NPASS Compound

Structure

NPC16468 OpenBabel06302215142D 68 77 0 0 1 0 0 0 0 0999 V2000 -2.5745 -8.9360 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5745 -8.9360 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.0745 -9.8020 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.0745 -9.8020 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.4255 -8.9360 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0745 -8.0700 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.0745 -8.0700 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.4255 -7.2039 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0745 -6.3379 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.4255 -5.4719 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.4255 -5.4719 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0745 -4.6059 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0745 -4.6059 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.5745 -5.4719 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0745 -6.3379 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.5745 -7.2039 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0745 -8.0700 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5745 -3.7398 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0745 -2.8738 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.0745 -2.8738 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.4255 -3.7398 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4255 -2.0078 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0745 -1.1418 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.0745 -1.1418 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5745 -2.0078 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.5745 -2.0078 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.0745 -2.8738 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4255 -0.2757 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0745 0.5903 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.4255 1.4563 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 1.4255 1.4563 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0745 2.3223 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0745 2.3223 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -1.5745 1.4563 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.0745 0.5903 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.5745 -0.2757 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0745 -1.1418 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5745 1.4563 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.5745 3.1884 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.0745 4.0544 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.5500 4.8780 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0745 5.7017 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1234 5.7017 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.6234 6.5677 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3521 4.8780 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1234 4.0544 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3032 4.8780 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7787 5.7017 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3032 6.5253 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.3521 6.5253 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.1234 7.3489 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3521 8.1726 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3032 8.1726 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 0.7154 7.3636 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3032 6.5545 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.2542 6.8636 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 2.2542 5.8636 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2542 7.8636 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 3.2053 8.1726 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 3.7931 7.3636 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2053 6.5545 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.7298 7.3489 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.7787 7.3489 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 2.2787 6.4829 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.3032 6.5253 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.4255 -10.6680 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0745 -11.5341 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5745 -10.6680 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 3 1 0 0 0 0 2 7 1 0 0 0 0 3 4 1 0 0 0 0 3 68 1 0 0 0 0 4 5 1 0 0 0 0 4 66 1 0 0 0 0 5 6 1 0 0 0 0 6 7 1 0 0 0 0 6 8 1 0 0 0 0 8 9 1 0 0 0 0 9 10 1 0 0 0 0 9 15 1 0 0 0 0 10 11 1 0 0 0 0 10 12 1 0 0 0 0 12 13 1 0 0 0 0 13 14 1 0 0 0 0 13 18 1 0 0 0 0 14 15 1 0 0 0 0 15 16 1 0 0 0 0 16 17 1 0 0 0 0 18 19 1 0 0 0 0 19 20 1 0 0 0 0 19 25 1 0 0 0 0 20 21 1 0 0 0 0 20 22 1 0 0 0 0 22 23 1 0 0 0 0 23 24 1 0 0 0 0 23 28 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 28 29 1 0 0 0 0 29 30 1 0 0 0 0 29 35 1 0 0 0 0 30 31 1 0 0 0 0 30 32 1 0 0 0 0 32 33 1 0 0 0 0 33 34 1 0 0 0 0 33 39 1 0 0 0 0 34 35 1 0 0 0 0 34 38 1 0 0 0 0 35 36 1 0 0 0 0 36 37 1 0 0 0 0 39 40 1 0 0 0 0 40 41 1 0 0 0 0 40 46 1 0 0 0 0 41 42 1 0 0 0 0 42 43 1 0 0 0 0 43 50 1 0 0 0 0 43 44 1 0 0 0 0 43 45 1 0 0 0 0 45 46 2 0 0 0 0 45 47 1 0 0 0 0 47 48 2 0 0 0 0 48 49 1 0 0 0 0 49 63 1 0 0 0 0 49 50 1 0 0 0 0 49 65 1 0 0 0 0 50 51 1 0 0 0 0 51 52 1 0 0 0 0 52 53 1 0 0 0 0 53 58 1 0 0 0 0 53 63 1 0 0 0 0 53 54 1 0 0 0 0 54 55 1 0 0 0 0 55 56 1 0 0 0 0 56 61 1 0 0 0 0 56 57 1 1 0 0 0 56 58 1 0 0 0 0 58 59 1 0 0 0 0 59 60 1 1 0 0 0 59 62 1 0 0 0 0 60 61 1 0 0 0 0 62 63 1 0 0 0 0 63 64 1 1 0 0 0 66 67 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	968.5
Volume:	932.237
LogP:	3.384
LogD:	2.757
LogS:	-4.873
# Rotatable Bonds:	12
TPSA:	219.37
# H-Bond Aceptor:	19
# H-Bond Donor:	4
# Rings:	10
# Heavy Atoms:	19

MedChem Properties

QED Drug-Likeness Score:	0.221
Synthetic Accessibility Score:	7.506
Fsp3:	0.918
Lipinski Rule-of-5:	Rejected
Pfizer Rule:	Accepted
GSK Rule:	Rejected
BMS Rule:	0
Golden Triangle Rule:	Rejected
Chelating Alert:	0
PAINS Alert:	0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:	-5.356
MDCK Permeability:	0.0001442610810045153
Pgp-inhibitor:	0.003
Pgp-substrate:	1.0
Human Intestinal Absorption (HIA):	0.009
20% Bioavailability (F20%):	0.001
30% Bioavailability (F30%):	0.01

