NP-MRD: Showing NP-Card for N-Formylcyclomicrobuxeine (NP0067721)

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Record Information

Version

2.0

Created at

2022-04-28 12:34:08 UTC

Updated at

2022-04-28 12:34:08 UTC

NP-MRD ID

NP0067721

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-Formylcyclomicrobuxeine

Description

N-[(1S,3R,6S,8R,11S,12S,16S)-15-acetyl-12,16-dimethyl-7-methylidenepentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadec-14-en-6-yl]-N-methylformamide belongs to the class of organic compounds known as 20-oxosteroids. These are steroid derivatives carrying a C=O group at the 20-position of the steroid skeleton. N-Formylcyclomicrobuxeine is found in Buxus papilosa. Based on a literature review very few articles have been published on N-[(1S,3R,6S,8R,11S,12S,16S)-15-acetyl-12,16-dimethyl-7-methylidenepentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadec-14-en-6-yl]-N-methylformamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214342D          

 28 32  0  0  1  0            999 V2000
   -0.5318   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2803   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5606   -2.3768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318   -1.4557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8121   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2803   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -0.5346    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1561   -1.1653    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8758   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682   -1.0201    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2485   -0.2441    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7167    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6195   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5794    0.3804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966    0.2675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685    1.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6083    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705   -1.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0924    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -1.1154    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1561   -0.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9682   -0.6299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9045   -1.8914    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
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
  9 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
  8 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 13 22  1  1  0  0  0
 12 23  1  6  0  0  0
  8 24  1  1  0  0  0
  6 24  1  1  0  0  0
  2 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 25 28  1  0  0  0  0
M  END

     RDKit          3D

 63 67  0  0  0  0  0  0  0  0999 V2000
   -3.9234    1.6329   -0.8878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3343    0.8533   -0.0256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0825   -0.1651    0.7155 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3107   -0.4399   -0.0222 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5981   -0.1459    0.5673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2417   -0.9982   -1.3190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1644   -1.2796   -1.9007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3244   -1.4617    0.8906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8490   -1.3287    0.9313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2759   -0.3463   -0.0565 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0001   -0.6999   -1.4456 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1263   -0.4088   -0.3990 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8805   -1.6019    0.0667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3255   -1.6598   -0.1953 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9757   -0.3689   -0.5440 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0286   -0.2400   -2.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3113   -0.1531   -0.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3570   -1.1607    0.2203 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6491   -0.7120    0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0948   -2.3506   -0.0743 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4419    1.1372    0.2552 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1704    1.8699   -0.0998 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1962    0.7407    0.1163 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0944    0.5098    1.5961 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8955    0.8457   -0.5752 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2045    2.1021   -0.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2616    2.1181   -0.5497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8928    0.9837    0.2216 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4367    2.4060   -1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0078    1.5376   -1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3621    0.2735    1.7027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2531   -1.0269    0.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5418    0.0440    1.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1046    0.7184    0.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1517   -1.1986   -1.8490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6424   -1.8513    1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6876   -2.2084    0.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4063   -2.3283    0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4895   -1.0799    1.9519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1156   -1.7631   -1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1133    0.0598   -2.2371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6977   -1.6937    1.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4080   -2.5422   -0.3468 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8641   -2.0804    0.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5510   -2.3840   -1.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2868   -0.9088   -2.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0063    0.7818   -2.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0296   -0.6628   -2.3536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9043    0.3183    0.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6890   -0.8237    1.8898 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4547   -1.3748    0.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264    1.6267    0.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0021    2.6156    0.6844 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1837    2.3018   -1.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5752    1.3462    2.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0073    0.5786    1.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5730   -0.4092    1.9475 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1164    0.9410   -1.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2587    2.2171    0.9272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7255    2.9714   -0.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4074    2.0377   -1.6316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6931    3.0612   -0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7398    1.2269    1.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
  4  6  1  0
  6  7  2  0
  4  3  1  0
  3  8  1  0
  8  9  1  0
 10  9  1  1
 10 11  1  0
 12 11  1  6
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28  2  1  0
  2  1  2  3
 17 18  1  0
 18 19  1  0
 18 20  2  0
  2  3  1  0
 12 10  1  0
 25 12  1  0
 28 10  1  0
 23 15  1  0
  5 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  3 31  1  1
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 11 40  1  0
 11 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 21 52  1  0
 22 53  1  0
 22 54  1  0
 24 55  1  0
 24 56  1  0
 24 57  1  0
 25 58  1  6
 26 59  1  0
 26 60  1  0
 27 61  1  0
 27 62  1  0
 28 63  1  1
  1 29  1  0
  1 30  1  0
 19 49  1  0
 19 50  1  0
 19 51  1  0
M  END


  Mrv1652304282214342D          

 28 32  0  0  1  0            999 V2000
   -0.5318   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2803   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5606   -2.3768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318   -1.4557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8121   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2803   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -0.5346    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1561   -1.1653    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8758   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682   -1.0201    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2485   -0.2441    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7167    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6195   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5794    0.3804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966    0.2675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685    1.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6083    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705   -1.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0924    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -1.1154    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1561   -0.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9682   -0.6299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9045   -1.8914    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
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
  9 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
  8 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 13 22  1  1  0  0  0
 12 23  1  6  0  0  0
  8 24  1  1  0  0  0
  6 24  1  1  0  0  0
  2 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 25 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067721

