NP-MRD: Showing NP-Card for (+)-Subamolide B (NP0077213)

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Record Information

Version

2.0

Created at

2022-04-28 22:21:20 UTC

Updated at

2022-04-28 22:21:20 UTC

NP-MRD ID

NP0077213

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Subamolide B

Description

SUBAMOLIDE B belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals. (+)-Subamolide B is found in Cinnamomum subavenium. (+)-Subamolide B was first documented in 2013 (PMID: 23573140). Based on a literature review very few articles have been published on SUBAMOLIDE B (PMID: 25495689).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 60 60  0  0  0  0  0  0  0  0999 V2000
    5.8021    3.3079   -0.3898 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1839    2.8055    0.8762 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6755    1.3396    0.6859 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8079    0.4640    0.3242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5700   -0.9568    0.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6641   -1.4462   -0.8678 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2452   -1.0609   -0.7794 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6171   -1.4780    0.5300 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1822   -1.0388    0.5669 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4272   -1.6664   -0.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0430   -1.2717   -0.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6683   -1.9832   -1.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1414   -1.6787   -1.8613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9089   -2.0844   -0.6743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5758   -1.1701   -0.0003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3876   -1.3747    1.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7167   -2.4835    1.6869 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7425   -0.1328    1.6999 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5550    0.8566    0.7203 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9313    1.1288    0.1095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0151    1.9720    1.3133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7942    3.0112    0.4084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6241    0.2552   -0.3350 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2076    0.5177   -1.5745 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8997    3.0446   -0.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6912    4.4010   -0.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3636    2.8618   -1.3006 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2624    3.3832    1.0951 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8698    2.7709    1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9222    1.4812   -0.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2776    1.0583    1.6678 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5912    0.5854    1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3147    0.8287   -0.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5875   -1.4696   -0.0480 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2780   -1.4628    1.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6679   -2.5988   -0.9180 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0429   -1.2069   -1.9216 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9069   -0.0908   -1.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7453   -1.7317   -1.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2154   -1.0690    1.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6240   -2.5999    0.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7326   -1.3988    1.5189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1757    0.0744    0.5213 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7873   -1.4242   -1.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4645   -2.7683   -0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0624   -0.1762   -0.7293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5439   -1.4842    0.3919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1062   -1.6758   -2.6358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5245   -3.0792   -1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2342   -0.6144   -2.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5465   -2.2439   -2.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9094   -3.1220   -0.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7399    1.5256   -0.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4687    1.8904    0.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4776    0.1683   -0.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1103    2.7564   -0.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4263    3.8991    0.9543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7838    3.2479   -0.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6142    0.7027   -0.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7361   -0.2958   -1.8076 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 23  1  0
 23 24  1  0
 23 19  1  0
 19 20  1  0
 19 21  1  1
 21 22  1  0
 19 18  1  0
 18 16  1  0
 16 17  2  0
 16 15  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  0
  8 41  1  0
  9 42  1  0
  9 43  1  0
 10 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 23 59  1  6
 24 60  1  0
 20 53  1  0
 20 54  1  0
 20 55  1  0
 22 56  1  0
 22 57  1  0
 22 58  1  0
M  END


  Mrv1652304292200212D          

 24 24  0  0  1  0            999 V2000
   -5.1252    2.8638    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3182    2.6923    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2320    1.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5175    1.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8030    1.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0886    1.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3741    1.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6596    1.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0549    1.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7693    1.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4838    1.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1983    1.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9127    1.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6272    1.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3417    1.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0562    1.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7706    1.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9856    1.5362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1572    0.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5377    2.1493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7051    3.2443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0475    3.6851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7875    3.3557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5446    3.0280    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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  1 20  1  0  0  0  0
  2 21  1  6  0  0  0
  1 22  1  6  0  0  0
  1 23  1  1  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0077213

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCC\C=C1/[C@@H](O)[C@](C)(OC)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H36O4/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(21)20(2,23-3)24-19(17)22/h16,18,21H,4-15H2,1-3H3/b17-16+/t18-,20-/m1/s1

