NPASS Compound

Natural Product: NPC481530

Natural Product ID	NPC481530
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	LSIXYKVIRINGAR-LXXAOEIBSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	n.a.
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0001551] Diterpenoids [CHEMONTID:0002875] Tigliane and ingenane diterpenoids

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 67 70 0 0 0 0 0 0 0 0999 V2000 5.3825 -0.2759 -1.0211 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0879 -1.7577 -1.0767 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2766 -2.2156 0.1133 C 0 0 2 0 0 0 0 0 0 0 0 0 4.0528 -3.7142 -0.0681 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9572 -1.5547 0.0751 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8664 -2.1900 0.0073 O 0 0 0 0 0 0 0 0 0 0 0 0 2.8100 -0.1959 0.1101 O 0 0 0 0 0 0 0 0 0 0 0 0 1.5531 0.4751 0.0750 C 0 0 2 0 0 0 0 0 0 0 0 0 0.5247 0.2811 1.0757 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.9012 0.3266 0.6739 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.7189 -0.6738 1.4152 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7230 -1.4575 1.1326 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4027 -1.5773 -0.1589 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.6851 -0.2594 -0.8170 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.5611 0.6232 -1.0827 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.8723 1.8582 -0.3116 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.0423 1.7784 0.2930 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6510 2.8587 1.1528 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6463 0.4914 -0.0009 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.7692 0.0818 0.3623 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.1780 0.1643 -0.7809 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.2588 1.1005 -1.5602 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.5419 1.0461 -3.0491 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1440 0.7310 -1.3230 C 0 0 1 0 0 0 0 0 0 0 0 0 2.0223 1.6745 -1.8747 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.9289 -1.1644 -1.0949 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.2678 -2.3472 2.2123 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6037 -2.0842 2.4764 O 0 0 0 0 0 0 0 0 0 0 0 0 1.4067 1.4763 1.1690 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4685 1.4924 2.2888 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9066 2.8633 0.8719 C 0 0 0 0 0 0 0 0 0 0 0 0 4.7038 0.2793 -1.6965 H 0 0 0 0 0 0 0 0 0 0 0 0 5.2314 0.1486 -0.0011 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4134 -0.0316 -1.3500 H 0 0 0 0 0 0 0 0 0 0 0 0 6.0490 -2.2837 -1.1676 H 0 0 0 0 0 0 0 0 0 0 0 0 4.5221 -1.9455 -2.0136 H 0 0 0 0 0 0 0 0 0 0 0 0 4.8633 -1.9870 1.0202 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2077 -4.0224 -1.1145 H 0 0 0 0 0 0 0 0 0 0 0 0 3.0164 -4.0069 0.2112 H 0 0 0 0 0 0 0 0 0 0 0 0 4.7445 -4.2456 0.6001 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7240 -0.4879 1.8832 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3397 1.3247 0.9751 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3834 -0.7676 2.4635 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9426 -2.3123 -0.8586 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4233 -2.0159 0.0444 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.2251 -0.5116 -1.7744 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5753 0.9608 -2.1638 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2432 2.7579 -0.2215 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.5078 3.2862 0.5916 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.0555 2.4155 2.0802 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9205 3.6635 1.3160 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5504 2.1252 -1.2516 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4364 1.2583 -3.5729 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8778 0.0808 -3.4060 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2160 1.8637 -3.3865 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3386 -0.2156 -1.9114 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3210 1.4268 -2.7785 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0512 -1.4036 -2.0213 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2103 -3.3809 1.8055 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6279 -2.2931 3.0959 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.7760 -1.8230 3.4139 H 0 0 0 0 0 0 0 0 0 0 0 0 2.1462 2.1625 3.0881 H 0 0 0 0 0 0 0 0 0 0 0 0 3.3859 1.8789 1.7971 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6118 0.4756 2.6733 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.1698 2.9904 0.9513 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3526 3.6508 1.5396 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3207 3.1293 -0.1454 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 3 5 1 0 5 6 2 0 5 7 1 0 8 7 1 6 8 9 1 0 9 10 1 0 10 11 1 0 11 12 2 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 17 19 1 0 19 20 2 0 15 21 1 0 21 22 1 0 22 23 1 0 22 24 1 0 24 25 1 0 21 26 1 6 12 27 1 0 27 28 1 0 9 29 1 0 29 30 1 0 29 31 1 0 24 8 1 0 29 8 1 0 21 10 1 0 19 14 1 0 1 32 1 0 1 33 1 0 1 34 1 0 2 35 1 0 2 36 1 0 3 37 1 1 4 38 1 0 4 39 1 0 4 40 1 0 9 41 1 1 10 42 1 1 11 43 1 0 13 44 1 0 13 45 1 0 14 46 1 6 15 47 1 6 16 48 1 0 18 49 1 0 18 50 1 0 18 51 1 0 22 52 1 1 23 53 1 0 23 54 1 0 23 55 1 0 24 56 1 6 25 57 1 0 26 58 1 0 27 59 1 0 27 60 1 0 28 61 1 0 30 62 1 0 30 63 1 0 30 64 1 0 31 65 1 0 31 66 1 0 31 67 1 0 M END

