NPASS Compound

Natural Product: NPC484718

Natural Product ID	NPC484718
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	MLNSIBIIWDOAGC-GRVQADPTSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	n.a.
PubChem CID	n.a.
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000258] Steroids and steroid derivatives [CHEMONTID:0001125] Steroid lactones [CHEMONTID:0001560] Withanolides and derivatives

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 79 83 0 0 0 0 0 0 0 0999 V2000 -4.9681 3.2176 -0.6650 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6374 1.7879 -0.3956 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4981 0.8273 -0.5932 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.8557 1.1332 -1.1082 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.1154 2.4449 -1.3466 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.1700 -0.5862 -0.2557 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.0447 -1.4584 -0.4807 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.9179 -0.8311 0.2813 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.3315 0.2676 0.9663 C 0 0 2 0 0 0 0 0 0 0 0 0 -3.2563 1.4354 0.0595 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1110 -0.0709 1.7665 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.7607 -0.8506 2.9685 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0773 -0.9418 1.1374 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.3671 -1.7252 2.3122 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9830 -2.0801 1.7137 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2819 -0.8091 1.0494 C 0 0 1 0 0 0 0 0 0 0 0 0 2.5135 -0.7090 0.2455 C 0 0 2 0 0 0 0 0 0 0 0 0 3.7039 -1.2703 0.9953 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9598 -0.7451 0.3704 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0205 0.2610 -0.4663 C 0 0 0 0 0 0 0 0 0 0 0 0 6.3498 0.6738 -1.0093 C 0 0 0 0 0 0 0 0 0 0 0 0 6.5767 2.0596 -0.5292 C 0 0 0 0 0 0 0 0 0 0 0 0 5.5486 2.8843 -0.4395 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1946 2.4839 -0.7954 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3664 3.4215 -0.9724 O 0 0 0 0 0 0 0 0 0 0 0 0 3.8472 1.0498 -0.9327 C 0 0 1 0 0 0 0 0 0 0 0 0 3.4625 0.7520 -2.3417 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6976 0.7942 0.0531 C 0 0 1 0 0 0 0 0 0 0 0 0 1.4790 1.5547 -0.2302 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1335 0.9753 -0.0414 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0142 -0.4719 0.3365 C 0 0 2 0 0 0 0 0 0 0 0 0 -0.0037 -1.2190 -1.0107 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1009 -2.5795 -0.9164 O 0 0 0 0 0 0 0 0 0 0 0 0 0.1112 -3.4688 -1.9331 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0182 -3.0622 -3.1096 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2313 -4.9243 -1.6785 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4481 0.1588 2.0893 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.7749 -1.9865 0.5250 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.6636 1.0619 2.3947 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.0403 3.8119 -0.3721 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.7397 3.6189 0.0239 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.1158 3.4538 -1.7198 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.6420 0.6501 -0.4596 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.9325 0.5878 -2.0942 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.6071 2.6332 -2.1798 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.1643 0.5874 1.6934 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6995 1.2473 -0.8830 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8194 2.3199 0.5486 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0789 -0.9615 3.7974 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5579 -0.1415 3.3203 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2767 -1.7356 2.6074 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.1694 -1.0576 3.1493 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9610 -2.5594 2.6490 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7489 -2.2172 2.5379 H 0 0 0 0 0 0 0 0 0 0 0 0 1.0145 -3.0007 1.1505 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5469 -1.1537 -0.7388 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7041 -2.3767 0.7854 H 0 0 0 0 0 0 0 0 0 0 0 0 3.6605 -1.1203 2.0716 H 0 0 0 0 0 0 0 0 0 0 0 0 5.9162 -1.2399 0.6303 H 0 0 0 0 0 0 0 0 0 0 0 0 6.2764 0.6749 -2.1016 H 0 0 0 0 0 0 0 0 0 0 0 0 7.1558 -0.0128 -0.6747 H 0 0 0 0 0 0 0 0 0 0 0 0 7.5639 2.4172 -0.2488 H 0 0 0 0 0 0 0 0 0 0 0 0 5.7461 3.9122 -0.0783 H 0 0 0 0 0 0 0 0 0 0 0 0 4.4237 0.6893 -2.9318 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9693 -0.2127 -2.4971 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9194 1.6041 -2.8270 H 0 0 0 0 0 0 0 0 0 0 0 0 3.1415 1.1240 1.0444 H 0 0 0 0 0 0 0 0 0 0 0 0 1.6062 1.9240 -1.3023 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5773 2.5544 0.3093 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4336 1.6752 0.6016 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3947 1.0970 -1.0410 H 0 0 0 0 0 0 0 0 0 0 0 0 0.8180 -0.8542 -1.6674 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9232 -0.9116 -1.5356 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0118 -5.5307 -2.5678 H 0 0 0 0 0 0 0 0 0 0 0 0 1.2852 -5.1141 -1.3715 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.3898 -5.2164 -0.7925 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9019 -0.2988 2.8309 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0475 -1.8862 -0.3745 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4599 1.5646 2.6949 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 2 0 3 4 1 0 4 5 1 0 3 6 1 0 6 7 2 0 6 8 1 0 8 9 1 0 9 10 1 0 9 11 1 0 11 12 1 0 11 13 1 0 13 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 17 18 1 0 18 19 1 0 19 20 2 0 20 21 1 0 21 22 1 0 22 23 2 0 23 24 1 0 24 25 2 0 24 26 1 0 26 27 1 6 26 28 1 0 28 29 1 0 29 30 1 0 30 31 1 0 31 32 1 6 32 33 1 0 33 34 1 0 34 35 2 0 34 36 1 0 16 37 1 1 13 38 1 6 11 39 1 1 10 2 1 0 31 13 1 0 31 16 1 0 28 17 1 0 26 20 1 0 1 40 1 0 1 41 1 0 1 42 1 0 4 43 1 0 4 44 1 0 5 45 1 0 9 46 1 1 10 47 1 0 10 48 1 0 12 49 1 0 12 50 1 0 12 51 1 0 14 52 1 0 14 53 1 0 15 54 1 0 15 55 1 0 17 56 1 6 18 57 1 0 18 58 1 0 19 59 1 0 21 60 1 0 21 61 1 0 22 62 1 0 23 63 1 0 27 64 1 0 27 65 1 0 27 66 1 0 28 67 1 1 29 68 1 0 29 69 1 0 30 70 1 0 30 71 1 0 32 72 1 0 32 73 1 0 36 74 1 0 36 75 1 0 36 76 1 0 37 77 1 0 38 78 1 0 39 79 1 0 M END

