Drug Information

Drug ID:  NPD11
Drug Name:  Calcium Pangamate
Molecular Formula:  2C10H19NO8.Ca
Canonical SMILES:  O[C@@H]([C@H]([C@@H]([C@H](C(=O)[O-])O)O)O)COC(=O)CN(C)C.O[C@@H]([C@H]([C@@H]([C@H](C(=O)[O-])O)O)O)COC(=O)CN(C)C.[Ca+2]
Standard InCHI:  InChI=1S/2C10H19NO8.Ca/c2*1-11(2)3-6(13)19-4-5(12)7(14)8(15)9(16)10(17)18;/h2*5,7-9,12,14-16H,3-4H2,1-2H3,(H,17,18);/q;;+2/p-2/t2*5-,7-,8+,9-;/m11./s1
Standard InCHIKey:  JWLAOERSRUNGEF-JQVJEGKNSA-L
Max Developmental Stage:  Approved
Max Developmental Stage Source:  ChEMBL

  Structural Similarity Between NPASS Natural Products and NPD11

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 0.7237 NPC32148
Intermediate Similarity 0.7183 NPC293692
Intermediate Similarity 0.7183 NPC220922
Intermediate Similarity 0.7101 NPC196612
Remote Similarity 0.6957 NPC277878
Remote Similarity 0.6711 NPC317651
Remote Similarity 0.6711 NPC258690
Remote Similarity 0.6543 NPC169976
Remote Similarity 0.6543 NPC33267
Remote Similarity 0.6543 NPC114640
Remote Similarity 0.6543 NPC324165
Remote Similarity 0.6543 NPC126366
Remote Similarity 0.6543 NPC170963
Remote Similarity 0.6533 NPC323945
Remote Similarity 0.6465 NPC227622
Remote Similarity 0.6447 NPC320296
Remote Similarity 0.6413 NPC292345
Remote Similarity 0.64 NPC179624
Remote Similarity 0.6373 NPC137453
Remote Similarity 0.6329 NPC322319
Remote Similarity 0.6329 NPC326651
Remote Similarity 0.6329 NPC325117
Remote Similarity 0.6292 NPC47135
Remote Similarity 0.6282 NPC268243
Remote Similarity 0.6207 NPC473984
Remote Similarity 0.6203 NPC472609
Remote Similarity 0.6184 NPC320032
Remote Similarity 0.6143 NPC247546
Remote Similarity 0.6143 NPC172086
Remote Similarity 0.6133 NPC198377
Remote Similarity 0.6129 NPC52533
Remote Similarity 0.6125 NPC12040
Remote Similarity 0.6125 NPC76881
Remote Similarity 0.6104 NPC17935
Remote Similarity 0.6098 NPC474298
Remote Similarity 0.6098 NPC474299
Remote Similarity 0.6098 NPC473985
Remote Similarity 0.6098 NPC28348
Remote Similarity 0.6098 NPC475808
Remote Similarity 0.6098 NPC320663
Remote Similarity 0.6098 NPC224700
Remote Similarity 0.6092 NPC474003
Remote Similarity 0.6087 NPC83839
Remote Similarity 0.6076 NPC325773
Remote Similarity 0.6071 NPC54460
Remote Similarity 0.6067 NPC219340
Remote Similarity 0.6056 NPC46254
Remote Similarity 0.6027 NPC35816
Remote Similarity 0.6027 NPC325180
Remote Similarity 0.6024 NPC477642
Remote Similarity 0.6022 NPC477728
Remote Similarity 0.6 NPC68743
Remote Similarity 0.6 NPC60830
Remote Similarity 0.5976 NPC206601
Remote Similarity 0.5974 NPC322855
Remote Similarity 0.596 NPC160066
Remote Similarity 0.5955 NPC474702
Remote Similarity 0.593 NPC125164
Remote Similarity 0.5909 NPC473741
Remote Similarity 0.5909 NPC477145
Remote Similarity 0.5904 NPC250619
Remote Similarity 0.5904 NPC97736
Remote Similarity 0.5904 NPC50228
Remote Similarity 0.5882 NPC477641
Remote Similarity 0.5882 NPC320865
Remote Similarity 0.5882 NPC42320
