1-Methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol
| Internal ID | d8285d78-43e6-4f7d-bc22-2b4cf6a80207 |
| Taxonomy | Organoheterocyclic compounds > Tetrahydroisoquinolines |
| IUPAC Name | 1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol |
| SMILES (Canonical) | CC1C2=CC(=C(C=C2CCN1)O)O |
| SMILES (Isomeric) | CC1C2=CC(=C(C=C2CCN1)O)O |
| InChI | InChI=1S/C10H13NO2/c1-6-8-5-10(13)9(12)4-7(8)2-3-11-6/h4-6,11-13H,2-3H2,1H3 |
| InChI Key | IBRKLUSXDYATLG-UHFFFAOYSA-N |
| Popularity | 377 references in papers |
| Molecular Formula | C10H13NO2 |
| Molecular Weight | 179.22 g/mol |
| Exact Mass | 179.094628657 g/mol |
| Topological Polar Surface Area (TPSA) | 52.50 Ų |
| XlogP | 1.00 |
| Atomic LogP (AlogP) | 1.30 |
| H-Bond Acceptor | 3 |
| H-Bond Donor | 3 |
| Rotatable Bonds | 0 |
| (RS)-Salsolinol |
| RefChem:1051127 |
| 1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol |
| 1-Methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline |
| (+/-)-SALSOLINOL |
| CHEMBL416732 |
| 1,2,3,4-TETRAHYDRO-1-METHYL-6,7-ISOQUINOLINEDIOL |
| CHEBI:88801 |
| (R)-Salsolinol |
| 1-Methyl-1,2,3,4-tetrahydro-isoquinoline-6,7-diol |
| There are more than 10 synonyms. If you wish to see them all click here. |
| Target | Value | Probability (raw) | Probability (%) |
|---|---|---|---|
| Human Intestinal Absorption | + | 0.9917 | 99.17% |
| Caco-2 | - | 0.5680 | 56.80% |
| Blood Brain Barrier | + | 0.6379 | 63.79% |
| Human oral bioavailability | + | 0.5857 | 58.57% |
| Subcellular localzation | Mitochondria | 0.3895 | 38.95% |
| OATP2B1 inhibitior | - | 0.8540 | 85.40% |
| OATP1B1 inhibitior | + | 0.9465 | 94.65% |
| OATP1B3 inhibitior | + | 0.9612 | 96.12% |
| MATE1 inhibitior | - | 0.9200 | 92.00% |
| OCT2 inhibitior | - | 0.5250 | 52.50% |
| BSEP inhibitior | - | 0.9732 | 97.32% |
| P-glycoprotein inhibitior | - | 0.9879 | 98.79% |
| P-glycoprotein substrate | - | 0.7630 | 76.30% |
| CYP3A4 substrate | - | 0.6172 | 61.72% |
| CYP2C9 substrate | - | 0.8108 | 81.08% |
| CYP2D6 substrate | + | 0.5589 | 55.89% |
| CYP3A4 inhibition | - | 0.9620 | 96.20% |
| CYP2C9 inhibition | - | 0.9647 | 96.47% |
| CYP2C19 inhibition | - | 0.9427 | 94.27% |
| CYP2D6 inhibition | - | 0.9231 | 92.31% |
| CYP1A2 inhibition | - | 0.9046 | 90.46% |
| CYP2C8 inhibition | - | 0.9314 | 93.14% |
| CYP inhibitory promiscuity | - | 0.9335 | 93.35% |
| UGT catelyzed | + | 0.8000 | 80.00% |
| Carcinogenicity (binary) | - | 0.9500 | 95.00% |
| Carcinogenicity (trinary) | Non-required | 0.6942 | 69.42% |
| Eye corrosion | - | 0.9813 | 98.13% |
| Eye irritation | - | 0.5902 | 59.02% |
| Skin irritation | - | 0.5972 | 59.72% |
| Skin corrosion | - | 0.8150 | 81.50% |
