NPASS Compound

Natural Product: NPC473735

Natural Product ID	NPC473735
Common Name ? The InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.	(3S,14R)-Petrocortyne G
IUPAC Name	(3S,4E,14R,21Z,28E,43Z)-hexatetraconta-4,21,28,43-tetraen-1,12,15,45-tetrayne-3,14,27-triol
Synonyms	(3S,14R)-Petrocortyne G
Synthetic Gene Cluster	n.a.
ChEMBL Identifier	CHEMBL450608
PubChem CID	10985247
Chemical Classification	CHEMONTID:0000000 [Organic compounds] [CHEMONTID:0000012] Lipids and lipid-like molecules [CHEMONTID:0003909] Fatty Acyls [CHEMONTID:0001334] Fatty alcohols

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 119118 0 0 0 0 0 0 0 0999 V2000 14.8067 -1.1177 3.2414 C 0 0 0 0 0 0 0 0 0 0 0 0 14.7080 0.1848 3.0119 C 0 0 0 0 0 0 0 0 0 0 0 0 14.6274 1.4857 2.7724 C 0 0 0 0 0 0 0 0 0 0 0 0 13.5950 1.7899 1.8516 C 0 0 0 0 0 0 0 0 0 0 0 0 12.8179 0.6438 1.3557 C 0 0 0 0 0 0 0 0 0 0 0 0 13.1610 0.3651 -0.0756 C 0 0 0 0 0 0 0 0 0 0 0 0 13.0237 1.4102 -1.1469 C 0 0 0 0 0 0 0 0 0 0 0 0 12.9018 0.8470 -2.5051 C 0 0 0 0 0 0 0 0 0 0 0 0 11.7579 0.1254 -3.0109 C 0 0 0 0 0 0 0 0 0 0 0 0 11.1626 -1.0828 -2.6025 C 0 0 0 0 0 0 0 0 0 0 0 0 10.5162 -1.5450 -1.4435 C 0 0 0 0 0 0 0 0 0 0 0 0 9.1424 -0.8834 -1.0612 C 0 0 0 0 0 0 0 0 0 0 0 0 8.2972 -0.8914 -2.3157 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9903 -0.3089 -2.2636 C 0 0 0 0 0 0 0 0 0 0 0 0 5.8586 -0.8792 -1.6480 C 0 0 0 0 0 0 0 0 0 0 0 0 5.5866 -1.3152 -0.2894 C 0 0 0 0 0 0 0 0 0 0 0 0 5.5024 -0.0121 0.5993 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2285 -0.3606 1.4470 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1495 0.0154 0.7931 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7176 -0.0869 0.9548 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8609 1.0487 0.5303 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7081 1.3285 -0.9126 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1187 0.2074 -1.6704 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0781 -0.4290 -0.8733 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1789 -0.4749 -1.9782 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3160 0.1081 -1.8728 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9007 0.8744 -0.7270 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.4897 0.3634 0.6424 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.7176 -1.1648 0.6280 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.2277 -1.4949 0.2230 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.0081 -1.2191 1.3907 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.6204 -0.9865 2.3071 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.4011 -0.6657 3.4723 C 0 0 1 0 0 0 0 0 0 0 0 0 -8.5516 0.1556 3.1478 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.5205 0.8739 2.8726 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.7528 1.7762 2.5030 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.5577 1.7243 0.9136 