Structure

Physi-Chem Properties

Molecular Weight:  244.16
Volume:  262.565
LogP:  1.43
LogD:  1.905
LogS:  -2.209
# Rotatable Bonds:  1
TPSA:  58.88
# H-Bond Aceptor:  3
# H-Bond Donor:  3
# Rings:  3
# Heavy Atoms:  3

MedChem Properties

QED Drug-Likeness Score:  0.742
Synthetic Accessibility Score:  5.181
Fsp3:  0.533
Lipinski Rule-of-5:  Accepted
Pfizer Rule:  Accepted
GSK Rule:  Accepted
BMS Rule:  0
Golden Triangle Rule:  Accepted
Chelating Alert:  0
PAINS Alert:  0

ADMET Properties (ADMETlab2.0)

ADMET: Absorption

Caco-2 Permeability:  -5.581
MDCK Permeability:  4.553418875730131e-06
Pgp-inhibitor:  0.0
Pgp-substrate:  0.992
Human Intestinal Absorption (HIA):  0.005
20% Bioavailability (F20%):  0.003
30% Bioavailability (F30%):  0.019

ADMET: Distribution

Blood-Brain-Barrier Penetration (BBB):  0.925
Plasma Protein Binding (PPB):  66.73539733886719%
Volume Distribution (VD):  0.766
Pgp-substrate:  40.45697021484375%

ADMET: Metabolism

CYP1A2-inhibitor:  0.192
CYP1A2-substrate:  0.826
CYP2C19-inhibitor:  0.214
CYP2C19-substrate:  0.259
CYP2C9-inhibitor:  0.163
CYP2C9-substrate:  0.399
CYP2D6-inhibitor:  0.101
CYP2D6-substrate:  0.822
CYP3A4-inhibitor:  0.755
CYP3A4-substrate:  0.291

ADMET: Excretion

Clearance (CL):  5.203
Half-life (T1/2):  0.832

ADMET: Toxicity

hERG Blockers:  0.082
Human Hepatotoxicity (H-HT):  0.38
Drug-inuced Liver Injury (DILI):  0.065
AMES Toxicity:  0.069
Rat Oral Acute Toxicity:  0.78
Maximum Recommended Daily Dose:  0.921
Skin Sensitization:  0.372
Carcinogencity:  0.126
Eye Corrosion:  0.006
Eye Irritation:  0.04
Respiratory Toxicity:  0.942

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General Info & Identifiers & Properties  
Structure MOL file  
Source Organisms  
Biological Activities  
Similar NPs/Drugs  

  Natural Product: NPC159319

Natural Product ID:  NPC159319
Common Name*:   SBVXFBLZBDSLKP-JNIYBQFBSA-N
IUPAC Name:   n.a.
Synonyms:  
Standard InCHIKey:  SBVXFBLZBDSLKP-JNIYBQFBSA-N
Standard InCHI:  InChI=1S/C15H20N2O/c1-3-11-10-6-9(2)8-15(11,16)12-4-5-14(18)17-13(12)7-10/h3-5,9-11H,1,6-8,16H2,2H3,(H,17,18)/t9-,10+,11-,15-/m1/s1
SMILES:  C=C[C@@H]1[C@H]2C[C@H](C[C@]1(N)c1c(C2)nc(cc1)O)C
Synthetic Gene Cluster:   n.a.
ChEMBL Identifier:   CHEMBL2409143
PubChem CID:   72193163
Chemical Classification**:  
  • CHEMONTID:0000000 [Organic compounds]
    • [CHEMONTID:0000002] Organoheterocyclic compounds
      • [CHEMONTID:0001253] Quinolines and derivatives
        • [CHEMONTID:0000056] Quinolones and derivatives

*Note: the InCHIKey will be temporarily assigned as the "Common Name" if no IUPAC name or alternative short name is available.
**Note: the Chemical Classification was calculated by NPClassifier Version 1.5. Reference: PMID:34662515.

