NPASS Compound

Natural Product: NPC70236

Natural Product ID	NPC70236
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,13R,14R,17S)-8,14,17-Trihydroxy-17-[(1S)-1-Hydroxyethyl]-3-[(2R,4S,5R,6R)-5-[(2S,4S,5R,6R)-5-[(2S,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3-Hydroxy-4-Methoxy-6-Methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl]Oxyoxan-2-Yl]Oxy-4-Methoxy-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,13R,14R,17S)-8,14,17-trihydroxy-17-[(1S)-1-hydroxyethyl]-3-[(2R,4S,5R,6R)-5-[(2S,4S,5R,6R)-5-[(2S,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3-hydroxy-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-methoxy-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	CHEMBL509848
PubChem CID	44566880
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 187196 0 0 0 0 0 0 0 0999 V2000 -0.5144 -4.3910 -3.1350 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6212 -4.0455 -1.8127 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.3572 -2.8453 -1.5962 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.5534 -3.3102 -0.7671 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.3807 -2.1597 -0.3404 C 0 0 2 0 0 0 0 0 0 0 0 0 -4.5808 -2.1161 -0.9775 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.6668 -1.8771 -0.2061 C 0 0 1 0 0 0 0 0 0 0 0 0 -6.4102 -0.6337 -0.5691 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.6717 -0.8634 -1.3780 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.6997 -1.6458 -0.5168 C 0 0 1 0 0 0 0 0 0 0 0 0 -7.8675 -2.2969 0.5160 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.0545 -2.2485 1.8146 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.1939 -1.4741 2.4027 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.2403 -1.1333 1.4108 C 0 0 2 0 0 0 0 0 0 0 0 0 -9.6736 -0.7308 0.0937 C 0 0 2 0 0 0 0 0 0 0 0 0 -10.8993 -0.4961 -0.7822 C 0 0 0 0 0 0 0 0 0 0 0 0 -11.4034 0.8836 -0.3995 C 0 0 1 0 0 0 0 0 0 0 0 0 -12.6563 1.1282 -1.0273 O 0 0 0 0 0 0 0 0 0 0 0 0 -12.9525 1.9992 -2.0057 C 0 0 0 0 0 0 0 0 0 0 0 0 -12.0743 2.7169 -2.5011 O 0 0 0 0 0 0 0 0 0 0 0 0 -14.3234 2.1658 -2.5518 C 0 0 0 0 0 0 0 0 0 0 0 0 -15.2956 1.4168 -2.0733 C 0 0 0 0 0 0 0 0 0 0 0 0 -16.6835 1.4205 -2.4513 C 0 0 0 0 0 0 0 0 0 0 0 0 -17.5649 0.5372 -1.8646 C 0 0 0 0 0 0 0 0 0 0 0 0 -18.9244 0.5115 -2.1893 C 0 0 0 0 0 0 0 0 0 0 0 0 -19.4335 1.3953 -3.1354 C 0 0 0 0 0 0 0 0 0 0 0 0 -18.5345 2.2671 -3.7075 C 0 0 0 0 0 0 0 0 0 0 0 0 -17.1948 2.2968 -3.3902 C 0 0 0 0 0 0 0 0 0 0 0 0 -11.4825 1.0749 1.0778 C 0 0 1 0 0 0 0 0 0 0 0 0 -11.2620 -0.1531 1.9165 C 0 0 1 0 0 0 0 0 0 0 0 0 -12.4707 -0.8294 2.0544 O 0 0 0 0 0 0 0 0 0 0 0 0 -10.9402 0.4477 3.2637 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.2432 1.7367 2.9816 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.8364 2.2529 1.6712 C 0 0 2 0 0 0 0 0 0 0 0 0 -11.8130 3.2213 2.0714 O 0 0 0 0 0 0 0 0 0 0 0 0 -9.8424 3.0399 0.8981 C 0 0 1 0 0 0 0 0 0 0 0 0 -10.3985 3.7075 -0.1906 O 0 0 0 0 0 0 0 0 0 0 0 0 -9.3813 4.1905 1.8291 C 0 0 0 0 0 0 0 0 0 0 0 0 -13.0180 1.3727 1.2896 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.8922 -2.3786 1.1447 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.6555 -3.0018 -0.0040 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.3281 -2.6513 -1.4609 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6877 -0.9633 -0.7437 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.4725 -0.9468 -0.0401 C 0 0 1 0 0 0 0 0 0 0 0 0 -0.5525 -1.8832 -0.7991 C 0 0 1 0 0 0 0 0 0 0 0 0 0.3321 -2.5726 0.0298 O 0 0 0 0 0 0 0 0 0 0 0 0 1.6233 -2.0882 -0.0731 C 0 0 1 0 0 0 0 0 0 0 0 0 2.2036 -1.6704 1.2389 