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN(C=O)[C@H]1CC[C@]23C[C@]22CC[C@]4(C)C(=CC[C@@]4(C)[C@@H]2CC[C@H]3C1=C)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H35NO2/c1-16-18-6-7-21-23(4)10-8-19(17(2)28)22(23,3)12-13-25(21)14-24(18,25)11-9-20(16)26(5)15-27/h8,15,18,20-21H,1,6-7,9-14H2,2-5H3/t18-,20-,21-,22+,23-,24+,25-/m0/s1

> <INCHI_KEY>
PEGHGSZQFPWEFQ-QNKFGOHQSA-N

> <FORMULA>
C25H35NO2

> <MOLECULAR_WEIGHT>
381.56

> <EXACT_MASS>
381.266779371

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
44.74319579776759

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(1S,3R,6S,8R,11S,12S,16S)-15-acetyl-12,16-dimethyl-7-methylidenepentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadec-14-en-6-yl]-N-methylformamide

> <ALOGPS_LOGP>
5.00

> <JCHEM_LOGP>
3.5113482163333325

> <ALOGPS_LOGS>
-5.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.656093482360276

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9181536002699245

> <JCHEM_POLAR_SURFACE_AREA>
37.38

> <JCHEM_REFRACTIVITY>
112.00919999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.15e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[(1S,3R,6S,8R,11S,12S,16S)-15-acetyl-12,16-dimethyl-7-methylidenepentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadec-14-en-6-yl]-N-methylformamide

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -0.993  -0.363   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.516  -1.811   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.523  -2.988   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.046  -4.437   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.993  -2.717   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.516  -1.269   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.523  -0.092   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.032  -0.998   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.025  -2.175   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.501  -3.624   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.985  -3.895   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.541  -1.904   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.064  -0.456   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.071   0.722   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.555   0.451   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.603  -0.506   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.031  -1.985   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.756  -2.849   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.548   0.710   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.074   0.499   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.968   2.137   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.736   0.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.172  -3.399   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.039   0.179   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      -3.032  -2.082   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      -4.025  -0.905   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -5.541  -1.176   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -3.555  -3.531   0.000  0.00  0.00           C+0
CONECT    1    2    7                                                       
CONECT    2    1    3   25                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   11                                                  
CONECT    6    5    7    8   24                                             
CONECT    7    6    1                                                       
CONECT    8    6    9   15   24                                             
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    5                                                       
CONECT   12    9   13   18   23                                             
CONECT   13   12   14   16   22                                             
CONECT   14   13   15                                                       
CONECT   15   14    8                                                       
CONECT   16   13   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17   12                                                       
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   13                                                            
CONECT   23   12                                                            
CONECT   24    8    6                                                       
CONECT   25    2   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₅NO₂

Average Mass

381.5600 Da

Monoisotopic Mass

381.26678 Da

IUPAC Name

N-[(1S,3R,6S,8R,11S,12S,16S)-15-acetyl-12,16-dimethyl-7-methylidenepentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadec-14-en-6-yl]-N-methylformamide

Traditional Name

N-[(1S,3R,6S,8R,11S,12S,16S)-15-acetyl-12,16-dimethyl-7-methylidenepentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadec-14-en-6-yl]-N-methylformamide

CAS Registry Number

Not Available

SMILES

CN(C=O)[C@H]1CC[C@]23C[C@]22CC[C@]4(C)C(=CC[C@@]4(C)[C@@H]2CC[C@H]3C1=C)C(C)=O

InChI Identifier

InChI=1S/C25H35NO2/c1-16-18-6-7-21-23(4)10-8-19(17(2)28)22(23,3)12-13-25(21)14-24(18,25)11-9-20(16)26(5)15-27/h8,15,18,20-21H,1,6-7,9-14H2,2-5H3/t18-,20-,21-,22+,23-,24+,25-/m0/s1

InChI Key

PEGHGSZQFPWEFQ-QNKFGOHQSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Buxus papilosa	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 20-oxosteroids. These are steroid derivatives carrying a C=O group at the 20-position of the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

20-oxosteroids

Alternative Parents

Substituents

20-oxosteroid
Tertiary carboxylic acid amide
Ketone
Carboxamide group
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5	ALOGPS
logP	3.51	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	19.66	ChemAxon
pKa (Strongest Basic)	-0.92	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	37.38 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	112.01 m³·mol⁻¹	ChemAxon
Polarizability	44.74 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163105494

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for N-Formylcyclomicrobuxeine (NP0067721)

MOL for NP0067721 (N-Formylcyclomicrobuxeine)

3D MOL for NP0067721 (N-Formylcyclomicrobuxeine)

3D SDF for NP0067721 (N-Formylcyclomicrobuxeine)

3D-SDF for NP0067721 (N-Formylcyclomicrobuxeine)

PDB for NP0067721 (N-Formylcyclomicrobuxeine)

3D PDB for NP0067721 (N-Formylcyclomicrobuxeine)

SMILES for NP0067721 (N-Formylcyclomicrobuxeine)

INCHI for NP0067721 (N-Formylcyclomicrobuxeine)

Structure for NP0067721 (N-Formylcyclomicrobuxeine)

3D Structure for NP0067721 (N-Formylcyclomicrobuxeine)