(3Z,7Z)-16,18-dichloro-11,22-dihydroxy-4,8,19,19-tetramethyl-20-oxatetracyclo[11.7.1.110,14.01,16]docosa-3,7,10,12,14(22)-pentaene-15,21-dione

Details

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Internal ID 673ad8cc-cad3-4449-a48c-6fc8f8bea0ed
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name (3Z,7Z)-16,18-dichloro-11,22-dihydroxy-4,8,19,19-tetramethyl-20-oxatetracyclo[11.7.1.110,14.01,16]docosa-3,7,10,12,14(22)-pentaene-15,21-dione
SMILES (Canonical) CC1=CCC23C(=O)C4=CC(=C(CC(=CCC1)C)C(=C4C(=O)C2(CC(C(O3)(C)C)Cl)Cl)O)O
SMILES (Isomeric) C/C/1=C/CC23C(=O)C4=CC(=C(C/C(=C\CC1)/C)C(=C4C(=O)C2(CC(C(O3)(C)C)Cl)Cl)O)O
InChI InChI=1S/C25H28Cl2O5/c1-13-6-5-7-14(2)10-15-17(28)11-16-19(20(15)29)22(31)24(27)12-18(26)23(3,4)32-25(24,9-8-13)21(16)30/h7-8,11,18,28-29H,5-6,9-10,12H2,1-4H3/b13-8-,14-7-
InChI Key JBVAFOMCWIFYSA-LUGOROIYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H28Cl2O5
Molecular Weight 479.40 g/mol
Exact Mass 478.1313794 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 4.50
Atomic LogP (AlogP) 5.62
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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SCHEMBL29377412
(3Z,7Z)-16,18-Dichloro-11,22-dihydroxy-4,8,19,19-tetramethyl-20-oxatetracyclo[11.7.1.110,14.01,16]docosa-3,7,10,12,14(22)-pentaene-15,21-dione

2D Structure

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2D Structure of (3Z,7Z)-16,18-dichloro-11,22-dihydroxy-4,8,19,19-tetramethyl-20-oxatetracyclo[11.7.1.110,14.01,16]docosa-3,7,10,12,14(22)-pentaene-15,21-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 - 0.5827 58.27%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7422 74.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8054 80.54%
OATP1B3 inhibitior + 0.8765 87.65%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9748 97.48%
P-glycoprotein inhibitior - 0.4463 44.63%
P-glycoprotein substrate - 0.6991 69.91%
CYP3A4 substrate + 0.6862 68.62%
CYP2C9 substrate - 0.6140 61.40%
CYP2D6 substrate - 0.8211 82.11%
CYP3A4 inhibition - 0.8462 84.62%
CYP2C9 inhibition - 0.6561 65.61%
CYP2C19 inhibition - 0.7168 71.68%
CYP2D6 inhibition - 0.8745 87.45%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition + 0.6960 69.60%
CYP inhibitory promiscuity - 0.7237 72.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8849 88.49%
Carcinogenicity (trinary) Non-required 0.6431 64.31%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9170 91.70%
Skin irritation - 0.6884 68.84%
Skin corrosion - 0.9150 91.50%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3953 39.53%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7581 75.81%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) IV 0.4590 45.90%
Estrogen receptor binding + 0.7775 77.75%
Androgen receptor binding + 0.6945 69.45%
Thyroid receptor binding + 0.6410 64.10%
Glucocorticoid receptor binding + 0.8669 86.69%
Aromatase binding + 0.8128 81.28%
PPAR gamma + 0.8162 81.62%
Honey bee toxicity - 0.7789 77.89%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.73% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 95.61% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.76% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.70% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 91.78% 96.21%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 91.13% 85.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.88% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.05% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.96% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.16% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.96% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.64% 92.94%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.71% 99.15%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 87.41% 96.38%
CHEMBL4208 P20618 Proteasome component C5 86.35% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.91% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 82.32% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.37% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.30% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 23305214
LOTUS LTS0153804
wikiData Q105124600