NPASS Compound

Structure

NPC154016 OpenBabel06302215422D 73 79 0 0 1 0 0 0 0 0999 V2000 15.2036 -4.8765 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.3589 -4.3889 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.5143 -4.8765 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.5143 -5.8519 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.6696 -4.3889 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.8250 -4.8765 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.6696 -3.4136 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 11.8250 -2.9259 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 11.8250 -1.9506 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 10.9803 -1.4630 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 12.6696 -0.4877 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.5143 -0.9753 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.1357 -1.9506 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 10.1357 -2.9259 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.9803 -3.4136 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.4680 -4.2582 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.4927 -4.2582 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2911 -1.4630 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.4464 -1.9506 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.6018 -1.4630 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.6018 -0.4877 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 6.7571 -0.0000 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 6.7571 -0.9753 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9125 -0.4877 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0679 -0.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0679 0.9753 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 5.9125 1.4630 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 5.4248 2.3076 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.7571 0.9753 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 7.6018 1.4630 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.4464 0.9753 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.4464 -0.0000 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 9.2911 0.4877 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2911 -0.4877 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 9.2911 1.4630 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.1357 -0.0000 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 10.9803 -0.4877 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 11.8250 -0.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.1357 0.9753 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.4001 2.3076 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9125 3.1522 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.3755 2.3076 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.8631 3.1522 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2232 1.4630 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.3786 0.9753 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.5339 1.4630 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.6893 0.9753 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 1.6893 -0.0000 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.5339 -0.4877 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.5339 -1.4630 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3786 -1.9506 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.6893 -1.9506 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.8446 -1.4630 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3786 -0.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.8446 -0.4877 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.8446 1.4630 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0000 0.9753 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8446 1.4630 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.6893 0.9753 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.6893 0.0000 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.8446 -0.4877 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0000 -0.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.5339 -0.4877 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.5339 1.4630 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8446 2.4383 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5339 2.4383 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.6696 -1.4630 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 13.5143 -1.9506 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.5143 -2.9259 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 14.3589 -1.4630 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.2036 -1.9506 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.2036 -2.9259 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.3589 -0.4877 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 3 2 0 0 0 0 3 4 1 0 0 0 0 3 5 1 0 0 0 0 5 6 2 0 0 0 0 5 7 1 0 0 0 0 8 7 1 6 0 0 0 8 9 1 0 0 0 0 8 15 1 0 0 0 0 9 10 1 0 0 0 0 9 67 1 0 0 0 0 10 37 1 0 0 0 0 10 11 1 6 0 0 0 10 13 1 0 0 0 0 11 12 1 0 0 0 0 13 14 1 1 0 0 0 13 18 1 0 0 0 0 14 15 1 0 0 0 0 15 16 1 0 0 0 0 15 17 1 0 0 0 0 18 34 1 0 0 0 0 18 19 2 0 0 0 0 19 20 1 0 0 0 0 20 21 1 0 0 0 0 21 32 1 0 0 0 0 21 22 1 0 0 0 0 22 29 1 0 0 0 0 22 23 1 6 0 0 0 22 24 1 0 0 0 0 24 25 1 0 0 0 0 25 26 1 0 0 0 0 26 27 1 0 0 0 0 26 44 1 6 0 0 0 27 28 1 6 0 0 0 27 29 1 0 0 0 0 27 40 1 0 0 0 0 29 30 1 0 0 0 0 30 31 1 0 0 0 0 31 32 1 0 0 0 0 32 33 1 6 0 0 0 32 34 1 0 0 0 0 34 35 1 0 0 0 0 34 36 1 0 0 0 0 36 37 1 0 0 0 0 36 39 1 0 0 0 0 37 38 1 0 0 0 0 40 41 2 0 0 0 0 40 42 1 0 0 0 0 42 43 1 0 0 0 0 45 44 1 6 0 0 0 45 46 1 0 0 0 0 45 54 1 0 0 0 0 46 47 1 0 0 0 0 46 66 1 1 0 0 0 47 48 1 0 0 0 0 47 56 1 6 0 0 0 48 49 1 0 0 0 0 48 55 1 1 0 0 0 49 50 1 6 0 0 0 49 54 1 0 0 0 0 50 51 2 0 0 0 0 50 52 1 0 0 0 0 52 53 1 0 0 0 0 57 56 1 6 0 0 0 57 58 1 0 0 0 0 57 62 1 0 0 0 0 58 59 1 0 0 0 0 58 65 1 1 0 0 0 59 60 1 0 0 0 0 59 64 1 6 0 0 0 60 61 1 0 0 0 0 60 63 1 6 0 0 0 61 62 1 0 0 0 0 67 68 1 0 0 0 0 68 69 2 0 0 0 0 68 70 1 0 0 0 0 70 71 2 0 0 0 0 70 73 1 0 0 0 0 71 72 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	1036.52
Volume:	1022.698
LogP:	2.433
LogD:	1.757
LogS:	-4.173
# Rotatable Bonds:	15
TPSA:	303.96
# H-Bond Aceptor:	20
# H-Bond Donor:	8
# Rings:	7
# Heavy Atoms:	20