| Ames mutagenesis | - | 0.7500 | 75.00% |
| Human Ether-a-go-go-Related Gene inhibition | - | 0.7327 | 73.27% |
| Micronuclear | - | 0.5700 | 57.00% |
| Hepatotoxicity | - | 0.5125 | 51.25% |
| skin sensitisation | - | 0.7267 | 72.67% |
| Respiratory toxicity | + | 0.5111 | 51.11% |
| Reproductive toxicity | + | 0.8556 | 85.56% |
| Mitochondrial toxicity | + | 0.8625 | 86.25% |
| Nephrotoxicity | - | 0.8615 | 86.15% |
| Acute Oral Toxicity (c) | III | 0.4878 | 48.78% |
| Estrogen receptor binding | - | 0.7244 | 72.44% |
| Androgen receptor binding | - | 0.7930 | 79.30% |
| Thyroid receptor binding | - | 0.5803 | 58.03% |
| Glucocorticoid receptor binding | - | 0.6158 | 61.58% |
| Aromatase binding | - | 0.8272 | 82.72% |
| PPAR gamma | - | 0.7922 | 79.22% |
| Honey bee toxicity | - | 0.9391 | 93.91% |
| Biodegradation | - | 0.7000 | 70.00% |
| Crustacea aquatic toxicity | + | 0.5500 | 55.00% |
| Fish aquatic toxicity | - | 0.8540 | 85.40% |
Proven Targets:
| CHEMBL ID | UniProt ID | Name | Min activity | Assay type | Source |
|---|---|---|---|---|---|
| CHEMBL217 | P14416 | Dopamine D2 receptor |
5400 nM |
Ki |
DOI: 10.1016/S0960-894X(97)00194-7
|
| CHEMBL234 | P35462 | Dopamine D3 receptor |
500 nM |
Ki |
via Super-PRED
|
| CHEMBL219 | P21917 | Dopamine D4 receptor |
6400 nM |
Ki |
DOI: 10.1016/S0960-894X(97)00194-7
|
| CHEMBL4159 | Q99714 | Endoplasmic reticulum-associated amyloid beta-peptide-binding protein |
251.2 nM |
Potency |
via Super-PRED
|
Predicted Targets (via Super-PRED):
| CHEMBL ID | UniProt ID | Name | Probability | Model accuracy |
|---|---|---|---|---|
| CHEMBL5619 | P27695 | DNA-(apurinic or apyrimidinic site) lyase | 98.08% | 91.11% |
| CHEMBL3251 | P19838 | Nuclear factor NF-kappa-B p105 subunit | 93.32% | 96.09% |
| CHEMBL3137262 | O60341 | LSD1/CoREST complex | 88.47% | 97.09% |
| CHEMBL2581 | P07339 | Cathepsin D | 87.29% | 98.95% |
| CHEMBL241 | Q14432 | Phosphodiesterase 3A | 87.01% | 92.94% |
| CHEMBL1951 | P21397 | Monoamine oxidase A | 85.63% | 91.49% |
| CHEMBL253 | P34972 | Cannabinoid CB2 receptor | 85.44% | 97.25% |
| CHEMBL5697 | Q9GZT9 | Egl nine homolog 1 | 83.53% | 93.40% |
| CHEMBL213 | P08588 | Beta-1 adrenergic receptor | 83.40% | 95.56% |
| CHEMBL4203 | Q9HAZ1 | Dual specificity protein kinase CLK4 | 80.80% | 94.45% |
| CHEMBL1994 | P08235 | Mineralocorticoid receptor | 80.70% | 100.00% |
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.
To see more specific details click the taxa you are interested in.
| Aconitum carmichaelii |
| Aconitum jaluense |
| Aconitum japonicum |
| Aconitum kusnezoffii |
| Aconitum volubile var. pubescens |
| PubChem | 54456 |
| NPASS | NPC302171 |
| ChEMBL | CHEMBL416732 |