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.4190 0.2120 0.6214 C 0 0 0 0 0 0 0 0 0 0 0 0 -11.4254 -0.5494 1.3928 C 0 0 0 0 0 0 0 0 0 0 0 0 -12.8216 -0.2400 0.9555 C 0 0 0 0 0 0 0 0 0 0 0 0 -13.8622 -0.7768 1.9931 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.2691 -0.6293 1.4031 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.4478 -0.1341 0.2598 C 0 0 0 0 0 0 0 0 0 0 0 0 -16.5836 0.1343 -0.6312 C 0 0 1 0 0 0 0 0 0 0 0 0 -16.1361 0.4449 -1.9985 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.7487 0.7018 -3.1913 C 0 0 0 0 0 0 0 0 0 0 0 0 -17.0849 -1.2299 -0.8720 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.9557 -1.8732 4.0198 O 0 0 0 0 0 0 0 0 0 0 0 0 1.4253 -1.1475 -0.0237 O 0 0 0 0 0 0 0 0 0 0 0 0 14.8965 -2.1261 3.4196 H 0 0 0 0 0 0 0 0 0 0 0 0 15.1285 2.3553 3.1138 H 0 0 0 0 0 0 0 0 0 0 0 0 13.3693 2.8010 1.6351 H 0 0 0 0 0 0 0 0 0 0 0 0 12.9079 -0.2539 1.9212 H 0 0 0 0 0 0 0 0 0 0 0 0 11.6796 0.8609 1.4318 H 0 0 0 0 0 0 0 0 0 0 0 0 12.9236 -0.6538 -0.3456 H 0 0 0 0 0 0 0 0 0 0 0 0 14.3453 0.2889 0.0764 H 0 0 0 0 0 0 0 0 0 0 0 0 12.2767 2.1634 -0.8750 H 0 0 0 0 0 0 0 0 0 0 0 0 14.0289 2.0434 -1.1276 H 0 0 0 0 0 0 0 0 0 0 0 0 13.4047 1.5010 -3.3082 H 0 0 0 0 0 0 0 0 0 0 0 0 13.7488 -0.0150 -2.4389 H 0 0 0 0 0 0 0 0 0 0 0 0 10.8550 0.8794 -3.1535 H 0 0 0 0 0 0 0 0 0 0 0 0 12.0426 -0.0716 -4.1573 H 0 0 0 0 0 0 0 0 0 0 0 0 11.8505 -2.0004 -3.0520 H 0 0 0 0 0 0 0 0 0 0 0 0 10.3058 -1.2574 -3.5003 H 0 0 0 0 0 0 0 0 0 0 0 0 11.0600 -1.4288 -0.4955 H 0 0 0 0 0 0 0 0 0 0 0 0 10.3671 -2.7033 -1.4771 H 0 0 0 0 0 0 0 0 0 0 0 0 8.6406 -1.5565 -0.2963 H 0 0 0 0 0 0 0 0 0 0 0 0 9.3283 0.0954 -0.6577 H 0 0 0 0 0 0 0 0 0 0 0 0 8.0614 -2.0777 -2.4987 H 0 0 0 0 0 0 0 0 0 0 0 0 8.8774 -0.6677 -3.2965 H 0 0 0 0 0 0 0 0 0 0 0 0 6.7053 -0.0408 -3.3875 H 0 0 0 0 0 0 0 0 0 0 0 0 7.2056 0.8328 -1.9485 H 0 0 0 0 0 0 0 0 0 0 0 0 5.0729 0.0767 -1.7416 H 0 0 0 0 0 0 0 0 0 0 0 0 5.3082 -1.5472 -2.4065 H 0 0 0 0 0 0 0 0 0 0 0 0 6.3905 -1.9836 0.1159 H 0 0 0 0 0 0 0 0 0 0 0 0 4.5928 -1.8156 -0.2760 H 0 0 0 0 0 0 0 0 0 0 0 0 6.3365 -0.0799 1.3442 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4170 0.8502 0.0957 H 0 0 0 0 0 0 0 0 0 0 0 0 4.1594 -0.8438 2.3231 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4020 0.8050 -0.0424 H 0 0 0 0 0 0 0 0 0 0 0 0 1.4121 -0.4367 1.9515 H 0 0 0 0 0 0 0 0 0 0 0 0 0.0005 1.2183 1.1713 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5572 1.9676 0.8815 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7857 1.5110 -1.3241 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1945 2.3072 -1.0138 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.4629 0.7514 -2.5217 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7443 -0.5210 -2.1584 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3487 0.2505 -0.1134 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9252 -1.4542 -0.6054 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.0442 -1.1165 -2.8445 