NP-MRD: Showing NP-Card for 2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid (NP0147659)

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Record Information

Version

2.0

Created at

2022-09-02 03:18:33 UTC

Updated at

2022-09-02 03:18:33 UTC

NP-MRD ID

NP0147659

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid

Description

(2,3-Dihydroxypropoxy)({2-[1-methyl-2-methylidene-9-(propan-2-yl)-5-azatricyclo[5.4.0.0³,⁸]Undecan-5-yl]ethoxy})phosphinic acid belongs to the class of organic compounds known as sesquiterpenoids. 2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid is found in Bipolaris victoriae. These are terpenes with three consecutive isoprene units (2,3-dihydroxypropoxy)({2-[1-methyl-2-methylidene-9-(propan-2-yl)-5-azatricyclo[5.4.0.0³,⁸]Undecan-5-yl]ethoxy})phosphinic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261505382D          

 28 30  0  0  0  0            999 V2000
   -0.8049    1.2685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0900    0.8567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6241    1.2698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0892    0.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8160   -0.4012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7488   -1.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0593   -1.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3373   -2.2196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8388   -0.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8271   -0.6554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9410   -0.0317    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9304    0.7932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2107    1.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2002    2.0215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4805    2.4248    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    3.1445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0771    1.7051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2392    2.8281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2498    3.6530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9695    4.0564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6786    3.6347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9800    4.8813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6997    5.2846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1488   -1.0251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2798   -1.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6846   -0.4273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6834   -1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7372   -2.8189    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  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  2  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  4 26  1  0  0  0  0
  9 26  1  0  0  0  0
 25 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 64 66  0  0  0  0  0  0  0  0999 V2000
   -0.7713   -2.2210    1.4791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7684   -1.5523    0.9251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9232   -0.0684    1.0832 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5548    0.4531    0.5615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5470    0.3709   -0.8263 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6210    0.5161   -1.5352 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8497    1.1346   -1.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4945    0.4143    0.0189 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0995    0.7411   -0.2047 P   0  0  1  0  0  5  0  0  0  0  0  0
    4.5352   -0.4181   -1.2446 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2504    2.1332   -1.2742 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2850    0.8591    0.8805 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1945   -0.2600    0.6788 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5193    0.3936    0.3998 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2007    1.2537   -0.7359 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4992   -0.5955   -0.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9802   -1.1690   -1.3510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3257   -0.6597   -1.4832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7243   -0.7853   -1.0019 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8944    0.3618    0.0083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2864    0.4185    0.4731 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6344    1.7161    1.1219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0678    2.8554    0.2654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1646    1.9645    1.0390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6581   -0.7977    1.2554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1380   -2.0436    0.6072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975   -1.9669   -0.0102 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4816   -3.2562   -0.7139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5526   -3.2535    1.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1088   -1.7215    2.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599    0.2766    2.0720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2731   -0.1355    1.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4700    1.4718    0.9581 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876    0.8762   -2.5976 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9744   -0.6191   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5650    1.4373   -1.7659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5748    2.1058   -0.4479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6608    2.8581   -0.7276 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2779   -0.6386    1.7579 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7867   -0.9479    0.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8536    1.0045    1.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7488    2.0409   -0.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4177   -0.0701   -0.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6451   -1.4430    0.5357 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1687   -1.6536   -1.1551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3327   -0.4354   -2.5757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7515   -1.6230   -1.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4864   -0.8150   -1.7710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5989    1.2910   -0.5205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9383    0.3887   -0.4717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3684    1.7796    2.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2357    2.6182   -0.7901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5914    3.8021    0.4943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9836    2.9900    0.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7412    1.0589    1.2384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3583    2.3496   -0.0072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3509    2.8163    1.7180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7266   -0.8388    1.4234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1818   -0.6533    2.2795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0878   -2.8374    1.3994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9157   -2.3719   -0.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2974   -3.9973   -0.5940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3164   -3.1298   -1.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5713   -3.7732   -0.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 24  1  0
 22 21  1  0
 21 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  6
 27 19  1  0
 19 18  1  0
 18  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  9  8  1  1
  9 11  1  0
  9 10  2  0
  9 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  5  4  1  0
  4  3  1  0
  3 20  1  0
  3  2  1  0
  2  1  2  3
 20 21  1  0
  2 27  1  0
 20 19  1  0
 23 52  1  0
 23 53  1  0
 23 54  1  0
 22 51  1  0
 24 55  1  0
 24 56  1  0
 24 57  1  0
 21 50  1  6
 25 58  1  0
 25 59  1  0
 26 60  1  0
 26 61  1  0
 28 62  1  0
 28 63  1  0
 28 64  1  0
 19 48  1  6
 18 46  1  0
 18 47  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  1
 15 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
  4 32  1  0
  4 33  1  0
  3 31  1  1
 20 49  1  6
  1 29  1  0
  1 30  1  0
M  END


