NP-MRD: Showing NP-Card for 1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid (NP0322965)

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Record Information

Version

2.0

Created at

2022-09-12 02:04:56 UTC

Updated at

2022-09-12 02:04:56 UTC

NP-MRD ID

NP0322965

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid

Description

1-({6-Hydroxy-5a,9-dimethyl-2-oxo-2H,3H,3aH,4H,5H,5aH,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton. 1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid is found in Saussurea costus. 1-({6-Hydroxy-5a,9-dimethyl-2-oxo-2H,3H,3aH,4H,5H,5aH,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251516082D          

 26 29  0  0  0  0            999 V2000
    2.2089   -2.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6043   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6490    0.6290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8636   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4736    0.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2982    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1228    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127   -0.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3140   -0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9440    0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7978    0.9726    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0549    1.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1667    2.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9787    2.2952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3687    1.5682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1861    1.4564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6916    2.1083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4979    0.6926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758   -1.6293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108   -1.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0781   -0.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  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
 17 18  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
  7 26  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -2.0310   -2.5605   -1.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7907   -1.4533   -0.4702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0903   -1.3808   -0.6691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9816   -0.3534   -0.0868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2446    0.6245    0.7892 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0952    0.0877    2.0652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8380    0.8406    0.2383 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9925    1.2672   -1.1856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1755    1.8679    1.1183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7946    2.0948    0.6264 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0600    0.8693    0.4594 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9758    1.0576   -0.7141 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4363    1.0671   -0.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0425   -0.0451    0.0967 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8886   -0.4887    1.4059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0993   -1.3535    1.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6708   -1.6920    0.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2933   -0.4704   -0.4319 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3552    0.5370   -0.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1456    1.6617    0.1721 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6227    0.2707   -0.8295 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7049   -0.0746   -1.6504 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921   -0.3803   -2.6298 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4302   -0.6920   -1.2176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6498   -0.3903    0.1470 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1128   -0.4539    0.3987 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1278   -2.8109   -0.5099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6454   -3.4952   -1.1433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7778   -2.3391   -2.1805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5695   -2.1258   -1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7976   -0.8081    0.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4875    0.1585   -0.9506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8077    1.5731    0.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9653   -0.3304    2.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4078    2.1723   -1.4312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6438    0.4717   -1.8898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0592    1.5298   -1.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1551    1.4792    2.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7226    2.8102    1.0840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7717    2.6853   -0.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2889    2.7825    1.3583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6642    0.7631    1.3744 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6634    1.9701   -1.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6457    2.0367    0.1139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9236    1.2443   -1.4760 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0213   -1.1694    1.5262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7958    0.3306    2.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8101   -0.7371    2.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8057   -2.2201    2.3369 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1191   -2.5422   -0.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7536   -1.8410    0.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1244   -0.8139   -1.4895 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9381    0.7980   -1.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1984   -1.2294    0.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2991   -0.8000    1.4574 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  6
  7  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  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 21  1  0
 19 20  2  0
 12 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26  2  1  0
 26  7  1  0
 25 11  1  0
 18 14  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  1
  6 34  1  0
  8 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  1
 12 43  1  6
 13 44  1  0
 13 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  6
 21 53  1  0
 25 54  1  1
 26 55  1  1
M  END


  Mrv1533004251516082D          

 26 29  0  0  0  0            999 V2000
    2.2089   -2.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6043   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6490    0.6290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8636   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4736    0.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2982    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1228    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127   -0.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3140   -0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9440    0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7978    0.9726    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0549    1.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1667    2.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9787    2.2952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3687    1.5682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1861    1.4564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6916    2.1083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4979    0.6926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758   -1.6293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108   -1.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0781   -0.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  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
 17 18  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
  7 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322965

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CCC(O)C2(C)CCC3C(CN4CCCC4C(O)=O)C(=O)OC3C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H29NO5/c1-11-5-6-15(22)20(2)8-7-12-13(19(25)26-17(12)16(11)20)10-21-9-3-4-14(21)18(23)24/h5,12-17,22H,3-4,6-10H2,1-2H3,(H,23,24)

