1-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline

Details

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Internal ID 8a5ed7c0-1eb8-4518-8b2d-3ecea8093ad4
Taxonomy Organoheterocyclic compounds > Tetrahydroisoquinolines
IUPAC Name 1-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H21NO4/c1-20-7-6-12-8-16(21-2)17(22-3)10-14(12)19(20)13-4-5-15-18(9-13)24-11-23-15/h4-5,8-10,19H,6-7,11H2,1-3H3
InChI Key JFTOOEZYKZTOEX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H21NO4
Molecular Weight 327.40 g/mol
Exact Mass 327.14705815 g/mol
Topological Polar Surface Area (TPSA) 40.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Oprea1_610557
Oprea1_664730
CBDivE_014822
SCHEMBL10325499
JFTOOEZYKZTOEX-UHFFFAOYSA-N
AKOS000558168
1-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline
1-Benzo[1,3]dioxol-5-yl-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

2D Structure

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2D Structure of 1-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9515 95.15%
Caco-2 + 0.9644 96.44%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.4460 44.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9387 93.87%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.7296 72.96%
P-glycoprotein inhibitior + 0.6825 68.25%
P-glycoprotein substrate - 0.7359 73.59%
CYP3A4 substrate + 0.5990 59.90%
CYP2C9 substrate - 0.6129 61.29%
CYP2D6 substrate + 0.7342 73.42%
CYP3A4 inhibition + 0.8169 81.69%
CYP2C9 inhibition + 0.7246 72.46%
CYP2C19 inhibition + 0.8264 82.64%
CYP2D6 inhibition + 0.5600 56.00%
CYP1A2 inhibition - 0.7675 76.75%
CYP2C8 inhibition - 0.8835 88.35%
CYP inhibitory promiscuity + 0.6196 61.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5389 53.89%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9347 93.47%
Skin irritation - 0.7847 78.47%
Skin corrosion - 0.9398 93.98%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8387 83.87%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8730 87.30%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6538 65.38%
Acute Oral Toxicity (c) III 0.7257 72.57%
Estrogen receptor binding + 0.7799 77.99%
Androgen receptor binding - 0.4920 49.20%
Thyroid receptor binding + 0.7379 73.79%
Glucocorticoid receptor binding + 0.8672 86.72%
Aromatase binding - 0.5615 56.15%
PPAR gamma + 0.5572 55.72%
Honey bee toxicity - 0.8685 86.85%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.8251 82.51%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.36% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.16% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.41% 96.77%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 94.37% 93.40%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.30% 93.99%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 92.03% 96.86%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.75% 92.62%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 90.14% 82.67%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 90.12% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.53% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.15% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.80% 98.95%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 88.76% 90.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.64% 95.89%
CHEMBL2056 P21728 Dopamine D1 receptor 87.35% 91.00%
CHEMBL3438 Q05513 Protein kinase C zeta 87.29% 88.48%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.57% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.51% 95.89%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 85.38% 95.78%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.83% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.00% 94.45%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.88% 90.24%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.29% 89.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.21% 97.09%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.09% 100.00%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 80.77% 80.96%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 80.48% 91.43%

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.
Cryptostylis arachnites

Cross-Links

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PubChem 3132927
LOTUS LTS0005271
wikiData Q105127004