  Species Source

Organism ID Organism Name Taxonomy Level Family SuperKingdom Isolation Part Collection Location Collection Time Reference
NPO32769 lycopodiastrum casuarinoides Species Lycopodiaceae Eukaryota n.a. n.a. n.a. PMID[23941108]

☑ 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 NP ID 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

Target ID Target Type Target Name Target Organism Activity Type Activity Relation Value Unit Reference
NPT610 Others Molecular identity unknown Activity = 12.02 % PMID[480780]
NPT610 Others Molecular identity unknown Activity = 55.47 % PMID[480780]
NPT610 Others Molecular identity unknown Activity = 49.06 % PMID[480780]

☑ Note for Activity Records:
☉ The quantitative biological activities were primarily integrated from ChEMBL (Version-30) database and were also directly collected from PubMed literature. PubMed PMID was provided as the reference link for each activity record.

  Chemically structural similarity: I. Similar Active Natural Products in NPASS

Top-200 similar NPs were calculated against the active-NP-set (includes 4,3285 NPs with experimentally-derived bioactivity available in NPASS)

Similarity level is defined by Tanimoto coefficient (Tc) between two molecules. Tc lies between [0, 1] where '1' indicates the highest similarity. What is Tanimoto coefficient

●  The left chart: Distribution of similarity level between NPC159319 and all remaining natural products in the NPASS database.
●  The right table: Most similar natural products (Tc>=0.56 or Top200).

