Costal

Details

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Internal ID 4bb88322-4c6d-496f-899b-87d0d5faebe2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 2-(4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enal
SMILES (Canonical) CC12CCCC(=C)C1CC(CC2)C(=C)C=O
SMILES (Isomeric) CC12CCCC(=C)C1CC(CC2)C(=C)C=O
InChI InChI=1S/C15H22O/c1-11-5-4-7-15(3)8-6-13(9-14(11)15)12(2)10-16/h10,13-14H,1-2,4-9H2,3H3
InChI Key QTCANKDTWWSCMR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Costic aldehyde
.beta.-Costal
(+)-Costal
(+)-.beta.-Costal
QTCANKDTWWSCMR-UHFFFAOYSA-N
Eudesma-4(14),11(13)-dien-12-al
2-((2R,4aR,8aS)-4a-Methyl-8-methylenedecahydronaphthalen-2-yl)acrylaldehyde
2-Naphthaleneacetaldehyde, decahydro-4a-methyl-.alpha.,8-bis(methylene)-, (2R,4aR,8aS)-
2-Naphthaleneacetaldehyde, decahydro-4a-methyl-.alpha.,8-bis(methylene)-, [2R-(2.alpha.,4a.alpha.,8a.beta.)]-

2D Structure

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2D Structure of Costal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.7347 73.47%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5075 50.75%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.8812 88.12%
OATP1B3 inhibitior + 0.8940 89.40%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8885 88.85%
P-glycoprotein inhibitior - 0.9324 93.24%
P-glycoprotein substrate - 0.9112 91.12%
CYP3A4 substrate + 0.5714 57.14%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7856 78.56%
CYP3A4 inhibition - 0.8112 81.12%
CYP2C9 inhibition - 0.7676 76.76%
CYP2C19 inhibition - 0.5830 58.30%
CYP2D6 inhibition - 0.9354 93.54%
CYP1A2 inhibition - 0.6798 67.98%
CYP2C8 inhibition - 0.7793 77.93%
CYP inhibitory promiscuity - 0.6771 67.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5204 52.04%
Eye corrosion - 0.8484 84.84%
Eye irritation - 0.6065 60.65%
Skin irritation - 0.5791 57.91%
Skin corrosion - 0.9578 95.78%
Ames mutagenesis - 0.7337 73.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6419 64.19%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5322 53.22%
skin sensitisation + 0.8575 85.75%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6863 68.63%
Acute Oral Toxicity (c) III 0.8456 84.56%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.5409 54.09%
Thyroid receptor binding - 0.6668 66.68%
Glucocorticoid receptor binding + 0.6342 63.42%
Aromatase binding - 0.6338 63.38%
PPAR gamma - 0.5189 51.89%
Honey bee toxicity - 0.8840 88.40%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5800 58.00%
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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.56% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.13% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.01% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.45% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.86% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.13% 100.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 83.75% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.13% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 82.45% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.95% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.71% 92.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.51% 94.45%

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.
Craspedia glauca
Fitchia speciosa
Thujopsis dolabrata

Cross-Links

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PubChem 14262761
LOTUS LTS0144285
wikiData Q104394493