N-[3-[(2,3-Di-O-sulfo-beta-D-glucopyranosyluronicacid)-(1->3)-(2-acetamido-2-deoxy-6-O-sulfo-alpha-D-galactopyranosyl)-(1->6)-(1-deoxy-D-glucitol-1-yl)amino]phenyl]-DL-alpha-lipoamide tetrasodium

ID: ALA3397497

PubChem CID: 118726751

Max Phase: Preclinical

Molecular Formula: C34H49N3Na4O26S5

Molecular Weight: 1080.13

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  CC(=O)N[C@H]1[C@@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)CNc2cccc(NC(=O)CCCCC3CCSS3)c2)O[C@H](COS(=O)(=O)[O-])[C@H](O)[C@@H]1O[C@@H]1O[C@H](C(=O)[O-])[C@@H](O)[C@H](OS(=O)(=O)[O-])[C@H]1OS(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+]

Standard InChI:  InChI=1S/C34H53N3O26S5.4Na/c1-15(38)36-23-28(60-34-31(63-68(54,55)56)29(62-67(51,52)53)27(45)30(61-34)32(46)47)26(44)21(14-58-66(48,49)50)59-33(23)57-13-20(40)25(43)24(42)19(39)12-35-16-5-4-6-17(11-16)37-22(41)8-3-2-7-18-9-10-64-65-18;;;;/h4-6,11,18-21,23-31,33-35,39-40,42-45H,2-3,7-10,12-14H2,1H3,(H,36,38)(H,37,41)(H,46,47)(H,48,49,50)(H,51,52,53)(H,54,55,56);;;;/q;4*+1/p-4/t18?,19-,20+,21+,23+,24+,25+,26-,27-,28+,29-,30-,31+,33-,34+;;;;/m0..../s1

Standard InChI Key:  MSMWXXJJUGLILU-JHNPOLKLSA-J

Molfile:  

     RDKit          2D

 73 72  0  0  0  0  0  0  0  0999 V2000
   12.9255    9.1549    0.0000 Na  0  0  0  0  0 15  0  0  0  0  0  0
   -7.4885   -1.0105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4944   -1.6827    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5799   -2.8796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1443   -1.0272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5737   -2.2073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3359   -3.9817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3390   -5.1817    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3800   -5.7786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3766   -4.5788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2501   -9.3878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2535   -8.1878    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.2159   -7.5851    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5550   -7.4403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2127   -8.7849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3905   -3.2480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0410   -5.9350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9010   -1.8679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2999   -2.2084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7246   -5.6913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5619   -2.9395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2622   -3.6884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2610   -5.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5594   -5.9395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8590   -5.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8603   -3.6906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1622   -2.9439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9974    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4928    0.7640    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4466    0.2840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0986    0.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1451    0.1034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0397   -1.3933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3071   -2.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5509   -1.2124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8188   12.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5750   11.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2270   12.4356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227   13.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3665   14.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7145   14.1125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6762   10.2802    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7753   14.5930    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6732   16.0904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3258   16.7514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6694   16.7594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2236   18.2488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1237   18.9098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2259   20.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5733   21.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8137   22.5359    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.2991   22.7451    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.9570   21.3971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8783   20.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4306    9.4430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0643    5.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1418    4.7738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3874    5.6110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2862    7.1084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5318    7.9456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6093    7.4174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2087    7.6366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4649    5.0828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2430    3.2764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -4.2087    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0271   -3.4459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1648   -1.9439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5954    2.2613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7654    2.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4933    2.7015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.4255    9.1549    0.0000 Na  0  0  0  0  0 15  0  0  0  0  0  0
   17.9255    9.1549    0.0000 Na  0  0  0  0  0 15  0  0  0  0  0  0
   15.4255    9.1549    0.0000 Na  0  0  0  0  0 15  0  0  0  0  0  0
  3  2  2  0
  4  3  2  0
  5  3  1  0
  3  6  1  0
  8  7  1  0
  9  8  2  0
  8 10  2  0
 12 11  2  0
 13 12  2  0
 14 12  1  0
 12 15  1  0
 18  5  1  0
 26 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
 22 19  1  0
 23 17  1  1
 24 14  1  6
 25 20  1  1
 35 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 18  1  1
 31 28  1  6
 32 29  1  6
 33 19  1  1
 34 16  1  1
 36 37  2  0
 37 38  1  0
 38 39  2  0
 39 40  1  0
 40 41  2  0
 41 36  1  0
 37 42  1  0
 39 43  1  0
 43 44  1  0
 44 45  1  0
 44 46  2  0
 45 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  1  0
 50 51  1  0
 51 52  1  0
 52 53  1  0
 53 54  1  0
 54 50  1  0
 42 55  1  0
 55 60  1  0
 57 56  1  6
 57 58  1  0
 58 59  1  0
 59 60  1  0
 60 61  1  1
 59 62  1  1
 58 63  1  1
 57 64  1  0
 64 28  1  0
 22 65  1  1
 27 66  2  0
 27 67  1  0
 29 68  1  0
 68 69  1  0
 68 70  2  0
 17  8  1  0
M  CHG  8   1   1   6  -1   7  -1  15  -1  67  -1  71   1  72   1  73   1
M  END

Associated Targets(Human)

FGF2 Tchem Basic fibroblast growth factor (185 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 1080.13Molecular Weight (Monoisotopic): 1079.1521AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Wakao M, Obata R, Miyachi K, Kaitsubata Y, Kondo T, Sakami C, Suda Y..  (2015)  Synthesis of a chondroitin sulfate disaccharide library and a GAG-binding protein interaction analysis.,  25  (7): [PMID:25765912] [10.1016/j.bmcl.2015.02.054]

Source