Similarity Score Similarity Level Natural Product ID
0.9867 High Similarity NPC32028
0.98 High Similarity NPC47298
0.98 High Similarity NPC315214
0.9487 High Similarity NPC259545
0.9484 High Similarity NPC126481
0.925 High Similarity NPC232340
0.9119 High Similarity NPC471294
0.8735 High Similarity NPC133306
0.8605 High Similarity NPC45850
0.848 Intermediate Similarity NPC183805
0.8312 Intermediate Similarity NPC60553
0.7988 Intermediate Similarity NPC84508
0.7987 Intermediate Similarity NPC161292
0.7907 Intermediate Similarity NPC88363
0.7853 Intermediate Similarity NPC246700
0.7853 Intermediate Similarity NPC128751
0.7844 Intermediate Similarity NPC473057
0.7809 Intermediate Similarity NPC469497
0.7809 Intermediate Similarity NPC106833
0.7797 Intermediate Similarity NPC206186
0.7791 Intermediate Similarity NPC153769
0.7785 Intermediate Similarity NPC245657
0.7784 Intermediate Similarity NPC94943
0.7771 Intermediate Similarity NPC212535
0.7727 Intermediate Similarity NPC190007
0.7722 Intermediate Similarity NPC280853
0.7701 Intermediate Similarity NPC72980
0.7674 Intermediate Similarity NPC474409
0.7673 Intermediate Similarity NPC285016
0.7658 Intermediate Similarity NPC471596
0.7657 Intermediate Similarity NPC478032
0.7561 Intermediate Similarity NPC288445
0.7554 Intermediate Similarity NPC153042
0.7547 Intermediate Similarity NPC471594
0.7531 Intermediate Similarity NPC471598
0.7529 Intermediate Similarity NPC97367
0.75 Intermediate Similarity NPC44161
0.7486 Intermediate Similarity NPC288943
0.7486 Intermediate Similarity NPC476319
0.7485 Intermediate Similarity NPC471178
0.7472 Intermediate Similarity NPC19679
0.7471 Intermediate Similarity NPC124542
0.7471 Intermediate Similarity NPC471177
0.7471 Intermediate Similarity NPC59779
0.7468 Intermediate Similarity NPC278451
0.7459 Intermediate Similarity NPC474188
0.7443 Intermediate Similarity NPC283152
0.744 Intermediate Similarity NPC141353
0.7435 Intermediate Similarity NPC477111
0.7433 Intermediate Similarity NPC249040
0.7432 Intermediate Similarity NPC114335
0.7432 Intermediate Similarity NPC280964
0.7432 Intermediate Similarity NPC141915
0.7429 Intermediate Similarity NPC303225
0.7425 Intermediate Similarity NPC26872
0.7414 Intermediate Similarity NPC105758
0.7414 Intermediate Similarity NPC476686
0.7414 Intermediate Similarity NPC476688
0.7396 Intermediate Similarity NPC26850
0.7371 Intermediate Similarity NPC208060
0.7368 Intermediate Similarity NPC475070
0.7366 Intermediate Similarity NPC243834
0.7366 Intermediate Similarity NPC70956
0.7348 Intermediate Similarity NPC171171
0.7348 Intermediate Similarity NPC314573
0.7344 Intermediate Similarity NPC470931
0.7341 Intermediate Similarity NPC98187
0.734 Intermediate Similarity NPC329747
0.7333 Intermediate Similarity NPC320394
0.7333 Intermediate Similarity NPC204717
0.733 Intermediate Similarity NPC477113
0.7316 Intermediate Similarity NPC223427
0.7308 Intermediate Similarity NPC66083
0.7299 Intermediate Similarity NPC278874
0.7293 Intermediate Similarity NPC314002
0.7278 Intermediate Similarity NPC220765
0.7263 Intermediate Similarity NPC475085
0.7263 Intermediate Similarity NPC291535
0.7263 Intermediate Similarity NPC475112
0.7259 Intermediate Similarity NPC469928
0.7259 Intermediate Similarity NPC330009
0.7256 Intermediate Similarity NPC470403
0.7256 Intermediate Similarity NPC470404
0.7256 Intermediate Similarity NPC470394
0.7254 Intermediate Similarity NPC475910
0.7253 Intermediate Similarity NPC194040
0.7249 Intermediate Similarity NPC329793
0.7245 Intermediate Similarity NPC478074
0.7243 Intermediate Similarity NPC99666
0.7243 Intermediate Similarity NPC324149
0.7241 Intermediate Similarity NPC108469
0.7238 Intermediate Similarity NPC62069
0.7232 Intermediate Similarity NPC329688
0.7232 Intermediate Similarity NPC189812
0.7228 Intermediate Similarity NPC95783
0.7228 Intermediate Similarity NPC3715
0.7222 Intermediate Similarity NPC144114