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6202 -2.1880 1.3509 C 0 0 2 0 0 0 0 0 0 0 0 0 4.1514 -1.5954 2.5006 O 0 0 0 0 0 0 0 0 0 0 0 0 4.6055 -2.6497 3.3183 C 0 0 0 0 0 0 0 0 0 0 0 0 4.3560 -1.7030 0.1062 C 0 0 1 0 0 0 0 0 0 0 0 0 3.5598 -2.0516 -1.1333 C 0 0 2 0 0 0 0 0 0 0 0 0 2.5239 -2.9305 -0.7303 O 0 0 0 0 0 0 0 0 0 0 0 0 4.4428 -2.7685 -2.0979 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6692 -0.3610 0.1884 O 0 0 0 0 0 0 0 0 0 0 0 0 5.9935 -0.0645 0.1914 C 0 0 1 0 0 0 0 0 0 0 0 0 6.2832 0.9293 -0.9010 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4400 1.8419 -0.5309 C 0 0 1 0 0 0 0 0 0 0 0 0 6.9606 2.8766 0.2663 O 0 0 0 0 0 0 0 0 0 0 0 0 7.1422 4.1303 -0.2592 C 0 0 0 0 0 0 0 0 0 0 0 0 8.4372 1.0797 0.3191 C 0 0 1 0 0 0 0 0 0 0 0 0 7.7139 0.6073 1.5511 C 0 0 2 0 0 0 0 0 0 0 0 0 6.3241 0.6127 1.3898 O 0 0 0 0 0 0 0 0 0 0 0 0 8.1253 1.2953 2.8171 C 0 0 0 0 0 0 0 0 0 0 0 0 8.9996 0.0192 -0.3475 O 0 0 0 0 0 0 0 0 0 0 0 0 10.3729 0.0415 -0.4652 C 0 0 2 0 0 0 0 0 0 0 0 0 10.6694 -0.0065 -1.8290 O 0 0 0 0 0 0 0 0 0 0 0 0 11.9827 -0.2377 -2.1263 C 0 0 2 0 0 0 0 0 0 0 0 0 12.1122 -1.4668 -3.0180 C 0 0 0 0 0 0 0 0 0 0 0 0 12.9268 -0.2804 -0.9749 C 0 0 2 0 0 0 0 0 0 0 0 0 12.4451 -1.0262 0.2288 C 0 0 2 0 0 0 0 0 0 0 0 0 10.9436 -1.2349 0.1181 C 0 0 1 0 0 0 0 0 0 0 0 0 10.3896 -1.6022 1.3205 O 0 0 0 0 0 0 0 0 0 0 0 0 12.6150 -0.1973 1.3537 O 0 0 0 0 0 0 0 0 0 0 0 0 13.3715 -0.7829 2.3359 C 0 0 0 0 0 0 0 0 0 0 0 0 13.3262 1.0169 -0.6581 O 0 0 0 0 0 0 0 0 0 0 0 0 14.6777 1.1596 -0.8610 C 0 0 2 0 0 0 0 0 0 0 0 0 15.2555 1.3872 0.3945 O 0 0 0 0 0 0 0 0 0 0 0 0 16.6250 1.4816 0.3280 C 0 0 2 0 0 0 0 0 0 0 0 0 17.1444 1.5989 1.7502 C 0 0 0 0 0 0 0 0 0 0 0 0 16.6080 2.7416 2.3131 O 0 0 0 0 0 0 0 0 0 0 0 0 16.9498 2.8068 -0.3742 C 0 0 2 0 0 0 0 0 0 0 0 0 16.4199 2.7262 -1.7767 C 0 0 1 0 0 0 0 0 0 0 0 0 14.9832 2.2472 -1.8369 C 0 0 1 0 0 0 0 0 0 0 0 0 14.7915 1.7601 -3.1438 O 0 0 0 0 0 0 0 0 0 0 0 0 16.4780 3.9984 -2.3437 O 0 0 0 0 0 0 0 0 0 0 0 0 18.3308 2.9944 -0.4346 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.9836 0.4738 -0.0694 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0766 -5.3612 -3.1438 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4486 -4.5548 -3.6749 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1965 -3.6876 -3.6721 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.7150 -2.4382 -2.5628 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2144 -3.9492 0.0815 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1483 -3.9480 -1.4940 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.4506 -2.1279 0.7730 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2551 -1.7112 0.8487 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.7620 0.0304 -1.1333 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.7556 -0.0747 0.3450 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.4856 -1.4270 -2.3092 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.0614 0.1251 -1.6710 H 0 0 0 0 0 0 0 0 0 0 0 0 -7.4102 -2.7541 2.5285 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.6580 -2.1808 3.1589 H 0 0 0 0 0 0 0 0 0 0 0 0 -8.7200 -0.6351 2.9375 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.1733 0.2532 0.2426 H 0 0 0 0 0 0 0 0 0 0 0 0 -10.6566 -0.4847 -1.8526 H 0 0 0 0 0 0 0 0 0 0 0 0 -11.6283 -1.2863 -0.5075 H 0 0 0 0 0 0 0 0 0 0 0 0 -10.6777 1.5827 -0.8381 H 0 0 0 0 0 0 0 0 0 0 0 0 -14.5519 2.8631 -3.3136 H 0 0 0 0 0 0 0 0 0 0 0 0 -14.9900 0.6994 -1.2855 H 0 0 0 0 0 0 0 0 0 0 0 0 -17.1966 -0.1685 -1.1246 H 0 0 0 0 0 0 0 0 0 0 0 0 -19.5843 -0.1837 -1.7129 H 0 0 0 0 0 0 0 0 0 0 0 0 -20.4896 1.3489 -3.3623 H 0 0 0 0 0 0 0 0 0 0 0 0 -18.9178 2.9724 -4.4598 H 0 0 0 0 0 0 0 0 0 0 0 0 -16.5026 2.9967 -3.8574 H 0 0 0 0 0 0 0 0 0 0 0 0 -12.7668 -0.8721 2.9987 H 0 0 0 0 0 0 0 0 0 0 0 0 -10.3686 -0.1641 3.9366 H 0 0 0 0 0 0 0 0 0 0 0 0 -11.8922 0.7032 3.8230 H 0 0 0 0 0 0 0 0 0 0 0 0 -10.4687 2.4843 3.7802 H 0 0 0 0 0 0 0 0 0 0 0 0 -9.1555 1.6681 2.9411 H 0 0 0 0 0 0 0 0 0 0 0 0 -11.9081 3.8441 1.3098 H 0 0 0 0 0 0 0 0 0 0 0 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0.6232 -2.7805 H 0 0 0 0 0 0 0 0 0 0 0 0 12.6626 -1.2569 -3.9606 H 0 0 0 0 0 0 0 0 0 0 0 0 11.0946 -1.7955 -3.3152 H 0 0 0 0 0 0 0 0 0 0 0 0 12.6463 -2.2895 -2.5099 H 0 0 0 0 0 0 0 0 0 0 0 0 13.8447 -0.8219 -1.3308 H 0 0 0 0 0 0 0 0 0 0 0 0 12.9707 -2.0005 0.3797 H 0 0 0 0 0 0 0 0 0 0 0 0 10.7699 -2.0738 -0.6040 H 0 0 0 0 0 0 0 0 0 0 0 0 10.0284 -2.5310 1.3192 H 0 0 0 0 0 0 0 0 0 0 0 0 13.4344 -0.0227 3.1714 H 0 0 0 0 0 0 0 0 0 0 0 0 12.7939 -1.6247 2.7904 H 0 0 0 0 0 0 0 0 0 0 0 0 14.3852 -1.0654 2.0614 H 0 0 0 0 0 0 0 0 0 0 0 0 15.1449 0.2140 -1.2328 H 0 0 0 0 0 0 0 0 0 0 0 0 17.1042 0.6334 -0.1979 H 0 0 0 0 0 0 0 0 0 0 0 0 18.2453 1.5424 1.7892 H 0 0 0 0 0 0 0 0 0 0 0 0 16.7535 0.7299 2.3529 H 0 0 0 0 0 0 0 0 0 0 0 0 16.8141 2.7585 3.2792 H 0 0 0 0 0 0 0 0 0 0 0 0 16.4354 3.5936 0.2022 H 0 0 0 0 0 0 0 0 0 0 0 0 17.0965 2.0328 -2.3345 H 0 0 0 0 0 0 0 0 0 0 0 0 14.3055 3.1220 -1.7046 H 0 0 0 0 0 0 0 0 0 0 0 0 15.3415 2.3095 -3.7881 H 0 0 0 0 0 0 0 0 0 0 0 0 15.6158 4.4817 -2.2928 H 0 0 0 0 0 0 0 0 0 0 0 0 18.5177 3.9508 -0.2280 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.5700 0.7424 -1.0707 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8346 1.1398 0.1632 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.1972 0.6903 0.6744 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 7 8 1 0 8 9 1 0 9 10 1 0 10 11 1 0 11 12 2 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 1 0 19 20 2 0 19 21 1 0 21 22 2 0 22 23 1 0 23 24 2 0 24 25 1 0 25 26 2 0 26 27 1 0 27 28 2 0 17 29 1 0 29 30 1 0 30 31 1 1 30 32 1 0 32 33 1 0 33 34 1 0 34 35 1 1 34 36 1 0 36 37 1 0 36 38 1 0 29 39 1 6 14 40 1 6 11 41 1 0 10 42 1 6 5 43 1 0 43 44 1 0 44 45 1 0 45 46 1 0 46 47 1 0 47 48 1 0 48 49 1 0 49 50 1 0 50 51 1 0 49 52 1 0 52 53 1 0 53 54 1 0 53 55 1 0 52 56 1 0 56 57 1 0 57 58 1 0 58 59 1 0 59 60 1 0 60 61 1 0 59 62 1 0 62 63 1 0 63 64 1 0 63 65 1 0 62 66 1 0 66 67 1 0 67 68 1 0 68 69 1 0 69 70 1 0 69 71 1 0 71 72 1 0 72 73 1 0 73 74 1 0 72 75 1 0 75 76 1 0 71 77 1 0 77 78 1 0 78 79 1 0 79 80 1 0 80 81 1 0 81 82 1 0 80 83 1 0 83 84 1 0 84 85 1 0 85 86 1 0 84 87 1 0 83 88 1 0 44 89 1 0 45 3 1 0 54 47 1 0 64 57 1 0 73 67 1 0 85 78 1 0 41 7 1 0 15 10 1 0 28 23 1 0 34 29 1 0 30 14 1 0 1 90 1 0 1 91 1 0 1 92 1 0 3 93 1 6 4 94 1 0 4 95 1 0 5 96 1 1 7 97 1 1 8 98 1 0 8 99 1 0 9100 1 0 9101 1 0 12102 1 0 13103 1 0 13104 1 0 15105 1 1 16106 1 0 16107 1 0 17108 1 6 21109 1 0 22110 1 0 24111 1 0 25112 1 0 26113 1 0 27114 1 0 28115 1 0 31116 1 0 32117 1 0 32118 1 0 33119 1 0 33120 1 0 35121 1 0 36122 1 6 37123 1 0 38124 1 0 38125 1 0 38126 1 0 39127 1 0 39128 1 0 39129 1 0 40130 1 0 41131 1 0 41132 1 0 42133 1 0 42134 1 0 42135 1 0 44136 1 1 45137 1 6 47138 1 6 48139 1 0 48140 1 0 49141 1 1 51142 1 0 51143 1 0 51144 1 0 52145 1 6 53146 1 6 55147 1 0 55148 1 0 55149 1 0 57150 1 6 58151 1 0 58152 1 0 59153 1 6 61154 1 0 61155 1 0 61156 1 0 62157 1 1 63158 1 1 65159 1 0 65160 1 0 65161 1 0 67162 1 1 69163 1 6 70164 1 0 70165 1 0 70166 1 0 71167 1 6 72168 1 1 73169 1 6 74170 1 0 76171 1 0 76172 1 0 76173 1 0 78174 1 6 80175 1 6 81176 1 0 81177 1 0 82178 1 0 83179 1 1 84180 1 6 85181 1 1 86182 1 0 87183 1 0 88184 1 0 89185 1 0 89186 1 0 89187 1 0 M END

