NP-MRD: Showing NP-Card for ondansetron-m2 (NP0030183)

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Record Information

Version

2.0

Created at

2021-06-19 21:36:23 UTC

Updated at

2021-06-29 23:58:00 UTC

NP-MRD ID

NP0030183

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ondansetron-m2

Provided By

JEOL Database JEOL Logo

Description

ondansetron-m2 is found in Mucor circinelloides. ondansetron-m2 was first documented in 2006 (Duan, M., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123363D          

 42 45  0  0  0  0            999 V2000
   -0.9160    4.2389    0.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3709    3.7693   -0.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834    4.5459   -1.7174 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0682    3.7111   -2.7641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362    2.4037   -2.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147    2.4472   -1.1161 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0425    1.2928   -0.3193 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1574    0.8071    0.6139 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4239    0.2464   -0.0821 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2412   -1.1421   -0.7124 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3752   -1.0395   -1.8279 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5721   -2.0375    0.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7831   -1.6156    1.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3444   -2.7723    2.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5342   -2.9824    3.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2987   -4.2839    3.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599   -5.3727    2.9530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6682   -5.1933    1.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8968   -3.8824    1.3741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6405   -3.4083    0.3070 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3804   -4.2620   -0.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -0.2022    1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8073    0.1814    2.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5539    3.8413    1.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9572    5.3315    0.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175    3.9335    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0965   -3.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9400    1.4778   -2.9662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6990    0.5093   -1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1542    1.5824    0.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4949    1.6490    1.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146    0.1723    0.6779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7810    0.9550   -0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2101   -1.5272   -1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1689   -1.9396   -2.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0947   -2.1364    3.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3266   -4.4414    4.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6685   -6.3784    3.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1016   -6.0528    1.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2789   -4.6075   -0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7488   -5.1075   -0.8837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6538   -3.7101   -1.4997 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0  0  0  0
 13 22  1  0  0  0  0
 12 10  1  0  0  0  0
 10  9  1  0  0  0  0
  9  8  1  0  0  0  0
  8 22  1  0  0  0  0
 16 17  1  0  0  0  0
 22 23  2  0  0  0  0
 20 21  1  0  0  0  0
 17 18  2  0  0  0  0
  8  7  1  0  0  0  0
 18 19  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
 13 12  2  0  0  0  0
 19 14  2  0  0  0  0
 19 20  1  0  0  0  0
 14 15  1  0  0  0  0
  5  4  2  0  0  0  0
  4  3  1  0  0  0  0
  3  2  2  0  0  0  0
  2  6  1  0  0  0  0
 20 12  1  0  0  0  0
  2  1  1  0  0  0  0
 15 16  2  0  0  0  0
 10 11  1  0  0  0  0
 15 36  1  0  0  0  0
 16 37  1  0  0  0  0
 17 38  1  0  0  0  0
 18 39  1  0  0  0  0
 10 34  1  6  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
  8 31  1  1  0  0  0
 21 40  1  0  0  0  0
 21 41  1  0  0  0  0
 21 42  1  0  0  0  0
  7 29  1  0  0  0  0
  7 30  1  0  0  0  0
  5 28  1  0  0  0  0
  4 27  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
 11 35  1  0  0  0  0
M  END

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
   -0.9160    4.2389    0.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3709    3.7693   -0.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834    4.5459   -1.7174 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0682    3.7111   -2.7641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362    2.4037   -2.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147    2.4472   -1.1161 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0425    1.2928   -0.3193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1574    0.8071    0.6139 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4239    0.2464   -0.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2412   -1.1421   -0.7124 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3752   -1.0395   -1.8279 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5721   -2.0375    0.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7831   -1.6156    1.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3444   -2.7723    2.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5342   -2.9824    3.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2987   -4.2839    3.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599   -5.3727    2.9530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6682   -5.1933    1.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8968   -3.8824    1.3741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6405   -3.4083    0.3070 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3804   -4.2620   -0.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -0.2022    1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8073    0.1814    2.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5539    3.8413    1.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9572    5.3315    0.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175    3.9335    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0965   -3.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9400    1.4778   -2.9662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6990    0.5093   -1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1542    1.5824    0.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4949    1.6490    1.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146    0.1723    0.6779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7810    0.9550   -0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2101   -1.5272   -1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1689   -1.9396   -2.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0947   -2.1364    3.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3266   -4.4414    4.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6685   -6.3784    3.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1016   -6.0528    1.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2789   -4.6075   -0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7488   -5.1075   -0.8837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6538   -3.7101   -1.4997 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0
 13 22  1  0
 12 10  1  0
 10  9  1  0
  9  8  1  0
  8 22  1  0
 16 17  1  0
 22 23  2  0
 20 21  1  0
 17 18  2  0
  8  7  1  0
 18 19  1  0
  7  6  1  0
  6  5  1  0
 13 12  2  0
 19 14  2  0
 19 20  1  0
 14 15  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  6  1  0
 20 12  1  0
  2  1  1  0
 15 16  2  0
 10 11  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 10 34  1  6
  9 32  1  0
  9 33  1  0
  8 31  1  1
 21 40  1  0
 21 41  1  0
 21 42  1  0
  7 29  1  0
  7 30  1  0
  5 28  1  0
  4 27  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 11 35  1  0
M  END


