NPASS Compound

Structure

NPC327158 OpenBabel06302215192D 62 68 0 0 1 0 0 0 0 0999 V2000 -3.4256 -3.7189 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9095 -2.8624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0908 -2.9392 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1248 -3.1980 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -0.2588 -2.6980 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5345 -3.3067 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.0000 -1.7321 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 1.0000 -1.7321 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 1.5000 -0.8660 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0000 -0.0000 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -0.0000 -0.0000 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -0.5000 -0.8660 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -1.4659 -0.6072 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -2.3320 -1.1072 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -2.5908 -2.0731 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.5146 -1.6904 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3841 -2.6819 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1029 -1.3933 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3600 -2.1744 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -4.3514 -2.3049 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.9602 -1.5116 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5775 -0.5877 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.9516 -1.6421 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -6.5604 -0.8487 0.0000 C 0 0 3 0 0 0 0 0 0 0 0 0 -6.1777 0.0751 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.7864 0.8685 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.4038 1.7924 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4123 1.9229 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.8036 1.1295 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1862 0.2057 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.5518 -0.9793 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 -8.1606 -0.1859 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.7779 0.7380 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -9.1520 -0.3164 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.5347 -1.2403 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.5261 -1.3708 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -11.1349 -0.5775 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.7522 0.3464 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.7608 0.4769 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.3343 -2.5660 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1192 -0.1301 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.5965 0.3842 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.5203 0.7669 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3137 0.1582 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.6509 1.7584 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.8575 2.3671 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9880 3.3586 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9119 3.7413 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7053 3.1325 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.5747 2.1411 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0000 1.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0000 1.0000 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.9659 -0.2588 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.2247 -1.2247 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5176 -1.9319 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.1907 -1.4836 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5000 -2.5981 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.9239 -1.3494 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9943 -4.1894 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7877 -4.7982 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7116 -4.4155 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.6571 -5.7896 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 19 1 0 0 0 0 2 3 2 0 0 0 0 3 15 1 0 0 0 0 3 4 1 0 0 0 0 4 5 1 0 0 0 0 4 59 1 0 0 0 0 5 6 2 0 0 0 0 5 7 1 0 0 0 0 7 12 1 0 0 0 0 7 8 1 0 0 0 0 7 58 1 0 0 0 0 8 9 1 0 0 0 0 8 57 1 0 0 0 0 9 10 1 0 0 0 0 10 52 1 0 0 0 0 10 11 1 0 0 0 0 11 12 1 0 0 0 0 11 51 1 0 0 0 0 11 53 1 0 0 0 0 12 13 1 0 0 0 0 13 14 1 0 0 0 0 13 42 1 0 0 0 0 14 15 1 0 0 0 0 14 18 1 0 0 0 0 14 41 1 0 0 0 0 15 16 1 0 0 0 0 15 17 1 0 0 0 0 18 19 1 0 0 0 0 19 20 1 0 0 0 0 20 21 1 0 0 0 0 21 22 2 0 0 0 0 21 23 1 0 0 0 0 23 24 1 0 0 0 0 23 40 1 0 0 0 0 24 25 1 0 0 0 0 24 31 1 0 0 0 0 25 30 1 0 0 0 0 25 26 2 0 0 0 0 26 27 1 0 0 0 0 27 28 2 0 0 0 0 28 29 1 0 0 0 0 29 30 2 0 0 0 0 31 32 1 0 0 0 0 32 33 2 0 0 0 0 32 34 1 0 0 0 0 34 39 1 0 0 0 0 34 35 2 0 0 0 0 35 36 1 0 0 0 0 36 37 2 0 0 0 0 37 38 1 0 0 0 0 38 39 2 0 0 0 0 42 43 1 0 0 0 0 43 44 2 0 0 0 0 43 45 1 0 0 0 0 45 50 1 0 0 0 0 45 46 2 0 0 0 0 46 47 1 0 0 0 0 47 48 2 0 0 0 0 48 49 1 0 0 0 0 49 50 2 0 0 0 0 51 52 1 0 0 0 0 53 54 1 0 0 0 0 54 55 2 0 0 0 0 54 56 1 0 0 0 0 59 60 1 0 0 0 0 60 61 2 0 0 0 0 60 62 1 0 0 0 0 M END $$$$

Physi-Chem Properties

Molecular Weight:	853.33
Volume:	853.449
LogP:	3.114
LogD:	2.277
LogS:	-3.948
# Rotatable Bonds:	15
TPSA:	221.29
# H-Bond Aceptor:	15
# H-Bond Donor:	4
# Rings:	7
# Heavy Atoms:	15

MedChem Properties

QED Drug-Likeness Score:	0.168
Synthetic Accessibility Score:	6.029
Fsp3:	0.447
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:	-5.377
MDCK Permeability:	3.8424528611358255e-05
Pgp-inhibitor:	1.0
Pgp-substrate:	0.952
Human Intestinal Absorption (HIA):	0.376
20% Bioavailability (F20%):	0.983
30% Bioavailability (F30%):	0.989

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.033
Plasma Protein Binding (PPB):	98.1620864868164%
Volume Distribution (VD):	0.565
Pgp-substrate:	4.450681686401367%

