NP-MRD: Showing NP-Card for (6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate (NP0237972)

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Record Information

Version

2.0

Created at

2022-09-06 21:16:33 UTC

Updated at

2022-09-06 21:16:33 UTC

NP-MRD ID

NP0237972

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate

Description

(6S,7R,8R)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2H,2'H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinoline]-8-yl acetate belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives. (6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate is found in Corydalis raddeana. Based on a literature review very few articles have been published on (6S,7R,8R)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2H,2'H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinoline]-8-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062223162D          

 31 35  0  0  1  0            999 V2000
    7.8154    1.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1510    0.8612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3952    1.1920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3039    2.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482    2.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8838    1.8538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9751    1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7308    0.7030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8221   -0.1169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5778   -0.4478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1280    2.1847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1331    1.3597    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6222    0.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3501    1.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0192    0.3442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1993    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102    0.9174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411    1.6731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8611    1.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3418    2.4348    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0821    3.2178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2740    3.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7258    2.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143    4.1674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4246    2.2213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7127    1.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8892    0.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0367    3.0047    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4202    3.5529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7012    3.4937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4569    3.1628    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
  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
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  2  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
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 17 27  1  0  0  0  0
 11 28  1  6  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
  5 31  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
    6.1873   -1.2206    0.1527 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3332   -0.4215    0.9651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9732   -0.3920    0.6156 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4720   -1.0944   -0.4561 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1116   -1.0435   -0.7773 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2415   -0.2791   -0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7625    0.3981    1.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1136    0.3672    1.3738 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5948    1.0848    2.4598 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6903    1.8502    3.2133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1481   -0.2705   -0.4036 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8921   -1.5976   -0.1213 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9182   -1.7918    1.2415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2319   -1.1648   -0.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2748   -1.8092   -1.3056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4103   -1.1420   -1.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5309    0.2282   -1.5037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5105    0.8904   -0.8766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3884    0.1925   -0.4736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1100    0.6324    0.2469 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3652    0.2767    1.5846 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4904    1.2475    2.5569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7588    0.9609    3.9875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3611    2.4291    2.1554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8222    2.2223   -0.7599 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2101    2.3443   -1.0002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5022    1.1776   -1.7827 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1364   -0.1852   -1.8426 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0386    1.0718   -2.4243 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3468   -1.3051   -2.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6344   -1.8201   -1.9532 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1424   -0.7634   -0.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8395   -2.2523    0.0560 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2226   -1.1923    0.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1707   -1.6824   -1.0341 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1532    1.0008    1.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1518    2.6080    2.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9004    1.2128    3.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2730    2.4065    3.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4869   -2.4381   -0.6676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9149   -2.7761    1.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2154   -2.8591   -1.4879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2267   -1.6465   -2.2174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9809    1.7184    0.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8663    1.1880    4.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5659    1.6605    4.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1160   -0.0571    4.1515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3607    3.2705   -1.5860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7313    2.3326   -0.0332 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8031    1.0910   -3.1595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9504    1.3032   -3.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1958    1.8527   -1.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4062   -2.1268   -2.6743 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5549   -0.9759   -3.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4562   -1.7872   -2.7349 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5967   -2.9242   -1.7135 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  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  6 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 27  1  0
 27 26  1  0
 26 25  1  0
 25 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 11 28  1  6
 28 29  1  0
 28 30  1  0
 30 31  1  0
  8  3  1  0
 20 11  1  0
 31  5  1  0
 19 14  1  0
 18 17  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  7 36  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
 12 40  1  6
 13 41  1  0
 15 42  1  0
 16 43  1  0
 26 48  1  0
 26 49  1  0
 20 44  1  1
 23 45  1  0
 23 46  1  0
 23 47  1  0
 29 50  1  0
 29 51  1  0
 29 52  1  0
 30 53  1  0
 30 54  1  0
 31 55  1  0
 31 56  1  0
M  END


  Mrv1652309062223162D          

 31 35  0  0  1  0            999 V2000
    7.8154    1.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1510    0.8612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3952    1.1920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3039    2.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482    2.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8838    1.8538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9751    1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7308    0.7030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8221   -0.1169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5778   -0.4478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1280    2.1847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1331    1.3597    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6222    0.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3501    1.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0192    0.3442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1993    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102    0.9174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411    1.6731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8611    1.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3418    2.4348    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0821    3.2178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2740    3.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7258    2.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143    4.1674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4246    2.2213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7127    1.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8892    0.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0367    3.0047    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4202    3.5529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7012    3.4937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4569    3.1628    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
  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
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  2  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
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 17 27  1  0  0  0  0
 11 28  1  6  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
  5 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237972