> <INCHI_KEY>
IOJCSUJBMIRADL-UHFFFAOYSA-N

> <FORMULA>
C20H29NO5

> <MOLECULAR_WEIGHT>
363.454

> <EXACT_MASS>
363.204573038

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
38.84146237456942

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-({6-hydroxy-5a,9-dimethyl-2-oxo-2H,3H,3aH,4H,5H,5aH,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid

> <ALOGPS_LOGP>
0.67

> <JCHEM_LOGP>
-1.2015352340578216

> <ALOGPS_LOGS>
-2.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.625857567011856

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2391167315971074

> <JCHEM_PKA_STRONGEST_BASIC>
10.156916453212036

> <JCHEM_POLAR_SURFACE_AREA>
87.07000000000001

> <JCHEM_REFRACTIVITY>
95.7774

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.81e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-({6-hydroxy-5a,9-dimethyl-2-oxo-3H,3aH,4H,5H,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       4.123  -4.254   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.395  -2.897   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.856  -2.849   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.128  -1.492   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.939  -0.183   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.211   1.174   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.479  -0.231   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.751   1.126   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.290   1.078   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.829   1.030   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.557  -0.327   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.053  -0.694   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.229   0.300   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       8.956   1.816   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       7.569   2.486   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.778   4.011   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.294   4.284   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.022   2.927   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.547   2.719   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.491   3.936   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      12.129   1.293   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.166  -2.230   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.475  -3.041   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.740  -2.812   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.746  -1.636   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.207  -1.588   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9   26                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   14   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   12   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   11   26                                                  
CONECT   26   25    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
1-({6-hydroxy-5a,9-dimethyl-2-oxo-2H,3H,3ah,4H,5H,5ah,6H,7H,9ah,9BH-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylate	Generator

Chemical Formula

C₂₀H₂₉NO₅

Average Mass

363.4540 Da

Monoisotopic Mass

363.20457 Da

IUPAC Name

1-({6-hydroxy-5a,9-dimethyl-2-oxo-2H,3H,3aH,4H,5H,5aH,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid

Traditional Name

1-({6-hydroxy-5a,9-dimethyl-2-oxo-3H,3aH,4H,5H,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1=CCC(O)C2(C)CCC3C(CN4CCCC4C(O)=O)C(=O)OC3C12

InChI Identifier

InChI=1S/C20H29NO5/c1-11-5-6-15(22)20(2)8-7-12-13(19(25)26-17(12)16(11)20)10-21-9-3-4-14(21)18(23)24/h5,12-17,22H,3-4,6-10H2,1-2H3,(H,23,24)

InChI Key

IOJCSUJBMIRADL-UHFFFAOYSA-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
Saussurea costus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Eudesmanolides, secoeudesmanolides, and derivatives

Alternative Parents

Substituents

Eudesmanolide
Sesquiterpenoid
Naphthofuran
Proline or derivatives
Alpha-amino acid or derivatives
Alpha-amino acid
Pyrrolidine carboxylic acid
Pyrrolidine carboxylic acid or derivatives
Dicarboxylic acid or derivatives
Gamma butyrolactone
N-alkylpyrrolidine
Tetrahydrofuran
Pyrrolidine
Amino acid
Lactone
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Carboxylic acid ester
Amino acid or derivatives
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organopnictogen compound
Organic nitrogen compound
Organic oxygen compound
Amine
Organooxygen compound
Organonitrogen 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	0.67	ALOGPS
logP	-1.2	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	1.24	ChemAxon
pKa (Strongest Basic)	10.16	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	87.07 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.78 m³·mol⁻¹	ChemAxon
Polarizability	38.84 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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

72767109

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid (NP0322965)

MOL for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

3D MOL for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

3D SDF for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

3D-SDF for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

PDB for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

3D PDB for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

SMILES for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

INCHI for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

Structure for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)

3D Structure for NP0322965 (1-({6-hydroxy-5a,9-dimethyl-2-oxo-3h,3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl)pyrrolidine-2-carboxylic acid)