Acutilobin D

ID: ALA4788129

PubChem CID: 162669384

Max Phase: Preclinical

Molecular Formula: C40H48O12

Molecular Weight: 720.81

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  C=C(C)[C@@]12O[C@@]3(/C=C/C=C/CCCCC)O[C@@H]1[C@@H]1[C@@H]4O[C@]4(CO)[C@@H](O)[C@]4(O)C(=O)C(C)=C[C@H]4[C@@]1(O3)[C@H](C)[C@H]2OC(=O)/C=C/c1ccc(O)c(OC)c1

Standard InChI:  InChI=1S/C40H48O12/c1-7-8-9-10-11-12-13-18-37-50-34-30-33-36(21-41,49-33)35(45)38(46)28(19-23(4)31(38)44)40(30,52-37)24(5)32(39(34,51-37)22(2)3)48-29(43)17-15-25-14-16-26(42)27(20-25)47-6/h11-20,24,28,30,32-35,41-42,45-46H,2,7-10,21H2,1,3-6H3/b12-11+,17-15+,18-13+/t24-,28-,30+,32-,33+,34-,35-,36+,37-,38-,39+,40+/m1/s1

Standard InChI Key:  IGWXJWQVKNVZHS-QYNSGBCPSA-N

Molfile:  

 
     RDKit          2D

 56 62  0  0  0  0  0  0  0  0999 V2000
   -1.2776   -0.7650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5971   -0.3647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0834   -0.7650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0834   -1.5544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8368   -1.7990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3013   -1.1577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8368   -0.5206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2783   -1.5569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5971   -1.9454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7835   -3.2526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2359   -2.6089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0104   -1.8467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6618   -1.3977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2928   -1.8805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0276   -2.6296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4677   -2.7237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9956   -3.3078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2265   -3.4764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4745   -3.2780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0473   -1.6560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1683   -3.9438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6355   -3.2868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8059   -1.0828    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0011   -4.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6868   -4.4872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1621   -2.5026    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6008   -1.1530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2866    0.0068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0455    0.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2747    0.5598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1185   -1.1578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5269   -1.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3441   -1.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7526   -2.5735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5698   -2.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9783   -3.2815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7955   -3.2816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2039   -3.9894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0211   -3.9895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9868   -0.3590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761   -2.3705    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3485   -2.7213    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0135    0.3452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6098    1.0557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0232    1.7606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2074    1.0613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8404    1.7550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2538    2.4598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8467    3.1667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2595    3.8711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0776    3.8659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4811    3.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0660    2.4490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4919    4.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8554    4.5814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0383    4.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  8  1  0
  1  2  1  0
  9  4  1  0
  3  2  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  3  1  0
  8  9  1  0
  9 16  1  0
  8 12  1  0
 17 10  1  0
 11 10  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 11  1  0
 17 16  1  0
 17 18  1  0
 16 18  1  0
 15 19  2  0
 14 20  1  0
 10 21  1  1
 11 22  1  1
 12 23  1  6
 17 24  1  1
 24 25  1  0
  9 26  1  1
  8 27  1  6
  6 27  1  0
  3 28  1  1
 28 29  1  0
 28 30  2  0
  6 31  1  6
 31 32  2  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
  1 40  1  6
  4 41  1  1
 16 42  1  1
  2 43  1  1
 43 44  1  0
 44 45  1  0
 44 46  2  0
 45 47  2  0
 47 48  1  0
 48 49  2  0
 49 50  1  0
 50 51  2  0
 51 52  1  0
 52 53  2  0
 53 48  1  0
 51 54  1  0
 50 55  1  0
 55 56  1  0
M  END

Alternative Forms

  1. Parent:

    ALA4788129

    ---

Associated Targets(Human)

MT4 (17854 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human immunodeficiency virus (3636 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: 720.81Molecular Weight (Monoisotopic): 720.3146AlogP: 3.82#Rotatable Bonds: 12
Polar Surface Area: 173.74Molecular Species: NEUTRALHBA: 12HBD: 4
#RO5 Violations: 2HBA (Lipinski): 12HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 9.86CX Basic pKa: CX LogP: 5.57CX LogD: 5.57
Aromatic Rings: 1Heavy Atoms: 52QED Weighted: 0.06Np Likeness Score: 3.21

References

1. Otsuki K,Li W,Miura K,Asada Y,Huang L,Chen CH,Lee KH,Koike K.  (2020)  Isolation, Structural Elucidation, and Anti-HIV Activity of Daphnane Diterpenoids from Daphne odora.,  83  (11): [PMID:32997496] [10.1021/acs.jnatprod.0c00540]

Source