NPASS Compound

Natural Product: NPC473797

Natural Product ID	NPC473797
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	[(3S,8S,9R,10R,12R,13S,14R,17R)-17-Acetyl-8,14,17-Trihydroxy-3-[(2R,4S,5R,6R)-5-[(2S,4S,5R,6R)-5-[(2S,3R,4R,5S,6R)-3-Hydroxy-4-Methoxy-5-[(2S,4R,5R,6R)-4-Methoxy-6-Methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl]Oxymethyl]Oxan-2-Yl]Oxyoxan-2-Yl]Oxy-6-Methyloxan-2-Yl]Oxy-4-Methoxy-6-Methyloxan-2-Yl]Oxy-4-Methoxy-6-Methyloxan-2-Yl]Oxy-10,13-Dimethyl-1,2,3,4,7,9,11,12,15,16-Decahydrocyclopenta[A]Phenanthren-12-Yl] (E)-3-Phenylprop-2-Enoate
IUPAC Name	[(3S,8S,9R,10R,12R,13S,14R,17R)-17-acetyl-8,14,17-trihydroxy-3-[(2R,4S,5R,6R)-5-[(2S,4S,5R,6R)-5-[(2S,3R,4R,5S,6R)-3-hydroxy-4-methoxy-5-[(2S,4R,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] (E)-3-phenylprop-2-enoate
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL451990
PubChem CID	44575239
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000258] Steroids and steroid derivatives [CHEMONTID:0001013] Steroidal glycosides

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 206216 0 0 0 0 0 0 0 0999 V2000 -2.7569 -0.4099 2.3441 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.6762 -0.2624 1.1437 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1719 -1.2231 0.0755 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7145 -2.5796 0.4699 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.2099 -2.5078 0.2370 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.6741 -1.0727 0.4509 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.9611 -0.6273 1.5839 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.0300 -0.9575 0.5632 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.5640 -0.0251 -0.3260 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.2134 1.1350 0.3144 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.6280 0.9552 0.7839 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.4735 0.2506 -0.2454 C 0 0 0 0 0 0 0 0 0 0 0 0 -11.8292 -0.1363 0.2116 C 0 0 0 0 0 0 0 0 0 0 0 0 -12.7560 -0.2474 -0.9439 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.1384 -0.7842 -0.6576 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.3663 -1.5291 0.5519 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.4090 -1.0590 1.5170 C 0 0 0 0 0 0 0 0 0 0 0 0 -14.6801 0.0758 2.2374 C 0 0 0 0 0 0 0 0 0 0 0 0 -13.3680 -0.6094 2.5873 C 0 0 0 0 0 0 0 0 0 0 0 0 -13.1843 -1.6484 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89 1 0 81 90 1 0 75 91 1 0 74 92 1 0 73 93 1 0 66 94 1 0 94 95 1 0 58 96 1 0 96 97 1 0 57 98 1 0 50 99 1 0 99100 1 0 7 2 1 0 77 72 1 0 85 80 1 0 25 9 1 0 24 12 1 0 21 13 1 0 20 16 1 0 43 38 1 0 53 48 1 0 61 56 1 0 69 64 1 0 1101 1 0 1102 1 0 1103 1 0 2104 1 0 3105 1 0 4106 1 0 5107 1 0 5108 1 0 6109 1 0 9110 1 0 10111 1 0 10112 1 0 11113 1 0 11114 1 0 13115 1 0 14116 1 0 14117 1 0 15118 1 0 18119 1 0 18120 1 0 19121 1 0 19122 1 0 22123 1 0 22124 1 0 23125 1 0 25126 1 0 25127 1 0 26128 1 0 27129 1 0 30130 1 0 30131 1 0 30132 1 0 31133 1 0 32134 1 0 32135 1 0 32136 1 0 36137 1 0 37138 1 0 39139 1 0 40140 1 0 41141 1 0 42142 1 0 43143 1 0 44144 1 0 44145 1 0 44146 1 0 46147 1 0 46148 1 0 46149 1 0 48150 1 0 49151 1 0 49152 1 0 50153 1 0 51154 1 0 52155 1 0 54156 1 0 54157 1 0 54158 1 0 56159 1 0 57160 1 0 58161 1 0 59162 1 0 60163 1 0 62164 1 0 62165 1 0 62166 1 0 64167 1 0 65168 1 0 65169 1 0 66170 1 0 67171 1 0 68172 1 0 70173 1 0 70174 1 0 70175 1 0 72176 1 0 73177 1 0 74178 1 0 75179 1 0 76180 1 0 78181 1 0 78182 1 0 80183 1 0 81184 1 0 82185 1 0 83186 1 0 84187 1 0 86188 1 0 86189 1 0 87190 1 0 88191 1 0 89192 1 0 90193 1 0 91194 1 0 92195 1 0 93196 1 0 95197 1 0 95198 1 0 95199 1 0 97200 1 0 97201 1 0 97202 1 0 98203 1 0 100204 1 0 100205 1 0 100206 1 0 M END