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.003
Plasma Protein Binding (PPB):	49.17817306518555%
Volume Distribution (VD):	-0.033
Pgp-substrate:	13.747185707092285%

ADMET: Metabolism

CYP1A2-inhibitor:	0.0
CYP1A2-substrate:	0.998
CYP2C19-inhibitor:	0.003
CYP2C19-substrate:	0.783
CYP2C9-inhibitor:	0.001
CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0
CYP2D6-substrate:	0.058
CYP3A4-inhibitor:	0.563
CYP3A4-substrate:	0.933

ADMET: Excretion

Clearance (CL):	1.074
Half-life (T1/2):	0.732

ADMET: Toxicity

hERG Blockers:	0.833
Human Hepatotoxicity (H-HT):	0.224
Drug-inuced Liver Injury (DILI):	0.7
AMES Toxicity:	0.456
Rat Oral Acute Toxicity:	0.864
Maximum Recommended Daily Dose:	0.986
Skin Sensitization:	0.978
Carcinogencity:	0.126
Eye Corrosion:	0.003
Eye Irritation:	0.006
Respiratory Toxicity:	0.976

Download Data

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

Natural Product: NPC16468

Natural Product ID:	NPC16468
*Common Name:**	CZCOTALTGQFFGO-QUVTWCLGSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	CZCOTALTGQFFGO-QUVTWCLGSA-N
Standard InCHI:	InChI=1S/C49H76O19/c1-23-37(50)29(54-7)18-34(60-23)65-39-24(2)61-35(19-30(39)55-8)66-40-25(3)62-36(20-31(40)56-9)67-41-26(4)63-44(38(51)42(41)57-10)64-28-12-14-45(5)27(17-28)11-16-48(52)33(45)13-15-47-22-59-46(6)43(47)32(21-58-46)68-49(47,48)53/h11,16-17,23-26,28-44,50-53H,12-15,18-22H2,1-10H3/t23-,24+,25+,26+,28-,29+,30-,31-,32+,33+,34-,35-,36-,37-,38+,39+,40+,41+,42+,43+,44-,45-,46+,47-,48+,49-/m0/s1
SMILES:	C[C@H]1[C@@H]([C@@H](C[C@@H](O1)O[C@@H]1[C@@H](C)O[C@H](C[C@@H]1OC)O[C@@H]1[C@@H](C)O[C@H](C[C@@H]1OC)O[C@@H]1[C@@H](C)O[C@H]([C@@H]([C@H]1OC)O)O[C@H]1CC[C@@]2(C)C(=C1)C=C[C@]1([C@@H]2CC[C@]23CO[C@]4(C)[C@H]2[C@@H](CO4)O[C@]13O)O)OC)O
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	71525119
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000258] Steroids and steroid derivatives [CHEMONTID:0001295] Hydroxysteroids [CHEMONTID:0004495] 14-hydroxysteroids

*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
NPO25999	Ferula communis	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[15620264]
NPO26982	Callyspongia siphonella	Species	Callyspongiidae	Eukaryota	n.a.	n.a.	n.a.	PMID[17488128]
NPO26982	Callyspongia siphonella	Species	Callyspongiidae	Eukaryota	n.a.	n.a.	n.a.	PMID[19534474]
NPO26953	Hebeloma senescens	Species	Cortinariaceae	Eukaryota	fruiting bodies	n.a.	n.a.	PMID[7561908]
NPO26455	Merwilla natalensis	Species	Hyacinthaceae	Eukaryota	n.a.	n.a.	n.a.	Database[Article]
NPO25823	Haminoea navicula	Species	Haminoeidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26324	Fevillea cordifolia	Species	Cucurbitaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO25927	Dictyota dentata	Species	Dictyotaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26885	Dictyosphaeria favulosa	Species	Siphonocladaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO25874	Tuber borchii	Species	Tuberaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO4538	Paysonia densipila	Species	Brassicaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26982	Callyspongia siphonella	Species	Callyspongiidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26809	Synoicum blochmanni	Species	Polyclinidae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO25999	Ferula communis	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26214	Baccharis artemisioides	Species	Asteraceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26953	Hebeloma senescens	Species	Cortinariaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO10658	Pedicularis rhinanthoides	Species	Orobanchaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO26455	Merwilla natalensis	Species	Hyacinthaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO25900	Pteris podophylla	Species	Pteridaceae	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 NPC16468 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	346
0.1-0.2	1827
0.2-0.3	5434
0.3-0.4	13135
0.4-0.5	10995
0.5-0.6	6659
0.6-0.7	2618
0.7-0.8	1427
0.8-0.85	225
0.85-0.9	31
0.9-0.95	0
0.95-1	0

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 NPC16468 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

range	Tanimoto Coefficient
0-0.1	283
0.1-0.2	1813
0.2-0.3	4193
0.3-0.4	1971
0.4-0.5	599
0.5-0.6	237
0.6-0.7	33
0.7-0.8	19
0.8-0.85	2
0.85-0.9	0
0.9-0.95	0
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