(+/-)-Radulapin E

ID: ALA4871384

PubChem CID: 164621143

Max Phase: Preclinical

Molecular Formula: C38H40O5

Molecular Weight: 576.73

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  CC1(C)Oc2cc(O)cc(CCc3ccccc3)c2C2OC3c4c(CCc5ccccc5)cc(O)cc4OC(C)(C)C3C21

Standard InChI:  InChI=1S/C38H40O5/c1-37(2)33-34-36(32-26(18-16-24-13-9-6-10-14-24)20-28(40)22-30(32)43-38(34,3)4)41-35(33)31-25(19-27(39)21-29(31)42-37)17-15-23-11-7-5-8-12-23/h5-14,19-22,33-36,39-40H,15-18H2,1-4H3

Standard InChI Key:  ZXEYRCCKJQNZHF-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

 43 49  0  0  0  0  0  0  0  0999 V2000
   29.8976  -12.4518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.6117  -12.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.6106  -12.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3788  -12.7408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.7957  -13.4548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2041  -12.7383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.3786  -15.1056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.3775  -15.9334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.0938  -16.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.8035  -15.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.0920  -14.6926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.8038  -15.1025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.0856  -13.8709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.6649  -16.3408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.5161  -16.3428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.5175  -17.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.8064  -17.5781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.0957  -17.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.3851  -17.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.3861  -18.3971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.1036  -18.8043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.8113  -18.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.5132  -13.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.5154  -14.6865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.2966  -14.9318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.2920  -13.6133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7703  -14.2726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4282  -12.7825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.9107  -13.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.5762  -14.1789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.0532  -14.8357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8606  -14.7524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.1887  -14.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.7137  -13.3530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.7199  -15.5859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1993  -16.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.0163  -16.1674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.4956  -16.8364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.3118  -16.7525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.6459  -16.0016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.1618  -15.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.3473  -15.4212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.0053  -13.9191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  3  2  1  0
  5  4  1  0
  6  5  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 11  7  1  0
 12 10  1  0
 11 12  2  0
 11 13  1  0
 12 24  1  0
 23  5  1  0
  5 13  1  0
  8 14  1  0
 10 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 17  1  0
 23 24  1  0
 24 25  1  0
 26 23  1  0
 27 25  1  0
 26 27  1  0
 26  2  1  0
 27 30  1  0
 29 28  1  0
 28  2  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  2  0
 34 29  1  0
 31 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  2  0
 38 39  1  0
 39 40  2  0
 40 41  1  0
 41 42  2  0
 42 37  1  0
 33 43  1  0
M  END

Alternative Forms

  1. Parent:

    ALA4871384

    ---

Associated Targets(Human)

PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1299 (3248 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: 576.73Molecular Weight (Monoisotopic): 576.2876AlogP: 8.06#Rotatable Bonds: 6
Polar Surface Area: 68.15Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 9.21CX Basic pKa: CX LogP: 8.62CX LogD: 8.61
Aromatic Rings: 4Heavy Atoms: 43QED Weighted: 0.24Np Likeness Score: 0.96

References

1. Zhang CY, Gao Y, Zhou JC, Xu ZJ, Qiao YN, Zhang JZ, Lou HX..  (2021)  Diverse Prenylated Bibenzyl Enantiomers from the Chinese Liverwort Radula apiculata and Their Cytotoxic Activities.,  84  (5.0): [PMID:33913326] [10.1021/acs.jnatprod.0c01264]

Source