[2-({1-[19-Amino-13-(4-azido-benzyl)-10-(2-carbamoyl-ethyl)-7-carbamoylmethyl-16-(4-hydroxy-benzyl)-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaaza-cycloicosane-4-carbonyl]-pyrrolidine-2-carbonyl}-amino)-5-guanidino-pentanoylamino]-acetic acid

ID: ALA2372421

PubChem CID: 73353251

Max Phase: Preclinical

Molecular Formula: C46H64N18O12S2

Molecular Weight: 1125.27

Molecule Type: Protein

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  [N-]=[N+]=Nc1ccc(C[C@@H]2NC(=O)[C@@H](Cc3ccc(O)cc3)NC(=O)[C@@H](N)CSSC[C@@H](C(=O)N3CCC[C@H]3C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC2=O)cc1

Standard InChI:  InChI=1S/C46H64N18O12S2/c47-27-21-77-78-22-33(45(76)64-16-2-4-34(64)44(75)57-28(3-1-15-54-46(51)52)39(70)55-20-37(50)68)61-43(74)32(19-36(49)67)60-40(71)29(13-14-35(48)66)56-41(72)31(17-23-5-9-25(10-6-23)62-63-53)59-42(73)30(58-38(27)69)18-24-7-11-26(65)12-8-24/h5-12,27-34,65H,1-4,13-22,47H2,(H2,48,66)(H2,49,67)(H2,50,68)(H,55,70)(H,56,72)(H,57,75)(H,58,69)(H,59,73)(H,60,71)(H,61,74)(H4,51,52,54)/t27-,28-,29-,30+,31-,32-,33-,34-/m0/s1

Standard InChI Key:  BQLRGCYAAWQNHV-DFJQZISPSA-N

Molfile:  

     RDKit          2D

 78 81  0  0  1  0  0  0  0  0999 V2000
    1.3144   -4.0258    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0096   -4.4794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7446   -4.1053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2313   -4.7707    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5156   -5.5123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5156   -0.2914    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4524   -1.7017    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4524   -4.1053    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9033   -5.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6879   -0.2914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9657   -1.0363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7106   -3.3173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3311   -5.1184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3003   -5.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1273   -5.5653    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6879   -5.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5463   -4.3238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7106   -2.4930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3003   -0.5496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9171   -5.7044    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5588   -6.3301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9657   -4.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9033   -0.5496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6503   -6.2109    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0960   -6.7174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0295   -9.8560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7875   -6.6247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6075   -4.9297    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3079   -7.5186    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4930   -2.4930    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.7446   -1.7017    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.7052   -6.5055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3210   -8.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9192   -6.7373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8241   -9.6375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9699   -5.3037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4635   -5.3369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5588    0.5231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5517   -0.4503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5259   -5.9924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5251   -3.4464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6744   -5.9924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4930   -3.3173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5251   -2.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6744    0.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6820   -6.1314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2313   -1.0363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6583   -7.4425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7237   -6.5254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1221   -8.7436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5517   -5.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4435   -9.2700    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1091   -7.7305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8110  -10.6505    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5259    0.1854    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2746   -3.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0844   -4.2841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1419   -6.1016    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3398   -6.1513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0415   -3.0028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5021    0.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7350   -9.1111    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7106   -7.5385    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.1508    0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3824   -3.5160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2700   -4.4132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8626   -2.8737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8761    0.9634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7502   -3.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9490   -0.4602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7734   -0.4205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7005    1.0097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0232   -3.6782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9752    0.3576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4767   -2.9896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2846   -7.0915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6587   -8.4721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0760   -7.8894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  3  2  1  6
  4  3  1  0
  5 16  1  0
  6 10  1  0
  7 11  1  0
  8 22  1  0
  9  4  1  0
 10 23  1  0
 11 19  1  0
 12  8  1  0
 17 13  1  6
 14  5  1  0
 15 28  2  0
 16  9  1  0
 17  1  1  0
 18 12  1  0
 19  6  1  0
 20 13  1  0
 16 21  1  1
 22 14  1  0
 23 47  1  0
 24 15  2  0
 32 25  1  0
 26 52  2  0
 27 21  1  0
 28 57  1  0
 29 25  1  0
 30 43  1  0
 31 30  1  0
 32 20  1  1
 33 53  1  0
 34 59  1  0
 35 26  1  0
 36  2  2  0
 37 13  2  0
 38 10  2  0
 39 11  2  0
 40  9  2  0
 41 12  2  0
 42 14  2  0
 43  3  1  0
 18 44  1  1
 19 45  1  6
 46 25  2  0
 47 31  1  0
 48 27  2  0
 49 34  2  0
 50 33  2  0
 22 51  1  1
 52 77  1  0
 53 29  1  0
 54 26  1  0
 23 55  1  6
 56  1  1  0
 57 66  2  0
 58 27  1  0
 59 51  1  0
 60 44  1  0
 61 45  1  0
 62 33  1  0
 63 34  1  0
 64 71  2  0
 65 67  2  0
 66 69  1  0
 67 60  1  0
 68 61  1  0
 69 60  2  0
 70 61  2  0
 71 70  1  0
 72 68  2  0
 73 17  1  0
 74 64  1  0
 75 56  1  0
 76 32  1  0
 77 78  1  0
 78 76  1  0
 75 73  1  0
  7 18  1  0
 72 64  1  0
 65 57  1  0
M  CHG  2  15   1  24  -1
M  END

Alternative Forms

Associated Targets(non-human)

Avpr1a Vasopressin V1a receptor (612 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: ProteinTopical: 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: 1125.27Molecular Weight (Monoisotopic): 1124.4393AlogP: #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. Barbeau D, Guay S, Neugebauer W, Escher E..  (1992)  Preparation and biological activities of potential vasopressin photoaffinity labels.,  35  (1): [PMID:1732523] [10.1021/jm00079a020]

Source