NP-MRD: Showing NP-Card for (1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate (NP0154330)

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Record Information

Version

2.0

Created at

2022-09-02 11:07:15 UTC

Updated at

2022-09-02 11:07:16 UTC

NP-MRD ID

NP0154330

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate

Description

12-O-acetylsarcostin belongs to the class of organic compounds known as gluco/mineralocorticoids, progestogins and derivatives. These are steroids with a structure based on a hydroxylated prostane moiety. Based on a literature review very few articles have been published on 12-O-acetylsarcostin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022213072D          

 30 33  0  0  1  0            999 V2000
    4.3959   -5.3296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6762   -4.5536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4883   -4.4084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1444   -3.9229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9853   -1.5952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4534   -0.9645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2655   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777   -0.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.7655   -1.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1731   -1.7404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1136   -0.9175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1278   -3.3123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2561   -2.6347    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7243   -2.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -3.4106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5330   -3.2587    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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  1  1  0  0  0
  8 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  6  0  0  0
 26 27  1  0  0  0  0
 26 28  1  1  0  0  0
 24 29  1  0  0  0  0
  5 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  1  0  0  0
M  END

     RDKit          3D

 66 69  0  0  0  0  0  0  0  0999 V2000
   -1.1935    2.4305    3.8277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5677    1.1791    3.1066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3185    0.3001    3.6020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0660    0.9894    1.8506 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3261   -0.1460    1.0332 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0526   -0.8976    0.8777 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8709   -0.4144   -0.1741 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3332    0.7557   -0.9592 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3706    1.9299   -0.2016 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1643    0.9468   -2.1831 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5897    1.0539   -1.8615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0622    0.5422   -0.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5349    0.6998   -0.4892 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1654   -0.5881   -0.0619 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4080   -0.3052    0.5333 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3702   -1.3814    0.9181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9180   -1.5224    0.5246 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2767   -0.1592    0.2903 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3669    0.6006    1.5757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0863    0.5301   -1.3739 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4809    1.6965   -2.0743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2836   -0.6115   -2.3160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4785   -1.4021   -1.8767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0826   -0.6483   -0.7000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1900    0.0460   -1.2290 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6379   -1.5953    0.3047 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7141   -2.4211   -0.4162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3106   -0.8942    1.3024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0162    0.2710   -0.1956 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7031    1.6157    0.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4772    2.3994    4.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7442    3.2605    3.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1199    2.6414    3.6592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0071   -0.7908    1.6641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3262   -1.9874    0.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4837   -0.8628    1.8572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9787   -1.2535   -0.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1839    2.4781   -0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0110    0.0749   -2.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8746    1.8422   -2.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2566    1.5669   -2.5756 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0629    1.0242   -1.4241 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7475    1.5040    0.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3710   -1.2073   -0.9645 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8778    0.4293    0.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4173   -0.9901    1.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7926   -2.4067    0.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3853   -1.9999    1.3531 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7751   -2.1112   -0.3851 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6445    1.4040    1.6962 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2626   -0.0769    2.4661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3773    1.0559    1.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9336    2.4739   -1.8082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4256   -1.2950   -2.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4949   -0.2736   -3.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2203   -1.5509   -2.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1767   -2.4387   -1.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0849    0.2319   -2.1787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9198   -2.3350    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4000   -2.8488    0.3458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2969   -1.7557   -1.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2603   -3.2788   -0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0563   -1.4082    1.6941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4322    1.8378   -0.7277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9158    2.3947    0.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1330    1.6517    1.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 28  1  0
 26 24  1  0
 24 25  1  6
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  1  6
 20 29  1  0
 29 30  1  1
 29  5  1  0
  5  6  1  0
  6  7  1  0
  7 18  1  0
 18 19  1  1
 18 17  1  0
 17 16  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10  8  1  0
  8  9  1  1
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 29 24  1  0
  8  7  1  0
  8 20  1  0
 12 18  1  0
 27 60  1  0
 27 61  1  0
 27 62  1  0
 26 59  1  1
 28 63  1  0
 25 58  1  0
 23 56  1  0
 23 57  1  0
 22 54  1  0
 22 55  1  0
 21 53  1  0
 30 64  1  0
 30 65  1  0
 30 66  1  0
  5 34  1  1
  6 35  1  0
  6 36  1  0
  7 37  1  6
 19 50  1  0
 19 51  1  0
 19 52  1  0
 17 48  1  0
 17 49  1  0
 16 46  1  0
 16 47  1  0
 14 44  1  6
 15 45  1  0
 13 42  1  0
 13 43  1  0
 11 41  1  0
 10 39  1  0
 10 40  1  0
  9 38  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
M  END