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1OC)[C@]1([C@@H](O)C3=CC=C4OCOC4=C3[C@H]1OC(C)=O)N(C)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C23H25NO7/c1-12(25)31-22-19-14(5-6-16-20(19)30-11-29-16)21(26)23(22)15-10-18(28-4)17(27-3)9-13(15)7-8-24(23)2/h5-6,9-10,21-22,26H,7-8,11H2,1-4H3/t21-,22+,23+/m0/s1

> <INCHI_KEY>
QBMUUVHMWQFUNH-YTFSRNRJSA-N

> <FORMULA>
C23H25NO7

> <MOLECULAR_WEIGHT>
427.453

> <EXACT_MASS>
427.163102149

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
44.002186073412645

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6S,7R,8R)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2H,2'H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinoline]-8-yl acetate

> <JCHEM_LOGP>
1.9021137543333322

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.356332543058265

> <JCHEM_PKA_STRONGEST_BASIC>
6.751311629288153

> <JCHEM_POLAR_SURFACE_AREA>
86.69000000000001

> <JCHEM_REFRACTIVITY>
110.40710000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(6S,7R,8R)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinoline]-8-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      14.589   2.520   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      13.348   1.607   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.938   2.225   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.767   3.756   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.357   4.373   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.116   3.460   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.287   1.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.697   1.312   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.868  -0.218   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      12.279  -0.836   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.706   4.078   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.715   2.538   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.628   1.298   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.254   2.053   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.636   0.643   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.105   0.472   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.192   1.712   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.810   3.123   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.341   3.294   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.238   4.545   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.753   6.007   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.245   6.318   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.222   5.167   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.760   7.779   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       2.659   4.146   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.330   3.368   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.660   1.864   0.000  0.00  0.00           O+0
HETATM   28  N   UNK     0       7.535   5.609   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       6.384   6.632   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.775   6.522   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.186   5.904   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    6   12   20   28                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   27                                                  
CONECT   18   17   19   25                                                  
CONECT   19   18   14   20                                                  
CONECT   20   19   11   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   18   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   17                                                       
CONECT   28   11   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30    5                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Value	Source
(6S,7R,8R)-6-Hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2H,2'H-spiro[indeno[4,5-D][1,3]dioxole-7,1'-isoquinoline]-8-yl acetic acid	Generator

Chemical Formula

C₂₃H₂₅NO₇

Average Mass

427.4530 Da

Monoisotopic Mass

427.16310 Da

IUPAC Name

(6S,7R,8R)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2H,2'H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinoline]-8-yl acetate

Traditional Name

(6S,7R,8R)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinoline]-8-yl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1OC)[C@]1([C@@H](O)C3=CC=C4OCOC4=C3[C@H]1OC(C)=O)N(C)CC2

InChI Identifier

InChI=1S/C23H25NO7/c1-12(25)31-22-19-14(5-6-16-20(19)30-11-29-16)21(26)23(22)15-10-18(28-4)17(27-3)9-13(15)7-8-24(23)2/h5-6,9-10,21-22,26H,7-8,11H2,1-4H3/t21-,22+,23+/m0/s1

InChI Key

QBMUUVHMWQFUNH-YTFSRNRJSA-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 raddeana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydroisoquinolines

Sub Class

Not Available

Direct Parent

Tetrahydroisoquinolines

Alternative Parents

Substituents

Tetrahydroisoquinoline
Indane
Benzodioxole
Anisole
Alkyl aryl ether
Aralkylamine
Benzenoid
1,2-aminoalcohol
Carboxylic acid ester
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Azacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Ether
Acetal
Organic nitrogen compound
Organonitrogen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Amine
Organopnictogen compound
Alcohol
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)	13.36	ChemAxon
pKa (Strongest Basic)	6.75	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	86.69 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	110.41 m³·mol⁻¹	ChemAxon
Polarizability	44 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

14218071

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate (NP0237972)

MOL for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

3D MOL for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

3D SDF for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

3D-SDF for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

PDB for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

3D PDB for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

SMILES for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

INCHI for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

Structure for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)

3D Structure for NP0237972 ((6s,7r,8r)-6-hydroxy-6',7'-dimethoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-8-yl acetate)