Ancistrocladeine

Details

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Internal ID 1926af65-12dc-4c27-b34e-63f9f23a207f
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Naphthylisoquinolines
IUPAC Name 5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethylisoquinolin-6-ol
SMILES (Canonical) CC1=CC(=C2C(=C1C3=C4C=C(N=C(C4=C(C=C3O)OC)C)C)C=CC=C2OC)OC
SMILES (Isomeric) CC1=CC(=C2C(=C1C3=C4C=C(N=C(C4=C(C=C3O)OC)C)C)C=CC=C2OC)OC
InChI InChI=1S/C25H25NO4/c1-13-10-20(29-5)25-16(8-7-9-19(25)28-4)22(13)24-17-11-14(2)26-15(3)23(17)21(30-6)12-18(24)27/h7-12,27H,1-6H3
InChI Key OHJNZUPFOVFQGI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H25NO4
Molecular Weight 403.50 g/mol
Exact Mass 403.17835828 g/mol
Topological Polar Surface Area (TPSA) 60.80 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.71
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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NSC656304
NSC-656304

2D Structure

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2D Structure of Ancistrocladeine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 + 0.6939 69.39%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7907 79.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8881 88.81%
OATP1B3 inhibitior + 0.9735 97.35%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8361 83.61%
P-glycoprotein inhibitior + 0.7008 70.08%
P-glycoprotein substrate - 0.7334 73.34%
CYP3A4 substrate + 0.6122 61.22%
CYP2C9 substrate - 0.8121 81.21%
CYP2D6 substrate + 0.3470 34.70%
CYP3A4 inhibition + 0.5657 56.57%
CYP2C9 inhibition - 0.8096 80.96%
CYP2C19 inhibition + 0.6225 62.25%
CYP2D6 inhibition + 0.5200 52.00%
CYP1A2 inhibition + 0.5247 52.47%
CYP2C8 inhibition + 0.7962 79.62%
CYP inhibitory promiscuity + 0.6446 64.46%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5588 55.88%
Eye corrosion - 0.9939 99.39%
Eye irritation + 0.6299 62.99%
Skin irritation - 0.8538 85.38%
Skin corrosion - 0.9790 97.90%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7675 76.75%
Micronuclear + 0.6759 67.59%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9576 95.76%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7028 70.28%
Acute Oral Toxicity (c) III 0.5214 52.14%
Estrogen receptor binding + 0.8952 89.52%
Androgen receptor binding + 0.6238 62.38%
Thyroid receptor binding + 0.8837 88.37%
Glucocorticoid receptor binding + 0.8075 80.75%
Aromatase binding + 0.7640 76.40%
PPAR gamma + 0.7603 76.03%
Honey bee toxicity - 0.9324 93.24%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity - 0.4695 46.95%

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 96.05% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.79% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.47% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.85% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.71% 99.15%
CHEMBL2535 P11166 Glucose transporter 92.42% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 90.91% 90.20%
CHEMBL2581 P07339 Cathepsin D 90.17% 98.95%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 89.75% 94.03%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.73% 93.99%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.70% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 88.61% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 88.57% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.48% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.97% 96.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.83% 93.65%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.47% 89.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.26% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.24% 99.17%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.97% 100.00%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.68% 100.00%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 81.32% 94.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.79% 92.62%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.28% 96.67%

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.
Ancistrocladus ealaensis

Cross-Links

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PubChem 135457245
LOTUS LTS0274681
wikiData Q105192109