NPASS Compound

Natural Product: NPC482026

Natural Product ID	NPC482026
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	HZYVKPMTUKWUOG-CYDBVHSLSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	101792015
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000261] Phenylpropanoids and polyketides [CHEMONTID:0000334] Flavonoids [CHEMONTID:0001111] Flavonoid glycosides [CHEMONTID:0001583] Flavonoid O-glycosides [CHEMONTID:0003531] Flavonoid-3-O-glycosides

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 86 91 0 0 0 0 0 0 0 0999 V2000 -4.2214 -2.7096 2.6676 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6186 -2.1949 1.3235 C 0 0 1 0 0 0 0 0 0 0 0 0 -5.9208 -1.4043 1.5206 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.5606 -1.4004 0.1504 C 0 0 2 0 0 0 0 0 0 0 0 0 -5.5018 -0.9908 -0.8463 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.2146 -0.5253 -0.2278 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.7237 -1.3305 0.7617 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.2379 -0.4765 -1.2386 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8025 0.8173 -1.4847 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.1016 1.2510 -2.8875 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.8166 1.5343 -3.6234 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.0790 2.6351 -2.9017 C 0 0 2 0 0 0 0 0 0 0 0 0 0.2805 2.8944 -3.5312 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9685 2.3239 -1.5679 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.3215 1.0153 -1.2462 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.9432 0.7793 0.1089 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2655 0.1310 0.3143 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2144 -1.2575 0.1966 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8170 -1.9051 -0.0641 O 0 0 0 0 0 0 0 0 0 0 0 0 1.3666 -1.9873 0.3759 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3697 -3.3611 0.2688 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5469 -4.0388 0.4559 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7367 -3.4088 0.7480 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7092 -2.0392 0.8499 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9789 -1.6461 1.1402 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7572 -2.7808 1.2099 C 0 0 0 0 0 0 0 0 0 0 0 0 7.2104 -2.8858 1.4988 C 0 0 0 0 0 0 0 0 0 0 0 0 7.6718 -4.3272 1.4743 C 0 0 0 0 0 0 0 0 0 0 0 0 7.9850 -2.1451 0.4309 C 0 0 0 0 0 0 0 0 0 0 0 0 7.5078 -2.3975 2.7709 O 0 0 0 0 0 0 0 0 0 0 0 0 4.9831 -3.8075 0.9711 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5279 -1.3048 0.6665 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5634 -0.0154 0.7756 O 0 0 0 0 0 0 0 0 0 0 0 0 1.4598 0.7343 0.6100 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5992 2.1763 0.7601 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8789 2.7147 0.7433 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0988 4.0530 0.9464 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0479 4.9168 1.1762 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7858 4.4088 1.1969 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5865 3.0463 0.9884 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2728 6.2812 1.3831 O 0 0 0 0 0 0 0 0 0 0 0 0 1.2768 7.2276 1.6212 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1697 -3.9829 -0.0249 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1374 1.9847 -4.9419 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.7975 0.2765 -3.6092 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.0603 0.0651 -1.5758 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.6925 -0.5916 0.1084 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.7175 -1.9874 2.4917 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.6469 -2.0811 3.5010 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1287 -2.7993 2.8026 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6704 -3.7166 2.7924 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.8208 -3.0264 0.5865 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.6802 -0.3464 1.7674 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.8762 -2.4493 -0.1247 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2952 -1.7916 -1.5873 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.3934 0.5314 0.1358 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.3841 1.5251 -0.8125 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7279 2.1798 -2.9227 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2090 0.6277 -3.8145 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.7292 3.5536 -3.0188 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0930 2.7999 -2.7759 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2728 3.9203 -3.9458 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4432 2.1194 -4.2979 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7562 0.3789 -1.9341 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5703 -5.1139 0.3766 H 0 0 0 0 0 0 0 0 0 0 0 0 5.3146 -0.6101 1.2901 H 0 0 0 0 0 0 0 0 0 0 0 0 8.7060 -4.4002 1.8193 H 0 0 0 0 0 0 0 0 0 0 0 0 6.9796 -4.9968 2.0349 H 0 0 0 0 0 0 0 0 0 0 0 0 7.6071 -4.6694 0.4034 H 0 0 0 0 0 0 0 0 0 0 0 0 7.5869 -1.1207 0.3199 H 0 0 0 0 0 0 0 0 0 0 0 0 9.0484 -2.1363 0.7588 H 0 0 0 0 0 0 0 0 0 0 0 0 7.9265 -2.7417 -0.4944 H 0 0 0 0 0 0 0 0 0 0 0 0 7.4077 -1.4312 2.8567 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7191 2.0671 0.5662 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1100 4.4593 0.9296 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0462 5.0803 1.3766 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4422 2.7319 1.0428 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7241 8.1032 2.1631 H 0 0 0 0 0 0 0 0 0 0 0 0 0.8757 7.6009 0.6334 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4265 6.8702 2.2219 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0417 -4.2674 -0.9758 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1118 1.8029 -5.1141 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2344 -0.5377 -3.6012 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.0282 0.0197 -1.5954 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.5064 -1.0803 0.3909 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.6787 -1.4199 3.3104 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 1 0 5 6 1 0 6 7 1 0 6 8 1 0 8 9 1 0 9 10 1 0 10 11 1 0 11 12 1 0 12 13 1 0 12 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 17 18 1 0 18 19 2 0 18 20 1 0 20 21 2 0 21 22 1 0 22 23 2 0 23 24 1 0 24 25 1 0 25 26 2 0 26 27 1 0 27 28 1 0 27 29 1 0 27 30 1 0 26 31 1 0 24 32 2 0 32 33 1 0 33 34 1 0 34 35 1 0 35 36 2 0 36 37 1 0 37 38 2 0 38 39 1 0 39 40 2 0 38 41 1 0 41 42 1 0 21 43 1 0 11 44 1 0 10 45 1 0 5 46 1 0 4 47 1 0 3 48 1 0 7 2 1 0 15 9 1 0 34 17 2 0 40 35 1 0 32 20 1 0 31 23 1 0 1 49 1 0 1 50 1 0 1 51 1 0 2 52 1 6 3 53 1 1 4 54 1 6 5 55 1 6 6 56 1 1 9 57 1 1 10 58 1 1 11 59 1 6 12 60 1 1 13 61 1 0 13 62 1 0 13 63 1 0 15 64 1 6 22 65 1 0 25 66 1 0 28 67 1 0 28 68 1 0 28 69 1 0 29 70 1 0 29 71 1 0 29 72 1 0 30 73 1 0 36 74 1 0 37 75 1 0 39 76 1 0 40 77 1 0 42 78 1 0 42 79 1 0 42 80 1 0 43 81 1 0 44 82 1 0 45 83 1 0 46 84 1 0 47 85 1 0 48 86 1 0 M END

