NP-MRD: Showing NP-Card for (2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane (NP0309155)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-11 03:32:15 UTC

Updated at

2022-09-11 03:32:15 UTC

NP-MRD ID

NP0309155

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane

Description

(1AS)-5beta-[(S)-Oxiranyl]-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1abeta,5,7bbeta-trimethyl-1H-cyclopropa[a]phenanthrene belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane is found in Laurencia saitoi. It was first documented in 2022 (PMID: 36122165). Based on a literature review a significant number of articles have been published on (1aS)-5beta-[(S)-Oxiranyl]-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1abeta,5,7bbeta-trimethyl-1H-cyclopropa[a]phenanthrene (PMID: 36122164) (PMID: 36122163) (PMID: 36122162) (PMID: 36122161).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 55  0  0  0  0  0  0  0  0999 V2000
   -3.7053    0.1195    2.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0957    0.4099    0.9956 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7440    1.6189    0.3125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9391    0.1752   -0.1462 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3345   -0.1396   -1.4548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8553    0.0429   -1.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1954   -0.5171   -0.3434 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5977   -1.9559   -0.1757 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2899   -0.4176   -0.3930 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9659    0.0532   -1.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4267    0.1772   -1.5330 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1278    0.0832   -0.2037 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1607    1.4726    0.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5609   -0.3405   -0.4520 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4044    0.5200   -1.3789 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5907    0.4730    0.0028 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4855   -0.8953    0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0166   -0.8836    0.8043 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5279   -0.1624    2.0509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9812   -0.1725    2.1146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6310    0.3076    0.8480 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7983    0.2912    2.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5869   -0.9658    2.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3124    0.7789    3.1476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1153    2.2863   -0.2862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6062    2.0992    0.7928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9515   -0.2575    0.0216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6597   -1.1551   -1.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7893    0.5690   -2.2115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6649    1.1380   -1.6757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5032   -0.5342   -2.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6989   -2.0535   -0.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3553   -2.3557    0.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0569   -2.5613   -0.9393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3937    0.3957   -2.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8131   -0.5986   -2.2260 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6570    1.1594   -2.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2857    1.3815    1.4919 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1732    1.9412    0.2204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9789    2.0826   -0.0717 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7706   -1.4380   -0.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9741    1.4747   -1.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1645    0.0154   -2.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8613   -1.9188    0.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8879   -0.6653    1.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6698   -1.9520    0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8911   -0.7533    2.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9530    0.8384    2.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2560    0.5800    2.9115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3801   -1.1335    2.4779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2168    1.3424    0.6608 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  1
  7 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 12  1  0
 12 13  1  1
 12 11  1  0
 11 10  1  0
 10  9  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
  4  2  1  0
  9  7  1  0
 16 14  1  0
 21  2  1  0
  9 18  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  1
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  8 32  1  0
  8 33  1  0
  8 34  1  0
 21 51  1  6
 20 49  1  0
 20 50  1  0
 19 47  1  0
 19 48  1  0
 18 46  1  1
 17 44  1  0
 17 45  1  0
 13 38  1  0
 13 39  1  0
 13 40  1  0
 11 36  1  0
 11 37  1  0
 10 35  1  0
 14 41  1  6
 15 42  1  0
 15 43  1  0
M  END


  Mrv1652309112205322D          

 21 25  0  0  1  0            999 V2000
    1.4472   -3.9987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5650   -3.1821    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7485   -3.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2588   -2.4161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7692   -1.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5857   -1.8857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8919   -2.6518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4022   -2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7084   -2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2188   -2.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0353   -2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3415   -3.0054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0428   -2.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8913   -3.6205    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6749   -3.8784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0598   -4.4281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8312   -3.6536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0146   -3.5357    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5043   -4.1839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6878   -4.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3816   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 16  1  1  0  0  0
 12 17  1  0  0  0  0
 18 17  1  1  0  0  0
  9 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  6  0  0  0
  2 21  1  0  0  0  0
  7 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0309155

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12C[C@H]1CC[C@]1(C)[C@@H]2CC[C@@H]2C[C@](C)(CC=C12)[C@H]1CO1

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O/c1-18(17-12-21-17)8-7-15-13(10-18)4-5-16-19(15,2)9-6-14-11-20(14,16)3/h7,13-14,16-17H,4-6,8-12H2,1-3H3/t13-,14-,16+,17-,18+,19+,20+/m1/s1

