Natural Product: NPC62507

Natural Product ID:  NPC62507
Common Name:   2,5-Dideoxy-2,5-Imino-D-Altritol
IUPAC Name:   (2R,3R,4S,5R)-2,5-bis(hydroxymethyl)pyrrolidine-3,4-diol
Synonyms:  
Molecular Formula:   C6H13NO4
Standard InCHIKey:  PFYHYHZGDNWFIF-KAZBKCHUSA-N
Standard InCHI:  InChI=1S/C6H13NO4/c8-1-3-5(10)6(11)4(2-9)7-3/h3-11H,1-2H2/t3-,4-,5-,6+/m1/s1
Canonical SMILES:  OC[C@H]1N[C@@H]([C@H]([C@H]1O)O)CO
First Find Year:  
Max Developmental Stage:  
Synthetic Gene Cluster:   ;

  Species Source

Organism ID Organism Name Taxonomy Level Family SuperKingdom Isolation Part Collection Location Collection Time Reference
NPO2647 Adenophora stricta Species Campanulaceae Eukaryota TM-MC*
NPO26838 Adenophora triphylla Species Campanulaceae Eukaryota TM-MC*

  Biological Activity

Target ID Target Type Target Name Target Organism Activity Type Activity Relation Value Unit Reference
NPT61 Individual Protein Beta-glucocerebrosidase Homo sapiens Ki = 200 nM 11327590
NPT61 Individual Protein Beta-glucocerebrosidase Homo sapiens Ki = 200 nM 11392550
NPT2 Others Unspecified IC50 = 7800 nM 16124768
NPT2 Others Unspecified IC50 = 3300 nM 16124768
NPT2 Others Unspecified IC50 = 66000 nM 20457528
NPT3543 Individual Protein Probable alpha-glucosidase Os06g0675700 Oryza sativa Japonica Group IC50 = 171000 nM 20457528
NPT2 Others Unspecified IC50 = 74000 nM 20457528
NPT2 Others Unspecified IC50 = 40000 nM 20457528
NPT1058 Individual Protein Beta-glucosidase A Caldicellulosiruptor saccharolyticus IC50 = 19000 nM 20457528
NPT2 Others Unspecified IC50 = 444000 nM 20457528
NPT1131 Individual Protein Alpha-galactosidase Coffea arabica IC50 = 780 nM 20457528
NPT501 Individual Protein Alpha-galactosidase A Homo sapiens IC50 = 690 nM 20457528
NPT2 Others Unspecified IC50 = 190000 nM 20457528
NPT1051 Individual Protein Lactase-glycosylceramidase Rattus norvegicus IC50 = 7200 nM 20457528
NPT2 Others Unspecified IC50 = 64000 nM 20457528
NPT506 Individual Protein Beta-mannosidase Rattus norvegicus Inhibition < 50 % 20457528
NPT496 Individual Protein Alpha-L-fucosidase 1 Bos taurus IC50 = 503000 nM 20457528
NPT2 Others Unspecified IC50 = 631000 nM 20457528
NPT2 Others Unspecified Inhibition < 50 % 20457528
NPT501 Individual Protein Alpha-galactosidase A Homo sapiens Ki = 500 nM 20457528
NPT501 Individual Protein Alpha-galactosidase A Homo sapiens Activity = 70 % 20457528
NPT501 Individual Protein Alpha-galactosidase A Homo sapiens Activity = 9.6 20457528

