NPASS Compound

Natural Product: NPC328122

Natural Product ID	NPC328122
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	Benzoylgomisin H
IUPAC Name	n.a.
Synonyms	Benzoylgomisin H
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL519932
PubChem CID	44575227
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000261] Phenylpropanoids and polyketides [CHEMONTID:0000238] Tannins [CHEMONTID:0001710] Hydrolyzable tannins

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 72 75 0 0 0 0 0 0 0 0999 V2000 -3.6690 2.6558 -2.3327 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6773 1.7660 -1.6051 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8238 2.1415 -0.1131 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4325 2.1170 0.4010 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1116 3.3024 0.9654 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1594 3.5183 1.4555 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1048 2.5178 1.3637 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8387 1.2882 0.7966 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4311 1.1109 0.3311 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4458 -0.2743 -0.1211 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8971 -0.8954 -1.3028 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6998 -2.2424 -1.4244 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0819 -2.9470 -0.4147 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3508 -2.3002 0.7506 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1641 -0.9509 0.8986 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5352 -0.2482 2.0130 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.2858 -0.0557 3.1485 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9759 -3.0650 1.7585 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2239 -3.6635 2.7913 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1440 -4.3097 -0.4894 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.2184 -5.1128 -1.5703 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6379 -0.3797 -2.4759 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8798 0.3241 -1.8784 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9726 0.1030 -2.9309 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.2524 -0.3963 -0.7701 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7395 0.2512 0.6456 O 0 0 0 0 0 0 0 0 0 0 0 0 2.4747 0.0573 -0.5226 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2292 0.9110 -1.4269 O 0 0 0 0 0 0 0 0 0 0 0 0 3.4406 -1.0021 -0.7363 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7890 -1.9301 0.2087 C 0 0 0 0 0 0 0 0 0 0 0 0 4.7209 -2.9358 -0.0607 C 0 0 0 0 0 0 0 0 0 0 0 0 5.3009 -2.9867 -1.3167 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9592 -2.0619 -2.2702 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0361 -1.0807 -1.9755 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3741 2.7688 1.8659 O 0 0 0 0 0 0 0 0 0 0 0 0 2.6473 2.4584 3.2195 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4551 4.7388 2.0295 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.5459 5.7263 2.0985 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3365 3.7015 -2.1597 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7026 2.3967 -3.4061 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.6381 2.5437 -1.8157 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6734 2.0567 -1.9874 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.3805 1.3427 0.4245 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2379 3.1396 0.0115 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8682 4.0802 1.0266 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0312 -2.7598 -2.3197 H 0 0 0 0 0 0 0 0 0 0 0 0 0.2598 -0.5434 4.0025 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4803 1.0111 3.3505 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2564 -0.5544 3.0441 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8667 -3.4490 2.6997 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5100 -3.2424 3.7970 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4646 -4.7269 2.8153 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0053 -4.6216 -2.5392 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2744 -5.4441 -1.5482 H 0 0 0 0 0 0 0 0 0 0 0 0 0.4030 -6.0322 -1.5318 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9560 -1.2416 -3.0991 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0728 0.3794 -3.0492 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.1471 -0.9923 -2.9545 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5639 0.4096 -3.9082 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.8671 0.6618 -2.6288 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.2404 -0.3466 -0.6393 H 0 0 0 0 0 0 0 0 0 0 0 0 3.3498 -1.8964 1.1938 H 0 0 0 0 0 0 0 0 0 0 0 0 4.9941 -3.6656 0.6834 H 0 0 0 0 0 0 0 0 0 0 0 0 6.0301 -3.7358 -1.5991 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4020 -2.0780 -3.2718 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7967 -0.3644 -2.7728 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8159 2.8011 3.8887 H 0 0 0 0 0 0 0 0 0 0 0 0 2.8160 1.3689 3.3701 H 0 0 0 0 0 0 0 0 0 0 0 0 3.5601 2.9957 3.5654 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.1765 6.6165 2.6595 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4239 5.2712 2.6237 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8145 6.0003 1.0704 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 2 0 5 6 1 0 6 7 2 0 7 8 1 0 8 9 2 0 9 10 1 0 10 11 2 0 11 12 1 0 12 13 2 0 13 14 1 0 14 15 2 0 15 16 1 0 16 17 1 0 14 18 1 0 18 19 1 0 13 20 1 0 20 21 1 0 11 22 1 0 22 23 1 0 23 24 1 0 23 25 1 0 8 26 1 0 26 27 1 0 27 28 2 0 27 29 1 0 29 30 2 0 30 31 1 0 31 32 2 0 32 33 1 0 33 34 2 0 7 35 1 0 35 36 1 0 6 37 1 0 37 38 1 0 23 2 1 0 34 29 1 0 9 4 1 0 15 10 1 0 1 39 1 0 1 40 1 0 1 41 1 0 2 42 1 0 3 43 1 0 3 44 1 0 5 45 1 0 12 46 1 0 17 47 1 0 17 48 1 0 17 49 1 0 19 50 1 0 19 51 1 0 19 52 1 0 21 53 1 0 21 54 1 0 21 55 1 0 22 56 1 0 22 57 1 0 24 58 1 0 24 59 1 0 24 60 1 0 25 61 1 0 30 62 1 0 31 63 1 0 32 64 1 0 33 65 1 0 34 66 1 0 36 67 1 0 36 68 1 0 36 69 1 0 38 70 1 0 38 71 1 0 38 72 1 0 M END

