Drug Information

Drug ID:  NPD4970
Drug Name:  Elzasonan
Molecular Formula:  C22H23Cl2N3OS
Canonical SMILES:  CN1CCN(CC1)c1ccccc1/C=C1/SCCN(C1=O)c1ccc(c(c1)Cl)Cl
Standard InCHI:  InChI=1S/C22H23Cl2N3OS/c1-25-8-10-26(11-9-25)20-5-3-2-4-16(20)14-21-22(28)27(12-13-29-21)17-6-7-18(23)19(24)15-17/h2-7,14-15H,8-13H2,1H3/b21-14+
Standard InCHIKey:  LHYMPSWMHXUWSK-KGENOOAVSA-N
Max Developmental Stage:  Phase 2
Max Developmental Stage Source:  ChEMBL

  Structural Similarity Between NPASS Natural Products and NPD4970

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
Tanimoto coefficient is calculated based on PubChem 881-bit substructure fingerprints.


  Similar Natural Products

High Similarity Level: Tc>=0.85; Intermediate Similarity Level: 0.7 <= Tc < 0.85; Remote Similarity Level: 0.65 <= Tc < 0.7

Similarity Level Similarity Score Natural Product ID
Intermediate Similarity 0.7368 NPC325599
Remote Similarity 0.6645 NPC473417
Remote Similarity 0.6619 NPC291610
Remote Similarity 0.6522 NPC469560
Remote Similarity 0.6478 NPC313352
Remote Similarity 0.6447 NPC475915
Remote Similarity 0.6442 NPC470301
Remote Similarity 0.638 NPC130251
Remote Similarity 0.6358 NPC228515
Remote Similarity 0.634 NPC257490
Remote Similarity 0.6301 NPC477887
Remote Similarity 0.6296 NPC471123
Remote Similarity 0.6275 NPC316582
Remote Similarity 0.6273 NPC316104
Remote Similarity 0.6273 NPC162417
Remote Similarity 0.6272 NPC109787
Remote Similarity 0.6257 NPC117032
Remote Similarity 0.6209 NPC177684
Remote Similarity 0.6209 NPC226143
Remote Similarity 0.6209 NPC291962
Remote Similarity 0.6169 NPC258531
Remote Similarity 0.6169 NPC161956
Remote Similarity 0.6169 NPC112373
Remote Similarity 0.6159 NPC473661
Remote Similarity 0.6149 NPC53044
Remote Similarity 0.6145 NPC301760
Remote Similarity 0.6145 NPC22082
Remote Similarity 0.6145 NPC186284
Remote Similarity 0.6139 NPC252794
Remote Similarity 0.6135 NPC300299
Remote Similarity 0.6133 NPC296163
Remote Similarity 0.6125 NPC187231
Remote Similarity 0.6105 NPC66936
Remote Similarity 0.6101 NPC469949
Remote Similarity 0.6078 NPC192209
Remote Similarity 0.6078 NPC313449
Remote Similarity 0.6071 NPC469537
Remote Similarity 0.6065 NPC317564
Remote Similarity 0.6056 NPC475248
Remote Similarity 0.6056 NPC63047
Remote Similarity 0.6054 NPC20322
Remote Similarity 0.6047 NPC473329
Remote Similarity 0.6038 NPC250476
Remote Similarity 0.6024 NPC83214
Remote Similarity 0.6022 NPC91895
Remote Similarity 0.6014 NPC75496
Remote Similarity 0.6012 NPC243756
Remote Similarity 0.6012 NPC154602
Remote Similarity 0.5988 NPC231382
Remote Similarity 0.5987 NPC268534
Remote Similarity 0.5974 NPC31651
Remote Similarity 0.5952 NPC471164
Remote Similarity 0.5934 NPC116961
Remote Similarity 0.5932 NPC222029
Remote Similarity 0.5922 NPC194881
Remote Similarity 0.5921 NPC187036
Remote Similarity 0.5918 NPC473418
Remote Similarity 0.5917 NPC238499
