NP-MRD: Showing NP-Card for methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate (NP0235754)

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Record Information

Version

2.0

Created at

2022-09-06 18:28:48 UTC

Updated at

2022-09-06 18:28:48 UTC

NP-MRD ID

NP0235754

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate

Description

Methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]Dodec-5-ene-5-carboxylate belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen. methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate is found in Negombata magnifica. Methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]Dodec-5-ene-5-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171523252D          

 26 28  0  0  0  0            999 V2000
   -0.3110   -1.1091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3565   -0.6242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2702    0.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4835    0.5319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377    0.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514    1.5017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189    1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987    1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7704    2.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8056    2.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5930    2.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1999    2.8581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9873    2.6120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5942    3.1708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1678    1.8070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661    1.5017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6198    1.8373    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.7799    0.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7713   -0.4389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9463   -0.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4614   -1.1064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6913    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3588    0.8306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0732    1.2431    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
  3  5  1  0  0  0  0
  5  6  2  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  0  0  0  0
  8 25  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
   -5.6327    3.4522    0.9842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3678    2.8898    0.7345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2280    1.5764    0.2760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2732    0.9337    0.1010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    0.9937    0.0172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8733    1.7712    0.2388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4503    1.2974    0.0129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5341   -0.1843    0.2086 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6917   -0.9518    0.4649 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4408   -1.9009    1.6595 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9464   -0.2605    0.7882 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6263    0.6507   -0.1080 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9026    1.1450    0.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0919    0.9369    0.0363 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2018    0.2093   -1.2368 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2961    1.4388    0.7324 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9384   -1.9409   -0.7046 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3351   -2.9374   -0.1597 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.2046   -2.8587   -0.9196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5457   -2.2301   -0.7992 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2159   -2.4654    0.3666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0674   -1.4215    0.6287 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4104   -1.8590    0.5448 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8717   -0.3953   -0.4657 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4482   -0.7194   -0.8675 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2148   -0.1832   -2.2187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9334    3.3910    2.0386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6457    4.4869    0.5896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3730    2.8880    0.3565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9767    2.7919    0.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1321    1.8096    0.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0985    1.6304   -0.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1396   -0.2392    1.1906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4487   -1.5046    2.2345 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2660   -1.8824    2.3926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2917   -2.9335    1.3747 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736    0.2413    1.8007 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6876   -1.0776    1.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9393    0.2494   -1.0917 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0855    1.5763   -0.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8291    1.6784    1.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6644    0.7997   -2.0333 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6959   -0.7825   -1.1945 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2563    0.1033   -1.5033 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0789    1.6344   -0.0160 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0275    2.4050    1.2148 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6725    0.7010    1.4833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2596   -1.4320   -1.6056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1212   -3.8486   -0.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1254   -3.1953   -2.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2421   -2.5194   -1.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9570   -1.0218    1.6485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6354   -2.1779   -0.3543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5802   -0.5693   -1.3115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9763    0.5928   -2.5262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2424    0.2375   -2.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3832   -1.0195   -2.9601 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8 25  1  0
 25 26  1  6
 25 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  0
 17  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24  5  1  0
  9  8  1  0
 24 25  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  1
 26 55  1  0
 26 56  1  0
 26 57  1  0
 20 51  1  6
 19 49  1  0
 19 50  1  0
 17 48  1  6
 10 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 15 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 16 47  1  0
 22 52  1  1
 23 53  1  0
 24 54  1  6
M  END


  Mrv1533004171523252D          

 26 28  0  0  0  0            999 V2000
   -0.3110   -1.1091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3565   -0.6242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2702    0.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4835    0.5319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377    0.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514    1.5017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189    1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987    1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7704    2.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8056    2.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5930    2.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1999    2.8581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9873    2.6120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5942    3.1708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1678    1.8070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661    1.5017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6198    1.8373    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.7799    0.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7713   -0.4389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9463   -0.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4614   -1.1064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6913    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3588    0.8306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0732    1.2431    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
  3  5  1  0  0  0  0
  5  6  2  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  0  0  0  0
  8 25  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0235754

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CCC2C3(C)C(CC(Cl)C2(C)CCC=C(C)C)OC(O)C13

> <INCHI_IDENTIFIER>
InChI=1S/C21H31ClO4/c1-12(2)7-6-10-20(3)14-9-8-13(18(23)25-5)17-19(24)26-16(11-15(20)22)21(14,17)4/h7-8,14-17,19,24H,6,9-11H2,1-5H3

> <INCHI_KEY>
SRJIDFQIECGKBW-UHFFFAOYSA-N

> <FORMULA>
C21H31ClO4

> <MOLECULAR_WEIGHT>
382.93

> <EXACT_MASS>
382.1910872

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
42.65095703533597

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate

> <ALOGPS_LOGP>
4.64

> <JCHEM_LOGP>
4.097647648

> <ALOGPS_LOGS>
-4.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.077536491838682

> <JCHEM_PKA_STRONGEST_BASIC>
-4.077085538469761

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
103.30299999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -0.580  -2.070   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.665  -1.165   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.504   0.366   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.902   0.993   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.750   1.272   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.589   2.803   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.835   3.708   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.242   3.082   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.971   3.708   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.171   5.025   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.104   4.752   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.574   4.292   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.706   5.335   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.176   4.876   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.309   5.919   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.513   3.373   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.217   2.803   0.000  0.00  0.00           C+0
HETATM   18 Cl   UNK     0       8.624   3.430   0.000  0.00  0.00          Cl+0
HETATM   19  C   UNK     0       7.056   1.272   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.649   0.645   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.173  -0.819   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.633  -0.819   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.728  -2.065   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.157   0.645   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.403   1.550   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.737   2.320   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   24                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   25                                                  
CONECT    9    8   10   11   17                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    9   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    5   25                                                  
CONECT   25   24    8   20   26                                             
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
Methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0,]dodec-5-ene-5-carboxylic acid	Generator
Methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylic acid	Generator

Chemical Formula

C₂₁H₃₁ClO₄

Average Mass

382.9300 Da

Monoisotopic Mass

382.19109 Da

IUPAC Name

methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate

Traditional Name

methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CCC2C3(C)C(CC(Cl)C2(C)CCC=C(C)C)OC(O)C13

InChI Identifier

InChI=1S/C21H31ClO4/c1-12(2)7-6-10-20(3)14-9-8-13(18(23)25-5)17-19(24)26-16(11-15(20)22)21(14,17)4/h7-8,14-17,19,24H,6,9-11H2,1-5H3

InChI Key

SRJIDFQIECGKBW-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
Negombata magnifica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydrofurans

Sub Class

Not Available

Direct Parent

Tetrahydrofurans

Alternative Parents

Substituents

Tetrahydrofuran
Methyl ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Hemiacetal
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Organochloride
Organohalogen compound
Alkyl chloride
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Alkyl halide
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	4.64	ALOGPS
logP	4.1	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	12.08	ChemAxon
pKa (Strongest Basic)	-4.1	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	5	ChemAxon
Refractivity	103.3 m³·mol⁻¹	ChemAxon
Polarizability	42.65 Å³	ChemAxon
Number of Rings	3	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate (NP0235754)

MOL for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

3D MOL for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

3D SDF for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

3D-SDF for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

PDB for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

3D PDB for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

SMILES for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

INCHI for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

Structure for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)

3D Structure for NP0235754 (methyl 10-chloro-3-hydroxy-9,12-dimethyl-9-(4-methylpent-3-en-1-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodec-5-ene-5-carboxylate)