  Mrv1652309022213072D          

 30 33  0  0  1  0            999 V2000
    4.3959   -5.3296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6762   -4.5536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4883   -4.4084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1444   -3.9229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9853   -1.5952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4534   -0.9645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2655   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777   -0.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.7655   -1.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1731   -1.7404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1136   -0.9175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1278   -3.3123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2561   -2.6347    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7243   -2.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -3.4106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5330   -3.2587    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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  1  1  0  0  0
  8 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  6  0  0  0
 26 27  1  0  0  0  0
 26 28  1  1  0  0  0
 24 29  1  0  0  0  0
  5 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0154330

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](O)[C@]1(O)CC[C@@]2(O)[C@]1(C)[C@@H](C[C@@H]1[C@@]3(C)CC[C@H](O)CC3=CC[C@@]21O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H36O7/c1-13(24)21(27)9-10-23(29)20(21,4)18(30-14(2)25)12-17-19(3)7-6-16(26)11-15(19)5-8-22(17,23)28/h5,13,16-18,24,26-29H,6-12H2,1-4H3/t13-,16-,17+,18+,19-,20+,21+,22-,23+/m0/s1

> <INCHI_KEY>
OWEULLLQUQJHMM-WXIGEINASA-N

> <FORMULA>
C23H36O7

> <MOLECULAR_WEIGHT>
424.534

> <EXACT_MASS>
424.246103499

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
45.4478828916601

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,5S,10S,11R,14S,15R,16R)-5,10,11,14-tetrahydroxy-14-[(1S)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-16-yl acetate

> <ALOGPS_LOGP>
0.97

> <JCHEM_LOGP>
-0.42600492066666656

> <ALOGPS_LOGS>
-2.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.455307440204805

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.78975285501463

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3972432787843028

> <JCHEM_POLAR_SURFACE_AREA>
127.45000000000002

> <JCHEM_REFRACTIVITY>
109.5741

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.68e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,10S,11R,14S,15R,16R)-5,10,11,14-tetrahydroxy-14-[(1S)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-16-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       8.206  -9.949   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.729  -8.500   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.245  -8.229   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.736  -7.323   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.313  -1.800   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      16.362  -3.071   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.679  -1.713   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.839  -6.183   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.211  -4.918   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.219  -3.741   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.688  -6.367   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9   10   20                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   12    7   19                                             
CONECT   19   18                                                            
CONECT   20    8   21   22   29                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   29                                             
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24    5   20   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₆O₇

Average Mass

424.5340 Da

Monoisotopic Mass

424.24610 Da

IUPAC Name

(1R,2R,5S,10S,11R,14S,15R,16R)-5,10,11,14-tetrahydroxy-14-[(1S)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-16-yl acetate

Traditional Name

(1R,2R,5S,10S,11R,14S,15R,16R)-5,10,11,14-tetrahydroxy-14-[(1S)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-16-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H](O)[C@]1(O)CC[C@@]2(O)[C@]1(C)[C@@H](C[C@@H]1[C@@]3(C)CC[C@H](O)CC3=CC[C@@]21O)OC(C)=O

InChI Identifier

InChI=1S/C23H36O7/c1-13(24)21(27)9-10-23(29)20(21,4)18(30-14(2)25)12-17-19(3)7-6-16(26)11-15(19)5-8-22(17,23)28/h5,13,16-18,24,26-29H,6-12H2,1-4H3/t13-,16-,17+,18+,19-,20+,21+,22-,23+/m0/s1

InChI Key

OWEULLLQUQJHMM-WXIGEINASA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gluco/mineralocorticoids, progestogins and derivatives. These are steroids with a structure based on a hydroxylated prostane moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Pregnane steroids

Direct Parent

Gluco/mineralocorticoids, progestogins and derivatives

Alternative Parents

Substituents

Progestogin-skeleton
Steroid ester
20-hydroxysteroid
3-hydroxy-delta-5-steroid
3-hydroxysteroid
17-hydroxysteroid
3-beta-hydroxysteroid
3-beta-hydroxy-delta-5-steroid
14-hydroxysteroid
Hydroxysteroid
Delta-5-steroid
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	0.97	ALOGPS
logP	-0.43	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	12.79	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	127.45 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	109.57 m³·mol⁻¹	ChemAxon
Polarizability	45.45 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

24698448

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44575619

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate (NP0154330)

MOL for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D MOL for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D SDF for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D-SDF for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

PDB for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D PDB for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

SMILES for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

INCHI for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

Structure for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D Structure for NP0154330 ((1s,3ar,3bs,7s,9ar,9br,11r,11ar)-1,3a,3b,7-tetrahydroxy-1-[(1s)-1-hydroxyethyl]-9a,11a-dimethyl-2h,3h,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)