Acetamide, N-(5,6,7,9-tetrahydro-2,10-dihydroxy-1,3-dimethoxy-9-oxobenzo(a)heptalen-7-yl)-, (S)-

Details

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Internal ID e81b6c38-8e86-4f4e-9155-a4e0b27da364
Taxonomy Hydrocarbon derivatives > Tropones > Tropolones
IUPAC Name N-[(7S)-2,10-dihydroxy-1,3-dimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide
SMILES (Canonical) CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)O)OC)O)OC
SMILES (Isomeric) CC(=O)N[C@H]1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)O)OC)O)OC
InChI InChI=1S/C20H21NO6/c1-10(22)21-14-6-4-11-8-17(26-2)19(25)20(27-3)18(11)12-5-7-15(23)16(24)9-13(12)14/h5,7-9,14,25H,4,6H2,1-3H3,(H,21,22)(H,23,24)/t14-/m0/s1
InChI Key VHIVSZXYLQFNPC-AWEZNQCLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H21NO6
Molecular Weight 371.40 g/mol
Exact Mass 371.13688739 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 2.27
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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33530-04-0
Acetamide, N-(5,6,7,9-tetrahydro-2,10-dihydroxy-1,3-dimethoxy-9-oxobenzo(a)heptalen-7-yl)-, (S)-
Acetamide, N-(5,6,7,9-tetrahydro-2,10-dihydroxy-1,3-dimethoxy-9-oxobenzo[a]heptalen-7-yl)-, (S)-
CHEMBL464647
DTXSID10187179
N-[(7S)-2,10-dihydroxy-1,3-dimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide

2D Structure

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2D Structure of Acetamide, N-(5,6,7,9-tetrahydro-2,10-dihydroxy-1,3-dimethoxy-9-oxobenzo(a)heptalen-7-yl)-, (S)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9565 95.65%
Caco-2 - 0.6097 60.97%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Nucleus 0.5545 55.45%
OATP2B1 inhibitior - 0.8654 86.54%
OATP1B1 inhibitior + 0.9238 92.38%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9572 95.72%
BSEP inhibitior + 0.6834 68.34%
P-glycoprotein inhibitior - 0.8158 81.58%
P-glycoprotein substrate + 0.9236 92.36%
CYP3A4 substrate + 0.7152 71.52%
CYP2C9 substrate - 0.8499 84.99%
CYP2D6 substrate - 0.8224 82.24%
CYP3A4 inhibition - 0.8740 87.40%
CYP2C9 inhibition - 0.9265 92.65%
CYP2C19 inhibition - 0.9458 94.58%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.9396 93.96%
CYP2C8 inhibition + 0.9099 90.99%
CYP inhibitory promiscuity - 0.9241 92.41%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6712 67.12%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.8366 83.66%
Skin irritation - 0.7813 78.13%
Skin corrosion - 0.9443 94.43%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7067 70.67%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.6573 65.73%
skin sensitisation - 0.9251 92.51%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.5903 59.03%
Acute Oral Toxicity (c) III 0.6069 60.69%
Estrogen receptor binding + 0.6824 68.24%
Androgen receptor binding + 0.8030 80.30%
Thyroid receptor binding + 0.6684 66.84%
Glucocorticoid receptor binding + 0.8165 81.65%
Aromatase binding - 0.6838 68.38%
PPAR gamma + 0.6868 68.68%
Honey bee toxicity - 0.8853 88.53%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6649 66.49%
Fish aquatic toxicity + 0.7505 75.05%

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 99.48% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.71% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 96.21% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.46% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL217 P14416 Dopamine D2 receptor 93.78% 95.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.66% 90.71%
CHEMBL2535 P11166 Glucose transporter 91.34% 98.75%
CHEMBL340 P08684 Cytochrome P450 3A4 90.48% 91.19%
CHEMBL2056 P21728 Dopamine D1 receptor 89.79% 91.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 89.54% 91.79%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.16% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.02% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.98% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.53% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.82% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.81% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.38% 95.89%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 83.07% 98.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.05% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.03% 93.03%
CHEMBL4208 P20618 Proteasome component C5 81.58% 90.00%
CHEMBL259 P32245 Melanocortin receptor 4 81.17% 95.38%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.82% 95.89%

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.
Colchicum robustum
Colchicum szovitsii

Cross-Links

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PubChem 453130
LOTUS LTS0063881
wikiData Q83058752