NPASS Compound

Natural Product: NPC320359

Natural Product ID	NPC320359
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	Cratoxyarborenone A
IUPAC Name	8-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,5,7-tetrahydroxy-2-(3-methylbut-2-enyl)xanthen-9-one
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL465205
PubChem CID	10367180
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000002] Organoheterocyclic compounds [CHEMONTID:0000123] Benzopyrans [CHEMONTID:0003410] 1-benzopyrans [CHEMONTID:0002817] Dibenzopyrans [CHEMONTID:0000200] Xanthenes [CHEMONTID:0000204] Xanthones [CHEMONTID:0003519] 8-prenylated xanthones

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 66 68 0 0 0 0 0 0 0 0999 V2000 -3.1741 0.4641 2.4401 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9360 -0.1273 1.2685 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1575 -0.4692 0.2562 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6540 -0.2752 0.2868 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9714 -1.5896 0.1942 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6119 -2.8070 0.2611 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.9868 -2.8125 0.4406 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.8888 -3.9829 0.1518 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4756 -4.0095 -0.0248 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1308 -2.7959 -0.0927 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4019 -1.6127 0.0173 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1484 -0.4611 -0.0610 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6285 0.6748 0.0238 O 0 0 0 0 0 0 0 0 0 0 0 0 2.5341 -0.4467 -0.2385 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1428 -1.6899 -0.3349 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4392 -2.7927 -0.2606 O 0 0 0 0 0 0 0 0 0 0 0 0 4.5221 -1.6995 -0.5126 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2396 -0.5242 -0.5879 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6213 0.7072 -0.4904 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2559 0.7220 -0.3144 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6122 1.9333 -0.2140 O 0 0 0 0 0 0 0 0 0 0 0 0 5.3426 2.0036 -0.5650 C 0 0 0 0 0 0 0 0 0 0 0 0 6.0724 2.3056 0.6945 C 0 0 0 0 0 0 0 0 0 0 0 0 7.3639 2.5216 0.8003 C 0 0 0 0 0 0 0 0 0 0 0 0 8.2849 2.4907 -0.3618 C 0 0 0 0 0 0 0 0 0 0 0 0 7.9813 2.8148 2.1223 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6112 -0.5794 -0.7652 O 0 0 0 0 0 0 0 0 0 0 0 0 1.2122 -5.1805 -0.1361 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.3828 -0.2218 1.3664 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.1762 -0.6917 0.2304 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.0661 0.2453 -0.9143 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.1807 0.8236 -1.4164 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.1612 1.7657 -2.5512 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.4892 0.4943 -0.7971 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7042 1.4222 2.1459 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.8984 0.6843 3.2450 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.4532 -0.2681 2.8470 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6368 -0.9084 -0.6077 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3386 0.2371 1.1895 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4970 0.3215 -0.6665 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4298 -3.6382 0.8622 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3922 -4.9398 0.2040 H 0 0 0 0 0 0 0 0 0 0 0 0 5.0247 -2.6659 -0.5912 H 0 0 0 0 0 0 0 0 0 0 0 0 2.1696 2.3759 -1.0036 H 0 0 0 0 0 0 0 0 0 0 0 0 5.9923 2.0629 -1.4538 H 0 0 0 0 0 0 0 0 0 0 0 0 4.5885 2.8299 -0.7221 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4757 2.3526 1.6234 H 0 0 0 0 0 0 0 0 0 0 0 0 9.3101 2.1881 -0.0379 H 0 0 0 0 0 0 0 0 0 0 0 0 8.3215 3.5383 -0.7815 H 0 0 0 0 0 0 0 0 0 0 0 0 7.9637 1.7642 -1.1007 H 0 0 0 0 0 0 0 0 0 0 0 0 7.4613 2.2709 2.9385 H 0 0 0 0 0 0 0 0 0 0 0 0 7.8633 3.9000 2.3213 H 0 0 0 0 0 0 0 0 0 0 0 0 9.0479 2.5189 2.1514 H 0 0 0 0 0 0 0 0 0 0 0 0 7.1831 -0.8039 0.0422 H 0 0 0 0 0 0 0 0 0 0 0 0 1.4454 -5.7775 0.6547 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.6136 -0.9094 2.2404 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.7975 0.7670 1.7396 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.9052 -1.6896 -0.1670 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.2484 -0.7665 0.5174 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.1643 0.5445 -1.4212 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.2174 1.7151 -3.1358 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.0448 1.6597 -3.2118 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.1911 2.8205 -2.1506 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.4764 0.8336 0.2434 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.3363 0.9702 -1.3503 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.6862 -0.6073 -0.9093 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 5 6 2 0 6 7 1 0 6 8 1 0 8 9 2 0 9 10 1 0 10 11 2 0 11 12 1 0 12 13 2 0 12 14 1 0 14 15 2 0 15 16 1 0 15 17 1 0 17 18 2 0 18 19 1 0 19 20 2 0 20 21 1 0 19 22 1 0 22 23 1 0 23 24 2 3 24 25 1 0 24 26 1 0 18 27 1 0 9 28 1 0 2 29 1 0 29 30 1 0 30 31 1 0 31 32 2 3 32 33 1 0 32 34 1 0 11 5 1 0 20 14 1 0 16 10 1 0 1 35 1 0 1 36 1 0 1 37 1 0 3 38 1 0 4 39 1 0 4 40 1 0 7 41 1 0 8 42 1 0 17 43 1 0 21 44 1 0 22 45 1 0 22 46 1 0 23 47 1 0 25 48 1 0 25 49 1 0 25 50 1 0 26 51 1 0 26 52 1 0 26 53 1 0 27 54 1 0 28 55 1 0 29 56 1 0 29 57 1 0 30 58 1 0 30 59 1 0 31 60 1 0 33 61 1 0 33 62 1 0 33 63 1 0 34 64 1 0 34 65 1 0 34 66 1 0 M END

