Asperazine G

ID: ALA5084095

PubChem CID: 166627922

Max Phase: Preclinical

Molecular Formula: C43H40N6O5

Molecular Weight: 720.83

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  CN1C(=O)[C@H](Cc2c[nH]c3cc([C@@]45C[C@H]6C(=O)N(C)[C@H](Cc7ccccc7)C(=O)N6[C@@H]4N(C=O)c4ccccc45)ccc23)NC(=O)[C@H]1Cc1ccccc1

Standard InChI:  InChI=1S/C43H40N6O5/c1-46-35(19-26-11-5-3-6-12-26)38(51)45-33(39(46)52)21-28-24-44-32-22-29(17-18-30(28)32)43-23-37-40(53)47(2)36(20-27-13-7-4-8-14-27)41(54)49(37)42(43)48(25-50)34-16-10-9-15-31(34)43/h3-18,22,24-25,33,35-37,42,44H,19-21,23H2,1-2H3,(H,45,51)/t33-,35+,36+,37-,42-,43+/m0/s1

Standard InChI Key:  DWDBEEFAYQKUNM-GRYGTWGOSA-N

Molfile:  

 
     RDKit          2D

 56 64  0  0  0  0  0  0  0  0999 V2000
    1.0799  -11.6635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0788  -12.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7909  -12.8961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5047  -12.4867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5019  -11.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7892  -11.2505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2122  -11.2445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9256  -11.6546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9261  -12.4731    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6354  -12.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6331  -11.2344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6291  -10.4131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6353  -13.7003    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2146  -12.8824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3469  -11.6489    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3511  -12.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1311  -12.7153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1244  -11.3892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6066  -12.0456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5957  -10.7291    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3734  -10.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3769  -11.7856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0817  -12.1849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7834  -11.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7759  -10.9616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0706  -10.5618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7038  -10.6771    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3448  -13.2855    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1121  -12.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7974  -13.4521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3021  -14.1012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9216  -12.5783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4241  -13.2242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1207  -13.9885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7540  -14.5121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4506  -14.0754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2450  -13.2779    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.7006  -15.3275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3801  -15.7815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3268  -16.5969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1130  -15.4200    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7925  -15.8740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5939  -16.9584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0063  -17.0509    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9529  -17.8663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7391  -16.6894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5254  -15.5125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4186  -17.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1515  -16.7819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8294  -17.2392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5617  -16.8784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6156  -16.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9312  -15.6080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2015  -15.9713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3361   -9.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8774   -9.3420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  5  7  1  0
  8  7  1  6
  8  9  1  0
  8 11  1  0
  9 10  1  0
 10 16  1  0
 15 11  1  0
 11 12  2  0
 10 13  2  0
  9 14  1  0
 15 16  1  0
 16 17  1  0
 17 19  1  0
 18 15  1  0
 18 19  1  0
 19 22  1  0
 21 20  1  0
 20 18  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 21  1  0
 18 27  1  1
 16 28  1  6
 19 29  1  1
 29 30  2  0
 30 31  1  0
 31 34  2  0
 33 32  2  0
 32 29  1  0
 33 34  1  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 33  1  0
 35 38  1  0
 39 38  1  6
 39 40  1  0
 39 41  1  0
 41 42  1  0
 40 43  2  0
 40 44  1  0
 44 45  1  0
 44 46  1  0
 42 46  1  0
 42 47  2  0
 46 48  1  1
 48 49  1  0
 49 50  2  0
 50 51  1  0
 51 52  2  0
 52 53  1  0
 53 54  2  0
 54 49  1  0
 20 55  1  0
 55 56  2  0
M  END

Alternative Forms

  1. Parent:

    ALA5084095

    ---

Associated Targets(Human)

HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Botrytis cinerea (4183 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fusarium graminearum (1554 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pyricularia grisea (1253 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 720.83Molecular Weight (Monoisotopic): 720.3060AlogP: 3.55#Rotatable Bonds: 8
Polar Surface Area: 126.13Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.13CX Basic pKa: CX LogP: 3.89CX LogD: 3.89
Aromatic Rings: 5Heavy Atoms: 54QED Weighted: 0.24Np Likeness Score: 0.99

References

1. Wang X, Serrano R, González-Menéndez V, Mackenzie TA, Ramos MC, Frisvad JC, Larsen TO..  (2022)  A Molecular Networking Based Discovery of Diketopiperazine Heterodimers and Aspergillicins from Aspergillus caelatus.,  85  (1.0): [PMID:35045259] [10.1021/acs.jnatprod.1c00526]

Source