Remote Similarity 0.5882 NPC188453
Remote Similarity 0.5882 NPC477643
Remote Similarity 0.5875 NPC88898
Remote Similarity 0.5875 NPC106216
Remote Similarity 0.5875 NPC145658
Remote Similarity 0.587 NPC320936
Remote Similarity 0.5867 NPC469937
Remote Similarity 0.5867 NPC53463
Remote Similarity 0.5867 NPC23155
Remote Similarity 0.5867 NPC6883
Remote Similarity 0.5867 NPC320588
Remote Similarity 0.5843 NPC150557
Remote Similarity 0.5833 NPC211428
Remote Similarity 0.5833 NPC285003
Remote Similarity 0.5833 NPC241265
Remote Similarity 0.5806 NPC192025
Remote Similarity 0.5806 NPC125253
Remote Similarity 0.5806 NPC253975
Remote Similarity 0.5804 NPC106791
Remote Similarity 0.5804 NPC201889
Remote Similarity 0.5795 NPC472594
Remote Similarity 0.5795 NPC330017
Remote Similarity 0.5783 NPC469925
Remote Similarity 0.5773 NPC476019
Remote Similarity 0.5773 NPC65359
Remote Similarity 0.5753 NPC198398
Remote Similarity 0.5753 NPC27359
Remote Similarity 0.5753 NPC295832
Remote Similarity 0.5747 NPC472595
Remote Similarity 0.5733 NPC19676
Remote Similarity 0.5733 NPC323401
Remote Similarity 0.5733 NPC65985
Remote Similarity 0.573 NPC233108
Remote Similarity 0.5714 NPC242655
Remote Similarity 0.5714 NPC270005
Remote Similarity 0.5714 NPC208537
Remote Similarity 0.5714 NPC471420
Remote Similarity 0.5714 NPC293551
Remote Similarity 0.5714 NPC38891
Remote Similarity 0.5714 NPC3547
Remote Similarity 0.5699 NPC95478
Remote Similarity 0.5699 NPC155670
Remote Similarity 0.5699 NPC196102
Remote Similarity 0.5699 NPC178758
Remote Similarity 0.5699 NPC145748
Remote Similarity 0.5698 NPC185419
Remote Similarity 0.5698 NPC184550
Remote Similarity 0.5698 NPC96322
Remote Similarity 0.5696 NPC68974
Remote Similarity 0.5688 NPC316984
Remote Similarity 0.5688 NPC30911
Remote Similarity 0.5682 NPC228411
Remote Similarity 0.5682 NPC473948
Remote Similarity 0.5667 NPC475616
Remote Similarity 0.5667 NPC470014
Remote Similarity 0.5652 NPC246005
Remote Similarity 0.5647 NPC476285
Remote Similarity 0.5647 NPC476291
Remote Similarity 0.5641 NPC112224
Remote Similarity 0.5641 NPC327895
Remote Similarity 0.5641 NPC43169
Remote Similarity 0.5641 NPC61567
Remote Similarity 0.5641 NPC93861
Remote Similarity 0.5638 NPC227051
Remote Similarity 0.5636 NPC1111
Remote Similarity 0.5636 NPC275100
Remote Similarity 0.5636 NPC261750
Remote Similarity 0.5632 NPC291228
Remote Similarity 0.5632 NPC206823
Remote Similarity 0.5632 NPC225748
Remote Similarity 0.5632 NPC39266
Remote Similarity 0.5632 NPC169085
Remote Similarity 0.5632 NPC163812
Remote Similarity 0.5632 NPC263281
Remote Similarity 0.5632 NPC178919
Remote Similarity 0.5632 NPC9763
Remote Similarity 0.5632 NPC308096
Remote Similarity 0.561 NPC160661

Drug Structure

External Identifiers

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

Drug Properties

Molecular Weight  280.10
ALogP  -3.1306
MLogP  1.57
XLogP  -3.955
HDA  9
HBD  4
Rotatable Bonds  16
TPSA  150.59
RO5 Violation  0