2-(9,32-dihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.11,4.14,7.012,17.017,23]pentatriaconta-10,13,22-trien-14-yl)-3-methyl-2H-furan-5-one

Details

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Internal ID 3ab430b3-d510-4c9d-8d11-dc566edcbc7b
Taxonomy Organoheterocyclic compounds > Azepines
IUPAC Name 2-(9,32-dihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.11,4.14,7.012,17.017,23]pentatriaconta-10,13,22-trien-14-yl)-3-methyl-2H-furan-5-one
SMILES (Canonical) CC1CC23CCC(=C(C2C=C(C(CC4CCC5(O4)CCC6(O5)C(CCC(O6)CC(=C)CCCC3=NCC1C)O)O)C)C)C7C(=CC(=O)O7)C
SMILES (Isomeric) CC1CC23CCC(=C(C2C=C(C(CC4CCC5(O4)CCC6(O5)C(CCC(O6)CC(=C)CCCC3=NCC1C)O)O)C)C)C7C(=CC(=O)O7)C
InChI InChI=1S/C41H59NO7/c1-24-8-7-9-35-39(22-27(4)28(5)23-42-35)14-13-32(38-26(3)20-37(45)46-38)29(6)33(39)19-25(2)34(43)21-31-12-15-40(47-31)16-17-41(49-40)36(44)11-10-30(18-24)48-41/h19-20,27-28,30-31,33-34,36,38,43-44H,1,7-18,21-23H2,2-6H3
InChI Key VFKBAIKPMPKSNW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C41H59NO7
Molecular Weight 677.90 g/mol
Exact Mass 677.42915322 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 7.44
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(9,32-dihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.11,4.14,7.012,17.017,23]pentatriaconta-10,13,22-trien-14-yl)-3-methyl-2H-furan-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9336 93.36%
Caco-2 - 0.8037 80.37%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5700 57.00%
OATP2B1 inhibitior - 0.7171 71.71%
OATP1B1 inhibitior + 0.8523 85.23%
OATP1B3 inhibitior + 0.9280 92.80%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9769 97.69%
P-glycoprotein inhibitior + 0.7951 79.51%
P-glycoprotein substrate + 0.7096 70.96%
CYP3A4 substrate + 0.7355 73.55%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.8911 89.11%
CYP3A4 inhibition - 0.9424 94.24%
CYP2C9 inhibition - 0.8528 85.28%
CYP2C19 inhibition - 0.8392 83.92%
CYP2D6 inhibition - 0.9309 93.09%
CYP1A2 inhibition - 0.8330 83.30%
CYP2C8 inhibition + 0.7128 71.28%
CYP inhibitory promiscuity - 0.9654 96.54%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5158 51.58%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.9230 92.30%
Skin irritation - 0.6500 65.00%
Skin corrosion - 0.9116 91.16%
Ames mutagenesis - 0.5964 59.64%
Human Ether-a-go-go-Related Gene inhibition + 0.7342 73.42%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5367 53.67%
skin sensitisation - 0.7995 79.95%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.9091 90.91%
Acute Oral Toxicity (c) III 0.4852 48.52%
Estrogen receptor binding + 0.7758 77.58%
Androgen receptor binding + 0.7202 72.02%
Thyroid receptor binding - 0.5315 53.15%
Glucocorticoid receptor binding + 0.7382 73.82%
Aromatase binding + 0.6930 69.30%
PPAR gamma + 0.6493 64.93%
Honey bee toxicity - 0.6971 69.71%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9529 95.29%

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 97.21% 91.11%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 96.29% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.60% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.55% 99.23%
CHEMBL5103 Q969S8 Histone deacetylase 10 94.45% 90.08%
CHEMBL2581 P07339 Cathepsin D 94.12% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.71% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.89% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.42% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.89% 89.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 87.62% 96.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.08% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.09% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.04% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.72% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 83.11% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.12% 94.80%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.12% 96.90%
CHEMBL3012 Q13946 Phosphodiesterase 7A 80.07% 99.29%

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 163075428
LOTUS LTS0084126
wikiData Q105285335