cis-6beta-Acetoxy-3alpha-(cinnamoyloxy)tropane

Details

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Internal ID 9ec99664-164a-45c5-8e0d-beec81ac8b56
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid esters
IUPAC Name [(1S,3S,5R,6S)-6-acetyloxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] (Z)-3-phenylprop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H23NO4/c1-13(21)23-18-11-15-10-16(12-17(18)20(15)2)24-19(22)9-8-14-6-4-3-5-7-14/h3-9,15-18H,10-12H2,1-2H3/b9-8-/t15-,16-,17+,18-/m0/s1
InChI Key QKTXQEDBXGTOFH-PKJXHJKLSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23NO4
Molecular Weight 329.40 g/mol
Exact Mass 329.16270821 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of cis-6beta-Acetoxy-3alpha-(cinnamoyloxy)tropane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9617 96.17%
Caco-2 + 0.8082 80.82%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.4527 45.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9357 93.57%
OATP1B3 inhibitior + 0.9359 93.59%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.4724 47.24%
P-glycoprotein inhibitior - 0.5545 55.45%
P-glycoprotein substrate - 0.6343 63.43%
CYP3A4 substrate + 0.5792 57.92%
CYP2C9 substrate - 0.6196 61.96%
CYP2D6 substrate - 0.7605 76.05%
CYP3A4 inhibition - 0.8826 88.26%
CYP2C9 inhibition - 0.8903 89.03%
CYP2C19 inhibition - 0.8752 87.52%
CYP2D6 inhibition - 0.6928 69.28%
CYP1A2 inhibition - 0.8476 84.76%
CYP2C8 inhibition - 0.7581 75.81%
CYP inhibitory promiscuity - 0.8731 87.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9107 91.07%
Carcinogenicity (trinary) Non-required 0.6018 60.18%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9760 97.60%
Skin irritation - 0.8164 81.64%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.6437 64.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7872 78.72%
Micronuclear + 0.5800 58.00%
Hepatotoxicity - 0.5343 53.43%
skin sensitisation - 0.8990 89.90%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7997 79.97%
Acute Oral Toxicity (c) III 0.7039 70.39%
Estrogen receptor binding - 0.6259 62.59%
Androgen receptor binding - 0.5517 55.17%
Thyroid receptor binding - 0.5802 58.02%
Glucocorticoid receptor binding - 0.6618 66.18%
Aromatase binding + 0.5949 59.49%
PPAR gamma - 0.6803 68.03%
Honey bee toxicity - 0.8629 86.29%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5855 58.55%
Fish aquatic toxicity + 0.9272 92.72%

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 97.48% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 96.62% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 96.23% 94.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.52% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.88% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.76% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.30% 91.11%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 90.07% 94.23%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.66% 97.21%
CHEMBL5028 O14672 ADAM10 85.32% 97.50%
CHEMBL1951 P21397 Monoamine oxidase A 82.22% 91.49%

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.
Erythroxylum zeylanicum

Cross-Links

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PubChem 101027040
LOTUS LTS0189226
wikiData Q105223327