Ancistrotectorine

Details

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Internal ID f1bf06e4-1243-4e31-aeb3-23171f66f44e
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Naphthylisoquinolines
IUPAC Name 2-[(1R,3S)-6,8-dimethoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-7-yl]-8-methoxy-3-methylnaphthalen-1-ol
SMILES (Canonical) CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC
SMILES (Isomeric) C[C@H]1CC2=CC(=C(C(=C2[C@H](N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC
InChI InChI=1S/C26H31NO4/c1-14-11-17-9-8-10-19(29-5)23(17)25(28)21(14)24-20(30-6)13-18-12-15(2)27(4)16(3)22(18)26(24)31-7/h8-11,13,15-16,28H,12H2,1-7H3/t15-,16+/m0/s1
InChI Key BHQAJMGEYYHIGV-JKSUJKDBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H31NO4
Molecular Weight 421.50 g/mol
Exact Mass 421.22530847 g/mol
Topological Polar Surface Area (TPSA) 51.20 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.48
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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98985-59-2
CHEMBL463908
CHEBI:31213
C12340
AC1L44PW
CTK3I7677
2-[(1R,3S)-6,8-dimethoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-7-yl]-8-methoxy-3-methyl-naphthalen-1-ol
DTXSID00243899
Q27114217

2D Structure

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2D Structure of Ancistrotectorine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9662 96.62%
Caco-2 + 0.7869 78.69%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5081 50.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9027 90.27%
OATP1B3 inhibitior + 0.9514 95.14%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6861 68.61%
BSEP inhibitior + 0.9744 97.44%
P-glycoprotein inhibitior + 0.8532 85.32%
P-glycoprotein substrate - 0.5280 52.80%
CYP3A4 substrate + 0.6467 64.67%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate + 0.8078 80.78%
CYP3A4 inhibition - 0.5688 56.88%
CYP2C9 inhibition - 0.8160 81.60%
CYP2C19 inhibition - 0.7004 70.04%
CYP2D6 inhibition + 0.5505 55.05%
CYP1A2 inhibition - 0.5554 55.54%
CYP2C8 inhibition + 0.5078 50.78%
CYP inhibitory promiscuity - 0.7225 72.25%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9510 95.10%
Carcinogenicity (trinary) Non-required 0.5289 52.89%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.8038 80.38%
Skin irritation - 0.8109 81.09%
Skin corrosion - 0.9447 94.47%
Ames mutagenesis + 0.5563 55.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8480 84.80%
Micronuclear + 0.5259 52.59%
Hepatotoxicity - 0.6219 62.19%
skin sensitisation - 0.9210 92.10%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.9157 91.57%
Acute Oral Toxicity (c) III 0.6861 68.61%
Estrogen receptor binding + 0.8563 85.63%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.8002 80.02%
Glucocorticoid receptor binding + 0.8086 80.86%
Aromatase binding + 0.6415 64.15%
PPAR gamma + 0.7512 75.12%
Honey bee toxicity - 0.8889 88.89%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8725 87.25%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.41% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.34% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.95% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.58% 95.56%
CHEMBL2535 P11166 Glucose transporter 93.12% 98.75%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 93.10% 89.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.60% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.50% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.96% 93.99%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.84% 93.56%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 89.23% 95.34%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.60% 99.15%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 88.48% 100.00%
CHEMBL2056 P21728 Dopamine D1 receptor 87.86% 91.00%
CHEMBL217 P14416 Dopamine D2 receptor 87.12% 95.62%
CHEMBL213 P08588 Beta-1 adrenergic receptor 86.64% 95.56%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 86.35% 91.79%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 85.26% 94.03%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 84.76% 97.31%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.72% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.53% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.73% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 83.61% 93.31%
CHEMBL4208 P20618 Proteasome component C5 83.11% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.41% 95.89%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 80.76% 96.39%
CHEMBL1795185 Q58F21 Bromodomain testis-specific protein 80.32% 89.76%

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 guineensis
Ancistrocladus korupensis
Ancistrocladus tanzaniensis
Ancistrocladus tectorius
Dioncophyllum thollonii

Cross-Links

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PubChem 179169
NPASS NPC79402
LOTUS LTS0198014
wikiData Q27114217