MedChem Properties

QED Drug-Likeness Score:	0.048
Synthetic Accessibility Score:	6.809
Fsp3:	0.811
Lipinski Rule-of-5:	Rejected
Pfizer Rule:	Accepted
GSK Rule:	Rejected
BMS Rule:	1
Golden Triangle Rule:	Rejected
Chelating Alert:	0
PAINS Alert:	0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:	-5.364
MDCK Permeability:	0.00018924410687759519
Pgp-inhibitor:	1.0
Pgp-substrate:	0.997
Human Intestinal Absorption (HIA):	0.901
20% Bioavailability (F20%):	0.007
30% Bioavailability (F30%):	0.99

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.068
Plasma Protein Binding (PPB):	75.180908203125%
Volume Distribution (VD):	0.864
Pgp-substrate:	7.662759780883789%

ADMET: Metabolism

CYP1A2-inhibitor:	0.001
CYP1A2-substrate:	0.354
CYP2C19-inhibitor:	0.005
CYP2C19-substrate:	0.504
CYP2C9-inhibitor:	0.037
CYP2C9-substrate:	0.013
CYP2D6-inhibitor:	0.007
CYP2D6-substrate:	0.052
CYP3A4-inhibitor:	0.519
CYP3A4-substrate:	0.128

ADMET: Excretion

Clearance (CL):	1.254
Half-life (T1/2):	0.266

ADMET: Toxicity

hERG Blockers:	0.111
Human Hepatotoxicity (H-HT):	0.312
Drug-inuced Liver Injury (DILI):	0.068
AMES Toxicity:	0.047
Rat Oral Acute Toxicity:	0.078
Maximum Recommended Daily Dose:	0.55
Skin Sensitization:	0.024
Carcinogencity:	0.029
Eye Corrosion:	0.003
Eye Irritation:	0.005
Respiratory Toxicity:	0.163

Download Data

Data Type	Select
General Info & Identifiers & Properties
Structure MOL file
Source Organisms
Biological Activities
Similar NPs/Drugs

Natural Product: NPC154016

Natural Product ID:	NPC154016
*Common Name:**	QCMIZNQBGXTSJB-ZEYACDJTSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	QCMIZNQBGXTSJB-ZEYACDJTSA-N
Standard InCHI:	InChI=1S/C53H80O20/c1-13-24(3)42(62)72-40-41(73-43(63)25(4)14-2)53(23-54)27(21-48(40,5)6)26-15-16-29-49(7)19-18-31(51(9,47(65)67-12)30(49)17-20-50(29,8)52(26,10)38(60)39(53)61)69-46-35(59)36(34(58)37(71-46)44(64)66-11)70-45-33(57)32(56)28(55)22-68-45/h13-15,27-41,45-46,54-61H,16-23H2,1-12H3/b24-13-,25-14-/t27-,28-,29?,30?,31-,32-,33+,34-,35+,36-,37-,38?,39?,40-,41?,45-,46+,49+,50+,51-,52?,53-/m0/s1
SMILES:	C/C=C(/C)C(=O)O[C@H]1C([C@@]2(CO)[C@@H](CC1(C)C)C1=CCC3[C@@]4(C)CC[C@@H]([C@](C)(C4CC[C@@]3(C)C1(C)C(C2O)O)C(=O)OC)O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](C(=O)OC)O1)O)O[C@H]1[C@@H]([C@H]([C@H](CO1)O)O)O)O)OC(=O)/C(=CC)/C
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	11969009
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0002049] Terpene glycosides [CHEMONTID:0001580] Triterpene glycosides [CHEMONTID:0002358] Triterpene saponins