Standard InCHIKey	BEAJFYKIOOQNTB-WTLBFJGFSA-N
Standard InCHI	InChI=1S/C64H98O25/c1-31-53(86-47-27-40(76-9)54(32(2)80-47)87-48-28-41(77-10)55(33(3)81-48)88-59-52(71)57(78-11)56(34(4)82-59)89-58-51(70)50(69)49(68)42(30-65)84-58)39(75-8)26-46(79-31)83-38-20-21-60(6)37(25-38)19-22-63(73)43(60)29-44(85-45(67)18-17-36-15-13-12-14-16-36)61(7)62(72,35(5)66)23-24-64(61,63)74/h12-19,31-35,38-44,46-59,65-66,68-74H,20-30H2,1-11H3/b18-17+/t31-,32-,33-,34-,35+,38+,39+,40+,41-,42-,43-,44-,46+,47+,48+,49-,50+,51-,52-,53-,54-,55-,56-,57+,58+,59+,60+,61-,62-,63+,64-/m1/s1
SMILES	CO[C@H]1C[C@H](O[C@H]2CC[C@]3(C(=CC[C@@]4([C@@H]3C[C@@H](OC(=O)/C=C/c3ccccc3)[C@]3([C@]4(O)CC[C@@]3(O)[C@@H](O)C)C)O)C2)C)O[C@@H]([C@H]1O[C@H]1C[C@H](OC)[C@@H]([C@H](O1)C)O[C@H]1C[C@@H](OC)[C@@H]([C@H](O1)C)O[C@@H]1O[C@H](C)[C@H]([C@H]([C@H]1O)OC)O[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O)C

