(+)-sinoracutine,C~17~H~17~NO~3~

Details

Top
Internal ID b82a13ca-9672-4b3d-aabf-9515851d969a
Taxonomy Benzenoids > Naphthalenes
IUPAC Name (1R,13R)-3-hydroxy-4-methoxy-14-methyl-14-azatetracyclo[8.6.0.01,13.02,7]hexadeca-2(7),3,5,8,10-pentaen-12-one
SMILES (Canonical) CN1CCC23C1C(=O)C=C2C=CC4=C3C(=C(C=C4)OC)O
SMILES (Isomeric) CN1CC[C@@]23[C@@H]1C(=O)C=C2C=CC4=C3C(=C(C=C4)OC)O
InChI InChI=1S/C17H17NO3/c1-18-8-7-17-11(9-12(19)16(17)18)5-3-10-4-6-13(21-2)15(20)14(10)17/h3-6,9,16,20H,7-8H2,1-2H3/t16-,17+/m0/s1
InChI Key LZMVKMPUAIZGJR-DLBZAZTESA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H17NO3
Molecular Weight 283.32 g/mol
Exact Mass 283.12084340 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (+)-sinoracutine,C~17~H~17~NO~3~

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9831 98.31%
Caco-2 + 0.8117 81.17%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6770 67.70%
OATP2B1 inhibitior - 0.8568 85.68%
OATP1B1 inhibitior + 0.9329 93.29%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6250 62.50%
BSEP inhibitior - 0.5181 51.81%
P-glycoprotein inhibitior - 0.9171 91.71%
P-glycoprotein substrate + 0.5473 54.73%
CYP3A4 substrate + 0.6818 68.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3481 34.81%
CYP3A4 inhibition - 0.6761 67.61%
CYP2C9 inhibition - 0.7014 70.14%
CYP2C19 inhibition - 0.7015 70.15%
CYP2D6 inhibition + 0.6188 61.88%
CYP1A2 inhibition + 0.5428 54.28%
CYP2C8 inhibition - 0.8027 80.27%
CYP inhibitory promiscuity + 0.5398 53.98%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5695 56.95%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9892 98.92%
Skin irritation - 0.7464 74.64%
Skin corrosion - 0.9121 91.21%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6856 68.56%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.5717 57.17%
skin sensitisation - 0.8376 83.76%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6023 60.23%
Acute Oral Toxicity (c) III 0.5393 53.93%
Estrogen receptor binding + 0.7377 73.77%
Androgen receptor binding + 0.5950 59.50%
Thyroid receptor binding + 0.5395 53.95%
Glucocorticoid receptor binding + 0.6543 65.43%
Aromatase binding + 0.5207 52.07%
PPAR gamma - 0.5361 53.61%
Honey bee toxicity - 0.8768 87.68%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9176 91.76%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.30% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.13% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.92% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.93% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.08% 93.40%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.47% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.23% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.06% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.33% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.75% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.12% 97.25%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.23% 91.07%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.06% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 82.09% 94.75%
CHEMBL2535 P11166 Glucose transporter 81.89% 98.75%
CHEMBL4208 P20618 Proteasome component C5 81.75% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 81.50% 90.20%
CHEMBL1951 P21397 Monoamine oxidase A 81.12% 91.49%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.38% 93.99%
CHEMBL2056 P21728 Dopamine D1 receptor 80.36% 91.00%

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.
Sinomenium acutum

Cross-Links

Top
PubChem 44179675
LOTUS LTS0188464
wikiData Q105160006