Standard InCHIKey	ZAXOSWZCOUYSSE-LICLKQGHSA-N
Standard InCHI	InChI=1S/C28H32O6/c1-15(2)7-6-8-17(5)10-12-18-20(29)13-22(31)28-24(18)27(33)25-23(34-28)14-21(30)19(26(25)32)11-9-16(3)4/h7,9-10,13-14,29-32H,6,8,11-12H2,1-5H3/b17-10+
SMILES	C/C(=CCc1c(O)cc(c2c1c(=O)c1c(o2)cc(c(c1O)CC=C(C)C)O)O)/CCC=C(C)C

Calculated Properties

Physi-Chem Properties

Molecular Weight:	464.22	Volume:	493.551 ? Van der Waals volume.
Dense:	0.941	LogP:	7.153 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	4.626 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-4.893 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	7.0	Rigid Bonds:	20.0
TPSA:	111.13 ? Topological Polar Surface Area.	H-Bond Acceptor:	6.0
H-Bond Donor:	4.0	Rings:	3.0
Heavy Atoms:	6.0

MedChem Properties

QED Drug-Likeness Score:	0.234	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	3.399	Fsp³:	0.321
MCE-18:	23.0 ? 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:	Rejected	BMS Rule:	0
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.994	Fluc inhibitor:	0.432 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.985 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.73 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.362	Promiscuous compounds:	0.173

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.067	MDCK Permeability:	-4.711
Pgp-inhibitor:	0.995	Pgp-substrate:	0.02
PAMPA:	0.026 ? 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):	0.069
20% Bioavailability (F20%):	0.945	30% Bioavailability (F30%):	0.999
50% Bioavailability (F50%):	1.0

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.0	MRP1:	0.87
Plasma Protein Binding (PPB):	96.484%	Volume Distribution (VD):	0.361
Fu:	3.568% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.999
OATP1B3 inhibitor:	0.994	BCRP inhibitor:	0.988
BSEP inhibitor:	0.968