ADMET: Metabolism

CYP1A2-inhibitor:	0.008
CYP1A2-substrate:	0.031
CYP2C19-inhibitor:	0.108
CYP2C19-substrate:	0.066
CYP2C9-inhibitor:	0.618
CYP2C9-substrate:	0.084
CYP2D6-inhibitor:	0.015
CYP2D6-substrate:	0.082
CYP3A4-inhibitor:	0.733
CYP3A4-substrate:	0.606

ADMET: Excretion

Clearance (CL):	2.993
Half-life (T1/2):	0.025

ADMET: Toxicity

hERG Blockers:	0.036
Human Hepatotoxicity (H-HT):	0.781
Drug-inuced Liver Injury (DILI):	0.96
AMES Toxicity:	0.01
Rat Oral Acute Toxicity:	0.989
Maximum Recommended Daily Dose:	0.14
Skin Sensitization:	0.022
Carcinogencity:	0.033
Eye Corrosion:	0.003
Eye Irritation:	0.004
Respiratory Toxicity:	0.014

Download Data

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

Natural Product: NPC327158

Natural Product ID:	NPC327158
*Common Name:**	RCINICONZNJXQF-PZZLNDKRSA-N
IUPAC Name:	n.a.
Synonyms:
Standard InCHIKey:	RCINICONZNJXQF-PZZLNDKRSA-N
Standard InCHI:	InChI=1S/C47H51NO14/c1-25-31(60-43(56)36(52)35(28-16-10-7-11-17-28)48-41(54)29-18-12-8-13-19-29)23-47(57)40(61-42(55)30-20-14-9-15-21-30)38-45(6,32(51)22-33-46(38,24-58-33)62-27(3)50)39(53)37(59-26(2)49)34(25)44(47,4)5/h7-21,31-33,35-38,40,51-52,57H,22-24H2,1-6H3,(H,48,54)/t31-,32-,33?,35?,36?,37+,38?,40?,45+,46?,47+/m0/s1
SMILES:	CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)C6=CC=CC=C6)O)O)OC(=O)C7=CC=CC=C7)(CO4)OC(=O)C)O)C)OC(=O)C
Synthetic Gene Cluster:	n.a.
ChEMBL Identifier:	n.a.
PubChem CID:	5321715
Chemical Classification:**	CHEMONTID:0000000 [Organic compounds]

*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
NPO31343	Taxus chinensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[12217376]
NPO29841	Taxus yunnanensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[12217376]
NPO29841	Taxus yunnanensis	Species	Taxaceae	Eukaryota	wood	n.a.	n.a.	PMID[12444707]
NPO24820	Taxus cuspidata	Species	Taxaceae	Eukaryota	n.a.	Japan	n.a.	PMID[14987066]
NPO24820	Taxus cuspidata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[15844936]
NPO24820	Taxus cuspidata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[15974623]
NPO24820	Taxus cuspidata	Species	Taxaceae	Eukaryota	n.a.	Japan	n.a.	PMID[15974623]
NPO23720	Taxus wallichiana	Species	Taxaceae	Eukaryota	needles	Himalayan	n.a.	PMID[16480866]
NPO27064	Taxus brevifolia	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[1955887]
NPO29841	Taxus yunnanensis	Species	Taxaceae	Eukaryota	n.a.	xylem	n.a.	PMID[21138310]
NPO29841	Taxus yunnanensis	Species	Taxaceae	Eukaryota	wood	Yunnang Province, China	2000-OCT	PMID[21138310]
NPO5067	Taxus baccata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[23265441]
NPO23720	Taxus wallichiana	Species	Taxaceae	Eukaryota	Stem Bark	n.a.	n.a.	PMID[28240909]
NPO23720	Taxus wallichiana	Species	Taxaceae	Eukaryota	Roots	n.a.	n.a.	PMID[28581744]
NPO27064	Taxus brevifolia	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[2878063]
NPO27064	Taxus brevifolia	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[7130988]
NPO23720	Taxus wallichiana	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[7264680]
NPO5067	Taxus baccata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[7561894]
NPO27064	Taxus brevifolia	Species	Taxaceae	Eukaryota	bark	n.a.	n.a.	PMID[7623034]
NPO5067	Taxus baccata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[7908950]
NPO31343	Taxus chinensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO15166	Cephalotaxus hainanensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO5067	Taxus baccata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO27064	Taxus brevifolia	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO29841	Taxus yunnanensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO23720	Taxus wallichiana	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO24820	Taxus cuspidata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO24820	Taxus cuspidata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO23720	Taxus wallichiana	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO5067	Taxus baccata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO27064	Taxus brevifolia	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO15166	Cephalotaxus hainanensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO23720	Taxus wallichiana	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO5067	Taxus baccata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO30249	Taxus malrei	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO15166	Cephalotaxus hainanensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO31343	Taxus chinensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO29841	Taxus yunnanensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO27064	Taxus brevifolia	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO24820	Taxus cuspidata	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO27064	Taxus brevifolia	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO23720	Taxus wallichiana	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO15166	Cephalotaxus hainanensis	Species	Taxaceae	Eukaryota	n.a.	n.a.	n.a.	Database[UNPD]
NPO24820	Taxus cuspidata	Species	Taxaceae	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 NPC327158 and all remaining natural products in the NPASS database.
● The right table: Most similar natural products (Tc>=0.56 or Top200).

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 NPC327158 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

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