(+)-(S)-N-Acetylcaaverine

Details

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Internal ID 356ccc78-852a-407b-b99d-d0ddd7decd60
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 1-[(6aS)-1-hydroxy-2-methoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-yl]ethanone
SMILES (Canonical) CC(=O)N1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)O)OC
SMILES (Isomeric) CC(=O)N1CCC2=CC(=C(C3=C2[C@@H]1CC4=CC=CC=C43)O)OC
InChI InChI=1S/C19H19NO3/c1-11(21)20-8-7-13-10-16(23-2)19(22)18-14-6-4-3-5-12(14)9-15(20)17(13)18/h3-6,10,15,22H,7-9H2,1-2H3/t15-/m0/s1
InChI Key CLLSFQOPDHRHKZ-HNNXBMFYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H19NO3
Molecular Weight 309.40 g/mol
Exact Mass 309.13649347 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.07
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-(S)-N-Acetylcaaverine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9602 96.02%
Caco-2 + 0.8636 86.36%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7806 78.06%
OATP2B1 inhibitior - 0.7186 71.86%
OATP1B1 inhibitior + 0.9129 91.29%
OATP1B3 inhibitior + 0.9551 95.51%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.6114 61.14%
BSEP inhibitior + 0.8932 89.32%
P-glycoprotein inhibitior - 0.8400 84.00%
P-glycoprotein substrate + 0.5075 50.75%
CYP3A4 substrate + 0.6572 65.72%
CYP2C9 substrate + 0.5905 59.05%
CYP2D6 substrate - 0.7232 72.32%
CYP3A4 inhibition - 0.8312 83.12%
CYP2C9 inhibition - 0.8832 88.32%
CYP2C19 inhibition - 0.7547 75.47%
CYP2D6 inhibition - 0.7996 79.96%
CYP1A2 inhibition + 0.7489 74.89%
CYP2C8 inhibition - 0.6473 64.73%
CYP inhibitory promiscuity - 0.7654 76.54%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6928 69.28%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.9925 99.25%
Skin irritation - 0.7765 77.65%
Skin corrosion - 0.9521 95.21%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4146 41.46%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.9061 90.61%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.7074 70.74%
Acute Oral Toxicity (c) III 0.6593 65.93%
Estrogen receptor binding - 0.4928 49.28%
Androgen receptor binding + 0.7378 73.78%
Thyroid receptor binding - 0.5377 53.77%
Glucocorticoid receptor binding + 0.7942 79.42%
Aromatase binding - 0.6658 66.58%
PPAR gamma + 0.5588 55.88%
Honey bee toxicity - 0.9000 90.00%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5404 54.04%
Fish aquatic toxicity + 0.8262 82.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.98% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.18% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.01% 91.11%
CHEMBL217 P14416 Dopamine D2 receptor 95.45% 95.62%
CHEMBL2056 P21728 Dopamine D1 receptor 94.93% 91.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.77% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.20% 86.33%
CHEMBL2535 P11166 Glucose transporter 90.51% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.70% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.31% 89.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.11% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.99% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 85.43% 91.19%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.50% 96.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.71% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.45% 82.69%
CHEMBL4208 P20618 Proteasome component C5 82.02% 90.00%
CHEMBL5028 O14672 ADAM10 81.73% 97.50%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 80.69% 96.39%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.62% 85.14%

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.
Avena fatua
Helichrysum fulvum
Illigera luzonensis
Piper sylvaticum

Cross-Links

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PubChem 52937890
NPASS NPC111588
LOTUS LTS0180900
wikiData Q104963603