NPASS Compound

Natural Product: NPC483211

Natural Product ID	NPC483211
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	WZYJEEIAFBHYJS-DDSWNALCSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	127030867
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0001283] Terpene lactones [CHEMONTID:0001538] Diterpene lactones

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 52 56 0 0 0 0 0 0 0 0999 V2000 -4.3496 -4.8652 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4679 -3.6517 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9679 -3.6517 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5413 -3.1881 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2294 -1.7209 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3442 -0.7172 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7707 -1.1807 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0826 -2.6480 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9314 -2.2251 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.3580 -1.7616 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.8855 -0.1771 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.3120 -0.6406 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.5736 1.2902 0.0000 O 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 -1.8351 3.2209 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 0.7062 2.6807 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0969 2.1188 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5010 3.9528 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 -0.0880 1.4842 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3907 1.0037 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.2546 0.7837 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8013 1.2525 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 0.5654 -0.4488 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.8413 -4.7084 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7395 -6.2355 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2798 -5.1189 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 0.9578 -3.2405 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3325 -4.6735 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 1.1613 -2.2828 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0721 0.0777 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.1617 -3.6899 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.5680 -2.4393 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.3758 2.6140 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0439 4.7063 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.3167 3.4556 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 -1.1128 5.0089 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4877 1.5569 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.8242 3.4307 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.4346 0.6573 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2959 5.2249 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.8605 3.3189 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3354 4.8968 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8886 1.3442 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5047 -0.8603 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 3.8173 0.5402 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3442 -2.2172 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5177 -0.9588 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0470 -0.6835 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 2 0 2 3 1 0 3 4 1 0 4 5 1 0 5 6 1 0 6 7 1 0 7 8 1 0 7 9 1 1 9 10 2 0 7 11 1 0 11 12 2 0 11 13 1 0 13 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 17 18 1 0 17 19 1 0 17 20 1 0 20 21 1 0 21 22 1 0 21 23 1 0 23 24 1 0 25 24 1 1 5 26 1 0 9 2 1 0 25 14 1 0 8 3 1 0 25 20 1 0 25 6 1 0 1 27 1 0 1 28 1 0 3 29 1 1 4 30 1 0 4 31 1 0 5 32 1 1 6 33 1 1 8 34 1 0 8 35 1 0 14 36 1 6 15 37 1 0 15 38 1 0 16 39 1 0 16 40 1 0 18 41 1 0 18 42 1 0 18 43 1 0 19 44 1 0 19 45 1 0 19 46 1 0 20 47 1 1 21 48 1 6 22 49 1 0 24 50 1 0 24 51 1 0 26 52 1 0 M END

Standard InCHIKey	WZYJEEIAFBHYJS-DDSWNALCSA-N
Standard InCHI	InChI=1S/C20H26O6/c1-9-10-6-11(21)13-19(7-10,15(9)22)17(24)26-12-4-5-18(2,3)14-16(23)25-8-20(12,13)14/h10-14,16,21,23H,1,4-8H2,2-3H3/t10-,11+,12-,13+,14+,16+,19-,20-/m0/s1
SMILES	C=C1[C@H]2C[C@H]([C@@H]3[C@@](C2)(C1=O)C(=O)O[C@H]1CCC(C)(C)[C@H]2[C@H](O)OC[C@@]312)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	362.17	Volume:	356.526 ? Van der Waals volume.
Dense:	1.016	LogP:	0.798 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	1.112 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-2.18 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	0.0	Rigid Bonds:	26.0
TPSA:	93.06 ? Topological Polar Surface Area.	H-Bond Acceptor:	6.0
H-Bond Donor:	2.0	Rings:	5.0
Heavy Atoms:	6.0

MedChem Properties

QED Drug-Likeness Score:	0.382	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	6.713	Fsp³:	0.8
MCE-18:	124.667 ? 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:	1
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.648	Fluc inhibitor:	0.0 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.031 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.001 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.204	Promiscuous compounds:	0.292

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-4.729	MDCK Permeability:	-4.786
Pgp-inhibitor:	0.039	Pgp-substrate:	0.85
PAMPA:	0.924 ? 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):	0.015
20% Bioavailability (F20%):	0.138	30% Bioavailability (F30%):	0.335
50% Bioavailability (F50%):	0.567

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.01	MRP1:	0.849
Plasma Protein Binding (PPB):	65.253%	Volume Distribution (VD):	-0.3
Fu:	34.292% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.842
OATP1B3 inhibitor:	0.936	BCRP inhibitor:	0.012
BSEP inhibitor:	0.82