Standard InCHIKey	LSIXYKVIRINGAR-LXXAOEIBSA-N
Standard InCHI	InChI=1S/C25H36O6/c1-7-12(2)22(29)31-25-20(23(25,5)6)18-10-15(11-26)9-16-17(8-13(3)19(16)27)24(18,30)14(4)21(25)28/h8,10,12,14,16-18,20-21,26,28,30H,7,9,11H2,1-6H3/t12-,14+,16+,17+,18-,20+,21+,24-,25+/m0/s1
SMILES	CC[C@H](C)C(=O)O[C@]12[C@H]([C@@H]3C=C(C[C@@H]4[C@@H](C=C(C)C4=O)[C@]3([C@H](C)[C@H]1O)O)CO)C2(C)C

Calculated Properties

Physi-Chem Properties

Molecular Weight:	432.25	Volume:	448.926 ? Van der Waals volume.
Dense:	0.963	LogP:	2.052 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	2.346 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-3.228 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	5.0	Rigid Bonds:	20.0
TPSA:	104.06 ? Topological Polar Surface Area.	H-Bond Acceptor:	6.0
H-Bond Donor:	3.0	Rings:	4.0
Heavy Atoms:	6.0

MedChem Properties

QED Drug-Likeness Score:	0.466	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	5.268	Fsp³:	0.76
MCE-18:	78.545 ? 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:	Rejected	BMS Rule:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.385	Fluc inhibitor:	0.002 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.01 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.0 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.304	Promiscuous compounds:	0.338

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.083	MDCK Permeability:	-4.827
Pgp-inhibitor:	0.006	Pgp-substrate:	0.807
PAMPA:	0.954 ? 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):	0.155
20% Bioavailability (F20%):	0.997	30% Bioavailability (F30%):	0.999
50% Bioavailability (F50%):	0.996

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.026	MRP1:	0.836
Plasma Protein Binding (PPB):	68.234%	Volume Distribution (VD):	0.007
Fu:	34.894% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.893
OATP1B3 inhibitor:	0.605	BCRP inhibitor:	0.0
BSEP inhibitor:	0.797

ADMET: Metabolism

CYP1A2-inhibitor:	0.001	CYP1A2-substrate:	0.007
CYP2C19-inhibitor:	0.005	CYP2C19-substrate:	0.003
CYP2C9-inhibitor:	0.001	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.093
CYP3A4-inhibitor:	0.99	CYP3A4-substrate:	0.552
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.646
HLM stability:	0.47 ? 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):

7.906

Half-life (T1/2):

1.424

ADMET: Toxicity

hERG Blockers:	0.058	hERG Blockers (10um):	0.21
Human Hepatotoxicity (H-HT):	0.656	Drug-induced Liver Injury (DILI):	0.647
AMES Toxicity:	0.749	Rat Oral Acute Toxicity:	0.439
Maximum Recommended Daily Dose:	0.287	Skin Sensitization:	0.989
Carcinogencity:	0.697	Eye Corrosion:	0.012
Eye Irritation:	0.654	Respiratory Toxicity:	0.773
Drug-induced Neurotoxicity:	0.423	Ototoxicity:	0.705
Hematotoxicity:	0.822	Drug-induced Nephrotoxicity:	0.647
Genotoxicity:	0.615	RPMI-8226 Immunitoxicity:	0.17
A549 Cytotoxicity:	0.555	Hek293 Cytotoxicity:	0.365
BCF:	0.651 ? 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:	3.315 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.053 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.466 ? 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
NPO40822	Croton damayeshu	Species	Euphorbiaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[31117522]

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
Inhibition	2

Activity Type	# Activity
Cell line	2

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	Inhibition	<	50.0	%	PMID[31117522]
NPT116	Cell line	HL-60	Homo sapiens	Inhibition	<	50.0	%	PMID[31117522]

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 NPC481530 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	16293
0.1-0.2	32050
0.2-0.3	1402
0.3-0.4	69
0.4-0.5	22
0.5-0.6	13
0.6-0.7	3
0.7-0.8	0
0.8-0.85	1
0.85-0.9	2
0.9-0.95	0
0.95-1	1

Similarity Score	Similarity Level	Natural Product ID
1.0	High Similarity	NPC472400
0.8929	High Similarity	NPC481521
0.8621	High Similarity	NPC481526
0.8	Intermediate Similarity	NPC481527
0.7097	Intermediate Similarity	NPC481529
0.6324	Remote Similarity	NPC472757
0.6324	Remote Similarity	NPC481522
0.6	Remote Similarity	NPC481520
0.5972	Remote Similarity	NPC471127
0.5972	Remote Similarity	NPC481531
0.5571	Remote Similarity	NPC482406
0.5513	Remote Similarity	NPC481523
0.5441	Remote Similarity	NPC156252
0.5385	Remote Similarity	NPC124676
0.5333	Remote Similarity	NPC481525
0.527	Remote Similarity	NPC234858
0.527	Remote Similarity	NPC179207
0.5205	Remote Similarity	NPC154363
0.5185	Remote Similarity	NPC146280
0.5065	Remote Similarity	NPC90814
0.5065	Remote Similarity	NPC189393

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC481530 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	6221
0.1-0.2	2870
0.2-0.3	59
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