(-)-Myrtenal

Details

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Internal ID 14d70b11-b348-4f66-b924-d5b0f88ee8da
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
SMILES (Canonical) CC1(C2CC=C(C1C2)C=O)C
SMILES (Isomeric) CC1([C@H]2CC=C([C@@H]1C2)C=O)C
InChI InChI=1S/C10H14O/c1-10(2)8-4-3-7(6-11)9(10)5-8/h3,6,8-9H,4-5H2,1-2H3/t8-,9-/m0/s1
InChI Key KMRMUZKLFIEVAO-IUCAKERBSA-N
Popularity 63 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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18486-69-6
(1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
(?)-Myrtenal
Myrtenal, (-)-
EH2E303QRY
8J97443QRZ
MFCD00074768
AI3-37785
FEMA No. 3395
Bicyclo(3.1.1)hept-2-ene-2-carboxaldehyde, 6,6-dimethyl-, (1R)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (-)-Myrtenal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7303 73.03%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4951 49.51%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8923 89.23%
OATP1B3 inhibitior + 0.9144 91.44%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9222 92.22%
P-glycoprotein inhibitior - 0.9738 97.38%
P-glycoprotein substrate - 0.9172 91.72%
CYP3A4 substrate - 0.5438 54.38%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8489 84.89%
CYP3A4 inhibition - 0.8969 89.69%
CYP2C9 inhibition - 0.7536 75.36%
CYP2C19 inhibition - 0.6083 60.83%
CYP2D6 inhibition - 0.8912 89.12%
CYP1A2 inhibition - 0.8513 85.13%
CYP2C8 inhibition - 0.9648 96.48%
CYP inhibitory promiscuity - 0.6204 62.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6131 61.31%
Eye corrosion - 0.7625 76.25%
Eye irritation + 0.9337 93.37%
Skin irritation + 0.6165 61.65%
Skin corrosion - 0.8467 84.67%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5845 58.45%
Micronuclear - 0.8651 86.51%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.8894 88.94%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7164 71.64%
Nephrotoxicity + 0.4495 44.95%
Acute Oral Toxicity (c) III 0.8378 83.78%
Estrogen receptor binding - 0.8385 83.85%
Androgen receptor binding - 0.8451 84.51%
Thyroid receptor binding - 0.8207 82.07%
Glucocorticoid receptor binding - 0.8304 83.04%
Aromatase binding - 0.9207 92.07%
PPAR gamma - 0.7392 73.92%
Honey bee toxicity - 0.7434 74.34%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.9876 98.76%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.76% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.71% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.87% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.89% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.27% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.01% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 81.47% 90.17%

Cross-Links

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PubChem 1201529
NPASS NPC105585
LOTUS LTS0147823
wikiData Q27270628