> <INCHI_KEY>
YLCXJNOKPGBEPM-DPBVHHOFSA-N

> <FORMULA>
C20H36O4

> <MOLECULAR_WEIGHT>
340.504

> <EXACT_MASS>
340.261359639

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
42.40179214587894

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3E,4R,5R)-4-hydroxy-5-methoxy-5-methyl-3-tetradecylideneoxolan-2-one

> <ALOGPS_LOGP>
6.23

> <JCHEM_LOGP>
6.163620403666666

> <ALOGPS_LOGS>
-5.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.402777536550555

> <JCHEM_PKA_STRONGEST_BASIC>
-3.934825105512787

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
97.58189999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.95e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E,4R,5R)-4-hydroxy-5-methoxy-5-methyl-3-tetradecylideneoxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -9.567   5.346   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.061   5.026   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.900   3.494   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.566   2.724   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.232   3.494   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.899   2.724   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.565   3.494   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.231   2.724   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.102   3.494   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.436   2.724   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.770   3.494   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.103   2.724   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.437   3.494   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.771   2.724   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.104   3.494   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.438   2.724   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.772   3.494   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -9.307   2.868   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -9.627   1.361   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0     -10.337   4.012   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -6.916   6.056   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -9.422   6.879   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0     -10.803   6.264   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0     -12.217   5.652   0.000  0.00  0.00           C+0
CONECT    1    2   20   22   23                                             
CONECT    2    1    3   21                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18    3   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    1                                                       
CONECT   21    2                                                            
CONECT   22    1                                                            
CONECT   23    1   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₆O₄

Average Mass

340.5040 Da

Monoisotopic Mass

340.26136 Da

IUPAC Name

(3E,4R,5R)-4-hydroxy-5-methoxy-5-methyl-3-tetradecylideneoxolan-2-one

Traditional Name

(3E,4R,5R)-4-hydroxy-5-methoxy-5-methyl-3-tetradecylideneoxolan-2-one

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCC\C=C1/[C@@H](O)[C@](C)(OC)OC1=O

InChI Identifier

InChI=1S/C20H36O4/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(21)20(2,23-3)24-19(17)22/h16,18,21H,4-15H2,1-3H3/b17-16+/t18-,20-/m1/s1

InChI Key

YLCXJNOKPGBEPM-DPBVHHOFSA-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
Cinnamomum subavenium	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Ketals

Alternative Parents

Substituents

Ketal
Gamma butyrolactone
Oxolane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	6.23	ALOGPS
logP	6.16	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	12.4	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	97.58 m³·mol⁻¹	ChemAxon
Polarizability	42.4 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00040402

Chemspider ID

17262751

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16104907

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hou YL, Chang HS, Wang HC, Wang SY, Chen TY, Lin CH, Chen IS: Sassarandainol: a new neolignan and anti-inflammatory constituents from the stem of Sassafras randaiense. Nat Prod Res. 2015;29(9):827-32. doi: 10.1080/14786419.2014.988713. Epub 2014 Dec 11. [PubMed:25495689 ]
Yang SY, Wang HM, Wu TW, Chen YJ, Shieh JJ, Lin JH, Ho TF, Luo RJ, Chen CY, Chang CC: Subamolide B Isolated from Medicinal Plant Cinnamomum subavenium Induces Cytotoxicity in Human Cutaneous Squamous Cell Carcinoma Cells through Mitochondrial and CHOP-Dependent Cell Death Pathways. Evid Based Complement Alternat Med. 2013;2013:630415. doi: 10.1155/2013/630415. Epub 2013 Mar 13. [PubMed:23573140 ]

Showing NP-Card for (+)-Subamolide B (NP0077213)

MOL for NP0077213 ((+)-Subamolide B)

3D MOL for NP0077213 ((+)-Subamolide B)

3D SDF for NP0077213 ((+)-Subamolide B)

3D-SDF for NP0077213 ((+)-Subamolide B)

PDB for NP0077213 ((+)-Subamolide B)

3D PDB for NP0077213 ((+)-Subamolide B)

SMILES for NP0077213 ((+)-Subamolide B)

INCHI for NP0077213 ((+)-Subamolide B)

Structure for NP0077213 ((+)-Subamolide B)

3D Structure for NP0077213 ((+)-Subamolide B)