NPASS Compound

Natural Product: NPC38376

Natural Product ID	NPC38376
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	WSSVJIGMYVWUJL-PSLKBDIJSA-N
IUPAC Name	n.a.
Synonyms
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL3613718
PubChem CID	n.a.
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0000259] Prenol lipids [CHEMONTID:0002049] Terpene glycosides [CHEMONTID:0001580] Triterpene glycosides [CHEMONTID:0002358] Triterpene saponins

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 102108 0 0 0 0 0 0 0 0999 V2000 -6.3811 1.9714 -0.4294 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.2480 1.1484 -1.3485 C 0 0 2 0 0 0 0 0 0 0 0 0 -8.3531 0.5311 -0.5321 C 0 0 1 0 0 0 0 0 0 0 0 0 -7.8852 -0.5712 0.3539 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.8612 -1.4610 -0.2899 C 0 0 2 0 0 0 0 0 0 0 0 0 -5.8708 -0.7377 -1.1530 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.5063 0.1931 -1.9588 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.8524 -0.1064 -0.4911 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.5626 -0.5289 -0.8702 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.8528 0.5149 -1.6761 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3730 0.5215 -1.5459 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.8958 0.5432 -0.0969 C 0 0 1 0 0 0 0 0 0 0 0 0 -1.3808 1.7824 0.5325 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3924 -0.7705 0.4350 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.8150 -1.0612 1.7826 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6799 -1.2475 1.5425 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3061 0.0725 1.1050 C 0 0 2 0 0 0 0 0 0 0 0 0 1.1575 1.0055 2.2539 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6199 0.4665 -0.1553 C 0 0 2 0 0 0 0 0 0 0 0 0 1.2199 1.6160 -0.8691 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4829 1.8757 -0.6918 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3560 1.1035 0.1742 C 0 0 1 0 0 0 0 0 0 0 0 0 4.6905 0.9631 -0.4300 C 0 0 2 0 0 0 0 0 0 0 0 0 4.9155 0.2905 -1.6902 C 0 0 0 0 0 0 0 0 0 0 0 0 6.3908 -0.0714 -1.8469 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6345 -1.5583 -1.6706 C 0 0 0 0 0 0 0 0 0 0 0 0 6.8743 0.2182 -3.2817 C 0 0 0 0 0 0 0 0 0 0 0 0 7.2736 0.7657 -0.9629 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9226 0.7118 0.4897 C 0 0 0 0 0 0 0 0 0 0 0 0 5.4898 0.6658 0.7899 C 0 0 1 0 0 0 0 0 0 0 0 0 4.9926 1.9410 1.5412 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6650 2.0012 1.2443 O 0 0 0 0 0 0 0 0 0 0 0 0 5.0671 -0.3683 1.7541 C 0 0 1 0 0 0 0 0 0 0 0 0 3.5878 -0.2869 2.0887 C 0 0 0 0 0 0 0 0 0 0 0 0 2.7702 -0.1081 0.8014 C 0 0 1 0 0 0 0 0 0 0 0 0 2.9454 -1.4158 0.1022 C 0 0 0 0 0 0 0 0 0 0 0 0 5.5781 -1.6299 1.6314 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8407 -1.0691 0.2919 C 0 0 1 0 0 0 0 0 0 0 0 0 -3.5889 -0.6221 1.5616 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0617 -2.5940 0.2770 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5584 -3.1165 -0.9054 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.5640 -2.3563 -1.1400 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.4492 -0.1811 1.5995 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.8991 1.5370 0.2990 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.4476 2.3037 -0.9037 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.2038 1.4729 0.5344 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.9771 2.8878 -0.1819 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.6535 1.8345 -2.1311 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.1786 0.2335 -1.2100 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.7854 -1.2299 0.5414 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.4171 -2.0924 0.5004 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.4104 -1.4819 -1.8875 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7794 -1.3438 -1.6297 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.2695 1.5029 -1.4093 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0627 0.4303 -2.7846 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9483 -0.4362 -1.9728 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9768 1.3114 -2.1724 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0172 2.4282 -0.1471 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.9465 1.7050 1.4575 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4783 2.4635 0.6518 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8703 -1.5192 -0.2488 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.0762 -0.4150 2.5960 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.1516 -2.0957 2.0878 H 0 0 0 0 0 0 0 0 0 0 0 0 0.6806 -1.9664 0.6666 H 0 0 0 0 0 0 0 0 0 0 0 0 1.1007 -1.6571 2.4512 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5476 0.4519 3.1640 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5690 2.0069 2.1390 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0932 1.1864 2.5763 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7751 -0.4083 -0.8672 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5969 2.2549 -1.5425 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9088 2.7218 -1.2248 H 0 0 0 0 0 0 0 0 0 0 0 0 4.9857 2.0560 -0.6544 H 0 0 0 0 0 0 0 0 0 0 0 0 4.7331 1.0060 -2.5641 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2621 -0.5353 -2.0109 H 0 0 0 0 0 0 0 0 0 0 0 0 5.7109 -2.1529 -1.6613 H 0 0 0 0 0 0 0 0 0 0 0 0 7.3970 -1.9550 -2.3730 H 0 0 0 0 0 0 0 0 0 0 0 0 7.0977 -1.6665 -0.6519 H 0 0 0 0 0 0 0 0 0 0 0 0 7.9759 0.1437 -3.2474 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4973 1.1918 -3.6215 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4836 -0.6190 -3.8966 H 0 0 0 0 0 0 0 0 0 0 0 0 8.3026 0.4396 -1.1018 H 0 0 0 0 0 0 0 0 0 0 0 0 7.1874 1.8171 -1.3057 H 0 0 0 0 0 0 0 0 0 0 0 0 7.3539 1.6460 0.9572 H 0 0 0 0 0 0 0 0 0 0 0 0 7.4787 -0.1196 0.9646 H 0 0 0 0 0 0 0 0 0 0 0 0 5.5594 2.7874 1.0740 H 0 0 0 0 0 0 0 0 0 0 0 0 5.2625 1.8935 2.5908 H 0 0 0 0 0 0 0 0 0 0 0 0 5.5611 -0.0454 2.7415 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4665 0.6921 2.6182 H 0 0 0 0 0 0 0 0 0 0 0 0 3.2550 -1.1449 2.6728 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6495 -2.2016 0.8693 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3926 -1.5394 -0.8298 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0278 -1.7273 -0.0142 H 0 0 0 0 0 0 0 0 0 0 0 0 6.5190 -1.6792 1.8586 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9534 0.4205 1.4616 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.5078 -1.2411 1.5982 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0418 -0.8365 2.4774 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.1539 -2.8137 0.2551 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5455 -3.0866 1.1021 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.1197 -2.4675 -1.4987 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.9664 -1.8449 -1.9052 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.4242 -1.0047 2.1760 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.4958 1.4597 1.2066 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 3 4 1 0 4 5 1 0 5 6 1 0 6 7 1 0 6 8 1 0 8 9 1 0 9 10 1 0 10 11 1 0 11 12 1 0 12 13 1 1 12 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 17 18 1 1 17 19 1 0 19 20 1 0 20 21 2 0 21 22 1 0 22 23 1 0 23 24 1 0 24 25 1 0 25 26 1 0 25 27 1 0 25 28 1 0 28 29 1 0 30 29 1 6 30 31 1 0 31 32 1 0 30 33 1 0 33 34 1 0 34 35 1 0 35 36 1 6 33 37 1 0 14 38 1 0 38 39 1 1 38 40 1 0 40 41 1 0 5 42 1 0 4 43 1 0 3 44 1 0 7 2 1 0 38 9 1 0 19 12 1 0 35 22 1 0 35 17 1 0 22 32 1 1 30 23 1 0 1 45 1 0 1 46 1 0 1 47 1 0 2 48 1 6 3 49 1 6 4 50 1 1 5 51 1 1 6 52 1 6 9 53 1 6 10 54 1 0 10 55 1 0 11 56 1 0 11 57 1 0 13 58 1 0 13 59 1 0 13 60 1 0 14 61 1 6 15 62 1 0 15 63 1 0 16 64 1 0 16 65 1 0 18 66 1 0 18 67 1 0 18 68 1 0 19 69 1 6 20 70 1 0 21 71 1 0 23 72 1 6 24 73 1 0 24 74 1 0 26 75 1 0 26 76 1 0 26 77 1 0 27 78 1 0 27 79 1 0 27 80 1 0 28 81 1 0 28 82 1 0 29 83 1 0 29 84 1 0 31 85 1 0 31 86 1 0 33 87 1 1 34 88 1 0 34 89 1 0 36 90 1 0 36 91 1 0 36 92 1 0 37 93 1 0 39 94 1 0 39 95 1 0 39 96 1 0 40 97 1 0 40 98 1 0 41 99 1 0 42100 1 0 43101 1 0 44102 1 0 M END