Standard InCHIKey	MLNSIBIIWDOAGC-GRVQADPTSA-N
Standard InCHI	InChI=1S/C30H40O9/c1-17-14-24(39-25(34)20(17)15-31)27(4,35)30(37)13-12-29(36)22-9-8-19-6-5-7-23(33)26(19,3)21(22)10-11-28(29,30)16-38-18(2)32/h5,7-8,21-22,24,31,35-37H,6,9-16H2,1-4H3/t21-,22+,24+,26-,27-,28+,29+,30+/m0/s1
SMILES	CC1=C(CO)C(=O)O[C@H](C1)[C@@](C)([C@@]1(CC[C@]2([C@@H]3CC=C4CC=CC(=O)[C@]4(C)[C@H]3CC[C@]12COC(=O)C)O)O)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	544.27	Volume:	547.947 ? Van der Waals volume.
Dense:	0.993	LogP:	1.37 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	1.694 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-3.453 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	6.0	Rigid Bonds:	29.0
TPSA:	150.59 ? Topological Polar Surface Area.	H-Bond Acceptor:	9.0
H-Bond Donor:	4.0	Rings:	5.0
Heavy Atoms:	9.0

MedChem Properties

QED Drug-Likeness Score:	0.301	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	5.545	Fsp³:	0.7
MCE-18:	99.412 ? 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:	0.133	Fluc inhibitor:	0.084 ? 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:	0.014 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.336	Promiscuous compounds:	0.508