Standard InCHIKey	HZYVKPMTUKWUOG-CYDBVHSLSA-N
Standard InCHI	InChI=1S/C33H38O15/c1-12-21(35)24(38)26(40)31(43-12)48-30-25(39)22(36)13(2)44-32(30)47-29-23(37)20-17(34)11-18-16(10-19(45-18)33(3,4)41)28(20)46-27(29)14-6-8-15(42-5)9-7-14/h6-13,21-22,24-26,30-32,34-36,38-41H,1-5H3/t12-,13-,21-,22-,24+,25+,26+,30+,31-,32-/m0/s1
SMILES	C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]1[C@@H]([C@H]([C@H](C)O[C@H]1Oc1c(=O)c2c(cc3c(cc(C(C)(C)O)o3)c2oc1c1ccc(cc1)OC)O)O)O)O)O)O

Calculated Properties

Physi-Chem Properties

MedChem Properties

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

ADMET: Distribution

ADMET: Metabolism

ADMET: Excretion

ADMET: Toxicity

Species Source

Organism ID	Organism Name	Taxonomy Level	Family	SuperKingdom	Isolation Part	Collection Location	Collection Time	Reference
NPO31054	Epimedium brevicornum	Species	Berberidaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[29338226]
NPO31054	Epimedium brevicornum	Species	Berberidaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO31054	Epimedium brevicornum	Species	Berberidaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO31054	Epimedium brevicornum	Species	Berberidaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]

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
GI	5
IC50	5

Activity Type	# Activity
Cell line	10

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
NPT116	Cell line	HL-60	Homo sapiens	GI	>	50.0	%	PMID[29338226]
NPT659	Cell line	SMMC-7721	Homo sapiens	GI	>	50.0	%	PMID[29338226]
NPT81	Cell line	A549	Homo sapiens	GI	>	50.0	%	PMID[29338226]
NPT83	Cell line	MCF7	Homo sapiens	GI	>	50.0	%	PMID[29338226]
NPT660	Cell line	SW480	Homo sapiens	GI	>	50.0	%	PMID[29338226]
NPT116	Cell line	HL-60	Homo sapiens	IC50	>	10000.0	nM	PMID[29338226]
NPT659	Cell line	SMMC-7721	Homo sapiens	IC50	>	10000.0	nM	PMID[29338226]
NPT81	Cell line	A549	Homo sapiens	IC50	>	10000.0	nM	PMID[29338226]
NPT83	Cell line	MCF7	Homo sapiens	IC50	>	10000.0	nM	PMID[29338226]
NPT660	Cell line	SW480	Homo sapiens	IC50	>	10000.0	nM	PMID[29338226]

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 NPC482026 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	18129
0.1-0.2	28267
0.2-0.3	2810
0.3-0.4	435
0.4-0.5	184
0.5-0.6	26
0.6-0.7	2
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
0.6237	Remote Similarity	NPC476215
0.6	Remote Similarity	NPC95866
0.596	Remote Similarity	NPC240306
0.5859	Remote Similarity	NPC470444
0.5816	Remote Similarity	NPC163242
0.5816	Remote Similarity	NPC272068
0.5728	Remote Similarity	NPC220173
0.5631	Remote Similarity	NPC142142
0.56	Remote Similarity	NPC155877
0.5534	Remote Similarity	NPC32641
0.5534	Remote Similarity	NPC256188
0.5437	Remote Similarity	NPC12013
0.5437	Remote Similarity	NPC11432
0.5437	Remote Similarity	NPC477613
0.5385	Remote Similarity	NPC35119
0.537	Remote Similarity	NPC89052
0.5321	Remote Similarity	NPC473072
0.5253	Remote Similarity	NPC170052
0.5253	Remote Similarity	NPC135846
0.5238	Remote Similarity	NPC122467
0.5185	Remote Similarity	NPC602448
0.5149	Remote Similarity	NPC473682
0.514	Remote Similarity	NPC473071
0.5128	Remote Similarity	NPC209550
0.5093	Remote Similarity	NPC221342
0.5093	Remote Similarity	NPC476470
0.505	Remote Similarity	NPC254855
0.505	Remote Similarity	NPC94610

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC482026 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4982
0.1-0.2	4106
0.2-0.3	55
0.3-0.4	2
0.4-0.5	5
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