0.7216 Intermediate Similarity NPC476116
0.7216 Intermediate Similarity NPC158129
0.7213 Intermediate Similarity NPC46580
0.7213 Intermediate Similarity NPC254762
0.7204 Intermediate Similarity NPC329541
0.7202 Intermediate Similarity NPC193777
0.72 Intermediate Similarity NPC154293
0.7198 Intermediate Similarity NPC42591
0.7172 Intermediate Similarity NPC183407
0.7169 Intermediate Similarity NPC470395
0.7168 Intermediate Similarity NPC224632
0.7168 Intermediate Similarity NPC177404
0.7159 Intermediate Similarity NPC473764
0.7159 Intermediate Similarity NPC314940
0.7135 Intermediate Similarity NPC312872
0.7128 Intermediate Similarity NPC205403
0.7127 Intermediate Similarity NPC477891
0.712 Intermediate Similarity NPC267423
0.7118 Intermediate Similarity NPC36168
0.7111 Intermediate Similarity NPC67659
0.7107 Intermediate Similarity NPC294620
0.7107 Intermediate Similarity NPC48353
0.7105 Intermediate Similarity NPC476167
0.7105 Intermediate Similarity NPC128823
0.7102 Intermediate Similarity NPC317430
0.709 Intermediate Similarity NPC77555
0.7088 Intermediate Similarity NPC176127
0.7085 Intermediate Similarity NPC477110
0.7083 Intermediate Similarity NPC257142
0.7081 Intermediate Similarity NPC242928
0.7079 Intermediate Similarity NPC34508
0.7074 Intermediate Similarity NPC195314
0.7074 Intermediate Similarity NPC276517
0.7069 Intermediate Similarity NPC16667
0.7068 Intermediate Similarity NPC11017
0.7065 Intermediate Similarity NPC61350
0.7062 Intermediate Similarity NPC280548
0.7056 Intermediate Similarity NPC9894
0.7056 Intermediate Similarity NPC184964
0.7056 Intermediate Similarity NPC208284
0.7056 Intermediate Similarity NPC220337
0.7053 Intermediate Similarity NPC306376
0.7053 Intermediate Similarity NPC192315
0.7049 Intermediate Similarity NPC84478
0.7047 Intermediate Similarity NPC476098
0.7044 Intermediate Similarity NPC162748
0.7037 Intermediate Similarity NPC70259
0.7037 Intermediate Similarity NPC472193
0.7035 Intermediate Similarity NPC285469
0.7033 Intermediate Similarity NPC314394
0.7029 Intermediate Similarity NPC118511
0.7016 Intermediate Similarity NPC476175
0.7011 Intermediate Similarity NPC131718
0.701 Intermediate Similarity NPC164374
0.701 Intermediate Similarity NPC137929
0.7005 Intermediate Similarity NPC469390
0.7005 Intermediate Similarity NPC471304
0.7005 Intermediate Similarity NPC5145
0.7 Intermediate Similarity NPC134586
0.7 Intermediate Similarity NPC150048
0.7 Intermediate Similarity NPC203754
0.699 Remote Similarity NPC18348
0.6989 Remote Similarity NPC32771
0.6984 Remote Similarity NPC43787
0.6984 Remote Similarity NPC205934
0.6983 Remote Similarity NPC472123
0.6983 Remote Similarity NPC313791
0.6978 Remote Similarity NPC198339
0.6974 Remote Similarity NPC304183
0.6974 Remote Similarity NPC474145
0.6974 Remote Similarity NPC476106
0.6974 Remote Similarity NPC475841
0.6966 Remote Similarity NPC164664
0.6965 Remote Similarity NPC476041
0.6965 Remote Similarity NPC304926
0.6963 Remote Similarity NPC72211
0.6961 Remote Similarity NPC96890
0.6961 Remote Similarity NPC211997
0.6959 Remote Similarity NPC477135
0.6959 Remote Similarity NPC284348
0.6947 Remote Similarity NPC242209
0.6943 Remote Similarity NPC476044
0.6941 Remote Similarity NPC124005
0.6936 Remote Similarity NPC184476
0.6932 Remote Similarity NPC476118
0.6931 Remote Similarity NPC289786
0.6927 Remote Similarity NPC32200
0.6927 Remote Similarity NPC280714
0.6923 Remote Similarity NPC470500
0.6923 Remote Similarity NPC472168
0.6923 Remote Similarity NPC270009
0.6919 Remote Similarity NPC473189
0.6914 Remote Similarity NPC120798
0.6911 Remote Similarity NPC156704
0.6907 Remote Similarity NPC135887
0.6907 Remote Similarity NPC199277
0.6906 Remote Similarity NPC56618
0.6905 Remote Similarity NPC242556
0.6904 Remote Similarity NPC39679
0.6901 Remote Similarity NPC33421
0.6897 Remote Similarity NPC116573
0.6895 Remote Similarity NPC131017
0.6889 Remote Similarity NPC97525

