26-(2-Hydroxy-2-methylpropyl)-5,5-dimethyl-6,15-dioxahexacyclo[12.12.0.02,7.08,13.016,25.018,23]hexacosa-1(14),2(7),3,8,10,12,16(25),18,20,22-decaene-17,24-dione

Details

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Internal ID bacf7eb0-a067-48c3-bbb2-474c7dc9d54a
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 26-(2-hydroxy-2-methylpropyl)-5,5-dimethyl-6,15-dioxahexacyclo[12.12.0.02,7.08,13.016,25.018,23]hexacosa-1(14),2(7),3,8,10,12,16(25),18,20,22-decaene-17,24-dione
SMILES (Canonical) CC1(C=CC2=C(O1)C3=CC=CC=C3C4=C2C(C5=C(O4)C(=O)C6=CC=CC=C6C5=O)CC(C)(C)O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C3=CC=CC=C3C4=C2C(C5=C(O4)C(=O)C6=CC=CC=C6C5=O)CC(C)(C)O)C
InChI InChI=1S/C30H26O5/c1-29(2,33)15-21-22-20-13-14-30(3,4)35-26(20)18-11-7-8-12-19(18)27(22)34-28-23(21)24(31)16-9-5-6-10-17(16)25(28)32/h5-14,21,33H,15H2,1-4H3
InChI Key OPQLAFFSVSLWJZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H26O5
Molecular Weight 466.50 g/mol
Exact Mass 466.17802393 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.99
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 26-(2-Hydroxy-2-methylpropyl)-5,5-dimethyl-6,15-dioxahexacyclo[12.12.0.02,7.08,13.016,25.018,23]hexacosa-1(14),2(7),3,8,10,12,16(25),18,20,22-decaene-17,24-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.5352 53.52%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7456 74.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8505 85.05%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9637 96.37%
P-glycoprotein inhibitior + 0.8033 80.33%
P-glycoprotein substrate - 0.5887 58.87%
CYP3A4 substrate + 0.6516 65.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8313 83.13%
CYP3A4 inhibition - 0.5691 56.91%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition - 0.5593 55.93%
CYP2D6 inhibition - 0.7501 75.01%
CYP1A2 inhibition - 0.7812 78.12%
CYP2C8 inhibition + 0.5178 51.78%
CYP inhibitory promiscuity - 0.7106 71.06%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5263 52.63%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.6613 66.13%
Skin irritation - 0.7266 72.66%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6878 68.78%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.5449 54.49%
skin sensitisation - 0.6309 63.09%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.5100 51.00%
Acute Oral Toxicity (c) III 0.6080 60.80%
Estrogen receptor binding + 0.8326 83.26%
Androgen receptor binding + 0.7764 77.64%
Thyroid receptor binding + 0.6038 60.38%
Glucocorticoid receptor binding + 0.7091 70.91%
Aromatase binding - 0.6040 60.40%
PPAR gamma + 0.8154 81.54%
Honey bee toxicity - 0.7198 71.98%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9665 96.65%

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 96.30% 95.56%
CHEMBL2581 P07339 Cathepsin D 96.14% 98.95%
CHEMBL1914 P06276 Butyrylcholinesterase 94.75% 95.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.97% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.93% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 92.30% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.90% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 90.18% 94.73%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.66% 85.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.24% 97.25%
CHEMBL2179 P04062 Beta-glucocerebrosidase 85.88% 85.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.53% 86.33%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 85.22% 95.71%
CHEMBL221 P23219 Cyclooxygenase-1 83.24% 90.17%
CHEMBL1937 Q92769 Histone deacetylase 2 82.82% 94.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.79% 97.14%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.44% 96.67%
CHEMBL1907 P15144 Aminopeptidase N 80.62% 93.31%

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.
Tabebuia heterophylla

Cross-Links

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PubChem 13989575
LOTUS LTS0112593
wikiData Q105196507