18 19 1 0 19 20 2 0 19 21 1 0 21 22 1 1 21 23 1 0 23 24 1 0 24 25 1 0 25 26 1 0 26 27 1 0 27 28 2 0 27 29 1 0 26 30 1 1 11 31 1 1 31 32 1 0 32 33 1 0 33 34 1 0 34 35 2 0 34 36 1 0 11 37 1 0 33 2 1 0 8 2 1 0 23 12 1 0 36 4 1 0 29 5 1 0 26 7 1 0 7 37 1 6 21 15 1 0 1 38 1 0 1 39 1 0 1 40 1 0 3 41 1 0 3 42 1 0 4 43 1 6 6 44 1 0 6 45 1 0 6 46 1 0 8 47 1 1 12 48 1 1 13 49 1 0 13 50 1 0 14 51 1 0 16 52 1 0 17 53 1 0 18 54 1 0 18 55 1 0 22 56 1 0 22 57 1 0 22 58 1 0 23 59 1 6 24 60 1 0 24 61 1 0 25 62 1 0 25 63 1 0 30 64 1 0 32 65 1 0 32 66 1 0 33 67 1 6 M END

Standard InCHIKey	HRUAQJXBUYEBPK-FMPMANLDSA-N
Standard InCHI	InChI=1S/C28H30O9/c1-23-11-18-25(3)28-19(23)20(30)27(37-28,34-12-16(23)21(31)35-18)15-8-7-13-5-4-6-17(29)24(13,2)14(15)9-10-26(28,33)22(32)36-25/h4-5,7,14-16,18-19,33H,6,8-12H2,1-3H3/t14-,15+,16+,18+,19-,23+,24-,25-,26-,27-,28-/m0/s1
SMILES	C[C@@]12C[C@@H]3[C@@]4(C)[C@@]56[C@H]2C(=O)[C@@]([C@@H]2CC=C7C=CCC(=O)[C@]7(C)[C@H]2CC[C@@]5(C(=O)O4)O)(OC[C@@H]1C(=O)O3)O6

Calculated Properties

Physi-Chem Properties

Molecular Weight:	510.19	Volume:	487.686 ? Van der Waals volume.
Dense:	1.046	LogP:	1.568 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	1.536 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-4.524 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	0.0	Rigid Bonds:	40.0
TPSA:	125.43 ? Topological Polar Surface Area.	H-Bond Acceptor:	9.0
H-Bond Donor:	1.0	Rings:	8.0
Heavy Atoms:	9.0

MedChem Properties

QED Drug-Likeness Score:	0.483	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	7.552	Fsp³:	0.714
MCE-18:	192.833 ? 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:	0.265	Fluc inhibitor:	0.048 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.008 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.034 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.205	Promiscuous compounds:	0.616

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.006	MDCK Permeability:	-4.773
Pgp-inhibitor:	0.365	Pgp-substrate:	0.007
PAMPA:	0.925 ? 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):	0.004
20% Bioavailability (F20%):	0.466	30% Bioavailability (F30%):	0.893
50% Bioavailability (F50%):	0.995

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.002	MRP1:	0.984
Plasma Protein Binding (PPB):	77.513%	Volume Distribution (VD):	-0.075
Fu:	19.639% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	1.0
OATP1B3 inhibitor:	1.0	BCRP inhibitor:	0.0
BSEP inhibitor:	1.0

ADMET: Metabolism

CYP1A2-inhibitor:	0.008	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.007	CYP2C19-substrate:	0.0
CYP2C9-inhibitor:	0.0	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.428
CYP3A4-inhibitor:	1.0	CYP3A4-substrate:	0.149
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.465
HLM stability:	0.845 ? 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):

4.661

Half-life (T1/2):

1.909

ADMET: Toxicity

hERG Blockers:	0.008	hERG Blockers (10um):	0.136
Human Hepatotoxicity (H-HT):	0.416	Drug-induced Liver Injury (DILI):	0.697
AMES Toxicity:	0.906	Rat Oral Acute Toxicity:	0.817
Maximum Recommended Daily Dose:	0.542	Skin Sensitization:	1.0
Carcinogencity:	0.965	Eye Corrosion:	0.003
Eye Irritation:	0.163	Respiratory Toxicity:	0.2
Drug-induced Neurotoxicity:	0.591	Ototoxicity:	0.438
Hematotoxicity:	0.363	Drug-induced Nephrotoxicity:	0.935
Genotoxicity:	0.998	RPMI-8226 Immunitoxicity:	0.232
A549 Cytotoxicity:	0.55	Hek293 Cytotoxicity:	0.841
BCF:	1.029 ? 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:	3.779 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.397 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.857 ? 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
NPO14304	Physalis alkekengi	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO14304	Physalis alkekengi	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO14304	Physalis alkekengi	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO14304	Physalis alkekengi	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO14304	Physalis alkekengi	Species	Solanaceae	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 NPC60666 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	20945
0.1-0.2	28032
0.2-0.3	820
0.3-0.4	19
0.4-0.5	10
0.5-0.6	7
0.6-0.7	21
0.7-0.8	0
0.8-0.85	0
0.85-0.9	0
0.9-0.95	0
0.95-1	2

Similarity Score	Similarity Level	Natural Product ID
1.0	High Similarity	NPC600158
1.0	High Similarity	NPC609951
0.7558	Intermediate Similarity	NPC188291
0.7558	Intermediate Similarity	NPC605653
0.7471	Intermediate Similarity	NPC264192
0.6966	Remote Similarity	NPC15215
0.6966	Remote Similarity	NPC242486
0.6739	Remote Similarity	NPC600931
0.663	Remote Similarity	NPC243014
0.6344	Remote Similarity	NPC100390
0.6344	Remote Similarity	NPC254614
0.6344	Remote Similarity	NPC600930
0.6344	Remote Similarity	NPC608769
0.6316	Remote Similarity	NPC79835
0.6316	Remote Similarity	NPC603465
0.6304	Remote Similarity	NPC484693
0.6277	Remote Similarity	NPC254146
0.6277	Remote Similarity	NPC33378
0.6277	Remote Similarity	NPC6274
0.6277	Remote Similarity	NPC486573
0.6277	Remote Similarity	NPC606278
0.6162	Remote Similarity	NPC601164
0.6146	Remote Similarity	NPC603368
0.6146	Remote Similarity	NPC610240
0.6042	Remote Similarity	NPC484694
0.6042	Remote Similarity	NPC600403
0.5769	Remote Similarity	NPC600933
0.5769	Remote Similarity	NPC601161
0.5686	Remote Similarity	NPC606873
0.5638	Remote Similarity	NPC600932
0.5567	Remote Similarity	NPC605654
0.54	Remote Similarity	NPC604937
0.5175	Remote Similarity	NPC602548

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC60666 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	7157
0.1-0.2	1978
0.2-0.3	15
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