  Chemically structural similarity: II. Similar Clinical/Approved Drugs

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

●  The left chart: Distribution of similarity level between NPC159319 and all drugs/candidates.
●  The right table: Most similar clinical/approved drugs (Tc>=0.56 or Top200).

Similarity Score Similarity Level Drug ID Developmental Stage
0.98 High Similarity NPD1685 Approved
0.98 High Similarity NPD1684 Approved
0.8212 Intermediate Similarity NPD5497 Clinical (unspecified phase)
0.8187 Intermediate Similarity NPD5522 Clinical (unspecified phase)
0.7791 Intermediate Similarity NPD6476 Clinical (unspecified phase)
0.7791 Intermediate Similarity NPD6158 Phase 2
0.7765 Intermediate Similarity NPD1325 Approved
0.7765 Intermediate Similarity NPD1326 Approved
0.7705 Intermediate Similarity NPD7889 Clinical (unspecified phase)
0.7692 Intermediate Similarity NPD925 Approved
0.7692 Intermediate Similarity NPD926 Approved
0.7683 Intermediate Similarity NPD2882 Phase 1
0.7644 Intermediate Similarity NPD6159 Phase 2
0.7568 Intermediate Similarity NPD2176 Approved
0.7568 Intermediate Similarity NPD2175 Phase 3
0.7568 Intermediate Similarity NPD2177 Approved
0.7526 Intermediate Similarity NPD2916 Discontinued
0.75 Intermediate Similarity NPD5936 Approved
0.75 Intermediate Similarity NPD1503 Clinical (unspecified phase)
0.75 Intermediate Similarity NPD5939 Approved
0.75 Intermediate Similarity NPD2383 Phase 1
0.7487 Intermediate Similarity NPD4511 Phase 1
0.7469 Intermediate Similarity NPD3525 Discontinued
0.7446 Intermediate Similarity NPD6491 Clinical (unspecified phase)
0.7442 Intermediate Similarity NPD425 Approved
0.7442 Intermediate Similarity NPD424 Approved
0.7416 Intermediate Similarity NPD4204 Approved
0.7416 Intermediate Similarity NPD4203 Approved
0.7414 Intermediate Similarity NPD1078 Clinical (unspecified phase)
0.7389 Intermediate Similarity NPD6344 Clinical (unspecified phase)
0.738 Intermediate Similarity NPD4118 Clinical (unspecified phase)
0.7356 Intermediate Similarity NPD7474 Suspended
0.7351 Intermediate Similarity NPD3810 Clinical (unspecified phase)
0.733 Intermediate Similarity NPD5065 Approved
0.733 Intermediate Similarity NPD6492 Phase 2
0.7326 Intermediate Similarity NPD863 Approved
0.7326 Intermediate Similarity NPD861 Approved
0.7326 Intermediate Similarity NPD862 Approved
0.7316 Intermediate Similarity NPD4044 Discontinued
0.7303 Intermediate Similarity NPD3920 Phase 2
0.7301 Intermediate Similarity NPD1592 Phase 3
0.7299 Intermediate Similarity NPD2781 Approved
0.7297 Intermediate Similarity NPD5575 Clinical (unspecified phase)
0.7292 Intermediate Similarity NPD6290 Phase 2
0.7288 Intermediate Similarity NPD2381 Approved
0.7288 Intermediate Similarity NPD2380 Approved
0.7288 Intermediate Similarity NPD5100 Phase 3
0.7288 Intermediate Similarity NPD2382 Approved
0.7283 Intermediate Similarity NPD2782 Approved
0.7283 Intermediate Similarity NPD2780 Approved
0.7273 Intermediate Similarity NPD7418 Discontinued
0.7254 Intermediate Similarity NPD6376 Discontinued
0.7251 Intermediate Similarity NPD604 Clinical (unspecified phase)
0.7251 Intermediate Similarity NPD5255 Approved
0.7238 Intermediate Similarity NPD5083 Clinical (unspecified phase)
0.7234 Intermediate Similarity NPD2727 Phase 2
0.7231 Intermediate Similarity NPD4502 Phase 2
0.7212 Intermediate Similarity NPD3813 Approved
0.7202 Intermediate Similarity NPD3930 Clinical (unspecified phase)
0.7198 Intermediate Similarity NPD2762 Phase 2