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.9737 0.1338 -2.8290 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.9045 1.2296 -0.8750 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.3353 1.9213 -0.8416 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.3929 0.6820 1.2834 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.6490 0.6930 1.1658 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6934 -1.4452 1.7463 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.9756 -1.7620 0.2146 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.4659 -0.7849 -0.5686 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.1717 -2.5207 -0.1269 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.8480 -0.1676 4.2410 H 0 0 0 0 0 0 0 0 0 0 0 0 -10.3870 2.8354 2.7332 H 0 0 0 0 0 0 0 0 0 0 0 0 -11.5611 1.4136 2.8835 H 0 0 0 0 0 0 0 0 0 0 0 0 -11.4394 2.1943 0.5390 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.5939 2.1448 0.6679 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.4221 -0.0584 0.8228 H 0 0 0 0 0 0 0 0 0 0 0 0 -10.6014 0.0486 -0.4734 H 0 0 0 0 0 0 0 0 0 0 0 0 -11.2461 -1.6249 1.1665 H 0 0 0 0 0 0 0 0 0 0 0 0 -11.3105 -0.4823 2.4579 H 0 0 0 0 0 0 0 0 0 0 0 0 -12.9844 -0.7794 0.0152 H 0 0 0 0 0 0 0 0 0 0 0 0 -13.0200 0.8524 0.7246 H 0 0 0 0 0 0 0 0 0 0 0 0 -13.7111 -1.7789 2.1527 H 0 0 0 0 0 0 0 0 0 0 0 0 -13.8357 -0.1698 2.9394 H 0 0 0 0 0 0 0 0 0 0 0 0 -16.1311 -0.9604 1.9419 H 0 0 0 0 0 0 0 0 0 0 0 0 -14.4899 0.1101 -0.3362 H 0 0 0 0 0 0 0 0 0 0 0 0 -17.3577 0.7448 -0.2476 H 0 0 0 0 0 0 0 0 0 0 0 0 -15.4126 0.9229 -4.2221 H 0 0 0 0 0 0 0 0 0 0 0 0 -16.3182 -1.7786 -1.1862 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.2774 -2.5706 3.7533 H 0 0 0 0 0 0 0 0 0 0 0 0 2.3185 -1.5013 -0.3496 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 3 0 2 3 1 0 3 4 2 0 4 5 1 0 5 6 1 0 6 7 1 0 7 8 1 0 8 9 1 0 9 10 1 0 10 11 1 0 11 12 1 0 12 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 2 0 19 20 1 0 20 21 1 0 21 22 1 0 22 23 1 0 23 24 1 0 24 25 1 0 25 26 2 0 26 27 1 0 27 28 1 0 28 29 1 0 29 30 1 0 30 31 1 0 31 32 3 0 32 33 1 0 33 34 1 0 34 35 3 0 35 36 1 0 36 37 1 0 37 38 1 0 38 39 1 0 39 40 1 0 40 41 1 0 41 42 1 0 42 43 2 0 43 44 1 0 44 45 1 0 45 46 3 0 44 47 1 0 33 48 1 0 20 49 1 0 1 50 1 0 3 51 1 0 4 52 1 0 5 53 1 0 5 54 1 0 6 55 1 0 6 56 1 0 7 57 1 0 7 58 1 0 8 59 1 0 8 60 1 0 9 61 1 0 9 62 1 0 10 63 1 0 10 64 1 0 11 65 1 0 11 66 1 0 12 67 1 0 12 68 1 0 13 69 1 0 13 70 1 0 14 71 1 0 14 72 1 0 15 73 1 0 15 74 1 0 16 75 1 0 16 76 1 0 17 77 1 0 17 78 1 0 18 79 1 0 19 80 1 0 20 81 1 0 21 82 1 0 21 83 1 0 22 84 1 0 22 85 1 0 23 86 1 0 23 87 1 0 24 88 1 0 24 89 1 0 25 90 1 0 26 91 1 0 27 92 1 0 27 93 1 0 28 94 1 0 28 95 1 0 29 96 1 0 29 97 1 0 30 98 1 0 30 99 1 0 33100 1 1 36101 1 0 36102 1 0 37103 1 0 37104 1 0 38105 1 0 38106 1 0 39107 1 0 39108 1 0 40109 1 0 40110 1 0 41111 1 0 41112 1 0 42113 1 0 43114 1 0 44115 1 1 46116 1 0 47117 1 0 48118 1 0 49119 1 0 M END

