Darlucin A

Details

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Internal ID 43fc0e9a-e20b-4bdf-8b33-1688baaebd37
Taxonomy Lignans, neolignans and related compounds
IUPAC Name 2-[2,3-diisocyano-4-(4-methoxyphenyl)but-2-enyl]benzene-1,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H16N2O3/c1-20-17(10-13-4-7-16(24-3)8-5-13)18(21-2)12-14-11-15(22)6-9-19(14)23/h4-9,11,22-23H,10,12H2,3H3
InChI Key IRXUFNXWOYXCEI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H16N2O3
Molecular Weight 320.30 g/mol
Exact Mass 320.11609238 g/mol
Topological Polar Surface Area (TPSA) 58.40 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.94
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Darlucin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9638 96.38%
Caco-2 + 0.5519 55.19%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8017 80.17%
OATP2B1 inhibitior - 0.5693 56.93%
OATP1B1 inhibitior + 0.9177 91.77%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6060 60.60%
P-glycoprotein inhibitior - 0.8037 80.37%
P-glycoprotein substrate - 0.7925 79.25%
CYP3A4 substrate - 0.5114 51.14%
CYP2C9 substrate - 0.8132 81.32%
CYP2D6 substrate - 0.7639 76.39%
CYP3A4 inhibition + 0.7098 70.98%
CYP2C9 inhibition - 0.5222 52.22%
CYP2C19 inhibition + 0.5207 52.07%
CYP2D6 inhibition - 0.7426 74.26%
CYP1A2 inhibition + 0.6795 67.95%
CYP2C8 inhibition + 0.6683 66.83%
CYP inhibitory promiscuity + 0.8977 89.77%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6728 67.28%
Carcinogenicity (trinary) Non-required 0.5316 53.16%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.6949 69.49%
Skin irritation - 0.7982 79.82%
Skin corrosion - 0.9311 93.11%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7861 78.61%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8191 81.91%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7114 71.14%
Acute Oral Toxicity (c) III 0.6133 61.33%
Estrogen receptor binding + 0.9196 91.96%
Androgen receptor binding + 0.7680 76.80%
Thyroid receptor binding + 0.7922 79.22%
Glucocorticoid receptor binding + 0.7922 79.22%
Aromatase binding + 0.8824 88.24%
PPAR gamma + 0.6777 67.77%
Honey bee toxicity - 0.8680 86.80%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9750 97.50%

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 97.26% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.99% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.94% 96.09%
CHEMBL4208 P20618 Proteasome component C5 92.46% 90.00%
CHEMBL2581 P07339 Cathepsin D 92.34% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.79% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.92% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.81% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.50% 96.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.58% 95.50%
CHEMBL2535 P11166 Glucose transporter 84.23% 98.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.53% 91.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.87% 86.33%
CHEMBL3820 P35557 Hexokinase type IV 82.66% 91.96%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.59% 92.68%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.44% 92.62%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 82.23% 96.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.36% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.14% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 80.56% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.53% 93.99%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.44% 90.24%

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 85079717
LOTUS LTS0132929
wikiData Q77420937