Standard InCHIKey	VBSFGTFDWOZVGT-QDKRDDSOSA-N
Standard InCHI	InChI=1S/C70H106O30/c1-32-58(40(84-8)26-48(89-32)93-39-20-21-66(6)38(25-39)19-22-69(82)45(66)29-46(96-47(73)18-17-37-15-13-12-14-16-37)67(7)68(81,36(5)72)23-24-70(67,69)83)97-49-27-41(85-9)60(34(3)90-49)100-65-57(80)62(87-11)61(35(4)92-65)98-50-28-42(86-10)59(33(2)91-50)99-64-56(79)54(77)52(75)44(95-64)31-88-63-55(78)53(76)51(74)43(30-71)94-63/h12-19,32-35,39-46,48-65,71,74-83H,20-31H2,1-11H3/b18-17+/t32-,33-,34-,35-,39+,40+,41+,42-,43-,44-,45-,46-,48+,49+,50+,51-,52-,53+,54+,55-,56-,57-,58-,59-,60-,61+,62-,63-,64+,65+,66+,67-,68+,69+,70-/m1/s1
SMILES	CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)(C(=O)C)O)C)OC(=O)C=CC6=CC=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)OC)OC)O)OC

Calculated Properties

Physi-Chem Properties

Molecular Weight:	1426.68	Volume:	1370.406 ? Van der Waals volume.
Dense:	1.041	LogP:	1.742 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	2.059 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-2.594 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	23.0	Rigid Bonds:	65.0
TPSA:	413.58 ? Topological Polar Surface Area.	H-Bond Acceptor:	30.0
H-Bond Donor:	11.0	Rings:	11.0
Heavy Atoms:	30.0

MedChem Properties

QED Drug-Likeness Score:	0.041	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	7.904	Fsp³:	0.829
MCE-18:	303.656 ? MCE-18 stands for medicinal chemistry evolution.MCE-18≥45 is considered a suitable value.	Lipinski Rule-of-5:	Accepted
Pfizer Rule:	Rejected	GSK Rule:	Accepted
Golden Triangle Rule:	Accepted	BMS Rule:	1
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.01	Fluc inhibitor:	0.28 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.004 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.351 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.397	Promiscuous compounds:	0.004

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-6.034	MDCK Permeability:	-5.236
Pgp-inhibitor:	0.0	Pgp-substrate:	1.0
PAMPA:	1.0 ? 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):	1.0
20% Bioavailability (F20%):	0.855	30% Bioavailability (F30%):	1.0
50% Bioavailability (F50%):	1.0

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.0	MRP1:	1.0
Plasma Protein Binding (PPB):	49.249%	Volume Distribution (VD):	-0.64
Fu:	37.458% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.0
OATP1B3 inhibitor:	0.016	BCRP inhibitor:	0.0
BSEP inhibitor:	0.009

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.993	CYP2C19-substrate:	0.0
CYP2C9-inhibitor:	0.994	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.0
CYP3A4-inhibitor:	0.041	CYP3A4-substrate:	0.0
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.0
HLM stability:	0.0 ? 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):