Standard InCHIKey	BBSNNCKQYMKHNA-KBIDCZRZSA-N
Standard InCHI	InChI=1S/C46H70O3/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-19-25-30-35-40-45(48)41-36-31-26-20-17-18-21-27-32-37-42-46(49)43-38-33-28-23-22-24-29-34-39-44(47)4-2/h1-2,5-6,17,20,34-35,39-40,44-49H,7-16,18-19,21-33,36,41H2/b6-5-,20-17-,39-34+,40-35+/t44-,45?,46+/m1/s1
SMILES	C#C/C=CCCCCCCCCCCCCC/C=C/C(CCCC/C=CCCCCC#C[C@@H](C#CCCCCCC/C=C/[C@@H](C#C)O)O)O

Calculated Properties

Physi-Chem Properties

Molecular Weight:	670.53	Volume:	798.905 ? Van der Waals volume.
Dense:	0.839	LogP:	8.851 ? The logarithm of the n-octanol/water distribution coefficients.
logD7.4:	4.892 ? The logarithm of the n-octanol/water distribution coefficient at pH=7.4.	LogS:	-8.897 ? The logarithm of aqueous solubility value.
Rotatable Bonds:	31.0	Rigid Bonds:	8.0
TPSA:	60.69 ? Topological Polar Surface Area.	H-Bond Acceptor:	3.0
H-Bond Donor:	3.0	Rings:	0.0
Heavy Atoms:	3.0

MedChem Properties

QED Drug-Likeness Score:	0.039	GASA:	1.0 ? GASA represents the probability of being difficult to synthesize, ranging from 0 to 1.
Synthetic Accessibility Score:	4.671	Fsp³:	0.652
MCE-18:	3.0 ? MCE-18 stands for medicinal chemistry evolution.MCE-18≥45 is considered a suitable value.	Lipinski Rule-of-5:	Accepted
Pfizer Rule:	Accepted	GSK Rule:	Accepted
Golden Triangle Rule:	Accepted	BMS Rule:	1
Chelating Alert:	0	PAINS Alert:	0
Colloidal aggregators:	0.665	Fluc inhibitor:	0.001 ? The fluc inhibitor value is the probability of being fLuc inhibitors, within the range of 0 to 1.
Blue fluorescence:	0.001 ? 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:	0.665	Promiscuous compounds:	0.033

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

Caco-2 Permeability:	-5.061	MDCK Permeability:	-4.565
Pgp-inhibitor:	0.058	Pgp-substrate:	0.0
PAMPA:	0.0 ? 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):	0.0
20% Bioavailability (F20%):	0.007	30% Bioavailability (F30%):	0.959
50% Bioavailability (F50%):	1.0

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):	0.0	MRP1:	0.0
Plasma Protein Binding (PPB):	101.488%	Volume Distribution (VD):	0.445
Fu:	0.004% ? The fraction unbound in plasms.	OATP1B1 inhibitor:	0.0
OATP1B3 inhibitor:	0.929	BCRP inhibitor:	0.999
BSEP inhibitor:	1.0

ADMET: Metabolism

CYP1A2-inhibitor:	0.0	CYP1A2-substrate:	1.0
CYP2C19-inhibitor:	0.032	CYP2C19-substrate:	1.0
CYP2C9-inhibitor:	1.0	CYP2C9-substrate:	0.0
CYP2D6-inhibitor:	0.386	CYP2D6-substrate:	1.0
CYP3A4-inhibitor:	0.0	CYP3A4-substrate:	1.0
CYP2B6-substrate:	0.0	CYP2C8-inhibitor:	1.0
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):

3.844

Half-life (T1/2):

1.663

ADMET: Toxicity

hERG Blockers:	0.077	hERG Blockers (10um):	0.744
Human Hepatotoxicity (H-HT):	0.837	Drug-induced Liver Injury (DILI):	0.001
AMES Toxicity:	0.054	Rat Oral Acute Toxicity:	0.512
Maximum Recommended Daily Dose:	0.992	Skin Sensitization:	1.0
Carcinogencity:	0.119	Eye Corrosion:	0.043
Eye Irritation:	0.479	Respiratory Toxicity:	1.0
Drug-induced Neurotoxicity:	0.013	Ototoxicity:	0.837
Hematotoxicity:	0.0	Drug-induced Nephrotoxicity:	0.923
Genotoxicity:	0.0	RPMI-8226 Immunitoxicity:	0.399
A549 Cytotoxicity:	0.83	Hek293 Cytotoxicity:	0.965
BCF:	-0.062 ? 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:	6.334 ? 48 hour Tetrahymena pyriformis IGC50. The unit of IGC50 is -log10[(mg/L)/(1000*MW)].
LC50DM:	8.832 ? 48 hour Daphnia magna LC50. The unit of LC50DM is -log10[(mg/L)/(1000*MW)].	LC50FM:	5.971 ? 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
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	(15-25 m depth) off Komun Island, Korea	1995-JUL	PMID[10217707]
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	n.a.	n.a.	PMID[10346968]
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	n.a.	n.a.	PMID[11170665]
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	n.a.	n.a.	PMID[11754614]
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	Indonesia	1996	PMID[18327911]
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	Miyako sea-knoll, southwestern Japan (2525.64' N, 12542.48' E), at a depth of 415 m	2009-OCT	PMID[21534590]
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	American Samoa	n.a.	PMID[23368996]
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	n.a.	n.a.	PMID[26821210]
NPO32667	Petrosia sp.	Species	Petrosiidae	Eukaryota	n.a.	n.a.	n.a.	PMID[9917297]
NPO32667	Petrosia sp.	Species	Petrosiidae	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
Inhibition	2
ED50	5