> <INCHI_KEY>
XYIJFUAEOWBFQQ-IZSQIBBJSA-N

> <FORMULA>
C20H30O

> <MOLECULAR_WEIGHT>
286.459

> <EXACT_MASS>
286.229665586

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
34.78945511351282

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-[(1R,5S,7R,10R,11S,13R)-1,5,11-trimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-5-yl]oxirane

> <JCHEM_LOGP>
4.364233303666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.182750638457991

> <JCHEM_POLAR_SURFACE_AREA>
12.53

> <JCHEM_REFRACTIVITY>
86.34499999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(1R,5S,7R,10R,11S,13R)-1,5,11-trimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-5-yl]oxirane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       2.701  -7.464   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.921  -5.940   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.397  -5.720   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.350  -4.510   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.302  -3.300   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.827  -3.520   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.398  -4.950   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.351  -3.740   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.922  -5.170   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.875  -3.960   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.399  -4.180   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.971  -5.610   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.280  -4.799   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.997  -6.758   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.460  -7.240   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      11.312  -8.266   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.018  -6.820   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.494  -6.600   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.541  -7.810   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.017  -7.590   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.446  -6.160   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   21                                             
CONECT    3    2    4                                                       
CONECT    4    3    2    5                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   21                                             
CONECT    8    7                                                            
CONECT    9    7   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   17                                             
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14   16                                                       
CONECT   16   15   14                                                       
CONECT   17   12   18                                                       
CONECT   18   17    9   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   21    0   50    0
END

View in JSmol

Synonyms

Value	Source
(1AS)-5b-[(S)-oxiranyl]-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1abeta,5,7bbeta-trimethyl-1H-cyclopropa[a]phenanthrene	Generator
(1AS)-5β-[(S)-oxiranyl]-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1abeta,5,7bbeta-trimethyl-1H-cyclopropa[a]phenanthrene	Generator

Chemical Formula

C₂₀H₃₀O

Average Mass

286.4590 Da

Monoisotopic Mass

286.22967 Da

IUPAC Name

(2S)-2-[(1R,5S,7R,10R,11S,13R)-1,5,11-trimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-5-yl]oxirane

Traditional Name

(2S)-2-[(1R,5S,7R,10R,11S,13R)-1,5,11-trimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-5-yl]oxirane

CAS Registry Number

Not Available

SMILES

C[C@]12C[C@H]1CC[C@]1(C)[C@@H]2CC[C@@H]2C[C@](C)(CC=C12)[C@H]1CO1

InChI Identifier

InChI=1S/C20H30O/c1-18(17-12-21-17)8-7-15-13(10-18)4-5-16-19(15,2)9-6-14-11-20(14,16)3/h7,13-14,16-17H,4-6,8-12H2,1-3H3/t13-,14-,16+,17-,18+,19+,20+/m1/s1

InChI Key

XYIJFUAEOWBFQQ-IZSQIBBJSA-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
Laurencia saitoi	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	4.36	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	12.53 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	86.34 m³·mol⁻¹	ChemAxon
Polarizability	34.79 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

8836258

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10660904

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Orrantia-Borunda E, Acuna-Aguilar LE, Ramirez-Valdespino CA: Nanomaterials for Breast Cancer. 2022 Aug 6. [PubMed:36122165 ]
Tecalco-Cruz AC, Ramirez-Jarquin JO, Zepeda-Cervantes J, Solleiro-Villavicencio H, Abraham-Juarez MJ: Ubiquitin-Specific Peptidase 18: A Multifaceted Protein Participating in Breast Cancer. 2022 Aug 6. [PubMed:36122164 ]
Berg AL, Rowson-Hodel A, Wheeler MR, Hu M, Free SR, Carraway KL III: Engaging the Lysosome and Lysosome-Dependent Cell Death in Cancer. 2022 Aug 6. [PubMed:36122163 ]
Sridhar J, Komati R, Kumar S: Targeting RPS6K1 for Refractory Breast Cancer Therapy. 2022 Aug 6. [PubMed:36122162 ]
Arzanova E, Mayrovitz HN: The Epidemiology of Breast Cancer. 2022 Aug 6. [PubMed:36122161 ]
LOTUS database [Link]

Showing NP-Card for (2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane (NP0309155)

MOL for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

3D MOL for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

3D SDF for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

3D-SDF for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

PDB for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

3D PDB for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

SMILES for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

INCHI for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

Structure for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)

3D Structure for NP0309155 ((2s)-2-[(1as,1br,3ar,5s,7br,9ar)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]oxirane)