NP-MRD: Showing NP-Card for (1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one (NP0298381)

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Record Information

Version

2.0

Created at

2022-09-10 09:35:44 UTC

Updated at

2022-09-10 09:35:44 UTC

NP-MRD ID

NP0298381

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one

Description

8-Oxocorynoline belongs to the class of organic compounds known as hexahydrobenzophenanthridine alkaloids. These are alkaloids containing a hexahydrobenzophenanthridine skeleton, which is a tetracyclic compound containing a benzene fused to a hexahydrophenanthridine moiety. (1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one is found in Corydalis incisa. (1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one was first documented in 2016 (PMID: 26805956). Based on a literature review very few articles have been published on 8-Oxocorynoline.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102211352D          

 28 33  0  0  1  0            999 V2000
    8.1844   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6894   -2.5147    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8703   -2.6133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5462   -3.3720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3754   -1.9533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6995   -1.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2045   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3855   -0.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0613   -1.3919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5563   -2.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0815   -2.7266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2931   -2.4835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2807   -1.6586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5186   -1.0960    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0236   -0.4359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8427   -0.3373    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3477    0.3227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6618   -0.2387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1567   -0.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9758   -0.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4708   -1.4601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1467   -2.2188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3276   -2.3174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8326   -1.6574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0135   -1.7560    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7680   -2.7615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4762   -2.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2925   -1.5339    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
  3  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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 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
  9 13  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25  2  1  1  0  0  0
 14 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 28  1  0  0  0  0
M  END

     RDKit          3D

 47 52  0  0  0  0  0  0  0  0999 V2000
    0.4037    0.3005   -2.6316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3523    0.5289   -1.4210 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7663    0.6952   -1.5014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3601    1.0934   -2.5265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5178    0.3701   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9081   -0.0724    0.8519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6784   -0.3519    1.9659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0247   -0.1939    1.9340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6634    0.2432    0.8101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8995    0.5231   -0.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7665    0.9443   -1.3007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1062    0.6537   -0.9343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9867    0.4999    0.4681 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4564   -0.2602    0.8978 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0291    0.1440    2.2766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1132   -1.7138    0.6447 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4318   -2.0387   -0.6625 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3289   -1.9966    0.9090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1987   -0.8987    0.3597 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5556   -1.0979    0.3202 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4380   -0.1466   -0.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9183    1.0469   -0.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5494    1.2516   -0.5915 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6759    0.2809   -0.0963 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2247    0.6075   -0.1024 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9919    1.8342   -1.0649 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1925    1.2808   -0.5628 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8144   -0.0616   -0.3303 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4144   -0.0547   -2.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4712    1.2280   -3.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0719   -0.4982   -3.2212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1952   -0.7016    2.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6154   -0.4189    2.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7982    1.4731   -1.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4210   -0.3242   -1.3685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5166    1.0925    2.5321 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1038    0.4038    2.2655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1366   -0.6527    3.0144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7298   -2.3627    1.3057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3362   -2.4824   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6221   -2.9230    0.3577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5523   -2.1807    1.9793 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9866   -2.0200    0.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1681    2.1898   -0.9574 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0605    1.6745    0.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9895    1.2664   -1.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4900    1.7979    0.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 25  1  0
 25 24  1  0
 24 23  2  0
 23 22  1  0
 22 21  2  0
 21 28  1  0
 28 27  1  0
 27 26  1  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16 14  1  0
 14 15  1  1
 14  6  1  0
  6  5  2  0
  5 10  1  0
 10  9  2  0
  9 13  1  0
 13 12  1  0
 12 11  1  0
  9  8  1  0
  8  7  2  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
 14 25  1  0
  7  6  1  0
 19 24  1  0
 11 10  1  0
 26 22  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 25 45  1  1
 23 44  1  0
 27 46  1  0
 27 47  1  0
 20 43  1  0
 18 41  1  0
 18 42  1  0
 16 39  1  1
 17 40  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 12 34  1  0
 12 35  1  0
  8 33  1  0
  7 32  1  0
M  END


  Mrv1652309102211352D          

 28 33  0  0  1  0            999 V2000
    8.1844   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6894   -2.5147    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8703   -2.6133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5462   -3.3720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3754   -1.9533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6995   -1.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2045   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3855   -0.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0613   -1.3919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5563   -2.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0815   -2.7266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2931   -2.4835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2807   -1.6586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5186   -1.0960    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0236   -0.4359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8427   -0.3373    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3477    0.3227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6618   -0.2387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1567   -0.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9758   -0.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4708   -1.4601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1467   -2.2188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3276   -2.3174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8326   -1.6574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0135   -1.7560    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7680   -2.7615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4762   -2.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2925   -1.5339    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
  3  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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 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
  9 13  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25  2  1  1  0  0  0
 14 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0298381

