(1S,4aS,10aR)-8-ethyl-1,4a,7-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde

Details

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Internal ID c7b0a432-d2b0-47e1-ab9f-a29c4c4f9f29
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1S,4aS,10aR)-8-ethyl-1,4a,7-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H28O/c1-5-15-14(2)7-9-17-16(15)8-10-18-19(3,13-21)11-6-12-20(17,18)4/h7,9,13,18H,5-6,8,10-12H2,1-4H3/t18-,19+,20+/m0/s1
InChI Key ICVPEPSOXXKVKV-XUVXKRRUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O
Molecular Weight 284.40 g/mol
Exact Mass 284.214015512 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.77
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4aS,10aR)-8-ethyl-1,4a,7-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde

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 + 0.8646 86.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.3881 38.81%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.8950 89.50%
OATP1B3 inhibitior + 0.9606 96.06%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7950 79.50%
P-glycoprotein inhibitior - 0.7252 72.52%
P-glycoprotein substrate - 0.7653 76.53%
CYP3A4 substrate + 0.5922 59.22%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate + 0.3848 38.48%
CYP3A4 inhibition - 0.9176 91.76%
CYP2C9 inhibition - 0.7620 76.20%
CYP2C19 inhibition - 0.6510 65.10%
CYP2D6 inhibition - 0.9146 91.46%
CYP1A2 inhibition - 0.5714 57.14%
CYP2C8 inhibition + 0.4436 44.36%
CYP inhibitory promiscuity + 0.5287 52.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6056 60.56%
Eye corrosion - 0.9243 92.43%
Eye irritation - 0.8914 89.14%
Skin irritation - 0.7341 73.41%
Skin corrosion - 0.9722 97.22%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7886 78.86%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6249 62.49%
skin sensitisation + 0.5509 55.09%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.5803 58.03%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.9173 91.73%
Acute Oral Toxicity (c) III 0.4565 45.65%
Estrogen receptor binding + 0.5661 56.61%
Androgen receptor binding + 0.6453 64.53%
Thyroid receptor binding + 0.8103 81.03%
Glucocorticoid receptor binding + 0.5650 56.50%
Aromatase binding - 0.6480 64.80%
PPAR gamma + 0.7465 74.65%
Honey bee toxicity - 0.9120 91.20%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.63% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.39% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.83% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.53% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.76% 89.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.84% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.20% 96.09%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 84.71% 90.24%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.14% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.89% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.35% 95.89%
CHEMBL1871 P10275 Androgen Receptor 80.51% 96.43%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.32% 96.00%

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.
Vellozia squamata

Cross-Links

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PubChem 13857906
LOTUS LTS0014638
wikiData Q105111186