  Similar Natural Products 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 NPC62507 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
1.0 High Similarity NPC8087
0.9649 High Similarity NPC474014
0.9649 High Similarity NPC57846
0.9649 High Similarity NPC30126
0.9492 High Similarity NPC474928
0.9333 High Similarity NPC77191
0.9333 High Similarity NPC69798
0.9333 High Similarity NPC116377
0.9333 High Similarity NPC101746
0.9333 High Similarity NPC473952
0.9286 High Similarity NPC311668
0.9286 High Similarity NPC10262
0.9286 High Similarity NPC65832
0.875 High Similarity NPC473710
0.875 High Similarity NPC272396
0.875 High Similarity NPC475694
0.8615 High Similarity NPC137554
0.8615 High Similarity NPC255535
0.8615 High Similarity NPC299603
0.8615 High Similarity NPC285014
0.8615 High Similarity NPC28959
0.8485 Intermediate Similarity NPC474468
0.8413 Intermediate Similarity NPC315980
0.8333 Intermediate Similarity NPC193593
0.8333 Intermediate Similarity NPC143809
0.8333 Intermediate Similarity NPC76726
0.8333 Intermediate Similarity NPC290106
0.8276 Intermediate Similarity NPC275727
0.8226 Intermediate Similarity NPC150680
0.8226 Intermediate Similarity NPC22774
0.8226 Intermediate Similarity NPC218150
0.8226 Intermediate Similarity NPC69669
0.8226 Intermediate Similarity NPC2432
0.8226 Intermediate Similarity NPC306462
0.7969 Intermediate Similarity NPC471780
0.7969 Intermediate Similarity NPC471892
0.7969 Intermediate Similarity NPC223386
0.7969 Intermediate Similarity NPC198341
0.7969 Intermediate Similarity NPC142290
0.7969 Intermediate Similarity NPC75435
0.7869 Intermediate Similarity NPC204709
0.7846 Intermediate Similarity NPC294883
0.7846 Intermediate Similarity NPC303798
0.7846 Intermediate Similarity NPC286851
0.7846 Intermediate Similarity NPC12514
0.7727 Intermediate Similarity NPC184150
0.7727 Intermediate Similarity NPC141156
0.7612 Intermediate Similarity NPC266242
0.7612 Intermediate Similarity NPC471418
0.7612 Intermediate Similarity NPC254617
0.7612 Intermediate Similarity NPC474469
0.7612 Intermediate Similarity NPC306763
0.7612 Intermediate Similarity NPC74555
0.75 Intermediate Similarity NPC475715
0.75 Intermediate Similarity NPC475127
0.75 Intermediate Similarity NPC473419
0.75 Intermediate Similarity NPC268922
0.7463 Intermediate Similarity NPC59221
0.7432 Intermediate Similarity NPC100204
0.7432 Intermediate Similarity NPC83248
0.7424 Intermediate Similarity NPC233034
0.7391 Intermediate Similarity NPC163538
0.7391 Intermediate Similarity NPC115800
0.7368 Intermediate Similarity NPC165119
0.7353 Intermediate Similarity NPC34291
0.7353 Intermediate Similarity NPC126664
0.7286 Intermediate Similarity NPC476695
0.7286 Intermediate Similarity NPC476694
0.7286 Intermediate Similarity NPC476696
0.7206 Intermediate Similarity NPC221764
0.7206 Intermediate Similarity NPC78312
0.7206 Intermediate Similarity NPC196359
0.7206 Intermediate Similarity NPC135539
0.7188 Intermediate Similarity NPC170172
0.7 Intermediate Similarity NPC306838
0.6875 Remote Similarity NPC8979
0.6765 Remote Similarity NPC471419
0.6765 Remote Similarity NPC163134
0.6714 Remote Similarity NPC322801
0.6714 Remote Similarity NPC129100
0.6714 Remote Similarity NPC291650
0.6667 Remote Similarity NPC469363
0.6623 Remote Similarity NPC98750
0.662 Remote Similarity NPC171850
0.662 Remote Similarity NPC107224
0.6618 Remote Similarity NPC17455
0.6538 Remote Similarity NPC70574
0.6406 Remote Similarity NPC277072
0.6406 Remote Similarity NPC178263
0.6375 Remote Similarity NPC36927
0.6375 Remote Similarity NPC271772
0.6364 Remote Similarity NPC293551
0.6269 Remote Similarity NPC11433
0.6269 Remote Similarity NPC245346
0.6269 Remote Similarity NPC302003
0.6267 Remote Similarity NPC185084
0.625 Remote Similarity NPC123814
0.625 Remote Similarity NPC219340
0.6197 Remote Similarity NPC160661
0.6176 Remote Similarity NPC233364
0.6176 Remote Similarity NPC471421
0.6129 Remote Similarity NPC121062
0.6129 Remote Similarity NPC29222
0.6129 Remote Similarity NPC96966
0.6061 Remote Similarity NPC471442
0.6061 Remote Similarity NPC471423
0.6047 Remote Similarity NPC275715
0.6026 Remote Similarity NPC244539
0.6 Remote Similarity NPC314510
0.6 Remote Similarity NPC474322
0.5949 Remote Similarity NPC313762
0.5921 Remote Similarity NPC306973
0.5915 Remote Similarity NPC145627
0.5882 Remote Similarity NPC471605
0.5882 Remote Similarity NPC471443
0.5867 Remote Similarity NPC15864
0.5867 Remote Similarity NPC223893
0.5857 Remote Similarity NPC319131
0.5789 Remote Similarity NPC327486
0.5789 Remote Similarity NPC223174
0.5789 Remote Similarity NPC327753
0.5769 Remote Similarity NPC315806
0.5753 Remote Similarity NPC472609
0.5753 Remote Similarity NPC41429
0.5747 Remote Similarity NPC52533
0.5733 Remote Similarity NPC316445
0.5732 Remote Similarity NPC318258
0.5714 Remote Similarity NPC276928
0.5714 Remote Similarity NPC64250
0.5714 Remote Similarity NPC268927
0.5641 Remote Similarity NPC55274
0.5638 Remote Similarity NPC315170
0.5632 Remote Similarity NPC313552
0.5625 Remote Similarity NPC477002
0.5625 Remote Similarity NPC470782
0.5625 Remote Similarity NPC62293
0.5625 Remote Similarity NPC140327
0.5625 Remote Similarity NPC212008
0.5625 Remote Similarity NPC51055
0.5625 Remote Similarity NPC3094
0.5616 Remote Similarity NPC88898
0.5616 Remote Similarity NPC106216
0.561 Remote Similarity NPC150557