ADMET: Metabolism

CYP1A2-inhibitor:	0.004	CYP1A2-substrate:	1.0
CYP2C19-inhibitor:	0.999	CYP2C19-substrate:	0.999
CYP2C9-inhibitor:	0.52	CYP2C9-substrate:	0.047
CYP2D6-inhibitor:	0.997	CYP2D6-substrate:	0.982
CYP3A4-inhibitor:	0.017	CYP3A4-substrate:	1.0
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	1.0
HLM stability:	1.0 ? 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):

1.828

Half-life (T1/2):

1.737

ADMET: Toxicity

hERG Blockers:	0.032	hERG Blockers (10um):	0.596
Human Hepatotoxicity (H-HT):	0.703	Drug-induced Liver Injury (DILI):	0.925
AMES Toxicity:	0.389	Rat Oral Acute Toxicity:	0.872
Maximum Recommended Daily Dose:	0.713	Skin Sensitization:	0.99
Carcinogencity:	0.519	Eye Corrosion:	0.0
Eye Irritation:	0.755	Respiratory Toxicity:	0.992
Drug-induced Neurotoxicity:	0.044	Ototoxicity:	0.396
Hematotoxicity:	0.152	Drug-induced Nephrotoxicity:	0.266
Genotoxicity:	0.986	RPMI-8226 Immunitoxicity:	0.115
A549 Cytotoxicity:	0.669	Hek293 Cytotoxicity:	0.728
BCF:	2.134 ? 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:	5.484 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	7.066 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	6.848 ? 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
NPO9520	Cratoxylum sumatranum	Species	Hypericaceae	Eukaryota	n.a.	twig	n.a.	PMID[11908969]
NPO9520	Cratoxylum sumatranum	Species	Hypericaceae	Eukaryota	n.a.	stem	n.a.	PMID[11908969]
NPO9520	Cratoxylum sumatranum	Species	Hypericaceae	Eukaryota	n.a.	leaf	n.a.	PMID[11908969]
NPO9520	Cratoxylum sumatranum	Species	Hypericaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO9520	Cratoxylum sumatranum	Species	Hypericaceae	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	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
EC50	1

Activity Type	# Activity
Cell line	1

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
NPT91	Cell line	KB	Homo sapiens	EC50	=	4.3	ug.mL-1	PMID[11908969]

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 NPC320359 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	23368
0.1-0.2	24160
0.2-0.3	1922
0.3-0.4	323
0.4-0.5	59
0.5-0.6	15
0.6-0.7	5
0.7-0.8	0
0.8-0.85	1
0.85-0.9	0
0.9-0.95	0
0.95-1	0

Similarity Score	Similarity Level	Natural Product ID
0.8361	Intermediate Similarity	NPC100123
0.7286	Intermediate Similarity	NPC236796
0.7101	Intermediate Similarity	NPC68093
0.6806	Remote Similarity	NPC227337
0.6447	Remote Similarity	NPC40491
0.6447	Remote Similarity	NPC278052
0.6324	Remote Similarity	NPC274730
0.6056	Remote Similarity	NPC488548
0.5974	Remote Similarity	NPC262286
0.5857	Remote Similarity	NPC142339
0.5854	Remote Similarity	NPC7483
0.5854	Remote Similarity	NPC74766
0.5789	Remote Similarity	NPC136674
0.5694	Remote Similarity	NPC119224
0.5513	Remote Similarity	NPC37684
0.5513	Remote Similarity	NPC212932
0.5316	Remote Similarity	NPC488731
0.5205	Remote Similarity	NPC186397
0.5181	Remote Similarity	NPC133392
0.5132	Remote Similarity	NPC228785
0.5132	Remote Similarity	NPC602307
0.5125	Remote Similarity	NPC25152
0.5059	Remote Similarity	NPC479155

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC320359 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4717
0.1-0.2	4413
0.2-0.3	19
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