NP-MRD: Showing NP-Card for 7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole (NP0295171)

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Record Information

Version

2.0

Created at

2022-09-10 04:01:55 UTC

Updated at

2022-09-10 04:01:55 UTC

NP-MRD ID

NP0295171

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole

Description

7-Bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-2H,3H,4H,4aH,9H,9aH-[1,2]oxazino[6,5-b]indole belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole is found in Flustra foliacea. Based on a literature review very few articles have been published on 7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-2H,3H,4H,4aH,9H,9aH-[1,2]oxazino[6,5-b]indole.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102206012D          

 25 27  0  0  0  0            999 V2000
    1.9339    3.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    3.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3629    3.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    2.7480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    2.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    1.5105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7674    0.7556    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.7054   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3464    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8570   -0.5127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3721   -1.1801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7076   -1.9338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5281   -2.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2227   -2.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925    0.5840    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995    0.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595    1.1971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  6 25  1  0  0  0  0
 14 25  1  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
    3.7258   -2.4538    0.5132 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2613   -2.0136   -0.8150 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2614   -1.9984   -1.9293 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0228   -1.6381   -1.0654 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9374   -1.6014   -0.0810 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803   -0.2575    0.0794 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5013    0.5722    1.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4217    0.6287    2.2786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3290    1.5485    3.3022 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5816    1.6237    4.7310 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.2883    2.4529    3.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6268    2.3937    2.2447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5355    1.4769    1.2234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3723    1.2148    0.0163 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5683    0.3713    0.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2345   -0.9160    0.9880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6329   -2.0380    0.4329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4317   -2.0117   -0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3013   -3.3623    1.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9051    2.4967   -0.5797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4172    2.6005   -2.0030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0150    2.3898   -2.1389 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7645    3.6105   -2.0800 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4938    1.3877   -1.4636 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3923    0.5042   -0.8838 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1663   -2.0800    1.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7837   -2.1258    0.6523 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7348   -3.5741    0.5094 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -3.0406   -2.3017 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9787   -1.3296   -2.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2754   -1.7430   -1.5545 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7776   -1.3265   -2.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2131   -2.0190    0.8904 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0957   -2.2509   -0.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2265   -0.0810    2.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1779    3.1989    4.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4478    3.1137    2.2467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1237    0.9715    1.1704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2813    0.3041   -0.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6569   -0.9644    1.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7240   -3.0141   -1.1527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8741   -1.5246   -1.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3653   -1.4178   -0.7045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6061   -3.9514    0.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8719   -3.2462    2.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2168   -3.9864    1.1746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5544    3.3402    0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0078    2.5332   -0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6406    3.6352   -2.3504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9462    1.9048   -2.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6676    3.4989   -1.4473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1304    4.4491   -1.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1198    3.8981   -3.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8964   -0.1535   -1.6205 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 14  1  0
 14 15  1  1
 15 16  1  0
 16 17  2  3
 17 18  1  0
 17 19  1  0
 14 25  1  0
 25 24  1  0
 25  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 24 22  1  0
 13  7  1  0
 13 14  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 21 49  1  0
 21 50  1  0
 20 47  1  0
 20 48  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
 18 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 19 46  1  0
 25 54  1  6
  5 33  1  0
  5 34  1  0
  4 32  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  8 35  1  0
 11 36  1  0
 12 37  1  0
M  END


  Mrv1652309102206012D          

 25 27  0  0  0  0            999 V2000
    1.9339    3.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    3.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3629    3.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    2.7480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    2.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    1.5105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7674    0.7556    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.7054   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3464    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8570   -0.5127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3721   -1.1801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7076   -1.9338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5281   -2.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2227   -2.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925    0.5840    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995    0.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595    1.1971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  6 25  1  0  0  0  0
 14 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0295171

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CCC2(CC=C(C)C)C(O1)N(CC=C(C)C)C1=CC(Br)=CC=C21

> <INCHI_IDENTIFIER>
InChI=1S/C21H29BrN2O/c1-15(2)8-10-21-11-13-23(5)25-20(21)24(12-9-16(3)4)19-14-17(22)6-7-18(19)21/h6-9,14,20H,10-13H2,1-5H3

> <INCHI_KEY>
NWEUSXXVDOPMJX-UHFFFAOYSA-N

> <FORMULA>
C21H29BrN2O

> <MOLECULAR_WEIGHT>
405.38

> <EXACT_MASS>
404.146327

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.21694724869231

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-2H,3H,4H,4aH,9H,9aH-[1,2]oxazino[6,5-b]indole

> <JCHEM_LOGP>
5.693350919333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
2.241469487272868

> <JCHEM_POLAR_SURFACE_AREA>
15.71

> <JCHEM_REFRACTIVITY>
110.58579999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3H,4H,9aH-[1,2]oxazino[6,5-b]indole

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       3.610   7.440   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.944   6.670   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.277   7.440   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.944   5.130   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.610   4.360   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       3.610   2.820   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       4.856   1.914   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.362   2.235   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.393   1.090   0.000  0.00  0.00           C+0
HETATM   10 Br   UNK     0       8.899   1.410   0.000  0.00  0.00          Br+0
HETATM   11  C   UNK     0       6.917  -0.374   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.410  -0.695   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.380   0.450   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.840   0.450   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.466  -0.957   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.561  -2.203   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.188  -3.610   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.719  -3.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.282  -4.856   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.810  -0.695   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.303  -0.374   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      -0.173   1.090   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      -1.679   1.410   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.858   2.235   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.364   1.914   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   25                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    7   14                                                  
CONECT   14   13   15   20   25                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24    6   14                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₉BrN₂O

Average Mass

405.3800 Da

Monoisotopic Mass

404.14633 Da

IUPAC Name

7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-2H,3H,4H,4aH,9H,9aH-[1,2]oxazino[6,5-b]indole

Traditional Name

7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3H,4H,9aH-[1,2]oxazino[6,5-b]indole

CAS Registry Number

Not Available

SMILES

CN1CCC2(CC=C(C)C)C(O1)N(CC=C(C)C)C1=CC(Br)=CC=C21

InChI Identifier

InChI=1S/C21H29BrN2O/c1-15(2)8-10-21-11-13-23(5)25-20(21)24(12-9-16(3)4)19-14-17(22)6-7-18(19)21/h6-9,14,20H,10-13H2,1-5H3

InChI Key

NWEUSXXVDOPMJX-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Flustra foliacea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Not Available

Direct Parent

Indoles and derivatives

Alternative Parents

Substituents

Indole or derivatives
Dialkylarylamine
1,2-oxazinane
Aryl bromide
Aryl halide
Oxazinane
Benzenoid
N-organohydroxylamine
Azacycle
Oxacycle
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organobromide
Organohalogen compound
Hydrocarbon derivative
Organopnictogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

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	5.69	ChemAxon
pKa (Strongest Basic)	2.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	15.71 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	110.59 m³·mol⁻¹	ChemAxon
Polarizability	42.22 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73811430

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole (NP0295171)

MOL for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

3D MOL for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

3D SDF for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

3D-SDF for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

PDB for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

3D PDB for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

SMILES for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

INCHI for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

Structure for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)

3D Structure for NP0295171 (7-bromo-2-methyl-4a,9-bis(3-methylbut-2-en-1-yl)-3h,4h,9ah-[1,2]oxazino[6,5-b]indole)