Calculated Properties

Physi-Chem Properties

MedChem Properties

ADMET Properties (ADMETlab3.0)

ADMET: Absorption

ADMET: Distribution

ADMET: Metabolism

ADMET: Excretion

ADMET: Toxicity

Species Source

Organism ID	Organism Name	Taxonomy Level	Family	SuperKingdom	Isolation Part	Collection Location	Collection Time	Reference
NPO33108	leptadenia hastata	Species	Apocynaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[7623046]
NPO33108	leptadenia hastata	Species	Apocynaceae	Eukaryota	n.a.	n.a.	n.a.	PMID[8786361]

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
Activity	6

Activity Type	# Activity
Cell line	6

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
NPT80	Cell line	Raji	Homo sapiens	Activity	=	59.0	%	PMID[24941130]
NPT80	Cell line	Raji	Homo sapiens	Activity	=	33.0	%	PMID[24992075]
NPT80	Cell line	Raji	Homo sapiens	Activity	=	16.0	%	PMID[24992075]
NPT80	Cell line	Raji	Homo sapiens	Activity	=	18.0	%	PMID[24992075]
NPT80	Cell line	Raji	Homo sapiens	Activity	=	10.0	%	PMID[24992075]

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 NPC70236 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	12620
0.1-0.2	31963
0.2-0.3	4862
0.3-0.4	354
0.4-0.5	18
0.5-0.6	14
0.6-0.7	6
0.7-0.8	0
0.8-0.85	9
0.85-0.9	1
0.9-0.95	3
0.95-1	0

Similarity Score	Similarity Level	Natural Product ID
0.9346	High Similarity	NPC475447
0.9048	High Similarity	NPC473641
0.9048	High Similarity	NPC475300
0.8879	High Similarity	NPC476092
0.8482	Intermediate Similarity	NPC473797
0.8333	Intermediate Similarity	NPC475175
0.8257	Intermediate Similarity	NPC475218
0.8137	Intermediate Similarity	NPC475358
0.8137	Intermediate Similarity	NPC473566
0.8036	Intermediate Similarity	NPC475437
0.8036	Intermediate Similarity	NPC475464
0.8017	Intermediate Similarity	NPC475531
0.8017	Intermediate Similarity	NPC475198
0.7963	Intermediate Similarity	NPC474564
0.7724	Intermediate Similarity	NPC476090
0.7589	Intermediate Similarity	NPC475613
0.729	Intermediate Similarity	NPC102015
0.7168	Intermediate Similarity	NPC475536
0.7054	Intermediate Similarity	NPC165234
0.7054	Intermediate Similarity	NPC481659
0.7054	Intermediate Similarity	NPC271687
0.6695	Remote Similarity	NPC481654
0.6667	Remote Similarity	NPC481661
0.6667	Remote Similarity	NPC481655
0.6667	Remote Similarity	NPC481650
0.6639	Remote Similarity	NPC475567
0.6172	Remote Similarity	NPC481660
0.5614	Remote Similarity	NPC473519
0.5484	Remote Similarity	NPC473468
0.5462	Remote Similarity	NPC473805
0.5439	Remote Similarity	NPC481657
0.5424	Remote Similarity	NPC481658
0.5424	Remote Similarity	NPC79250
0.5424	Remote Similarity	NPC290746
0.542	Remote Similarity	NPC478508
0.542	Remote Similarity	NPC478510
0.542	Remote Similarity	NPC478509
0.5414	Remote Similarity	NPC481648
0.536	Remote Similarity	NPC481662
0.5267	Remote Similarity	NPC473557
0.5042	Remote Similarity	NPC479287

Similar Clinical/Approved Drugs

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

● The left chart: Distribution of similarity level between NPC70236 and all drugs/candidates.
● The right table: Most similar clinical/approved drugs (Tc>=0.5 or Top200).

range	Tanimoto Coefficient
0-0.1	4949
0.1-0.2	4127
0.2-0.3	72
0.3-0.4	2
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