*Note: the InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.
**Note: the Chemical Classification was calculated by NPClassifier Version 1.5. Reference: PMID:34662515.

Species Source

Organism ID	Organism Name	Taxonomy Level	Family	SuperKingdom	Isolation Part	Collection Location	Collection Time	Reference
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	fruits	n.a.	n.a.	PMID[12467621]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	n.a.	root	n.a.	PMID[16212233]
NPO22874	Bombyx mori	Species	Bombycidae	Eukaryota	n.a.	n.a.	n.a.	PMID[18071251]
NPO22874	Bombyx mori	Species	Bombycidae	Eukaryota	n.a.	faeces	n.a.	PMID[18323202]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	rhizome	n.a.	PMID[18787781]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[21302967]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	root bark	n.a.	n.a.	PMID[23282106]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	Root Bark	n.a.	n.a.	PMID[26982999]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[27228227]
NPO4554	Isatis tinctoria	Species	Brassicaceae	Eukaryota	Roots	n.a.	n.a.	PMID[32004936]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	fruits	n.a.	n.a.	PMID[9090870]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	PMID[9544564]
NPO22874	Bombyx mori	Species	Bombycidae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO8258.1	Camellia sinensis var. assamica	Varieties	Theaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO4554	Isatis tinctoria	Species	Brassicaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO26396	Coprinopsis atramentaria	Species	Psathyrellaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO8258.1	Camellia sinensis var. assamica	Varieties	Theaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO4554	Isatis tinctoria	Species	Brassicaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO22874	Bombyx mori	Species	Bombycidae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO22874	Bombyx mori	Species	Bombycidae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO4554	Isatis tinctoria	Species	Brassicaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO22874	Bombyx mori	Species	Bombycidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO16087	Atractylodes lancea	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26396	Coprinopsis atramentaria	Species	Psathyrellaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO17823	Lycium chinense	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO4554	Isatis tinctoria	Species	Brassicaceae	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	NP ID	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

Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference

☑ Note for Activity Records:
☉ The quantitative biological activities were primarily integrated from ChEMBL (Version-30) database and were also directly collected from PubMed literature. PubMed PMID was provided as the reference link for each activity record.

Chemically structural similarity: I. Similar Active Natural Products in NPASS

Top-200 similar NPs were calculated against the active-NP-set (includes 4,3285 NPs with experimentally-derived bioactivity available in NPASS)

Similarity level is defined by Tanimoto coefficient (Tc) between two molecules. Tc lies between [0, 1] where '1' indicates the highest similarity. What is Tanimoto coefficient

● The left chart: Distribution of similarity level between NPC154016 and all remaining natural products in the NPASS database.
● The right table: Most similar natural products (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	324
0.1-0.2	1886
0.2-0.3	4703
0.3-0.4	7897
0.4-0.5	11983
0.5-0.6	8569
0.6-0.7	4426
0.7-0.8	2032
0.8-0.85	307
0.85-0.9	336
0.9-0.95	141
0.95-1	93

Similarity Score	Similarity Level	Natural Product ID

Chemically structural similarity: II. Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC154016 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	307
0.1-0.2	2080
0.2-0.3	3672
0.3-0.4	1972
0.4-0.5	671
0.5-0.6	280
0.6-0.7	133
0.7-0.8	33
0.8-0.85	0
0.85-0.9	0
0.9-0.95	2
0.95-1	0

Similarity Score	Similarity Level	Drug ID	Developmental Stage

Bioactivity similarity: Similar Natural Products in NPASS

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