NP-MRD: Showing NP-Card for reserpiline (NP0198994)

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Record Information

Version

2.0

Created at

2022-09-04 17:33:10 UTC

Updated at

2022-09-04 17:33:10 UTC

NP-MRD ID

NP0198994

Secondary Accession Numbers

None

Natural Product Identification

Common Name

reserpiline

Description

AC1L5T3B belongs to the class of organic compounds known as yohimbine alkaloids. These are alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor. reserpiline is found in Ochrosia elliptica and Rauvolfia salicifolia. AC1L5T3B is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241502382D          

 30 34  0  0  0  0            999 V2000
    3.1037   -1.1001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8316   -1.8790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3700   -2.5041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1805   -2.3503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0978   -3.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2873   -3.4366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0151   -4.2154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5535   -4.8405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2814   -5.6193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3641   -4.6868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9025   -5.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7131   -5.1582    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2515   -5.7833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0620   -5.6295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3342   -4.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7957   -4.2256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2239   -3.5204    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0269   -3.7096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7048   -3.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4509   -3.5916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1289   -3.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0607   -2.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5191   -4.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2652   -4.7658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3334   -5.5880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8411   -4.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0950   -4.5318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9852   -4.3793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4468   -3.7542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6362   -3.9080    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  2  0  0  0  0
 15 27  1  0  0  0  0
 18 27  1  0  0  0  0
 16 28  1  0  0  0  0
 12 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
 10 30  1  0  0  0  0
M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
   -2.9320    3.7635   -1.4621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0087    2.3784   -1.1712 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1486    1.8152   -0.6453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1370    2.5495   -0.4212 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2252    0.3666   -0.3424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3524   -0.0888    0.1584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4768   -1.4348    0.4594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3225   -2.1780    0.7024 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8160   -1.9469    2.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3284   -1.8835   -0.3966 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1431   -2.7803   -0.1952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8831   -2.1035   -0.1543 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2682   -1.9732   -1.4601 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2265   -1.9799   -1.2178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4967   -0.8481   -0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5255   -0.3469    0.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1173    0.6486    1.2804 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3953    0.7804    0.9242 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4394    1.6229    1.3204 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7012    1.5201    0.7510 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7294    2.3464    1.1378 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6524    3.3509    2.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9631    0.5839   -0.2227 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2296    0.4648   -0.8091 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4455   -0.5155   -1.8068 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9361   -0.2396   -0.6073 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6612   -0.1471   -0.0426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8762   -0.8931    0.5865 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8839    0.1133    0.1402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0340   -0.4641   -0.6226 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5080    4.3175   -0.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8566    4.0659   -1.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2795    4.0072   -2.4824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1999    0.6070    0.3380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5695   -3.2695    0.6173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7009   -2.0301    2.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3753   -0.9723    2.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1060   -2.7165    2.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8481   -2.2536   -1.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0544   -3.5549   -1.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2255   -3.3875    0.7347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5878   -2.7579   -2.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5190   -0.9619   -1.8400 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4620   -2.9099   -0.6368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8161   -1.8843   -2.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6213    1.2268    2.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2230    2.3544    2.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6453    3.5097    2.6162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9663    3.0118    2.9149 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3547    4.3391    1.6998 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3898   -1.5547   -1.3857 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6320   -0.4785   -2.5883 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3822   -0.3496   -2.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0848   -0.9864   -1.3613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0615   -1.1467    1.6684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3374    0.8642   -0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2153    0.7083    1.0302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8158   -0.2787   -1.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  2  0
 23 24  1  0
 24 25  1  0
 23 26  1  0
 26 27  2  0
 16 28  1  0
 28 29  1  0
 29 30  1  0
 30  5  1  0
 30 10  1  0
 28 12  1  0
 27 15  1  0
 27 18  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  6 34  1  0
  8 35  1  1
  9 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  6
 11 40  1  0
 11 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 17 46  1  0
 19 47  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 26 54  1  0
 28 55  1  1
 29 56  1  0
 29 57  1  0
 30 58  1  6
M  END


  Mrv1533004241502382D          

 30 34  0  0  0  0            999 V2000
    3.1037   -1.1001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8316   -1.8790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3700   -2.5041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1805   -2.3503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0978   -3.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2873   -3.4366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0151   -4.2154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5535   -4.8405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2814   -5.6193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3641   -4.6868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9025   -5.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7131   -5.1582    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2515   -5.7833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0620   -5.6295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3342   -4.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7957   -4.2256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2239   -3.5204    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0269   -3.7096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7048   -3.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4509   -3.5916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1289   -3.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0607   -2.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5191   -4.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2652   -4.7658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3334   -5.5880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8411   -4.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0950   -4.5318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9852   -4.3793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4468   -3.7542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6362   -3.9080    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  2  0  0  0  0
 15 27  1  0  0  0  0
 18 27  1  0  0  0  0
 16 28  1  0  0  0  0
 12 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
 10 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198994