  Similar Clinical/Approved Drugs

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

●  The left chart: Distribution of similarity level between NPC62507 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
0.8226 Intermediate Similarity NPD9027 Phase 3
0.8226 Intermediate Similarity NPD9028 Phase 2
0.8226 Intermediate Similarity NPD9026 Phase 2
0.8226 Intermediate Similarity NPD9029 Phase 3
0.7903 Intermediate Similarity NPD9239 Approved
0.7903 Intermediate Similarity NPD9240 Approved
0.7612 Intermediate Similarity NPD9444 Discontinued
0.7424 Intermediate Similarity NPD9440 Discontinued
0.7353 Intermediate Similarity NPD9443 Clinical (unspecified phase)
0.7231 Intermediate Similarity NPD9024 Phase 2
0.7231 Intermediate Similarity NPD9022 Phase 2
0.7206 Intermediate Similarity NPD8868 Approved
0.7077 Intermediate Similarity NPD9455 Approved
0.697 Remote Similarity NPD393 Approved
0.675 Remote Similarity NPD9401 Discovery
0.6714 Remote Similarity NPD9033 Approved
0.6714 Remote Similarity NPD9031 Approved
0.6714 Remote Similarity NPD9032 Approved
0.6714 Remote Similarity NPD9030 Approved
0.6463 Remote Similarity NPD394 Phase 3
0.6269 Remote Similarity NPD8865 Approved
0.625 Remote Similarity NPD3215 Phase 1
0.6184 Remote Similarity NPD67 Phase 2
0.6184 Remote Similarity NPD9034 Approved
0.6098 Remote Similarity NPD883 Phase 2
0.6098 Remote Similarity NPD882 Phase 2
0.5968 Remote Similarity NPD398 Approved
0.5968 Remote Similarity NPD399 Approved
0.5968 Remote Similarity NPD400 Approved
0.5938 Remote Similarity NPD3214 Discontinued
0.5926 Remote Similarity NPD9429 Discontinued
0.5823 Remote Similarity NPD9407 Approved
0.5789 Remote Similarity NPD9445 Approved
0.5769 Remote Similarity NPD9653 Clinical (unspecified phase)
0.5765 Remote Similarity NPD9640 Clinical (unspecified phase)
0.5714 Remote Similarity NPD9446 Approved

Structure

External Identifiers

PubChem CID   10261406
ChEMBL   CHEMBL469844
ZINC  

Physicochemical Properties

Molecular Weight:  163.08
ALogP:  -2.44
MLogP:  1.57
XLogP:  -0.929
# Rotatable Bonds:  6
Polar Surface Area:  92.95
# H-Bond Aceptor:  5
# H-Bond Donor:  5
# Rings:  1
# Heavy Atoms:  11

Download Data

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Structure MOL file  
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Similar NPs/Drugs