Curtisian V

Details

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Internal ID cb52dd65-e03e-48a2-9958-a735fc70cde5
Taxonomy Benzenoids > Benzene and substituted derivatives > Terphenyls > P-terphenyls
IUPAC Name [5-acetyloxy-2-[(3R)-3-hydroxybutanoyl]oxy-3,6-bis(4-hydroxyphenyl)-4-(3-phenylpropanoyloxy)phenyl] (3R)-3-hydroxybutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H36O12/c1-21(38)19-30(44)48-36-32(25-10-14-27(41)15-11-25)34(46-23(3)40)35(47-29(43)18-9-24-7-5-4-6-8-24)33(26-12-16-28(42)17-13-26)37(36)49-31(45)20-22(2)39/h4-8,10-17,21-22,38-39,41-42H,9,18-20H2,1-3H3/t21-,22-/m1/s1
InChI Key OLIWVBBLGVEWMF-FGZHOGPDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C37H36O12
Molecular Weight 672.70 g/mol
Exact Mass 672.22067658 g/mol
Topological Polar Surface Area (TPSA) 186.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.25
H-Bond Acceptor 12
H-Bond Donor 4
Rotatable Bonds 13

Synonyms

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CHEMBL553159

2D Structure

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2D Structure of Curtisian V

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9683 96.83%
Caco-2 - 0.8224 82.24%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.8967 89.67%
OATP2B1 inhibitior - 0.7100 71.00%
OATP1B1 inhibitior + 0.8809 88.09%
OATP1B3 inhibitior - 0.2679 26.79%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.8471 84.71%
P-glycoprotein substrate - 0.6148 61.48%
CYP3A4 substrate + 0.5683 56.83%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.7909 79.09%
CYP3A4 inhibition - 0.9179 91.79%
CYP2C9 inhibition - 0.7070 70.70%
CYP2C19 inhibition - 0.8687 86.87%
CYP2D6 inhibition - 0.8887 88.87%
CYP1A2 inhibition - 0.5099 50.99%
CYP2C8 inhibition + 0.7941 79.41%
CYP inhibitory promiscuity - 0.9002 90.02%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7122 71.22%
Carcinogenicity (trinary) Non-required 0.6788 67.88%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.9074 90.74%
Skin irritation - 0.8701 87.01%
Skin corrosion - 0.9398 93.98%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7097 70.97%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9234 92.34%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.4861 48.61%
Acute Oral Toxicity (c) III 0.7334 73.34%
Estrogen receptor binding + 0.7760 77.60%
Androgen receptor binding + 0.8911 89.11%
Thyroid receptor binding + 0.5480 54.80%
Glucocorticoid receptor binding + 0.7653 76.53%
Aromatase binding - 0.5589 55.89%
PPAR gamma + 0.6964 69.64%
Honey bee toxicity - 0.7504 75.04%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9866 98.66%

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
CHEMBL2581 P07339 Cathepsin D 99.33% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.14% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 95.26% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.27% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.08% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 92.47% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.00% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.00% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.81% 91.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.03% 97.21%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.28% 99.15%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.99% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.65% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 84.25% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.62% 96.95%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 80.02% 100.00%

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 45271723
LOTUS LTS0252164
wikiData Q105193995