NPASS Compound

Natural Product: NPC601035

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 49 50 0 0 0 0 0 0 0 0999 V2000 4.5393 2.0228 2.4042 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4027 1.4306 2.6415 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9660 1.1743 4.0259 C 0 0 0 0 0 0 0 0 0 0 0 0 2.7799 -0.1811 4.2831 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5791 1.0294 1.5193 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9003 1.2214 0.3198 O 0 0 0 0 0 0 0 0 0 0 0 0 1.3452 0.3887 1.6796 O 0 0 0 0 0 0 0 0 0 0 0 0 0.5383 -0.0034 0.5707 C 0 0 1 0 0 0 0 0 0 0 0 0 0.3992 -1.5414 0.5576 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1431 -1.8828 -0.8290 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8497 -1.6607 -1.9511 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2934 -2.4064 -1.0563 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9220 -2.7564 -2.4186 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9786 -1.5570 -2.4853 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1479 -0.3599 -2.4015 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5740 0.3219 -3.5369 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6400 -0.3970 -4.2259 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1556 -0.0292 -1.1618 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4106 1.0611 -0.7371 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.2710 2.0792 -0.3248 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.0757 2.5385 0.9218 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5806 3.5654 1.4743 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.1373 1.6159 1.5802 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.7550 1.7814 2.8232 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8090 0.5894 0.6523 C 0 0 2 0 0 0 0 0 0 0 0 0 4.8652 2.2131 1.4060 H 0 0 0 0 0 0 0 0 0 0 0 0 5.1599 2.3250 3.2316 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6918 1.5302 4.7825 H 0 0 0 0 0 0 0 0 0 0 0 0 2.0243 1.7223 4.2385 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6738 -0.5636 4.4370 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0560 0.2846 -0.3290 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3414 -2.0573 0.6744 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4129 -1.8117 1.2522 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8285 -2.0682 -1.5353 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0371 -0.5919 -2.1377 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6443 -2.2865 -2.8152 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9569 -2.6855 -0.2084 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2858 -2.7944 -3.2361 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5382 -3.5982 -2.2549 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.3664 -1.6341 -3.4622 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6165 -1.7239 -1.6883 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.1100 1.3169 -3.2657 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4087 0.6673 -4.2499 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8981 -0.6655 -5.1431 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7721 -0.5642 -0.3658 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6325 1.5258 -1.3172 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0734 1.0931 3.2710 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0967 2.5944 3.4500 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5600 -0.2724 0.9405 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 2 5 1 0 5 6 2 0 5 7 1 0 7 8 1 0 8 9 1 0 9 10 1 0 10 11 1 0 10 12 2 0 12 13 1 0 13 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 15 18 2 0 18 19 1 0 19 20 1 0 20 21 1 0 21 22 2 0 21 23 1 0 23 24 2 0 23 25 1 0 25 8 1 0 25 19 1 0 1 26 1 0 1 27 1 0 3 28 1 0 3 29 1 0 4 30 1 0 8 31 1 6 9 32 1 0 9 33 1 0 11 34 1 0 11 35 1 0 11 36 1 0 12 37 1 0 13 38 1 0 13 39 1 0 14 40 1 0 14 41 1 0 16 42 1 0 16 43 1 0 17 44 1 0 18 45 1 0 19 46 1 6 24 47 1 0 24 48 1 0 25 49 1 1 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 NPC601035 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	17229
0.1-0.2	28379
0.2-0.3	3617
0.3-0.4	425
0.4-0.5	145
0.5-0.6	46
0.6-0.7	6
0.7-0.8	0
0.8-0.85	1
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	NPC158756
0.8235	Intermediate Similarity	NPC469910
0.7647	Intermediate Similarity	NPC481909
0.7115	Intermediate Similarity	NPC473390
0.7037	Intermediate Similarity	NPC470755
0.7037	Intermediate Similarity	NPC298801
0.68	Remote Similarity	NPC611318
0.66	Remote Similarity	NPC171204
0.66	Remote Similarity	NPC606745
0.6552	Remote Similarity	NPC481911
0.6296	Remote Similarity	NPC116177
0.6038	Remote Similarity	NPC24417
0.5965	Remote Similarity	NPC482126
0.5965	Remote Similarity	NPC482131
0.5893	Remote Similarity	NPC477921
0.5893	Remote Similarity	NPC600706
0.5893	Remote Similarity	NPC602288
0.5862	Remote Similarity	NPC482130
0.5862	Remote Similarity	NPC482128
0.5862	Remote Similarity	NPC482129
0.5857	Remote Similarity	NPC605837
0.5833	Remote Similarity	NPC481910
0.5833	Remote Similarity	NPC476804
0.5833	Remote Similarity	NPC476803
0.5833	Remote Similarity	NPC602701
0.5833	Remote Similarity	NPC609128
0.5789	Remote Similarity	NPC607796
0.5789	Remote Similarity	NPC608869
0.5789	Remote Similarity	NPC610116
0.5763	Remote Similarity	NPC131669
0.5714	Remote Similarity	NPC250940
0.5714	Remote Similarity	NPC169575
0.5667	Remote Similarity	NPC486031
0.5636	Remote Similarity	NPC270126
0.5593	Remote Similarity	NPC599997
0.5593	Remote Similarity	NPC601440
0.5593	Remote Similarity	NPC601519
0.5593	Remote Similarity	NPC603351
0.5574	Remote Similarity	NPC134725
0.5574	Remote Similarity	NPC48657
0.5507	Remote Similarity	NPC608871
0.55	Remote Similarity	NPC482127
0.55	Remote Similarity	NPC269509
0.5439	Remote Similarity	NPC7563
0.541	Remote Similarity	NPC477922
0.5385	Remote Similarity	NPC475819
0.5385	Remote Similarity	NPC474232
0.5357	Remote Similarity	NPC476028
0.5352	Remote Similarity	NPC607890
0.5345	Remote Similarity	NPC488296
0.5246	Remote Similarity	NPC212486
0.5231	Remote Similarity	NPC476805
0.5185	Remote Similarity	NPC97516
0.5167	Remote Similarity	NPC320630
0.5156	Remote Similarity	NPC288876
0.5152	Remote Similarity	NPC486033
0.5077	Remote Similarity	NPC486037
0.5077	Remote Similarity	NPC482132

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC601035 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	6533
0.1-0.2	2574
0.2-0.3	40
0.3-0.4	3
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