Standard InCHIKey	WSSVJIGMYVWUJL-PSLKBDIJSA-N
Standard InCHI	InChI=1S/C36H58O8/c1-20-26(39)27(40)28(41)29(43-20)44-25-10-11-31(4)21(32(25,5)18-37)8-12-33(6)22(31)9-13-36-23-16-30(2,3)14-15-35(23,19-42-36)24(38)17-34(33,36)7/h9,13,20-29,37-41H,8,10-12,14-19H2,1-7H3/t20-,21-,22-,23-,24-,25+,26+,27+,28-,29+,31+,32+,33-,34+,35-,36+/m1/s1
SMILES	C[C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2C=C[C@]24[C@@H]5CC(C)(C)CC[C@]5(CO4)[C@@H](C[C@@]32C)O)[C@]1(C)CO)O)O)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	618.41	Volume:	639.002 ? Van der Waals volume.
Dense:	0.968	LogP:	1.912 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	2.22 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-3.56 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	3.0	Rigid Bonds:	35.0
TPSA:	128.84 ? Topological Polar Surface Area.	H-Bond Acceptor:	8.0
H-Bond Donor:	5.0	Rings:	7.0
Heavy Atoms:	8.0

MedChem Properties

QED Drug-Likeness Score:	0.238	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	6.827	Fsp³:	0.944
MCE-18:	194.629 ? 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:	0.842	Fluc inhibitor:	0.0 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.008 ? The blue fluorescence value is the probability of being blue fluorescence, within the range of 0 to 1	Green fluorescence:	0.0 ? The green fluorescence value is the probability of being green fluorescence, within the range of 0 to 1
Reactive compounds:	0.196	Promiscuous compounds:	0.056

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.722	MDCK Permeability:	-4.992
Pgp-inhibitor:	0.051	Pgp-substrate:	0.317
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):	0.0
20% Bioavailability (F20%):	0.069	30% Bioavailability (F30%):	0.043
50% Bioavailability (F50%):	0.97

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.011	MRP1:	0.233
Plasma Protein Binding (PPB):	82.648%	Volume Distribution (VD):	-0.327
Fu:	13.934% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	1.0
OATP1B3 inhibitor:	0.986	BCRP inhibitor:	0.053
BSEP inhibitor:	0.995

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	0.0
CYP2C19-inhibitor:	0.114	CYP2C19-substrate:	0.0
CYP2C9-inhibitor:	0.0	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.0	CYP2D6-substrate:	0.001
CYP3A4-inhibitor:	0.352	CYP3A4-substrate:	0.242
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	0.961
HLM stability:	0.813 ? 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):

2.972

Half-life (T1/2):

