NP-MRD: Showing NP-Card for (1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one (NP0184657)

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Record Information

Version

2.0

Created at

2022-09-03 23:50:15 UTC

Updated at

2022-09-03 23:50:15 UTC

NP-MRD ID

NP0184657

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one

Description

1Beta,2alpha-Dimethyl-3alpha-hydroxy-2,3-dihydro-1H-carbazole-4(9H)-one belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. Based on a literature review a small amount of articles have been published on 1beta,2alpha-Dimethyl-3alpha-hydroxy-2,3-dihydro-1H-carbazole-4(9H)-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
   -1.8106    2.1593   -0.7288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5607    1.0848    0.2909 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1227    0.7073    0.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9012    1.3730    0.9495 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0305    0.6821    0.7520 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3155    0.9410    1.1622 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3171    0.0294    0.8057 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0270   -1.1037    0.0603 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7093   -1.3253   -0.3337 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7080   -0.4410    0.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3548   -0.4440   -0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5675   -1.3188   -0.9750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1685   -2.4617   -1.2956 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9143   -0.7766   -1.2639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7816   -1.7448   -1.7540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4220   -0.1162   -0.0178 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4223   -1.0409    1.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2347    3.0598   -0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5273    1.8569   -1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8593    2.4136   -1.2606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8583    1.4283    1.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8109    2.2819    1.4839 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6230    1.7985    1.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3194    0.1992    1.1062 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7975   -1.8089   -0.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4948   -2.2106   -0.9137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7654    0.0327   -2.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5795   -1.8353   -2.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4524    0.2580   -0.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0946   -1.9042    1.0243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4038   -1.3146    1.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8637   -0.4591    2.0251 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16  2  1  0
  2  1  1  0
  2  3  1  0
  3 11  2  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
  4  3  1  0
  5 10  1  0
 17 30  1  0
 17 31  1  0
 17 32  1  0
 16 29  1  6
  2 21  1  1
  1 18  1  0
  1 19  1  0
  1 20  1  0
  9 26  1  0
  8 25  1  0
  7 24  1  0
  6 23  1  0
  4 22  1  0
 14 27  1  6
 15 28  1  0
M  END


  Mrv1652309042201502D          

 17 19  0  0  1  0            999 V2000
    2.0171    0.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720   -0.4349    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0790   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7464   -0.1215    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4139   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2208   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7729   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5179   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1589   -1.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3339   -1.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7819   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0368   -2.7887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9749   -1.8326    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4229   -2.4457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200   -1.0479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9130   -0.8764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  3 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0184657

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H](C)C2=C(C3=CC=CC=C3N2)C(=O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C14H15NO2/c1-7-8(2)13(16)14(17)11-9-5-3-4-6-10(9)15-12(7)11/h3-8,13,15-16H,1-2H3/t7-,8-,13-/m0/s1

> <INCHI_KEY>
QCKVUTCVXGLZQC-UPFKWVMWSA-N

> <FORMULA>
C14H15NO2

> <MOLECULAR_WEIGHT>
229.279

> <EXACT_MASS>
229.110278727

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
24.91760536745987

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3S)-3-hydroxy-1,2-dimethyl-2,3,4,9-tetrahydro-1H-carbazol-4-one

> <JCHEM_LOGP>
2.0028600570000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.21413889589181

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.440439884594149

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6580591193239975

> <JCHEM_POLAR_SURFACE_AREA>
53.089999999999996

> <JCHEM_REFRACTIVITY>
65.8801

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       3.765   0.653   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.241  -0.812   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.747  -1.132   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       6.993  -0.227   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       8.239  -1.132   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.746  -0.812   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.776  -1.956   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.300  -3.421   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.794  -3.741   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.763  -2.597   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.223  -2.597   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.193  -3.741   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.669  -5.206   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.687  -3.421   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.656  -4.565   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.211  -1.956   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.704  -1.636   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10    3   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    2   17                                                  
CONECT   17   16                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

View in JSmol

Synonyms

Value	Source
1b,2a-Dimethyl-3a-hydroxy-2,3-dihydro-1H-carbazole-4(9H)-one	Generator
1Β,2α-dimethyl-3α-hydroxy-2,3-dihydro-1H-carbazole-4(9H)-one	Generator

Chemical Formula

C₁₄H₁₅NO₂

Average Mass

229.2790 Da

Monoisotopic Mass

229.11028 Da

IUPAC Name

(1S,2S,3S)-3-hydroxy-1,2-dimethyl-2,3,4,9-tetrahydro-1H-carbazol-4-one

Traditional Name

(1S,2S,3S)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H](C)C2=C(C3=CC=CC=C3N2)C(=O)[C@H]1O

InChI Identifier

InChI=1S/C14H15NO2/c1-7-8(2)13(16)14(17)11-9-5-3-4-6-10(9)15-12(7)11/h3-8,13,15-16H,1-2H3/t7-,8-,13-/m0/s1

InChI Key

QCKVUTCVXGLZQC-UPFKWVMWSA-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 carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
Indole
Aryl ketone
Aryl alkyl ketone
Benzenoid
Pyrrole
Heteroaromatic compound
Vinylogous amide
Ketone
Secondary alcohol
Azacycle
Organic oxide
Organooxygen compound
Organonitrogen compound
Alcohol
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2	ChemAxon
pKa (Strongest Acidic)	12.44	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	53.09 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	65.88 m³·mol⁻¹	ChemAxon
Polarizability	24.92 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

78437075

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101537394

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one (NP0184657)

MOL for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

3D MOL for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

3D SDF for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

3D-SDF for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

PDB for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

3D PDB for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

SMILES for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

INCHI for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

Structure for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)

3D Structure for NP0184657 ((1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one)