Activity Type	# Activity
Cell line	5
Nucleic acid	2

Molecular-level activity

Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference
NPT317	Nucleic acid	Nucleic Acid	n.a.	Inhibition	=	8.0	%	DOI[10.6019/CHEMBL1201861]
NPT317	Nucleic acid	Nucleic Acid	n.a.	Inhibition	=	55.0	%	PMID[20805391]

In vitro activity

Target ID	Target Type	Target Name	Target Organism	Activity Type	Activity Relation	Value	Unit	Reference
NPT81	Cell line	A549	Homo sapiens	ED50	=	4.0	ug ml-1	PMID[23398362]
NPT146	Cell line	SK-OV-3	Homo sapiens	ED50	=	1.2	ug ml-1	PMID[23398362]
NPT147	Cell line	SK-MEL-2	Homo sapiens	ED50	=	0.5	ug ml-1	DOI[10.6019/CHEMBL1201861]
NPT574	Cell line	XF498	Homo sapiens	ED50	=	3.5	ug ml-1	PMID[20160052]
NPT148	Cell line	HCT-15	Homo sapiens	ED50	=	1.4	ug ml-1	PMID[17455978]

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 NPC473735 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	43576
0.1-0.2	5790
0.2-0.3	351
0.3-0.4	68
0.4-0.5	21
0.5-0.6	23
0.6-0.7	7
0.7-0.8	0
0.8-0.85	0
0.85-0.9	5
0.9-0.95	0
0.95-1	6

Similarity Score	Similarity Level	Natural Product ID
1.0	High Similarity	NPC473896
0.975	High Similarity	NPC473847
0.975	High Similarity	NPC473721
0.975	High Similarity	NPC473725
0.975	High Similarity	NPC473910
0.975	High Similarity	NPC475384
0.8718	High Similarity	NPC89824
0.8718	High Similarity	NPC475477
0.8718	High Similarity	NPC256656
0.8718	High Similarity	NPC294278
0.8718	High Similarity	NPC477723
0.7955	Intermediate Similarity	NPC473532
0.7727	Intermediate Similarity	NPC329608
0.7561	Intermediate Similarity	NPC197272
0.7381	Intermediate Similarity	NPC26102
0.7381	Intermediate Similarity	NPC477724
0.7234	Intermediate Similarity	NPC473652
0.7111	Intermediate Similarity	NPC224148
0.7111	Intermediate Similarity	NPC477725
0.68	Remote Similarity	NPC168407
0.6585	Remote Similarity	NPC161838
0.6304	Remote Similarity	NPC48058
0.6279	Remote Similarity	NPC187361
0.619	Remote Similarity	NPC55383
0.6047	Remote Similarity	NPC471960
0.6047	Remote Similarity	NPC477727
0.5714	Remote Similarity	NPC477726
0.5614	Remote Similarity	NPC594
0.5614	Remote Similarity	NPC48968
0.5385	Remote Similarity	NPC170776
0.5385	Remote Similarity	NPC9273
0.5385	Remote Similarity	NPC165447
0.5385	Remote Similarity	NPC471959
0.5385	Remote Similarity	NPC199286
0.5385	Remote Similarity	NPC489046
0.5385	Remote Similarity	NPC76198
0.5385	Remote Similarity	NPC610719
0.537	Remote Similarity	NPC470967
0.537	Remote Similarity	NPC470968
0.5294	Remote Similarity	NPC470969
0.5273	Remote Similarity	NPC601905
0.5273	Remote Similarity	NPC603973
0.5263	Remote Similarity	NPC475984
0.525	Remote Similarity	NPC607242
0.5192	Remote Similarity	NPC470965
0.5128	Remote Similarity	NPC125122
0.5128	Remote Similarity	NPC471276
0.5128	Remote Similarity	NPC471280
0.5128	Remote Similarity	NPC471281

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC473735 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	8746
0.1-0.2	388
0.2-0.3	16
0.3-0.4	0
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