  Mrv1652306192123363D          

 42 45  0  0  0  0            999 V2000
   -0.9160    4.2389    0.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3709    3.7693   -0.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834    4.5459   -1.7174 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0682    3.7111   -2.7641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362    2.4037   -2.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147    2.4472   -1.1161 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0425    1.2928   -0.3193 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1574    0.8071    0.6139 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4239    0.2464   -0.0821 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2412   -1.1421   -0.7124 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3752   -1.0395   -1.8279 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5721   -2.0375    0.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7831   -1.6156    1.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3444   -2.7723    2.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5342   -2.9824    3.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2987   -4.2839    3.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599   -5.3727    2.9530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6682   -5.1933    1.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8968   -3.8824    1.3741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6405   -3.4083    0.3070 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3804   -4.2620   -0.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -0.2022    1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8073    0.1814    2.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5539    3.8413    1.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9572    5.3315    0.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175    3.9335    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0965   -3.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9400    1.4778   -2.9662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6990    0.5093   -1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1542    1.5824    0.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4949    1.6490    1.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146    0.1723    0.6779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7810    0.9550   -0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2101   -1.5272   -1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1689   -1.9396   -2.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0947   -2.1364    3.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3266   -4.4414    4.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6685   -6.3784    3.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1016   -6.0528    1.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2789   -4.6075   -0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7488   -5.1075   -0.8837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6538   -3.7101   -1.4997 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0  0  0  0
 13 22  1  0  0  0  0
 12 10  1  0  0  0  0
 10  9  1  0  0  0  0
  9  8  1  0  0  0  0
  8 22  1  0  0  0  0
 16 17  1  0  0  0  0
 22 23  2  0  0  0  0
 20 21  1  0  0  0  0
 17 18  2  0  0  0  0
  8  7  1  0  0  0  0
 18 19  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
 13 12  2  0  0  0  0
 19 14  2  0  0  0  0
 19 20  1  0  0  0  0
 14 15  1  0  0  0  0
  5  4  2  0  0  0  0
  4  3  1  0  0  0  0
  3  2  2  0  0  0  0
  2  6  1  0  0  0  0
 20 12  1  0  0  0  0
  2  1  1  0  0  0  0
 15 16  2  0  0  0  0
 10 11  1  0  0  0  0
 15 36  1  0  0  0  0
 16 37  1  0  0  0  0
 17 38  1  0  0  0  0
 18 39  1  0  0  0  0
 10 34  1  6  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
  8 31  1  1  0  0  0
 21 40  1  0  0  0  0
 21 41  1  0  0  0  0
 21 42  1  0  0  0  0
  7 29  1  0  0  0  0
  7 30  1  0  0  0  0
  5 28  1  0  0  0  0
  4 27  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
 11 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0030183

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C2=C(C3=C(C([H])=C([H])C([H])=C3[H])N2C([H])([H])[H])C(=O)[C@@]([H])(C([H])([H])N2C([H])=C([H])N=C2C([H])([H])[H])C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H19N3O2/c1-11-19-7-8-21(11)10-12-9-15(22)17-16(18(12)23)13-5-3-4-6-14(13)20(17)2/h3-8,12,15,22H,9-10H2,1-2H3/t12-,15-/m1/s1

> <INCHI_KEY>
VBUMWRZTWGNELX-IUODEOHRSA-N

> <FORMULA>
C18H19N3O2

> <MOLECULAR_WEIGHT>
309.369

> <EXACT_MASS>
309.147726864

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
33.84292700445802

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3R)-1-hydroxy-9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-2,3,4,9-tetrahydro-1H-carbazol-4-one

> <ALOGPS_LOGP>
1.02

> <JCHEM_LOGP>
1.2750615633333333

> <ALOGPS_LOGS>
-2.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.603647142376175