0.7196 Intermediate Similarity NPD8396 Approved
0.7196 Intermediate Similarity NPD8395 Approved
0.7193 Intermediate Similarity NPD4671 Clinical (unspecified phase)
0.7193 Intermediate Similarity NPD4669 Clinical (unspecified phase)
0.7193 Intermediate Similarity NPD4670 Clinical (unspecified phase)
0.7191 Intermediate Similarity NPD6375 Clinical (unspecified phase)
0.7186 Intermediate Similarity NPD4703 Approved
0.7186 Intermediate Similarity NPD4702 Approved
0.7184 Intermediate Similarity NPD5744 Clinical (unspecified phase)
0.7181 Intermediate Similarity NPD7948 Phase 1
0.7151 Intermediate Similarity NPD3404 Approved
0.715 Intermediate Similarity NPD3932 Clinical (unspecified phase)
0.7143 Intermediate Similarity NPD4554 Clinical (unspecified phase)
0.7127 Intermediate Similarity NPD7414 Clinical (unspecified phase)
0.7126 Intermediate Similarity NPD444 Approved
0.7111 Intermediate Similarity NPD3417 Phase 1
0.7105 Intermediate Similarity NPD3814 Phase 1
0.7083 Intermediate Similarity NPD3928 Approved
0.7083 Intermediate Similarity NPD3931 Approved
0.7074 Intermediate Similarity NPD6590 Discontinued
0.7062 Intermediate Similarity NPD5530 Phase 1
0.7044 Intermediate Similarity NPD947 Approved
0.7043 Intermediate Similarity NPD6281 Approved
0.7022 Intermediate Similarity NPD5934 Clinical (unspecified phase)
0.7015 Intermediate Similarity NPD8109 Clinical (unspecified phase)
0.7006 Intermediate Similarity NPD6872 Clinical (unspecified phase)
0.6995 Remote Similarity NPD6975 Discontinued
0.699 Remote Similarity NPD7671 Approved
0.699 Remote Similarity NPD7672 Approved
0.6983 Remote Similarity NPD3224 Phase 2
0.6977 Remote Similarity NPD5257 Clinical (unspecified phase)
0.6971 Remote Similarity NPD972 Clinical (unspecified phase)
0.6961 Remote Similarity NPD5751 Clinical (unspecified phase)
0.6959 Remote Similarity NPD9706 Clinical (unspecified phase)
0.6959 Remote Similarity NPD6991 Approved
0.6957 Remote Similarity NPD1251 Discontinued
0.6946 Remote Similarity NPD3717 Discontinued
0.6944 Remote Similarity NPD9690 Approved
0.694 Remote Similarity NPD7867 Phase 1
0.6939 Remote Similarity NPD7222 Phase 2
0.6935 Remote Similarity NPD3330 Phase 1
0.6932 Remote Similarity NPD5140 Approved
0.6932 Remote Similarity NPD5138 Approved
0.6923 Remote Similarity NPD1620 Clinical (unspecified phase)
0.6923 Remote Similarity NPD5398 Clinical (unspecified phase)
0.6919 Remote Similarity NPD4889 Approved
0.6919 Remote Similarity NPD6227 Discontinued
0.6915 Remote Similarity NPD5912 Clinical (unspecified phase)
0.6915 Remote Similarity NPD5913 Phase 3
0.6914 Remote Similarity NPD9705 Discontinued
0.6914 Remote Similarity NPD112 Approved
0.6912 Remote Similarity NPD7726 Phase 1
0.691 Remote Similarity NPD2844 Phase 3
0.6901 Remote Similarity NPD4462 Approved
0.6901 Remote Similarity NPD4463 Approved
0.69 Remote Similarity NPD3243 Approved
0.6895 Remote Similarity NPD6251 Discontinued
0.689 Remote Similarity NPD1254 Approved
0.689 Remote Similarity NPD1255 Approved
0.689 Remote Similarity NPD1253 Approved
0.689 Remote Similarity NPD1256 Approved
0.6889 Remote Similarity NPD4112 Clinical (unspecified phase)
0.6884 Remote Similarity NPD6220 Phase 3
0.6878 Remote Similarity NPD3924 Approved
0.6878 Remote Similarity NPD6569 Phase 2
0.6878 Remote Similarity NPD3923 Approved
0.6878 Remote Similarity NPD3921 Approved
0.6878 Remote Similarity NPD3922 Approved
0.6875 Remote Similarity NPD5352 Clinical (unspecified phase)
0.6872 Remote Similarity NPD4724 Clinical (unspecified phase)
