NP-MRD: Showing NP-Card for (1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate (NP0295751)

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Record Information

Version

2.0

Created at

2022-09-10 04:54:55 UTC

Updated at

2022-09-10 04:54:55 UTC

NP-MRD ID

NP0295751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate

Description

1-O-Acetylbulbisine belongs to the class of organic compounds known as phenanthridines and derivatives. These are polycyclic compounds containing a phenanthridine moiety, which is a tricyclic system with two benzene rings joined by a pyridine forming a non-linear skeleton. Hydrogenated derivatives are also included. (1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate is found in Crinum asiaticum. (1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate was first documented in 2011 (PMID: 21314165). Based on a literature review very few articles have been published on 1-O-Acetylbulbisine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102206542D          

 26 30  0  0  1  0            999 V2000
    5.7471   -1.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9428   -1.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6994   -0.9488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8950   -0.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6517    0.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2127    0.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170    0.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2604   -0.3438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0853   -0.3560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3518    0.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6915    0.9195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8836    0.3241    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1693   -0.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0465   -0.9044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6078   -1.5090    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305   -1.4471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5667   -0.4376    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7486   -0.5439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2474    0.1114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5644    0.8731    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0632    1.5284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3825    0.9795    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6994    1.7411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5175    1.8475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8345    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0187    1.1922    0.0000 O   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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 17 15  1  6  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
M  END

     RDKit          3D

 49 53  0  0  0  0  0  0  0  0999 V2000
    4.1022   -0.4975    2.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8203   -0.8088    1.1855 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8039   -0.1846    0.4755 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5247   -0.6585    0.4332 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5052   -0.0452   -0.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8292    1.0952   -0.9497 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1337    1.6122   -0.9295 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1102    0.9726   -0.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3202    1.6735   -0.3504 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1197    2.7291   -1.2386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7289    2.7158   -1.5072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8494   -0.5779   -0.2943 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8935   -1.5243   -1.4793 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2315   -2.4628   -0.9860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0897   -2.5153    0.4524 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147   -1.9122    1.1673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0373   -1.6650    0.7926 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3171   -2.3772    0.6517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4868   -1.6419    0.1457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2465   -0.3657   -0.5694 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3130   -0.4537   -1.9595 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9760    0.3306   -0.1002 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8940    1.6258   -0.5763 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0223    2.7367    0.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9338    4.1316   -0.2803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2260    2.5325    1.4784 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1938   -1.4805    3.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0553    0.0517    2.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2395    0.0571    2.9924 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1176    1.6643   -1.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6516    2.5473   -2.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4009    3.7213   -0.8482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7760   -2.1525   -1.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5736   -1.0558   -2.4160 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1040   -3.4683   -1.4173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2034   -2.0711   -1.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8627   -1.6106    2.1771 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0747   -2.5909    1.2364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9143   -1.2228    1.7922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5731   -2.7851    1.6798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1256   -3.3331    0.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2627   -1.5022    0.9574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0223   -2.3159   -0.5923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0754    0.3557   -0.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9346   -1.1998   -2.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584    0.4228    1.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4605    4.7871    0.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4772    4.2235   -1.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8884    4.4926   -0.3375 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
  4 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 12 13  1  6
 12 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  2  0
 12  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  8  3  1  0
  5  4  1  0
 11  7  1  0
 17 15  1  0
 22 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
 16 37  1  0
 16 38  1  0
 14 35  1  0
 14 36  1  0
 13 33  1  0
 13 34  1  0
 17 39  1  1
 18 40  1  0
 18 41  1  0
 19 42  1  0
 19 43  1  0
 20 44  1  1
 21 45  1  0
 22 46  1  1
 25 47  1  0
 25 48  1  0
 25 49  1  0
  6 30  1  0
 10 31  1  0
 10 32  1  0
M  END


  Mrv1652309102206542D          

 26 30  0  0  1  0            999 V2000
    5.7471   -1.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9428   -1.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6994   -0.9488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8950   -0.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6517    0.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2127    0.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170    0.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2604   -0.3438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0853   -0.3560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3518    0.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6915    0.9195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8836    0.3241    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1693   -0.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0465   -0.9044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6078   -1.5090    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305   -1.4471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5667   -0.4376    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7486   -0.5439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2474    0.1114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5644    0.8731    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0632    1.5284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3825    0.9795    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6994    1.7411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5175    1.8475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8345    2.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0187    1.1922    0.0000 O   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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 17 15  1  6  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0295751

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2CN3CC[C@@]4([C@H]3CC[C@H](O)[C@@H]4OC(C)=O)C2=CC2=C1OCO2

