Isochromophilone D

Details

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Internal ID 81c07141-b73f-4649-b890-d2e9f4fb5fee
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name (6aR,8R,9S,9aS)-9-acetyl-5-chloro-3-[(1E,3E,5S)-3,5-dimethylhepta-1,3-dienyl]-8-methoxy-6a,8-dimethyl-9,9a-dihydrofuro[2,3-h]isochromen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H31ClO5/c1-8-14(2)11-15(3)9-10-17-12-18-19(13-30-17)21-20(16(4)27)25(6,29-7)31-24(21,5)23(28)22(18)26/h9-14,20-21H,8H2,1-7H3/b10-9+,15-11+/t14-,20+,21+,24+,25+/m0/s1
InChI Key HVVWQGQUCAAUGE-CAIZGLRYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H31ClO5
Molecular Weight 447.00 g/mol
Exact Mass 446.1860018 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 4.30
Atomic LogP (AlogP) 5.38
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Isochromophilone D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.5729 57.29%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5335 53.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7918 79.18%
OATP1B3 inhibitior + 0.8844 88.44%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9681 96.81%
P-glycoprotein inhibitior + 0.7750 77.50%
P-glycoprotein substrate - 0.6260 62.60%
CYP3A4 substrate + 0.6886 68.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8776 87.76%
CYP3A4 inhibition - 0.5585 55.85%
CYP2C9 inhibition - 0.7293 72.93%
CYP2C19 inhibition - 0.7050 70.50%
CYP2D6 inhibition - 0.8949 89.49%
CYP1A2 inhibition - 0.7877 78.77%
CYP2C8 inhibition + 0.7152 71.52%
CYP inhibitory promiscuity + 0.6651 66.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8819 88.19%
Carcinogenicity (trinary) Danger 0.6584 65.84%
Eye corrosion - 0.9790 97.90%
Eye irritation - 0.9520 95.20%
Skin irritation - 0.6682 66.82%
Skin corrosion - 0.9030 90.30%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8661 86.61%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.5071 50.71%
skin sensitisation - 0.7611 76.11%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.6381 63.81%
Acute Oral Toxicity (c) III 0.5640 56.40%
Estrogen receptor binding + 0.8505 85.05%
Androgen receptor binding + 0.6642 66.42%
Thyroid receptor binding + 0.7522 75.22%
Glucocorticoid receptor binding + 0.7025 70.25%
Aromatase binding + 0.5927 59.27%
PPAR gamma + 0.6825 68.25%
Honey bee toxicity - 0.7429 74.29%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6152 61.52%
Fish aquatic toxicity + 0.9879 98.79%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.38% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.28% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.61% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 92.60% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.19% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.97% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 90.23% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.97% 96.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.22% 97.25%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.13% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.98% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.36% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.16% 86.92%
CHEMBL226 P30542 Adenosine A1 receptor 85.59% 95.93%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.66% 89.34%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.66% 83.57%
CHEMBL340 P08684 Cytochrome P450 3A4 82.72% 91.19%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 82.69% 89.05%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 82.07% 80.00%
CHEMBL5957 P21589 5'-nucleotidase 81.83% 97.78%
CHEMBL1937 Q92769 Histone deacetylase 2 81.37% 94.75%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.70% 94.80%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 80.23% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139589933
LOTUS LTS0185652
wikiData Q105034464