0.6859 Remote Similarity NPD6594 Discontinued
0.6859 Remote Similarity NPD5512 Phase 3
0.6853 Remote Similarity NPD5429 Discontinued
0.685 Remote Similarity NPD2794 Discontinued
0.6845 Remote Similarity NPD6506 Clinical (unspecified phase)
0.6845 Remote Similarity NPD6141 Clinical (unspecified phase)
0.6842 Remote Similarity NPD1038 Approved
0.6839 Remote Similarity NPD6026 Approved
0.6832 Remote Similarity NPD6803 Clinical (unspecified phase)
0.6828 Remote Similarity NPD3082 Discontinued
0.6828 Remote Similarity NPD6610 Clinical (unspecified phase)
0.6825 Remote Similarity NPD5040 Clinical (unspecified phase)
0.6824 Remote Similarity NPD6148 Clinical (unspecified phase)
0.6821 Remote Similarity NPD5669 Clinical (unspecified phase)
0.6818 Remote Similarity NPD9398 Clinical (unspecified phase)
0.6811 Remote Similarity NPD5596 Phase 2
0.6809 Remote Similarity NPD6965 Clinical (unspecified phase)
0.6807 Remote Similarity NPD852 Discontinued
0.6802 Remote Similarity NPD4305 Clinical (unspecified phase)
0.68 Remote Similarity NPD2581 Approved
0.68 Remote Similarity NPD2582 Approved
0.6796 Remote Similarity NPD6824 Clinical (unspecified phase)
0.6791 Remote Similarity NPD5256 Discontinued
0.6788 Remote Similarity NPD7419 Discontinued
0.6786 Remote Similarity NPD4886 Phase 2
0.6786 Remote Similarity NPD5020 Approved
0.6768 Remote Similarity NPD7453 Approved
0.6768 Remote Similarity NPD7452 Approved
0.6761 Remote Similarity NPD1554 Clinical (unspecified phase)
0.6754 Remote Similarity NPD5428 Discontinued
0.6754 Remote Similarity NPD9695 Approved
0.6754 Remote Similarity NPD6361 Phase 2
0.6754 Remote Similarity NPD1304 Clinical (unspecified phase)
0.6754 Remote Similarity NPD802 Phase 2
0.6751 Remote Similarity NPD4122 Approved
0.6751 Remote Similarity NPD4039 Approved
0.6751 Remote Similarity NPD4034 Approved
0.6751 Remote Similarity NPD4037 Approved
0.6751 Remote Similarity NPD31 Approved
0.6751 Remote Similarity NPD4795 Phase 2
0.6751 Remote Similarity NPD4038 Approved
0.6751 Remote Similarity NPD4033 Approved
0.6751 Remote Similarity NPD32 Approved
0.6751 Remote Similarity NPD4035 Approved
0.6751 Remote Similarity NPD6138 Clinical (unspecified phase)
0.6751 Remote Similarity NPD4036 Approved
0.6743 Remote Similarity NPD2789 Approved
0.674 Remote Similarity NPD5680 Clinical (unspecified phase)
0.6737 Remote Similarity NPD6630 Clinical (unspecified phase)
0.6736 Remote Similarity NPD5003 Discontinued
0.6735 Remote Similarity NPD6208 Discontinued
0.6734 Remote Similarity NPD5658 Approved
0.6733 Remote Similarity NPD2616 Phase 3
0.6733 Remote Similarity NPD2615 Phase 3
0.6725 Remote Similarity NPD1683 Approved
0.6725 Remote Similarity NPD7469 Discontinued
0.6723 Remote Similarity NPD5599 Discontinued
0.6722 Remote Similarity NPD5021 Discontinued
0.672 Remote Similarity NPD9714 Clinical (unspecified phase)
0.6719 Remote Similarity NPD5975 Clinical (unspecified phase)
0.6718 Remote Similarity NPD1739 Approved
0.6718 Remote Similarity NPD484 Approved
0.6718 Remote Similarity NPD1740 Approved
0.6718 Remote Similarity NPD6389 Clinical (unspecified phase)
0.6715 Remote Similarity NPD7219 Approved
0.6715 Remote Similarity NPD7221 Approved
0.6708 Remote Similarity NPD9284 Approved
0.6708 Remote Similarity NPD9080 Approved
0.6707 Remote Similarity NPD2323 Clinical (unspecified phase)
0.6703 Remote Similarity NPD6452 Discontinued

  Bioactivity similarity: Similar Natural Products in NPASS

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