NPASS Compound

Natural Product: NPC603555

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 57 59 0 0 0 0 0 0 0 0999 V2000 6.3411 3.0262 -0.8745 C 0 0 0 0 0 0 0 0 0 0 0 0 5.8382 1.7976 -0.2298 C 0 0 0 0 0 0 0 0 0 0 0 0 6.1965 0.4749 -0.7911 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0706 1.8796 0.8468 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5238 0.7172 1.5568 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0402 0.6877 1.6339 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3462 -0.1703 0.7521 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9921 -0.2727 0.7384 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1900 -1.1131 -0.1399 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1421 -1.1104 0.0112 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.9483 -1.8200 -0.7188 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3228 -1.7327 -0.4665 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7423 -0.8210 0.6451 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.6782 0.6026 0.2985 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7679 1.3405 0.3640 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7009 2.7733 0.0141 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.0872 0.7673 0.7867 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.2366 -2.4560 -1.2029 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.5894 -2.3603 -0.9425 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.7853 -3.2773 -2.2027 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.4218 -3.3665 -2.4551 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9569 -4.2091 -3.4804 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.4976 -2.6528 -1.7308 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1461 -2.7121 -1.9492 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3111 -3.4390 -2.8392 O 0 0 0 0 0 0 0 0 0 0 0 0 0.6715 -1.9209 -1.1261 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0307 -1.9909 -1.3578 O 0 0 0 0 0 0 0 0 0 0 0 0 0.3113 0.5354 1.6657 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9932 1.3692 2.5218 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3646 1.4659 2.5274 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0571 2.3047 3.3879 O 0 0 0 0 0 0 0 0 0 0 0 0 5.7363 3.9244 -0.5981 H 0 0 0 0 0 0 0 0 0 0 0 0 7.4167 3.1947 -0.6635 H 0 0 0 0 0 0 0 0 0 0 0 0 6.2466 2.8922 -1.9900 H 0 0 0 0 0 0 0 0 0 0 0 0 5.2895 -0.1233 -1.0548 H 0 0 0 0 0 0 0 0 0 0 0 0 6.8341 -0.0922 -0.0706 H 0 0 0 0 0 0 0 0 0 0 0 0 6.8185 0.6347 -1.6909 H 0 0 0 0 0 0 0 0 0 0 0 0 4.8298 2.8648 1.2268 H 0 0 0 0 0 0 0 0 0 0 0 0 4.8910 0.6490 2.6154 H 0 0 0 0 0 0 0 0 0 0 0 0 4.8712 -0.1922 1.0102 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9260 -0.7605 0.0726 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.8013 -1.1172 0.8866 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1849 -1.0766 1.5884 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7568 1.0590 -0.0085 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6487 3.1689 0.1172 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.3294 3.4071 0.7037 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.0577 2.9583 -1.0070 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.8606 1.5675 0.8463 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.0022 0.2669 1.7759 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.4405 0.0664 0.0151 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.2965 -2.6001 -1.6284 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4607 -3.8486 -2.7905 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8691 -5.2090 -3.3465 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5026 -1.6354 -2.1797 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7732 0.4780 1.6819 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4491 1.9932 3.2394 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4157 3.2132 3.1311 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 2 4 2 3 4 5 1 0 5 6 1 0 6 7 2 0 7 8 1 0 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 2 3 15 16 1 0 15 17 1 0 12 18 1 0 18 19 1 0 18 20 2 0 20 21 1 0 21 22 1 0 21 23 2 0 23 24 1 0 24 25 2 0 24 26 1 0 26 27 1 0 8 28 2 0 28 29 1 0 29 30 2 0 30 31 1 0 30 6 1 0 26 9 2 0 23 11 1 0 1 32 1 0 1 33 1 0 1 34 1 0 3 35 1 0 3 36 1 0 3 37 1 0 4 38 1 0 5 39 1 0 5 40 1 0 7 41 1 0 13 42 1 0 13 43 1 0 14 44 1 0 16 45 1 0 16 46 1 0 16 47 1 0 17 48 1 0 17 49 1 0 17 50 1 0 19 51 1 0 20 52 1 0 22 53 1 0 27 54 1 0 28 55 1 0 29 56 1 0 31 57 1 0 M END

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

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 NPC603555 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	24335
0.1-0.2	22594
0.2-0.3	2461
0.3-0.4	349
0.4-0.5	82
0.5-0.6	25
0.6-0.7	7
0.7-0.8	0
0.8-0.85	0
0.85-0.9	0
0.9-0.95	0
0.95-1	1

Similarity Score	Similarity Level	Natural Product ID
1.0	High Similarity	NPC293053
0.7931	Intermediate Similarity	NPC9117
0.7931	Intermediate Similarity	NPC63187
0.7705	Intermediate Similarity	NPC59162
0.7581	Intermediate Similarity	NPC200694
0.7419	Intermediate Similarity	NPC216978
0.6875	Remote Similarity	NPC273538
0.6769	Remote Similarity	NPC270708
0.625	Remote Similarity	NPC482025
0.6232	Remote Similarity	NPC3980
0.6029	Remote Similarity	NPC301217
0.6029	Remote Similarity	NPC475799
0.6	Remote Similarity	NPC220062
0.5942	Remote Similarity	NPC80962
0.5942	Remote Similarity	NPC13779
0.5915	Remote Similarity	NPC326500
0.5909	Remote Similarity	NPC88804
0.5882	Remote Similarity	NPC482074
0.5882	Remote Similarity	NPC601414
0.5821	Remote Similarity	NPC190637
0.5797	Remote Similarity	NPC269420
0.5694	Remote Similarity	NPC269285
0.5658	Remote Similarity	NPC273843
0.5652	Remote Similarity	NPC216538
0.5652	Remote Similarity	NPC205046
0.5606	Remote Similarity	NPC606140
0.5362	Remote Similarity	NPC172986
0.5352	Remote Similarity	NPC59210
0.5217	Remote Similarity	NPC227122
0.5217	Remote Similarity	NPC157784
0.5217	Remote Similarity	NPC24821
0.5211	Remote Similarity	NPC261227
0.5211	Remote Similarity	NPC96565
0.5139	Remote Similarity	NPC304295
0.5132	Remote Similarity	NPC193200
0.5075	Remote Similarity	NPC603348
0.5067	Remote Similarity	NPC605541
0.5063	Remote Similarity	NPC187354

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC603555 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4540
0.1-0.2	4574
0.2-0.3	33
0.3-0.4	1
0.4-0.5	1
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
0.6875	Remote Similarity	NPD4378	Phase 3

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