Standard InCHIKey	AZQOQICAWOAGEN-UHFFFAOYSA-N
Standard InCHI	InChI=1S/C30H34O8/c1-17-13-19-14-21(33-3)26(36-6)28(38-29(31)18-11-9-8-10-12-18)23(19)24-20(16-30(17,2)32)15-22(34-4)25(35-5)27(24)37-7/h8-12,14-15,17,32H,13,16H2,1-7H3
SMILES	CC1Cc2cc(c(c(c2-c2c(cc(c(c2OC)OC)OC)CC1(C)O)OC(=O)c1ccccc1)OC)OC

Calculated Properties

Physi-Chem Properties

Molecular Weight:	522.23	Volume:	537.167 ? Van der Waals volume.
Dense:	0.972	LogP:	4.093 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	3.959 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-5.503 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	8.0	Rigid Bonds:	25.0
TPSA:	92.68 ? Topological Polar Surface Area.	H-Bond Acceptor:	8.0
H-Bond Donor:	1.0	Rings:	4.0
Heavy Atoms:	8.0

MedChem Properties

QED Drug-Likeness Score:	0.338	GASA:	0.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	3.484	Fsp³:	0.367
MCE-18:	89.463 ? 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:	Accepted	BMS Rule:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.381	Fluc inhibitor:	0.316 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.585 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.793 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.092	Promiscuous compounds:	0.174

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-4.764	MDCK Permeability:	-4.708
Pgp-inhibitor:	0.215	Pgp-substrate:	0.056
PAMPA:	0.035 ? 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):	0.0
20% Bioavailability (F20%):	0.001	30% Bioavailability (F30%):	0.003
50% Bioavailability (F50%):	0.195

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.094	MRP1:	0.998
Plasma Protein Binding (PPB):	97.007%	Volume Distribution (VD):	0.113
Fu:	2.649% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.94
OATP1B3 inhibitor:	0.991	BCRP inhibitor:	0.008
BSEP inhibitor:	0.996

ADMET: Metabolism

CYP1A2-inhibitor:	0.455	CYP1A2-substrate:	0.005
CYP2C19-inhibitor:	0.998	CYP2C19-substrate:	0.014
CYP2C9-inhibitor:	0.15	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.01	CYP2D6-substrate:	0.053
CYP3A4-inhibitor:	1.0	CYP3A4-substrate:	0.01
CYP2B6-substrate:	0.001	CYP2C8-inhibitor:	0.59
HLM stability:	0.141 ? 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):

2.723

Half-life (T1/2):

1.02

ADMET: Toxicity

hERG Blockers:	0.264	hERG Blockers (10um):	0.815
Human Hepatotoxicity (H-HT):	0.159	Drug-induced Liver Injury (DILI):	0.273
AMES Toxicity:	0.164	Rat Oral Acute Toxicity:	0.234
Maximum Recommended Daily Dose:	0.359	Skin Sensitization:	0.695
Carcinogencity:	0.804	Eye Corrosion:	0.0
Eye Irritation:	0.189	Respiratory Toxicity:	0.622
Drug-induced Neurotoxicity:	0.555	Ototoxicity:	0.493
Hematotoxicity:	0.097	Drug-induced Nephrotoxicity:	0.077
Genotoxicity:	0.028	RPMI-8226 Immunitoxicity:	0.114
A549 Cytotoxicity:	0.328	Hek293 Cytotoxicity:	0.551
BCF:	1.329 ? 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:	3.918 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.576 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.575 ? 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
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[16562834]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	fruit	n.a.	PMID[24155209]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[24959987]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[25302569]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO8187	Schisandra chinensis	Species	Schisandraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]

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
IC50	1

Activity Type	# Activity
Cell line	1

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	IC50	=	41200.0	nM	PMID[16562834]

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 NPC328122 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	15981
0.1-0.2	30881
0.2-0.3	2864
0.3-0.4	88
0.4-0.5	29
0.5-0.6	5
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	0

Similarity Score	Similarity Level	Natural Product ID
0.7255	Intermediate Similarity	NPC102256
0.6667	Remote Similarity	NPC249070
0.6333	Remote Similarity	NPC137352
0.6333	Remote Similarity	NPC183083
0.6333	Remote Similarity	NPC485503
0.6271	Remote Similarity	NPC53722
0.6271	Remote Similarity	NPC201404
0.6271	Remote Similarity	NPC290714
0.6	Remote Similarity	NPC240279
0.5645	Remote Similarity	NPC180602
0.5469	Remote Similarity	NPC55239
0.527	Remote Similarity	NPC83049
0.527	Remote Similarity	NPC320471
0.527	Remote Similarity	NPC118162

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC328122 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	2225
0.1-0.2	6632
0.2-0.3	292
0.3-0.4	1
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