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.433434556928852

> <JCHEM_PKA_STRONGEST_BASIC>
7.344302473722427

> <JCHEM_POLAR_SURFACE_AREA>
60.05

> <JCHEM_REFRACTIVITY>
88.141

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.04e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R)-1-hydroxy-9-methyl-3-[(2-methylimidazol-1-yl)methyl]-2,3-dihydro-1H-carbazol-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
   -0.9160    4.2389    0.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3709    3.7693   -0.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834    4.5459   -1.7174 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0682    3.7111   -2.7641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362    2.4037   -2.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147    2.4472   -1.1161 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0425    1.2928   -0.3193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1574    0.8071    0.6139 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4239    0.2464   -0.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2412   -1.1421   -0.7124 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3752   -1.0395   -1.8279 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5721   -2.0375    0.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7831   -1.6156    1.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3444   -2.7723    2.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5342   -2.9824    3.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2987   -4.2839    3.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599   -5.3727    2.9530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6682   -5.1933    1.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8968   -3.8824    1.3741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6405   -3.4083    0.3070 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3804   -4.2620   -0.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -0.2022    1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8073    0.1814    2.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5539    3.8413    1.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9572    5.3315    0.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175    3.9335    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0965   -3.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9400    1.4778   -2.9662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6990    0.5093   -1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1542    1.5824    0.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4949    1.6490    1.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146    0.1723    0.6779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7810    0.9550   -0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2101   -1.5272   -1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1689   -1.9396   -2.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0947   -2.1364    3.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3266   -4.4414    4.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6685   -6.3784    3.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1016   -6.0528    1.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2789   -4.6075   -0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7488   -5.1075   -0.8837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6538   -3.7101   -1.4997 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0
 13 22  1  0
 12 10  1  0
 10  9  1  0
  9  8  1  0
  8 22  1  0
 16 17  1  0
 22 23  2  0
 20 21  1  0
 17 18  2  0
  8  7  1  0
 18 19  1  0
  7  6  1  0
  6  5  1  0
 13 12  2  0
 19 14  2  0
 19 20  1  0
 14 15  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  6  1  0
 20 12  1  0
  2  1  1  0
 15 16  2  0
 10 11  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 10 34  1  6
  9 32  1  0
  9 33  1  0
  8 31  1  1
 21 40  1  0
 21 41  1  0
 21 42  1  0
  7 29  1  0
  7 30  1  0
  5 28  1  0
  4 27  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 11 35  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.916   4.239   0.599  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.371   3.769  -0.734  0.00  0.00           C+0
HETATM    3  N   UNK     0      -1.783   4.546  -1.717  0.00  0.00           N+0
HETATM    4  C   UNK     0      -2.068   3.711  -2.764  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.836   2.404  -2.417  0.00  0.00           C+0
HETATM    6  N   UNK     0      -1.415   2.447  -1.116  0.00  0.00           N+0
HETATM    7  C   UNK     0      -1.042   1.293  -0.319  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.157   0.807   0.614  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.424   0.246  -0.082  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.241  -1.142  -0.712  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.375  -1.040  -1.828  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.572  -2.038   0.266  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.783  -1.616   1.322  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.344  -2.772   2.023  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.534  -2.982   3.158  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.299  -4.284   3.611  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.860  -5.373   2.953  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.668  -5.193   1.827  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.897  -3.882   1.374  0.00  0.00           C+0
HETATM   20  N   UNK     0      -2.640  -3.408   0.307  0.00  0.00           N+0
HETATM   21  C   UNK     0      -3.380  -4.262  -0.599  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.530  -0.202   1.576  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.807   0.181   2.495  0.00  0.00           O+0
HETATM   24  H   UNK     0      -1.554   3.841   1.393  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.957   5.332   0.652  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.118   3.934   0.788  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.421   4.096  -3.711  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.940   1.478  -2.966  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.699   0.509  -1.002  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.154   1.582   0.256  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.495   1.649   1.233  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.215   0.172   0.678  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.781   0.955  -0.837  0.00  0.00           H+0
HETATM   34  H   UNK     0      -4.210  -1.527  -1.044  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.169  -1.940  -2.131  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.095  -2.136   3.681  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.327  -4.441   4.487  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.669  -6.378   3.320  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.102  -6.053   1.325  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.279  -4.607  -0.082  0.00  0.00           H+0
HETATM   41  H   UNK     0      -2.749  -5.107  -0.884  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.654  -3.710  -1.500  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    3    6    1                                                  
CONECT    3    4    2                                                       
CONECT    4    5    3   27                                                  
CONECT    5    6    4   28                                                  
CONECT    6    7    5    2                                                  
CONECT    7    8    6   29   30                                             
CONECT    8    9   22    7   31                                             
CONECT    9   10    8   32   33                                             
CONECT   10   12    9   11   34                                             
CONECT   11   10   35                                                       
CONECT   12   10   13   20                                                  
CONECT   13   14   22   12                                                  
CONECT   14   13   19   15                                                  
CONECT   15   14   16   36                                                  
CONECT   16   17   15   37                                                  
CONECT   17   16   18   38                                                  
CONECT   18   17   19   39                                                  
CONECT   19   18   14   20                                                  
CONECT   20   21   19   12                                                  
CONECT   21   20   40   41   42                                             
CONECT   22   13    8   23                                                  
CONECT   23   22                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    4                                                            
CONECT   28    5                                                            
CONECT   29    7                                                            
CONECT   30    7                                                            
CONECT   31    8                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34   10                                                            
CONECT   35   11                                                            
CONECT   36   15                                                            
CONECT   37   16                                                            
CONECT   38   17                                                            
CONECT   39   18                                                            
CONECT   40   21                                                            
CONECT   41   21                                                            
CONECT   42   21                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