Remote Similarity 0.5912 NPC17497
Remote Similarity 0.5912 NPC305602
Remote Similarity 0.5909 NPC125416
Remote Similarity 0.5901 NPC476950
Remote Similarity 0.5899 NPC276085
Remote Similarity 0.5889 NPC478182
Remote Similarity 0.5889 NPC328270
Remote Similarity 0.5872 NPC470440
Remote Similarity 0.587 NPC242269
Remote Similarity 0.5862 NPC326792
Remote Similarity 0.586 NPC279385
Remote Similarity 0.586 NPC179605
Remote Similarity 0.5848 NPC470822
Remote Similarity 0.5844 NPC288232
Remote Similarity 0.5838 NPC478186
Remote Similarity 0.5823 NPC103292
Remote Similarity 0.5817 NPC57051
Remote Similarity 0.5812 NPC17273
Remote Similarity 0.5812 NPC135601
Remote Similarity 0.5812 NPC141612
Remote Similarity 0.5808 NPC267508
Remote Similarity 0.5802 NPC478079
Remote Similarity 0.58 NPC302790
Remote Similarity 0.5799 NPC315051
Remote Similarity 0.5798 NPC286994
Remote Similarity 0.5797 NPC53492
Remote Similarity 0.5795 NPC122106
Remote Similarity 0.5795 NPC285381
Remote Similarity 0.5789 NPC308197
Remote Similarity 0.5787 NPC476464
Remote Similarity 0.5786 NPC39818
Remote Similarity 0.5765 NPC471574
Remote Similarity 0.5765 NPC2823
Remote Similarity 0.5765 NPC315348
Remote Similarity 0.5765 NPC32002
Remote Similarity 0.5763 NPC478076
Remote Similarity 0.5758 NPC207428
Remote Similarity 0.5754 NPC104345
Remote Similarity 0.5754 NPC113946
Remote Similarity 0.5732 NPC9856
Remote Similarity 0.5732 NPC320656
Remote Similarity 0.5722 NPC293487
Remote Similarity 0.5722 NPC128582
Remote Similarity 0.5722 NPC477591
Remote Similarity 0.5706 NPC207554
Remote Similarity 0.5699 NPC161861
Remote Similarity 0.5699 NPC473743
Remote Similarity 0.5698 NPC469536
Remote Similarity 0.5698 NPC478040
Remote Similarity 0.5691 NPC14325
Remote Similarity 0.5691 NPC28848
Remote Similarity 0.5689 NPC184437
Remote Similarity 0.5683 NPC472106
Remote Similarity 0.5674 NPC281094
Remote Similarity 0.5671 NPC209389
Remote Similarity 0.5665 NPC136002
Remote Similarity 0.5665 NPC20144
Remote Similarity 0.5659 NPC472120
Remote Similarity 0.5659 NPC472101
Remote Similarity 0.5657 NPC212799
Remote Similarity 0.5657 NPC254798
Remote Similarity 0.5652 NPC475920
Remote Similarity 0.5652 NPC478183
Remote Similarity 0.5648 NPC473615
Remote Similarity 0.5645 NPC318183
Remote Similarity 0.5635 NPC471122
Remote Similarity 0.5633 NPC264580
Remote Similarity 0.5629 NPC79618
Remote Similarity 0.5625 NPC242000
Remote Similarity 0.5625 NPC321617
Remote Similarity 0.5619 NPC229484
Remote Similarity 0.5617 NPC192533
Remote Similarity 0.5611 NPC29285
Remote Similarity 0.5611 NPC84317
Remote Similarity 0.5607 NPC277157
Remote Similarity 0.5604 NPC320064

Drug Structure

External Identifiers

TTD  
DrugBank  
ChEMBL  
IUPHAR/BPS  
PharmaGKB  
KEGG Drug  
PubChem CID  
ChEBI  
CAS Number  

Drug Properties

Molecular Weight  447.09
ALogP  1.6637
MLogP  3.11
XLogP  4.969
HDA  4
HBD  0
Rotatable Bonds  6
TPSA  52.09
RO5 Violation  0