> <INCHI_IDENTIFIER>
InChI=1S/C19H23NO6/c1-10(21)26-18-13(22)3-4-15-19(18)5-6-20(15)8-11-12(19)7-14-17(16(11)23-2)25-9-24-14/h7,13,15,18,22H,3-6,8-9H2,1-2H3/t13-,15+,18-,19-/m0/s1

> <INCHI_KEY>
UTIPPRKETJBQNW-UAFONNFLSA-N

> <FORMULA>
C19H23NO6

> <MOLECULAR_WEIGHT>
361.394

> <EXACT_MASS>
361.152537465

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.468025485711244

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,13R,16S,17R)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0^{1,13}.0^{2,10}.0^{4,8}]nonadeca-2,4(8),9-trien-17-yl acetate

> <JCHEM_LOGP>
0.744885003

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.141847013074063

> <JCHEM_PKA_STRONGEST_BASIC>
8.18071163753766

> <JCHEM_POLAR_SURFACE_AREA>
77.46000000000001

> <JCHEM_REFRACTIVITY>
91.04860000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,13R,16S,17R)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0^{1,13}.0^{2,10}.0^{4,8}]nonadeca-2,4(8),9-trien-17-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

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      10.728  -3.585   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.227  -3.242   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.772  -1.771   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.271  -1.429   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.816   0.043   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.864   1.172   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.365   0.830   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.819  -0.642   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      11.359  -0.665   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.857   0.793   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.624   1.716   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.383   0.605   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.049  -0.165   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.820  -1.688   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       4.868  -2.817   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       6.404  -2.701   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.791  -0.817   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.264  -1.015   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.328   0.208   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.920   1.630   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.985   2.853   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.447   1.828   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.039   3.250   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.566   3.449   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.158   4.870   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.502   2.225   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    7                                                       
CONECT   12    5   13   17   22                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15    4                                                       
CONECT   17   15   12   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   12   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₃NO₆

Average Mass

361.3940 Da

Monoisotopic Mass

361.15254 Da

IUPAC Name

(1S,13R,16S,17R)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0^{1,13}.0^{2,10}.0^{4,8}]nonadeca-2,4(8),9-trien-17-yl acetate

Traditional Name

(1S,13R,16S,17R)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0^{1,13}.0^{2,10}.0^{4,8}]nonadeca-2,4(8),9-trien-17-yl acetate

CAS Registry Number

Not Available

SMILES

COC1=C2CN3CC[C@@]4([C@H]3CC[C@H](O)[C@@H]4OC(C)=O)C2=CC2=C1OCO2

InChI Identifier

InChI=1S/C19H23NO6/c1-10(21)26-18-13(22)3-4-15-19(18)5-6-20(15)8-11-12(19)7-14-17(16(11)23-2)25-9-24-14/h7,13,15,18,22H,3-6,8-9H2,1-2H3/t13-,15+,18-,19-/m0/s1

InChI Key

UTIPPRKETJBQNW-UAFONNFLSA-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
Crinum asiaticum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthridines and derivatives. These are polycyclic compounds containing a phenanthridine moiety, which is a tricyclic system with two benzene rings joined by a pyridine forming a non-linear skeleton. Hydrogenated derivatives are also included.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Benzoquinolines

Direct Parent

Phenanthridines and derivatives

Alternative Parents

Substituents

Phenanthridine
Benzazepine
Tetrahydroisoquinoline
Benzodioxole
Indole or derivatives
Anisole
Alkyl aryl ether
Azepine
Aralkylamine
Benzenoid
N-alkylpyrrolidine
Pyrrolidine
Cyclic alcohol
Tertiary amine
Secondary alcohol
Tertiary aliphatic amine
Amino acid or derivatives
Carboxylic acid ester
Acetal
Azacycle
Monocarboxylic acid or derivatives
Oxacycle
Ether
Carboxylic acid derivative
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organonitrogen compound
Amine
Organic nitrogen 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	0.74	ChemAxon
pKa (Strongest Acidic)	14.14	ChemAxon
pKa (Strongest Basic)	8.18	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	77.46 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	91.05 m³·mol⁻¹	ChemAxon
Polarizability	37.47 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

70698017

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chen CK, Lin FH, Tseng LH, Jiang CL, Lee SS: Comprehensive study of alkaloids from Crinum asiaticum var. sinicum assisted by HPLC-DAD-SPE-NMR. J Nat Prod. 2011 Mar 25;74(3):411-9. doi: 10.1021/np100819n. Epub 2011 Feb 11. [PubMed:21314165 ]
LOTUS database [Link]

Showing NP-Card for (1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate (NP0295751)

MOL for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

3D MOL for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

3D SDF for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

3D-SDF for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

PDB for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

3D PDB for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

SMILES for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

INCHI for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

Structure for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)

3D Structure for NP0295751 ((1s,13r,16s,17r)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9-trien-17-yl acetate)