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=COC(C)C2CN3CCC4=C(NC5=CC(OC)=C(OC)C=C45)C3CC12

> <INCHI_IDENTIFIER>
InChI=1S/C23H28N2O5/c1-12-16-10-25-6-5-13-15-8-20(27-2)21(28-3)9-18(15)24-22(13)19(25)7-14(16)17(11-30-12)23(26)29-4/h8-9,11-12,14,16,19,24H,5-7,10H2,1-4H3

> <INCHI_KEY>
FGWJRZQNNZVCHR-UHFFFAOYSA-N

> <FORMULA>
C23H28N2O5

> <MOLECULAR_WEIGHT>
412.486

> <EXACT_MASS>
412.19982201

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
45.51848559318806

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 6,7-dimethoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁵,²⁰]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate

> <ALOGPS_LOGP>
2.76

> <JCHEM_LOGP>
2.2373838596666658

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.610620225988658

> <JCHEM_PKA_STRONGEST_BASIC>
7.094483586335143

> <JCHEM_POLAR_SURFACE_AREA>
73.02000000000001

> <JCHEM_REFRACTIVITY>
112.76279999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.46e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
reserpiline

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       5.794  -2.054   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.286  -3.507   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.291  -4.674   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.804  -4.387   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.783  -6.128   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.270  -6.415   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.762  -7.869   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.767  -9.036   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.259 -10.489   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.280  -8.749   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.285  -9.916   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       8.798  -9.629   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       9.803 -10.795   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.316 -10.508   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.824  -9.055   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.819  -7.888   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0      11.618  -6.571   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0      13.117  -6.925   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.382  -6.047   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.775  -6.704   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      17.041  -5.827   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      16.913  -4.292   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      15.902  -8.239   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      17.295  -8.896   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      17.422 -10.431   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.637  -9.117   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.244  -8.459   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.306  -8.175   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.301  -7.008   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.788  -7.295   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   30                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   30                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   28                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   27                                                  
CONECT   16   15   17   28                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27                                                       
CONECT   27   26   15   18                                                  
CONECT   28   16   12   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29    5   10                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Value	Source
Methyl 6,7-dimethoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁵,²⁰]henicosa-2(10),4,6,8,18-pentaene-19-carboxylic acid	Generator
Methyl 6,7-dimethoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.0,.0,.0,]henicosa-2(10),4,6,8,18-pentaene-19-carboxylic acid	Generator

Chemical Formula

C₂₃H₂₈N₂O₅

Average Mass

412.4860 Da

Monoisotopic Mass

412.19982 Da

IUPAC Name

methyl 6,7-dimethoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁵,²⁰]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate

Traditional Name

reserpiline

CAS Registry Number

Not Available

SMILES

COC(=O)C1=COC(C)C2CN3CCC4=C(NC5=CC(OC)=C(OC)C=C45)C3CC12

InChI Identifier

InChI=1S/C23H28N2O5/c1-12-16-10-25-6-5-13-15-8-20(27-2)21(28-3)9-18(15)24-22(13)19(25)7-14(16)17(11-30-12)23(26)29-4/h8-9,11-12,14,16,19,24H,5-7,10H2,1-4H3

InChI Key

FGWJRZQNNZVCHR-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
Ochrosia elliptica	LOTUS Database	35616633
Rauvolfia salicifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as yohimbine alkaloids. These are alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Yohimbine alkaloids

Sub Class

Not Available

Direct Parent

Yohimbine alkaloids

Alternative Parents

Substituents

Ajmalicine-skeleton
18-oxayohimban
Corynanthean skeleton
Yohimbine alkaloid
Pyridoindole
Beta-carboline
3-alkylindole
Indole
Indole or derivatives
Anisole
Alkyl aryl ether
Aralkylamine
Piperidine
Benzenoid
Methyl ester
Vinylogous ester
Heteroaromatic compound
Pyrrole
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid derivative
Oxacycle
Ether
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Amine
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Organopnictogen compound
Organic oxide
Organonitrogen compound
Organooxygen 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	2.76	ALOGPS
logP	2.24	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	16.61	ChemAxon
pKa (Strongest Basic)	7.09	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	73.02 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	112.76 m³·mol⁻¹	ChemAxon
Polarizability	45.52 Å³	ChemAxon
Number of Rings	5	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

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

234846

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for reserpiline (NP0198994)

MOL for NP0198994 (reserpiline)

3D MOL for NP0198994 (reserpiline)

3D SDF for NP0198994 (reserpiline)

3D-SDF for NP0198994 (reserpiline)

PDB for NP0198994 (reserpiline)

3D PDB for NP0198994 (reserpiline)

SMILES for NP0198994 (reserpiline)

INCHI for NP0198994 (reserpiline)

Structure for NP0198994 (reserpiline)

3D Structure for NP0198994 (reserpiline)