2.785

ADMET: Toxicity

hERG Blockers:	0.05	hERG Blockers (10um):	0.334
Human Hepatotoxicity (H-HT):	0.203	Drug-induced Liver Injury (DILI):	0.059
AMES Toxicity:	0.502	Rat Oral Acute Toxicity:	0.237
Maximum Recommended Daily Dose:	0.207	Skin Sensitization:	0.881
Carcinogencity:	0.499	Eye Corrosion:	0.0
Eye Irritation:	0.076	Respiratory Toxicity:	0.168
Drug-induced Neurotoxicity:	0.001	Ototoxicity:	0.9
Hematotoxicity:	0.099	Drug-induced Nephrotoxicity:	0.572
Genotoxicity:	0.024	RPMI-8226 Immunitoxicity:	0.114
A549 Cytotoxicity:	0.083	Hek293 Cytotoxicity:	0.316
BCF:	2.066 ? 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:	3.947 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	5.252 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	4.676 ? 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
NPO29401	Bupleurum chinense	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	DOI[10.1016/j.indcrop.2008.08.002]
NPO29401	Bupleurum chinense	Species	Apiaceae	Eukaryota	roots	n.a.	n.a.	PMID[26259802]
NPO29401	Bupleurum chinense	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[Article]
NPO29401	Bupleurum chinense	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[COCONUT]
NPO29401	Bupleurum chinense	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[HerDing]
NPO29401	Bupleurum chinense	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCMID]
NPO29401	Bupleurum chinense	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TCM_Taiwan]
NPO29401	Bupleurum chinense	Species	Apiaceae	Eukaryota	n.a.	n.a.	n.a.	Database[TM-MC]
NPO29401	Bupleurum chinense	Species	Apiaceae	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
IC50	5

Activity Type	# Activity
Cell line	4
Non-molecular	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
NPT81	Cell line	A549	Homo sapiens	IC50	>	50000.0	nM	DrugMatrix in vivo data: Biochemistry
NPT65	Cell line	HepG2	Homo sapiens	IC50	=	9340.0	nM	DrugMatrix in vivo data: Hematology
NPT1872	Cell line	Bcap37	Homo sapiens	IC50	=	32010.0	nM	PMID[18178085]
NPT83	Cell line	MCF7	Homo sapiens	IC50	=	48990.0	nM	PMID[23268606]
NPT20529	Non-molecular	NON-PROTEIN TARGET	n.a.	IC50	=	20390.0	nM	PMID[26259802]

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 NPC38376 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	22846
0.1-0.2	23266
0.2-0.3	3144
0.3-0.4	521
0.4-0.5	60
0.5-0.6	4
0.6-0.7	4
0.7-0.8	0
0.8-0.85	4
0.85-0.9	0
0.9-0.95	0
0.95-1	1

Similarity Score	Similarity Level	Natural Product ID
1.0	High Similarity	NPC80210
0.8333	Intermediate Similarity	NPC473125
0.8193	Intermediate Similarity	NPC180459
0.8193	Intermediate Similarity	NPC195116
0.8193	Intermediate Similarity	NPC221110
0.764	Intermediate Similarity	NPC40133
0.764	Intermediate Similarity	NPC49413
0.764	Intermediate Similarity	NPC600293
0.7586	Intermediate Similarity	NPC110494
0.7391	Intermediate Similarity	NPC476305
0.7356	Intermediate Similarity	NPC285253
0.7333	Intermediate Similarity	NPC157474
0.7033	Intermediate Similarity	NPC473128
0.6966	Remote Similarity	NPC290608
0.6774	Remote Similarity	NPC44298
0.6711	Remote Similarity	NPC92885
0.6277	Remote Similarity	NPC473130
0.5455	Remote Similarity	NPC473129
0.5455	Remote Similarity	NPC99627
0.5275	Remote Similarity	NPC473123
0.5192	Remote Similarity	NPC171741

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC38376 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	7362
0.1-0.2	1726
0.2-0.3	61
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