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-4.932	MDCK Permeability:	-4.635
Pgp-inhibitor:	0.002	Pgp-substrate:	0.106
PAMPA:	0.989 ? 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):	0.02
20% Bioavailability (F20%):	0.394	30% Bioavailability (F30%):	0.758
50% Bioavailability (F50%):	0.95

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.048	MRP1:	0.941
Plasma Protein Binding (PPB):	92.153%	Volume Distribution (VD):	0.019
Fu:	5.876% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.996
OATP1B3 inhibitor:	0.998	BCRP inhibitor:	0.001
BSEP inhibitor:	0.985

ADMET: Metabolism

CYP1A2-inhibitor:	0.162	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.001	CYP2C19-substrate:	0.0
CYP2C9-inhibitor:	0.016	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.0
CYP3A4-inhibitor:	0.031	CYP3A4-substrate:	0.342
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.996
HLM stability:	0.322 ? 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):

2.366

Half-life (T1/2):

2.038

ADMET: Toxicity

hERG Blockers:	0.015	hERG Blockers (10um):	0.136
Human Hepatotoxicity (H-HT):	0.542	Drug-induced Liver Injury (DILI):	0.138
AMES Toxicity:	0.353	Rat Oral Acute Toxicity:	0.149
Maximum Recommended Daily Dose:	0.741	Skin Sensitization:	0.988
Carcinogencity:	0.88	Eye Corrosion:	0.0
Eye Irritation:	0.077	Respiratory Toxicity:	0.183
Drug-induced Neurotoxicity:	0.113	Ototoxicity:	0.542
Hematotoxicity:	0.253	Drug-induced Nephrotoxicity:	0.657
Genotoxicity:	0.821	RPMI-8226 Immunitoxicity:	0.099
A549 Cytotoxicity:	0.059	Hek293 Cytotoxicity:	0.448
BCF:	0.597 ? 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:	3.415 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.273 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.468 ? 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
NPO40288	Physalis crassifolia	Species	Solanaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[27071003]

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	5

Activity Type	# Activity
Cell line	5

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
NPT858	Cell line	LNCaP	Homo sapiens	IC50	=	3700.0	nM	PMID[27071003]
NPT83	Cell line	MCF7	Homo sapiens	IC50	>	5000.0	nM	PMID[27071003]
NPT397	Cell line	NCI-H460	Homo sapiens	IC50	>	5000.0	nM	PMID[27071003]
NPT395	Cell line	SF-268	Homo sapiens	IC50	>	5000.0	nM	PMID[27071003]
NPT23103	Cell line	PC-3M	Homo sapiens	IC50	>	5000.0	nM	PMID[27071003]

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 NPC484718 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	18589
0.1-0.2	27285
0.2-0.3	3869
0.3-0.4	79
0.4-0.5	13
0.5-0.6	11
0.6-0.7	7
0.7-0.8	0
0.8-0.85	1
0.85-0.9	1
0.9-0.95	0
0.95-1	0

Similarity Score	Similarity Level	Natural Product ID
0.8873	High Similarity	NPC5292
0.8267	Intermediate Similarity	NPC484725
0.7917	Intermediate Similarity	NPC107493
0.7089	Intermediate Similarity	NPC484717
0.6933	Remote Similarity	NPC153440
0.6667	Remote Similarity	NPC46570
0.6667	Remote Similarity	NPC103045
0.6538	Remote Similarity	NPC191620
0.6375	Remote Similarity	NPC470961
0.6136	Remote Similarity	NPC484715
0.6105	Remote Similarity	NPC484726
0.5926	Remote Similarity	NPC79579
0.5814	Remote Similarity	NPC55621
0.5802	Remote Similarity	NPC176840
0.5802	Remote Similarity	NPC190286
0.5714	Remote Similarity	NPC484716
0.5476	Remote Similarity	NPC29133
0.5476	Remote Similarity	NPC44428
0.5476	Remote Similarity	NPC78691
0.5422	Remote Similarity	NPC484742
0.5238	Remote Similarity	NPC225826
0.5053	Remote Similarity	NPC484720

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC484718 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	6643
0.1-0.2	2399
0.2-0.3	107
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