ADMET: Metabolism

CYP1A2-inhibitor:	0.007	CYP1A2-substrate:	0.001
CYP2C19-inhibitor:	0.011	CYP2C19-substrate:	0.0
CYP2C9-inhibitor:	0.0	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.024
CYP3A4-inhibitor:	0.382	CYP3A4-substrate:	0.006
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.038
HLM stability:	0.033 ? 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):

4.157

Half-life (T1/2):

2.904

ADMET: Toxicity

hERG Blockers:	0.049	hERG Blockers (10um):	0.369
Human Hepatotoxicity (H-HT):	0.661	Drug-induced Liver Injury (DILI):	0.727
AMES Toxicity:	0.713	Rat Oral Acute Toxicity:	0.524
Maximum Recommended Daily Dose:	0.821	Skin Sensitization:	0.976
Carcinogencity:	0.643	Eye Corrosion:	0.003
Eye Irritation:	0.408	Respiratory Toxicity:	0.917
Drug-induced Neurotoxicity:	0.337	Ototoxicity:	0.778
Hematotoxicity:	0.775	Drug-induced Nephrotoxicity:	0.899
Genotoxicity:	0.968	RPMI-8226 Immunitoxicity:	0.157
A549 Cytotoxicity:	0.163	Hek293 Cytotoxicity:	0.345
BCF:	0.516 ? 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:	3.253 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	4.964 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.121 ? 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
NPO25255	Isodon phyllostachys	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[26757019]
NPO25255	Isodon phyllostachys	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO25255	Isodon phyllostachys	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO25255	Isodon phyllostachys	Species	Lamiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO25255	Isodon phyllostachys	Species	Lamiaceae	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	6
GI	5

Activity Type	# Activity
Cell line	7
Non-molecular	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
NPT81	Cell line	A549	Homo sapiens	IC50	=	14300.0	nM	PMID[26757019]
NPT83	Cell line	MCF7	Homo sapiens	IC50	=	14000.0	nM	PMID[26757019]
NPT660	Cell line	SW480	Homo sapiens	IC50	=	10900.0	nM	PMID[26757019]
NPT81	Cell line	A549	Homo sapiens	GI	=	50.0	%	PMID[26757019]
NPT83	Cell line	MCF7	Homo sapiens	GI	=	50.0	%	PMID[26757019]
NPT660	Cell line	SW480	Homo sapiens	GI	=	50.0	%	PMID[26757019]
NPT113	Cell line	RAW264.7	Mus musculus	IC50	=	3560.0	nM	PMID[26757019]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	IC50	=	11400.0	nM	PMID[26757019]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	IC50	=	10300.0	nM	PMID[26757019]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	GI	=	50.0	%	PMID[26757019]

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 NPC483211 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	18088
0.1-0.2	26829
0.2-0.3	4739
0.3-0.4	144
0.4-0.5	28
0.5-0.6	16
0.6-0.7	9
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	NPC96333
1.0	High Similarity	NPC88833
0.7705	Intermediate Similarity	NPC483232
0.7377	Intermediate Similarity	NPC483212
0.7377	Intermediate Similarity	NPC101842
0.6935	Remote Similarity	NPC483228
0.6875	Remote Similarity	NPC148279
0.6615	Remote Similarity	NPC193785
0.6471	Remote Similarity	NPC483251
0.6471	Remote Similarity	NPC483252
0.6418	Remote Similarity	NPC483222
0.6418	Remote Similarity	NPC483221
0.6364	Remote Similarity	NPC98069
0.6364	Remote Similarity	NPC483216
0.5882	Remote Similarity	NPC61071
0.5882	Remote Similarity	NPC483215
0.5714	Remote Similarity	NPC96217
0.5672	Remote Similarity	NPC285927
0.5571	Remote Similarity	NPC483234
0.5522	Remote Similarity	NPC483227
0.5522	Remote Similarity	NPC483225
0.5294	Remote Similarity	NPC483214
0.5286	Remote Similarity	NPC483206
0.5286	Remote Similarity	NPC42776
0.5286	Remote Similarity	NPC483209
0.5286	Remote Similarity	NPC88469
0.5286	Remote Similarity	NPC483210
0.5278	Remote Similarity	NPC49730
0.5211	Remote Similarity	NPC130302
0.5068	Remote Similarity	NPC124053

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC483211 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	6205
0.1-0.2	2869
0.2-0.3	76
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