Drug Information

Drug ID:  NPD9352
Drug Name:  Sulfacetamide Sodium
Molecular Formula:  C8H10N2O3S.Na
Canonical SMILES:  [O-]C(=NS(=O)(=O)c1ccc(cc1)N)C.[Na+]
Standard InCHI:  InChI=1S/C8H10N2O3S.Na/c1-6(11)10-14(12,13)8-4-2-7(9)3-5-8;/h2-5H,9H2,1H3,(H,10,11);/q;+1/p-1
Standard InCHIKey:  PQMSFAORUFMASU-UHFFFAOYSA-M
Max Developmental Stage:  Approved
Max Developmental Stage Source:  ChEMBL

  Structural Similarity Between NPASS Natural Products and NPD9352

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
High Similarity 0.9222 NPC315403
High Similarity 0.8587 NPC43655
Intermediate Similarity 0.8404 NPC107135
Intermediate Similarity 0.7576 NPC92689
Intermediate Similarity 0.7553 NPC307456
Intermediate Similarity 0.7396 NPC15839
Intermediate Similarity 0.7283 NPC301874
Intermediate Similarity 0.7222 NPC271732
Intermediate Similarity 0.7204 NPC35599
Intermediate Similarity 0.72 NPC297532
Remote Similarity 0.6989 NPC66775
Remote Similarity 0.6983 NPC218710
Remote Similarity 0.6893 NPC78154
Remote Similarity 0.6857 NPC476483
Remote Similarity 0.67 NPC134825
Remote Similarity 0.6602 NPC262295
Remote Similarity 0.6569 NPC229477
Remote Similarity 0.6538 NPC30445
Remote Similarity 0.6538 NPC111233
Remote Similarity 0.6476 NPC173991
Remote Similarity 0.646 NPC328877
Remote Similarity 0.6415 NPC191444
Remote Similarity 0.6372 NPC474430
Remote Similarity 0.6321 NPC176858
Remote Similarity 0.6279 NPC321053
Remote Similarity 0.6273 NPC317400
Remote Similarity 0.6162 NPC302129
Remote Similarity 0.6154 NPC37584
Remote Similarity 0.6154 NPC76327
Remote Similarity 0.6147 NPC108800
Remote Similarity 0.6106 NPC75496
Remote Similarity 0.6066 NPC205652
Remote Similarity 0.6066 NPC470550
Remote Similarity 0.6053 NPC326792
Remote Similarity 0.605 NPC255721
Remote Similarity 0.6048 NPC31651
Remote Similarity 0.6031 NPC328590
Remote Similarity 0.6019 NPC240134
Remote Similarity 0.6017 NPC172170
Remote Similarity 0.6 NPC9336
Remote Similarity 0.5983 NPC313362
Remote Similarity 0.5983 NPC313810
Remote Similarity 0.5948 NPC178681
Remote Similarity 0.5913 NPC70201
Remote Similarity 0.5877 NPC317642
Remote Similarity 0.5854 NPC264782
Remote Similarity 0.5854 NPC314141
Remote Similarity 0.5833 NPC302790
Remote Similarity 0.5812 NPC311660
Remote Similarity 0.5802 NPC474926
Remote Similarity 0.5798 NPC24060
Remote Similarity 0.5784 NPC325662
Remote Similarity 0.5784 NPC98269
Remote Similarity 0.5772 NPC316910
Remote Similarity 0.5763 NPC256838
Remote Similarity 0.5763 NPC38262
Remote Similarity 0.575 NPC20322
Remote Similarity 0.5745 NPC473429
Remote Similarity 0.5738 NPC226914
Remote Similarity 0.5691 NPC181390
Remote Similarity 0.569 NPC316435
Remote Similarity 0.5669 NPC476440
Remote Similarity 0.56 NPC322735

Drug Structure

External Identifiers

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

Drug Properties

Molecular Weight  213.03
ALogP  -2.5708
MLogP  1.68
XLogP  0.71
HDA  5
HBD  1
Rotatable Bonds  5
TPSA  103.96
RO5 Violation  0