NP-MRD: Showing NP-Card for 5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol (NP0228076)

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Record Information

Version

2.0

Created at

2022-09-06 07:36:17 UTC

Updated at

2022-09-06 07:36:17 UTC

NP-MRD ID

NP0228076

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol

Description

5-(3-Hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol is found in Gypothamnium pinifolium. 5-(3-Hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241512042D          

 29 29  0  0  0  0            999 V2000
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    8.6625    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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  4  0  0  0
 16 17  2  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
 21 20  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 65 65  0  0  0  0  0  0  0  0999 V2000
   -5.6400    3.6089   -0.4905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6279    2.8323    0.1178 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8950    1.5320    0.5206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1473    0.9788    0.3346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4234   -0.3195    0.7339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7336   -0.9383    0.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7662   -0.3624    0.0127 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0542   -1.0844   -0.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0927   -0.4359    0.5626 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3901   -1.0014    1.3143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1173   -0.4967    1.5257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1472   -1.2775    2.1299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8680    0.7896    1.1209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6254    1.3742    1.2914 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6779    1.4259    0.2118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3910    0.0457   -0.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203   -0.5617   -0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0953   -1.9959   -0.6813 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0342    0.0685    0.2352 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9793    0.0353   -0.9769 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2889    0.6489   -0.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3879   -0.0617   -0.7429 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3147   -1.4793   -1.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7001    0.5413   -0.4169 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3928   -0.1917    0.7202 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6942    0.5189    0.9404 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8587   -0.0727    0.8205 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0949    0.7202    1.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9435   -1.5220    0.4487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9359    3.2092   -1.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3519    4.6692   -0.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5604    3.5611    0.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9371    1.5727   -0.1356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8196   -1.9799    0.9165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7061    0.6488   -0.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9799   -2.1047    0.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3341   -1.2494   -1.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8682   -1.0739    0.5112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5564   -2.0176    1.6426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2427   -0.8784    2.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1888    2.0112   -0.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8096    1.9958    0.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2859   -0.5192   -0.5702 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3013   -1.9787   -1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1202   -2.4307   -0.6440 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5674   -2.5604    0.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5314   -0.5299    1.0536 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9464    1.1084    0.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4605    0.5538   -1.8072 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0717   -1.0340   -1.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3522    1.6775   -0.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2934   -1.9599   -1.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8121   -1.5613   -2.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6782   -2.0040   -0.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5371    1.5833   -0.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3374    0.4790   -1.3372 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5200   -1.2560    0.5295 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7863   -0.0596    1.6401 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6102    1.5655    1.2082 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0527    1.6894    0.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9596    0.1363    0.6848 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2379    1.0011    2.1070 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4426   -1.6199   -0.5489 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4159   -2.1573    1.1842 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0059   -1.8070    0.3099 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
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
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 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  3
 27 28  1  0
 27 29  1  0
 13  3  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  6 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  0
 12 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 23 52  1  0
 23 53  1  0
 23 54  1  0
 24 55  1  0
 24 56  1  0
 25 57  1  0
 25 58  1  0
 26 59  1  0
 28 60  1  0
 28 61  1  0
 28 62  1  0
 29 63  1  0
 29 64  1  0
 29 65  1  0
M  END


  Mrv1533004241512042D          

 29 29  0  0  0  0            999 V2000
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    8.6625    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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  4  0  0  0
 16 17  2  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
 21 20  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0228076

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C=CCO)=CC(O)=C1OCC=C(C)CCC=C(C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O4/c1-19(2)9-6-10-20(3)11-7-12-21(4)14-16-29-25-23(27)17-22(13-8-15-26)18-24(25)28-5/h8-9,11,13-14,17-18,26-27H,6-7,10,12,15-16H2,1-5H3

> <INCHI_KEY>
OWYVGANMNUNBLO-UHFFFAOYSA-N

> <FORMULA>
C25H36O4

> <MOLECULAR_WEIGHT>
400.559

> <EXACT_MASS>
400.261359639

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
48.73580006864183

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol

> <ALOGPS_LOGP>
6.05

> <JCHEM_LOGP>
5.877578508666666

> <ALOGPS_LOGS>
-5.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.622962517207863

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.857291998485387

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5264874122123775

> <JCHEM_POLAR_SURFACE_AREA>
58.92

> <JCHEM_REFRACTIVITY>
124.82320000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.31e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.001   8.470   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.335   9.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.335  10.780   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.001  11.550   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.668  11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.668  13.090   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -8.002  13.860   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -8.002  15.400   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -9.336  16.170   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -6.668  16.170   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    5   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    3   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₆O₄

Average Mass

400.5590 Da

Monoisotopic Mass

400.26136 Da

IUPAC Name

5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol

Traditional Name

5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol

CAS Registry Number

Not Available

SMILES

COC1=CC(C=CCO)=CC(O)=C1OCC=C(C)CCC=C(C)CCC=C(C)C

InChI Identifier

InChI=1S/C25H36O4/c1-19(2)9-6-10-20(3)11-7-12-21(4)14-16-29-25-23(27)17-22(13-8-15-26)18-24(25)28-5/h8-9,11,13-14,17-18,26-27H,6-7,10,12,15-16H2,1-5H3

InChI Key

OWYVGANMNUNBLO-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
Gypothamnium pinifolium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Farsesane sesquiterpenoid
Cinnamyl alcohol
Methoxyphenol
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Phenol
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Ether
Primary alcohol
Alcohol
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	6.05	ALOGPS
logP	5.88	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	9.86	ChemAxon
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.92 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	124.82 m³·mol⁻¹	ChemAxon
Polarizability	48.74 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

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 5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol (NP0228076)

MOL for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

3D MOL for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

3D SDF for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

3D-SDF for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

PDB for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

3D PDB for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

SMILES for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

INCHI for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

Structure for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)

3D Structure for NP0228076 (5-(3-hydroxyprop-1-en-1-yl)-3-methoxy-2-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]phenol)