N-Hormyldehydrocaaverine

Details

Top
Internal ID 0324a947-8da6-4142-8426-d6a26c82499c
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 16-hydroxy-15-methoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,8,13,15-heptaene-10-carbaldehyde
SMILES (Canonical) COC1=C(C2=C3C(=C1)CCN(C3=CC4=CC=CC=C42)C=O)O
SMILES (Isomeric) COC1=C(C2=C3C(=C1)CCN(C3=CC4=CC=CC=C42)C=O)O
InChI InChI=1S/C18H15NO3/c1-22-15-9-12-6-7-19(10-20)14-8-11-4-2-3-5-13(11)17(16(12)14)18(15)21/h2-5,8-10,21H,6-7H2,1H3
InChI Key CBULCCZPHJKXAA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H15NO3
Molecular Weight 293.30 g/mol
Exact Mass 293.10519334 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of N-Hormyldehydrocaaverine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9632 96.32%
Caco-2 + 0.9021 90.21%
Blood Brain Barrier + 0.7317 73.17%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7644 76.44%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.8888 88.88%
OATP1B3 inhibitior + 0.9604 96.04%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5564 55.64%
BSEP inhibitior + 0.7281 72.81%
P-glycoprotein inhibitior - 0.7812 78.12%
P-glycoprotein substrate - 0.5769 57.69%
CYP3A4 substrate + 0.6090 60.90%
CYP2C9 substrate - 0.7853 78.53%
CYP2D6 substrate + 0.3845 38.45%
CYP3A4 inhibition - 0.5277 52.77%
CYP2C9 inhibition - 0.7071 70.71%
CYP2C19 inhibition - 0.6379 63.79%
CYP2D6 inhibition - 0.8280 82.80%
CYP1A2 inhibition + 0.8401 84.01%
CYP2C8 inhibition + 0.4688 46.88%
CYP inhibitory promiscuity - 0.6018 60.18%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5926 59.26%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.9022 90.22%
Skin irritation - 0.7371 73.71%
Skin corrosion - 0.9543 95.43%
Ames mutagenesis + 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5397 53.97%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.5321 53.21%
skin sensitisation - 0.9182 91.82%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.9212 92.12%
Acute Oral Toxicity (c) III 0.7765 77.65%
Estrogen receptor binding + 0.8079 80.79%
Androgen receptor binding + 0.7004 70.04%
Thyroid receptor binding + 0.5900 59.00%
Glucocorticoid receptor binding + 0.8378 83.78%
Aromatase binding + 0.6660 66.60%
PPAR gamma + 0.7396 73.96%
Honey bee toxicity - 0.9166 91.66%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.5583 55.83%

Targets

Top

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 99.18% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.31% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.84% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.95% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.79% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.79% 92.94%
CHEMBL2581 P07339 Cathepsin D 88.72% 98.95%
CHEMBL2056 P21728 Dopamine D1 receptor 88.39% 91.00%
CHEMBL2535 P11166 Glucose transporter 88.23% 98.75%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.07% 98.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.02% 85.14%
CHEMBL4208 P20618 Proteasome component C5 83.01% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.38% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.31% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.59% 99.17%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 81.28% 97.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.34% 96.67%

Plants that contains it

Top
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

Top
PubChem 52937893
NPASS NPC16402
LOTUS LTS0024217
wikiData Q104952855