1-hydroxy-6,8a-dimethyl-5-methylidene-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde

Details

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Internal ID fa735684-aa83-425a-bbc7-c8f629c37135
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-hydroxy-6,8a-dimethyl-5-methylidene-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde
SMILES (Canonical) CC1CCC2(C(C1=C)CC=C(C2(C=O)O)C=O)C
SMILES (Isomeric) CC1CCC2(C(C1=C)CC=C(C2(C=O)O)C=O)C
InChI InChI=1S/C15H20O3/c1-10-6-7-14(3)13(11(10)2)5-4-12(8-16)15(14,18)9-17/h4,8-10,13,18H,2,5-7H2,1,3H3
InChI Key LDAIOVKPAKFZHM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O3
Molecular Weight 248.32 g/mol
Exact Mass 248.14124450 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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NSC-294574

2D Structure

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2D Structure of 1-hydroxy-6,8a-dimethyl-5-methylidene-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.6828 68.28%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8197 81.97%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8321 83.21%
OATP1B3 inhibitior + 0.9070 90.70%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.5948 59.48%
BSEP inhibitior - 0.8393 83.93%
P-glycoprotein inhibitior - 0.9486 94.86%
P-glycoprotein substrate - 0.8621 86.21%
CYP3A4 substrate + 0.5881 58.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8654 86.54%
CYP3A4 inhibition - 0.7648 76.48%
CYP2C9 inhibition - 0.8158 81.58%
CYP2C19 inhibition - 0.8399 83.99%
CYP2D6 inhibition - 0.9189 91.89%
CYP1A2 inhibition - 0.7552 75.52%
CYP2C8 inhibition - 0.7481 74.81%
CYP inhibitory promiscuity - 0.9191 91.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5015 50.15%
Eye corrosion - 0.9865 98.65%
Eye irritation - 0.7298 72.98%
Skin irritation + 0.5457 54.57%
Skin corrosion - 0.9334 93.34%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6023 60.23%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5295 52.95%
skin sensitisation - 0.5585 55.85%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5644 56.44%
Acute Oral Toxicity (c) III 0.5877 58.77%
Estrogen receptor binding - 0.4930 49.30%
Androgen receptor binding - 0.4821 48.21%
Thyroid receptor binding - 0.5350 53.50%
Glucocorticoid receptor binding - 0.4843 48.43%
Aromatase binding + 0.6474 64.74%
PPAR gamma - 0.6229 62.29%
Honey bee toxicity - 0.8831 88.31%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5000 50.00%
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 93.52% 95.56%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 92.20% 83.57%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.78% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.50% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.64% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.83% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.81% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.43% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.40% 92.94%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.24% 86.00%

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.
Canella winterana
Warburgia salutaris
Warburgia stuhlmannii

Cross-Links

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PubChem 325604
LOTUS LTS0233645
wikiData Q105150117