NPASS Compound

Natural Product: NPC606216

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 104109 0 0 0 0 0 0 0 0999 V2000 1.5318 -3.7388 1.2886 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4709 -2.6354 0.7585 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6891 -3.4089 0.2756 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8665 -1.8417 1.9553 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0606 -0.6137 2.2025 C 0 0 0 0 0 0 0 0 0 0 0 0 1.9448 0.2254 0.9434 C 0 0 2 0 0 0 0 0 0 0 0 0 3.3051 0.5656 0.4244 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5906 1.7833 0.2845 O 0 0 0 0 0 0 0 0 0 0 0 0 4.2981 -0.3028 0.0771 O 0 0 0 0 0 0 0 0 0 0 0 0 5.5625 0.0257 -0.4039 C 0 0 2 0 0 0 0 0 0 0 0 0 5.7957 -0.3977 -1.7125 O 0 0 0 0 0 0 0 0 0 0 0 0 6.7542 0.4649 -2.2374 C 0 0 2 0 0 0 0 0 0 0 0 0 6.9099 0.3631 -3.7141 C 0 0 0 0 0 0 0 0 0 0 0 0 7.2869 -0.8840 -4.1567 O 0 0 0 0 0 0 0 0 0 0 0 0 8.0724 0.3668 -1.5217 C 0 0 1 0 0 0 0 0 0 0 0 0 8.7864 1.5461 -1.8263 O 0 0 0 0 0 0 0 0 0 0 0 0 7.9517 0.2765 -0.0433 C 0 0 2 0 0 0 0 0 0 0 0 0 9.0988 -0.2788 0.5198 O 0 0 0 0 0 0 0 0 0 0 0 0 6.7038 -0.4361 0.4327 C 0 0 1 0 0 0 0 0 0 0 0 0 6.5337 -0.1682 1.7888 O 0 0 0 0 0 0 0 0 0 0 0 0 1.2981 1.5621 1.2458 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0123 1.7916 0.5865 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9360 0.6605 0.8005 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.3218 0.6353 2.2607 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2738 -0.6140 0.3599 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1044 -1.6706 0.3131 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5335 -1.5477 0.6685 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0589 -2.6200 1.0322 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.1527 -0.2299 0.5590 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.5526 -0.1755 0.0185 C 0 0 1 0 0 0 0 0 0 0 0 0 -4.6416 -0.8584 -1.2807 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4465 -0.8483 1.0717 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.8909 -0.8000 0.7074 C 0 0 1 0 0 0 0 0 0 0 0 0 -7.6367 -0.8231 1.8980 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.3100 0.2944 -0.1879 C 0 0 2 0 0 0 0 0 0 0 0 0 -7.5749 -0.1153 -1.5170 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.4305 1.5124 -0.1682 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.6850 2.2222 -1.5095 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.9855 2.4766 0.8757 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.2753 3.6391 0.9994 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.9905 1.2674 0.0722 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.0923 2.2194 -0.6741 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7284 2.1625 -0.0345 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2033 0.7414 -0.0383 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.8766 0.4553 -1.4798 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1309 -0.6078 -0.0059 C 0 0 2 0 0 0 0 0 0 0 0 0 1.7599 -1.9266 -0.3156 C 0 0 1 0 0 0 0 0 0 0 0 0 2.7019 -1.6832 -1.3591 O 0 0 0 0 0 0 0 0 0 0 0 0 2.0945 -4.4663 1.8994 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0626 -4.2771 0.4452 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7096 -3.2889 1.8930 H 0 0 0 0 0 0 0 0 0 0 0 0 4.4827 -3.4322 1.0676 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4674 -4.4534 0.0302 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1647 -2.9568 -0.6072 H 0 0 0 0 0 0 0 0 0 0 0 0 2.7661 -2.4581 2.9035 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9352 -1.5561 1.9690 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0609 -0.9338 2.5030 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5060 -0.0653 3.0452 H 0 0 0 0 0 0 0 0 0 0 0 0 5.6037 1.1539 -0.4435 H 0 0 0 0 0 0 0 0 0 0 0 0 6.3613 1.5023 -2.0240 H 0 0 0 0 0 0 0 0 0 0 0 0 7.5640 1.1835 -4.0510 H 0 0 0 0 0 0 0 0 0 0 0 0 5.9020 0.5771 -4.1778 H 0 0 0 0 0 0 0 0 0 0 0 0 7.0952 -0.9054 -5.1483 H 0 0 0 0 0 0 0 0 0 0 0 0 8.6566 -0.4632 -1.9846 H 0 0 0 0 0 0 0 0 0 0 0 0 8.8038 2.1622 -1.0560 H 0 0 0 0 0 0 0 0 0 0 0 0 7.8792 1.3233 0.3646 H 0 0 0 0 0 0 0 0 0 0 0 0 9.8014 0.4312 0.5738 H 0 0 0 0 0 0 0 0 0 0 0 0 6.8913 -1.5301 0.2612 H 0 0 0 0 0 0 0 0 0 0 0 0 7.0385 -0.8057 2.3246 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3028 1.6695 2.3576 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9454 2.4348 0.9216 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1686 2.0604 -0.4710 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4602 2.7013 1.0563 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0578 1.4078 2.5209 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5980 -0.3959 2.6215 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4416 0.8829 2.9296 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6813 -2.5874 0.0042 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2904 0.0943 1.6548 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.3723 -1.7198 -1.1714 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7080 -1.3975 -1.5748 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.9169 -0.2320 -2.1535 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.1810 -1.8805 1.2786 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2710 -0.2666 2.0057 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.1539 -1.7743 0.1981 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.1263 -0.4840 2.6700 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.3353 0.6305 0.1607 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.3554 -0.7109 -1.4776 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.1173 3.1447 -1.6056 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.7743 2.5142 -1.4695 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.6000 1.5219 -2.3559 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.9101 1.9284 1.8553 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.0759 2.6497 0.7133 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.6154 4.3004 0.3257 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.7951 1.5400 1.1610 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.1189 2.1270 -1.7536 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4695 3.2557 -0.4022 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0307 2.7699 -0.6406 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7899 2.6042 0.9595 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0972 1.2049 -1.8399 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4981 -0.5312 -1.7122 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7488 0.7307 -2.1427 H 0 0 0 0 0 0 0 0 0 0 0 0 1.1668 0.0102 -0.9775 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0119 -2.5481 -0.8552 H 0 0 0 0 0 0 0 0 0 0 0 0 2.7577 -2.4276 -1.9771 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 2 4 1 0 4 5 1 0 5 6 1 0 6 7 1 6 7 8 2 0 7 9 1 0 9 10 1 0 10 11 1 0 11 12 1 0 12 13 1 0 13 14 1 0 12 15 1 0 15 16 1 0 15 17 1 0 17 18 1 0 17 19 1 0 19 20 1 0 6 21 1 0 21 22 1 0 22 23 1 0 23 24 1 1 23 25 1 0 25 26 2 0 26 27 1 0 27 28 2 0 27 29 1 0 29 30 1 0 30 31 1 6 30 32 1 0 32 33 1 0 33 34 1 0 33 35 1 0 35 36 1 0 35 37 1 0 37 38 1 6 37 39 1 0 39 40 1 0 37 41 1 0 41 42 1 0 42 43 1 0 43 44 1 0 44 45 1 6 25 46 1 0 46 47 1 0 47 48 1 0 47 2 1 0 46 6 1 0 19 10 1 0 44 23 1 0 44 29 1 0 41 30 1 0 1 49 1 0 1 50 1 0 1 51 1 0 3 52 1 0 3 53 1 0 3 54 1 0 4 55 1 0 4 56 1 0 5 57 1 0 5 58 1 0 10 59 1 6 12 60 1 6 13 61 1 0 13 62 1 0 14 63 1 0 15 64 1 6 16 65 1 0 17 66 1 1 18 67 1 0 19 68 1 1 20 69 1 0 21 70 1 0 21 71 1 0 22 72 1 0 22 73 1 0 24 74 1 0 24 75 1 0 24 76 1 0 26 77 1 0 29 78 1 1 31 79 1 0 31 80 1 0 31 81 1 0 32 82 1 0 32 83 1 0 33 84 1 6 34 85 1 0 35 86 1 1 36 87 1 0 38 88 1 0 38 89 1 0 38 90 1 0 39 91 1 0 39 92 1 0 40 93 1 0 41 94 1 1 42 95 1 0 42 96 1 0 43 97 1 0 43 98 1 0 45 99 1 0 45100 1 0 45101 1 0 46102 1 6 47103 1 6 48104 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 NPC606216 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	19392
0.1-0.2	25169
0.2-0.3	4474
0.3-0.4	676
0.4-0.5	113
0.5-0.6	19
0.6-0.7	8
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	NPC187056
1.0	High Similarity	NPC607023
0.775	Intermediate Similarity	NPC116794
0.6786	Remote Similarity	NPC605954
0.6477	Remote Similarity	NPC102914
0.6364	Remote Similarity	NPC68419
0.6292	Remote Similarity	NPC271138
0.6292	Remote Similarity	NPC110139
0.6292	Remote Similarity	NPC108709
0.6222	Remote Similarity	NPC220984
0.6047	Remote Similarity	NPC191763
0.5806	Remote Similarity	NPC256798
0.5686	Remote Similarity	NPC473401
0.5652	Remote Similarity	NPC7870
0.5652	Remote Similarity	NPC212968
0.5652	Remote Similarity	NPC75747
0.5638	Remote Similarity	NPC128925
0.5543	Remote Similarity	NPC199457
0.5495	Remote Similarity	NPC285576
0.5484	Remote Similarity	NPC310014
0.5484	Remote Similarity	NPC269315
0.5269	Remote Similarity	NPC237503
0.5243	Remote Similarity	NPC161674
0.5234	Remote Similarity	NPC134835
0.5213	Remote Similarity	NPC37739
0.5189	Remote Similarity	NPC148417
0.5185	Remote Similarity	NPC73318
0.5158	Remote Similarity	NPC137917
0.5158	Remote Similarity	NPC604133
0.5109	Remote Similarity	NPC240125

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC606216 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	7053
0.1-0.2	2012
0.2-0.3	79
0.3-0.4	6
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