Rel-Myrtucommulone K

Details

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Internal ID e7a45a87-7d93-43ce-be30-fa02d6ae2d22
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (8R,8aS,9S,10aS)-8-(2,2-dimethylcyclopentyl)-2,2,4,4,10a-pentamethyl-7-methylidene-9-propan-2-yl-6,8,8a,9-tetrahydro-5H-xanthene-1,3-dione
SMILES (Canonical) CC(C)C1C2C(C(=C)CCC2(OC3=C1C(=O)C(C(=O)C3(C)C)(C)C)C)C4CCCC4(C)C
SMILES (Isomeric) CC(C)[C@H]1[C@@H]2[C@H](C(=C)CC[C@@]2(OC3=C1C(=O)C(C(=O)C3(C)C)(C)C)C)C4CCCC4(C)C
InChI InChI=1S/C29H44O3/c1-16(2)19-21-23(30)27(6,7)25(31)28(8,9)24(21)32-29(10)15-13-17(3)20(22(19)29)18-12-11-14-26(18,4)5/h16,18-20,22H,3,11-15H2,1-2,4-10H3/t18?,19-,20-,22-,29+/m1/s1
InChI Key TUBFXKZFEGFKBF-URAKOGNMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C29H44O3
Molecular Weight 440.70 g/mol
Exact Mass 440.32904526 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 7.20
Atomic LogP (AlogP) 6.91
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEMBL2011677

2D Structure

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2D Structure of Rel-Myrtucommulone K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.5331 53.31%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7286 72.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8574 85.74%
OATP1B3 inhibitior + 0.8579 85.79%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.5268 52.68%
P-glycoprotein inhibitior + 0.6736 67.36%
P-glycoprotein substrate - 0.7987 79.87%
CYP3A4 substrate + 0.6540 65.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8316 83.16%
CYP3A4 inhibition - 0.6807 68.07%
CYP2C9 inhibition - 0.7742 77.42%
CYP2C19 inhibition - 0.7281 72.81%
CYP2D6 inhibition - 0.9518 95.18%
CYP1A2 inhibition - 0.7226 72.26%
CYP2C8 inhibition - 0.6318 63.18%
CYP inhibitory promiscuity - 0.8103 81.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5758 57.58%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.7692 76.92%
Skin irritation - 0.5334 53.34%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4719 47.19%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6703 67.03%
skin sensitisation - 0.6377 63.77%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.8413 84.13%
Acute Oral Toxicity (c) III 0.4844 48.44%
Estrogen receptor binding + 0.6475 64.75%
Androgen receptor binding + 0.6947 69.47%
Thyroid receptor binding + 0.5915 59.15%
Glucocorticoid receptor binding + 0.7260 72.60%
Aromatase binding + 0.6279 62.79%
PPAR gamma + 0.6563 65.63%
Honey bee toxicity - 0.7840 78.40%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9947 99.47%

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 96.65% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 96.00% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.22% 94.45%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 93.44% 96.38%
CHEMBL2581 P07339 Cathepsin D 93.07% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 92.91% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.87% 95.89%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.38% 93.40%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.22% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.99% 85.14%
CHEMBL1871 P10275 Androgen Receptor 89.11% 96.43%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.75% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 88.35% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.12% 96.09%
CHEMBL5600 P27448 Serine/threonine-protein kinase c-TAK1 87.21% 88.81%
CHEMBL5103 Q969S8 Histone deacetylase 10 87.10% 90.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.52% 95.56%
CHEMBL1914 P06276 Butyrylcholinesterase 85.92% 95.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.61% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.33% 93.04%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 83.53% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.50% 99.23%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 83.34% 97.50%
CHEMBL237 P41145 Kappa opioid receptor 83.08% 98.10%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.80% 92.88%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.75% 99.18%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.71% 93.03%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.62% 91.24%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.73% 90.24%
CHEMBL3310 Q96DB2 Histone deacetylase 11 80.37% 88.56%

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.
Myrtus communis

Cross-Links

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PubChem 57333286
LOTUS LTS0183347
wikiData Q105264656