RDKit          3D

42 45  0  0  0  0  0  0  0  0999 V2000
   -0.9160    4.2389    0.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3709    3.7693   -0.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834    4.5459   -1.7174 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0682    3.7111   -2.7641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362    2.4037   -2.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147    2.4472   -1.1161 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0425    1.2928   -0.3193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1574    0.8071    0.6139 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4239    0.2464   -0.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2412   -1.1421   -0.7124 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3752   -1.0395   -1.8279 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5721   -2.0375    0.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7831   -1.6156    1.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3444   -2.7723    2.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5342   -2.9824    3.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2987   -4.2839    3.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599   -5.3727    2.9530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6682   -5.1933    1.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8968   -3.8824    1.3741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6405   -3.4083    0.3070 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3804   -4.2620   -0.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -0.2022    1.5763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8073    0.1814    2.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5539    3.8413    1.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9572    5.3315    0.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175    3.9335    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0965   -3.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9400    1.4778   -2.9662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6990    0.5093   -1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1542    1.5824    0.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4949    1.6490    1.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146    0.1723    0.6779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7810    0.9550   -0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2101   -1.5272   -1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1689   -1.9396   -2.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0947   -2.1364    3.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3266   -4.4414    4.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6685   -6.3784    3.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1016   -6.0528    1.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2789   -4.6075   -0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7488   -5.1075   -0.8837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6538   -3.7101   -1.4997 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0
 13 22  1  0
 12 10  1  0
 10  9  1  0
  9  8  1  0
  8 22  1  0
 16 17  1  0
 22 23  2  0
 20 21  1  0
 17 18  2  0
  8  7  1  0
 18 19  1  0
  7  6  1  0
  6  5  1  0
 13 12  2  0
 19 14  2  0
 19 20  1  0
 14 15  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  6  1  0
 20 12  1  0
  2  1  1  0
 15 16  2  0
 10 11  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 10 34  1  6
  9 32  1  0
  9 33  1  0
  8 31  1  1
 21 40  1  0
 21 41  1  0
 21 42  1  0
  7 29  1  0
  7 30  1  0
  5 28  1  0
  4 27  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 11 35  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₉N₃O₂

Average Mass

309.3690 Da

Monoisotopic Mass

309.14773 Da

IUPAC Name

(1R,3R)-1-hydroxy-9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-2,3,4,9-tetrahydro-1H-carbazol-4-one

Traditional Name

(1R,3R)-1-hydroxy-9-methyl-3-[(2-methylimidazol-1-yl)methyl]-2,3-dihydro-1H-carbazol-4-one

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])C2=C(C3=C(C([H])=C([H])C([H])=C3[H])N2C([H])([H])[H])C(=O)[C@@]([H])(C([H])([H])N2C([H])=C([H])N=C2C([H])([H])[H])C1([H])[H]

InChI Identifier

InChI=1S/C18H19N3O2/c1-11-19-7-8-21(11)10-12-9-15(22)17-16(18(12)23)13-5-3-4-6-14(13)20(17)2/h3-8,12,15,22H,9-10H2,1-2H3/t12-,15-/m1/s1

InChI Key

VBUMWRZTWGNELX-IUODEOHRSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Mucor circinelloides	JEOL database	Duan, M., et al, Magn. Reson. Chem. 44, 972 (2006)

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.02	ALOGPS
logP	1.28	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	13.43	ChemAxon
pKa (Strongest Basic)	7.34	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	60.05 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	88.14 m³·mol⁻¹	ChemAxon
Polarizability	33.84 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Duan, M., et al. (2006). Duan, M., et al, Magn. Reson. Chem. 44, 972 (2006). Mag. Reson. Chem..

Showing NP-Card for ondansetron-m2 (NP0030183)

MOL for NP0030183 (ondansetron-m2)

3D MOL for NP0030183 (ondansetron-m2)

3D SDF for NP0030183 (ondansetron-m2)

3D-SDF for NP0030183 (ondansetron-m2)

PDB for NP0030183 (ondansetron-m2)

3D PDB for NP0030183 (ondansetron-m2)

SMILES for NP0030183 (ondansetron-m2)

INCHI for NP0030183 (ondansetron-m2)

Structure for NP0030183 (ondansetron-m2)

3D Structure for NP0030183 (ondansetron-m2)