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1[C@@H]2C3=CC4=C(OCO4)C=C3C[C@H](O)[C@]2(C)C2=C(C3=C(OCO3)C=C2)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H19NO6/c1-21-12-3-4-13-18(28-9-25-13)17(12)20(24)22(2)19(21)11-7-15-14(26-8-27-15)5-10(11)6-16(21)23/h3-5,7,16,19,23H,6,8-9H2,1-2H3/t16-,19+,21-/m0/s1

> <INCHI_KEY>
KUCVHCLYIAWDLU-SCWSEQNSSA-N

> <FORMULA>
C21H19NO6

> <MOLECULAR_WEIGHT>
381.384

> <EXACT_MASS>
381.121237336

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
38.99055456423508

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,12S,13R)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one

> <JCHEM_LOGP>
1.903691966666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.376619169882662

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4444831100059274

> <JCHEM_POLAR_SURFACE_AREA>
77.46000000000001

> <JCHEM_REFRACTIVITY>
97.68020000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,12S,13R)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one

> <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      15.277  -5.926   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      14.354  -4.694   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      12.825  -4.878   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      12.220  -6.294   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.901  -3.646   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.506  -2.230   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.582  -0.998   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.053  -1.182   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.448  -2.598   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.372  -3.830   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.485  -5.090   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.014  -4.636   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.991  -3.096   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      14.035  -2.046   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.111  -0.814   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.640  -0.630   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.716   0.602   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      16.169  -0.446   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.093  -1.678   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.622  -1.493   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      19.545  -2.726   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      18.940  -4.142   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      17.411  -4.326   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.488  -3.094   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      14.959  -3.278   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      20.100  -5.155   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      21.422  -4.365   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      21.079  -2.863   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10                                                  
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9                                                       
CONECT   14    6   15   16   25                                             
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   28                                                  
CONECT   22   21   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24    2   14                                                  
CONECT   26   22   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   21                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₉NO₆

Average Mass

381.3840 Da

Monoisotopic Mass

381.12124 Da

IUPAC Name

(1R,12S,13R)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one

Traditional Name

(1R,12S,13R)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one

CAS Registry Number

Not Available

SMILES

CN1[C@@H]2C3=CC4=C(OCO4)C=C3C[C@H](O)[C@]2(C)C2=C(C3=C(OCO3)C=C2)C1=O

InChI Identifier

InChI=1S/C21H19NO6/c1-21-12-3-4-13-18(28-9-25-13)17(12)20(24)22(2)19(21)11-7-15-14(26-8-27-15)5-10(11)6-16(21)23/h3-5,7,16,19,23H,6,8-9H2,1-2H3/t16-,19+,21-/m0/s1

InChI Key

KUCVHCLYIAWDLU-SCWSEQNSSA-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
Corydalis incisa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexahydrobenzophenanthridine alkaloids. These are alkaloids containing a hexahydrobenzophenanthridine skeleton, which is a tetracyclic compound containing a benzene fused to a hexahydrophenanthridine moiety.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Benzophenanthridine alkaloids

Sub Class

Hexahydrobenzophenanthridine alkaloids

Direct Parent

Hexahydrobenzophenanthridine alkaloids

Alternative Parents

Substituents

Hexahydrobenzophenanthridine alkaloid skeleton
Benzoquinoline
Phenanthridine
Isoquinolone
Quinoline
Tetralin
Tetrahydroisoquinoline
Benzodioxole
Benzenoid
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Organic oxygen 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	1.9	ChemAxon
pKa (Strongest Acidic)	14.38	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	77.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	97.68 m³·mol⁻¹	ChemAxon
Polarizability	38.99 Å³	ChemAxon
Number of Rings	6	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

132558697

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Liu L, Yu X, Wang Z, Sun J, Pan R, Yang C, Wu L: Simultaneous determination and pharmacokinetics of five alkaloids in rat plasma by ultra high performance liquid chromatography with tandem mass spectrometry after the oral administration of Corydalis bungeana Turcz extract. J Sep Sci. 2016 Jan;39(2):296-305. doi: 10.1002/jssc.201500889. Epub 2015 Nov 26. [PubMed:26805956 ]
LOTUS database [Link]

Showing NP-Card for (1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one (NP0298381)

MOL for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

3D MOL for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

3D SDF for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

3D-SDF for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

PDB for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

3D PDB for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

SMILES for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

INCHI for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

Structure for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)

3D Structure for NP0298381 ((1r,12s,13r)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁴,²².0¹⁷,²¹]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one)