-0.515

Half-life (T1/2):

7.201

ADMET: Toxicity

hERG Blockers:	0.171	hERG Blockers (10um):	0.444
Human Hepatotoxicity (H-HT):	0.463	Drug-induced Liver Injury (DILI):	0.782
AMES Toxicity:	0.949	Rat Oral Acute Toxicity:	0.792
Maximum Recommended Daily Dose:	0.867	Skin Sensitization:	0.41
Carcinogencity:	0.003	Eye Corrosion:	0.0
Eye Irritation:	0.0	Respiratory Toxicity:	0.0
Drug-induced Neurotoxicity:	0.727	Ototoxicity:	1.0
Hematotoxicity:	0.002	Drug-induced Nephrotoxicity:	0.018
Genotoxicity:	0.727	RPMI-8226 Immunitoxicity:	0.591
A549 Cytotoxicity:	0.184	Hek293 Cytotoxicity:	0.993
BCF:	0.411 ? 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:	3.679 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.887 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.352 ? 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
NPO32487	leptadenia pyrotechnica	Species	Apocynaceae	Eukaryota	whole plant	Dogon region, Mali	2002-Apr	PMID[16643040]
NPO32487	leptadenia pyrotechnica	Species	Apocynaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]

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	3

Activity Type	# Activity
Cell line	3

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
NPT71	Cell line	HEK293	Homo sapiens	IC50	=	590.0	nM	PMID[15646539]
NPT3470	Cell line	WEHI-164	Mus musculus	IC50	=	950.0	nM	PMID[12161115]
NPT1182	Cell line	J774.A1	Mus musculus	IC50	=	620.0	nM	DOI[10.1584/jpestics.28.183]

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 NPC473797 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	13230
0.1-0.2	31245
0.2-0.3	4828
0.3-0.4	486
0.4-0.5	32
0.5-0.6	11
0.6-0.7	7
0.7-0.8	0
0.8-0.85	2
0.85-0.9	1
0.9-0.95	3
0.95-1	2

Similarity Score	Similarity Level	Natural Product ID
0.9533	High Similarity	NPC475437
0.9533	High Similarity	NPC475464
0.9346	High Similarity	NPC473641
0.9346	High Similarity	NPC475300
0.9107	High Similarity	NPC475447
0.8661	High Similarity	NPC476092
0.8482	Intermediate Similarity	NPC70236
0.8151	Intermediate Similarity	NPC475175
0.7895	Intermediate Similarity	NPC475613
0.7851	Intermediate Similarity	NPC475531
0.7851	Intermediate Similarity	NPC475198
0.7615	Intermediate Similarity	NPC102015
0.7478	Intermediate Similarity	NPC475536
0.7442	Intermediate Similarity	NPC476090
0.7368	Intermediate Similarity	NPC165234
0.7368	Intermediate Similarity	NPC481659
0.7368	Intermediate Similarity	NPC271687
0.7209	Intermediate Similarity	NPC481650
0.7167	Intermediate Similarity	NPC475218
0.6991	Remote Similarity	NPC481661
0.6991	Remote Similarity	NPC481655
0.6842	Remote Similarity	NPC475358
0.6842	Remote Similarity	NPC473566
0.675	Remote Similarity	NPC474564
0.6535	Remote Similarity	NPC475567
0.632	Remote Similarity	NPC481654
0.597	Remote Similarity	NPC481660
0.5948	Remote Similarity	NPC473519
0.594	Remote Similarity	NPC481648
0.5785	Remote Similarity	NPC473805
0.5776	Remote Similarity	NPC481657
0.575	Remote Similarity	NPC481658
0.575	Remote Similarity	NPC79250
0.575	Remote Similarity	NPC290746
0.5448	Remote Similarity	NPC473557
0.5426	Remote Similarity	NPC473468
0.5076	Remote Similarity	NPC481662

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC473797 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4962
0.1-0.2	4117
0.2-0.3	68
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