  Mrv1533004261505382D          

 28 30  0  0  0  0            999 V2000
   -0.8049    1.2685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0900    0.8567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6241    1.2698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0892    0.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8160   -0.4012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7488   -1.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0593   -1.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3373   -2.2196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8388   -0.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8271   -0.6554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9410   -0.0317    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9304    0.7932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2107    1.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2002    2.0215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4805    2.4248    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    3.1445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0771    1.7051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2392    2.8281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2498    3.6530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9695    4.0564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6786    3.6347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9800    4.8813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6997    5.2846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1488   -1.0251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2798   -1.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6846   -0.4273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6834   -1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7372   -2.8189    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  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  2  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  4 26  1  0  0  0  0
  9 26  1  0  0  0  0
 25 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0147659

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1CCC2(C)C3CN(CCOP(O)(=O)OCC(O)CO)CC(C13)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C20H36NO6P/c1-13(2)16-5-6-20(4)14(3)17-9-21(10-18(20)19(16)17)7-8-26-28(24,25)27-12-15(23)11-22/h13,15-19,22-23H,3,5-12H2,1-2,4H3,(H,24,25)

> <INCHI_KEY>
FMUUEXPZVSOMDJ-UHFFFAOYSA-N

> <FORMULA>
C20H36NO6P

> <MOLECULAR_WEIGHT>
417.483

> <EXACT_MASS>
417.228024881

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
44.527015120015506

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2,3-dihydroxypropoxy)({2-[1-methyl-2-methylidene-9-(propan-2-yl)-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl]ethoxy})phosphinic acid

> <ALOGPS_LOGP>
1.11

> <JCHEM_LOGP>
-0.11432019538776383

> <ALOGPS_LOGS>
-3.17

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.641400785158883

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7357541649604578

> <JCHEM_PKA_STRONGEST_BASIC>
10.199486726917288

> <JCHEM_POLAR_SURFACE_AREA>
99.46000000000001

> <JCHEM_REFRACTIVITY>
107.5688

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.84e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      -1.502   2.368   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.168   1.599   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.165   2.370   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.167   0.059   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.523  -0.749   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.398  -2.280   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.111  -2.793   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.630  -4.143   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.566  -1.772   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.411  -1.223   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       3.623  -0.059   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       3.603   1.481   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.260   2.234   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.240   3.773   0.000  0.00  0.00           O+0
HETATM   15  P   UNK     0       0.897   4.526   0.000  0.00  0.00           P+0
HETATM   16  O   UNK     0       1.650   5.870   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.144   3.183   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -0.447   5.279   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.466   6.819   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.810   7.572   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -3.133   6.785   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.829   9.112   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.173   9.865   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.011  -1.914   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.389  -2.566   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.278  -0.798   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.276  -3.725   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.376  -5.262   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   26                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   27                                             
CONECT    8    7                                                            
CONECT    9    7   10   26                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   24                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22                                                            
CONECT   24   11   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25    4    9                                                  
CONECT   27   25    7   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
(2,3-Dihydroxypropoxy)({2-[1-methyl-2-methylidene-9-(propan-2-yl)-5-azatricyclo[5.4.0.0,]undecan-5-yl]ethoxy})phosphinate	Generator
(2,3-Dihydroxypropoxy)({2-[1-methyl-2-methylidene-9-(propan-2-yl)-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl]ethoxy})phosphinate	Generator

Chemical Formula

C₂₀H₃₆NO₆P

Average Mass

417.4830 Da

Monoisotopic Mass

417.22802 Da

IUPAC Name

(2,3-dihydroxypropoxy)({2-[1-methyl-2-methylidene-9-(propan-2-yl)-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl]ethoxy})phosphinic acid

Traditional Name

2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid

CAS Registry Number

Not Available

SMILES

CC(C)C1CCC2(C)C3CN(CCOP(O)(=O)OCC(O)CO)CC(C13)C2=C

InChI Identifier

InChI=1S/C20H36NO6P/c1-13(2)16-5-6-20(4)14(3)17-9-21(10-18(20)19(16)17)7-8-26-28(24,25)27-12-15(23)11-22/h13,15-19,22-23H,3,5-12H2,1-2,4H3,(H,24,25)

InChI Key

FMUUEXPZVSOMDJ-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
Cochliobolus victoriae	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
Phosphoethanolamine
Azepane
Dialkyl phosphate
Organic phosphoric acid derivative
Phosphoric acid ester
Piperidine
Alkyl phosphate
1,2-diol
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Amine
Alcohol
Primary alcohol
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	1.11	ALOGPS
logP	-0.11	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	1.74	ChemAxon
pKa (Strongest Basic)	10.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.46 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	107.57 m³·mol⁻¹	ChemAxon
Polarizability	44.53 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	Yes	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

75061211

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid (NP0147659)

MOL for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

3D MOL for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

3D SDF for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

3D-SDF for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

PDB for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

3D PDB for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

SMILES for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

INCHI for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

Structure for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)

3D Structure for NP0147659 (2,3-dihydroxypropoxy(2-{9-isopropyl-1-methyl-2-methylidene-5-azatricyclo[5.4.0.0³,⁸]undecan-5-yl}ethoxy)phosphinic acid)