(4bS)-1-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-fluorene-3,4-dione

Details

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Internal ID 01888e21-6246-4340-ace9-fd34a6b0fef8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4bS)-1-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-fluorene-3,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H24O3/c1-10(2)13-15(20)11-9-12-18(3,4)7-6-8-19(12,5)14(11)17(22)16(13)21/h9-10,20H,6-8H2,1-5H3/t19-/m0/s1
InChI Key WMWMKDIHCOZLTG-IBGZPJMESA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O3
Molecular Weight 300.40 g/mol
Exact Mass 300.17254462 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4bS)-1-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-fluorene-3,4-dione

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 + 0.8597 85.97%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7593 75.93%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.8844 88.44%
OATP1B3 inhibitior + 0.9514 95.14%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.9177 91.77%
P-glycoprotein inhibitior - 0.8938 89.38%
P-glycoprotein substrate - 0.8427 84.27%
CYP3A4 substrate + 0.5245 52.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8811 88.11%
CYP3A4 inhibition - 0.9409 94.09%
CYP2C9 inhibition - 0.7471 74.71%
CYP2C19 inhibition - 0.8503 85.03%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition - 0.6868 68.68%
CYP2C8 inhibition - 0.9106 91.06%
CYP inhibitory promiscuity - 0.8399 83.99%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4826 48.26%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.5823 58.23%
Skin irritation + 0.6229 62.29%
Skin corrosion - 0.9255 92.55%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7898 78.98%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5995 59.95%
skin sensitisation + 0.5308 53.08%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.4512 45.12%
Acute Oral Toxicity (c) III 0.5134 51.34%
Estrogen receptor binding + 0.5370 53.70%
Androgen receptor binding + 0.5710 57.10%
Thyroid receptor binding + 0.6618 66.18%
Glucocorticoid receptor binding + 0.6475 64.75%
Aromatase binding - 0.6679 66.79%
PPAR gamma + 0.8248 82.48%
Honey bee toxicity - 0.8110 81.10%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9919 99.19%

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 96.21% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.58% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.62% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.42% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.35% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 90.83% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.65% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.30% 90.71%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.90% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.79% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.48% 93.99%

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.
Salvia dichroantha

Cross-Links

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PubChem 5316656
LOTUS LTS0267502
wikiData Q105308883