19-Nor-4-hydroxyabieta-8,11,13-trien-7-one

Details

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Internal ID a4c0d76f-1342-4646-ac5c-eec474d53e88
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1S,4aS,10aR)-1-hydroxy-1,4a-dimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one
SMILES (Canonical) CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)O)C
SMILES (Isomeric) CC(C)C1=CC2=C(C=C1)[C@]3(CCC[C@]([C@@H]3CC2=O)(C)O)C
InChI InChI=1S/C19H26O2/c1-12(2)13-6-7-15-14(10-13)16(20)11-17-18(15,3)8-5-9-19(17,4)21/h6-7,10,12,17,21H,5,8-9,11H2,1-4H3/t17-,18-,19+/m1/s1
InChI Key PTQFIYQNKVSVGM-QRVBRYPASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H26O2
Molecular Weight 286.40 g/mol
Exact Mass 286.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.21
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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19-Nor-4-hydroxyabieta-8,11,13-trien-7-one
(1S,4aS,10aR)-1-hydroxy-1,4a-dimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one
PTQFIYQNKVSVGM-QRVBRYPASA-N
AKOS032962387
4-Hydroxy-19-norabieta-8,11,13-trien-7-one
(1S,4AS,10aR)-1-hydroxy-7-isopropyl-1,4a-dimethyl-2,3,4,4a,10,10a-hexahydrophenanthren-9(1H)-one

2D Structure

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2D Structure of 19-Nor-4-hydroxyabieta-8,11,13-trien-7-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8520 85.20%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8075 80.75%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.9326 93.26%
OATP1B3 inhibitior + 0.9644 96.44%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.4533 45.33%
P-glycoprotein inhibitior - 0.8776 87.76%
P-glycoprotein substrate - 0.7396 73.96%
CYP3A4 substrate + 0.5337 53.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7968 79.68%
CYP3A4 inhibition - 0.8454 84.54%
CYP2C9 inhibition - 0.6890 68.90%
CYP2C19 inhibition - 0.7103 71.03%
CYP2D6 inhibition - 0.9281 92.81%
CYP1A2 inhibition + 0.6148 61.48%
CYP2C8 inhibition - 0.8751 87.51%
CYP inhibitory promiscuity - 0.9461 94.61%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7911 79.11%
Carcinogenicity (trinary) Non-required 0.6390 63.90%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.9402 94.02%
Skin irritation - 0.5151 51.51%
Skin corrosion - 0.9475 94.75%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4789 47.89%
Micronuclear - 0.9941 99.41%
Hepatotoxicity - 0.5011 50.11%
skin sensitisation - 0.6473 64.73%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8225 82.25%
Acute Oral Toxicity (c) III 0.8750 87.50%
Estrogen receptor binding - 0.4741 47.41%
Androgen receptor binding + 0.5633 56.33%
Thyroid receptor binding + 0.7043 70.43%
Glucocorticoid receptor binding + 0.6029 60.29%
Aromatase binding - 0.5284 52.84%
PPAR gamma + 0.8522 85.22%
Honey bee toxicity - 0.7934 79.34%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9790 97.90%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.90% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.53% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.10% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.98% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.62% 90.71%
CHEMBL1937 Q92769 Histone deacetylase 2 90.07% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.21% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.70% 96.09%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 86.14% 85.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.83% 93.99%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.20% 93.04%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.63% 93.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.49% 95.89%
CHEMBL2535 P11166 Glucose transporter 84.33% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.09% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.43% 100.00%
CHEMBL4208 P20618 Proteasome component C5 82.16% 90.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.60% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.20% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.82% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 80.54% 97.79%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.40% 96.67%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.35% 85.30%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.34% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Asparagus racemosus
Brucea antidysenterica
Juniperus chinensis
Phagnalon bicolor
Pinus yunnanensis
Squamopappus skutchii

Cross-Links

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PubChem 91884799
NPASS NPC43293
LOTUS LTS0201139
wikiData Q105214822