Damascenine

Details

Top
Internal ID 6620f429-d163-4678-87ae-96186d71e9cc
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > M-methoxybenzoic acids and derivatives
IUPAC Name methyl 3-methoxy-2-(methylamino)benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H13NO3/c1-11-9-7(10(12)14-3)5-4-6-8(9)13-2/h4-6,11H,1-3H3
InChI Key ZRWJIZYZTLTXJI-UHFFFAOYSA-N
Popularity 23 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H13NO3
Molecular Weight 195.21 g/mol
Exact Mass 195.08954328 g/mol
Topological Polar Surface Area (TPSA) 47.60 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
methyl 3-methoxy-2-(methylamino)benzoate
483-64-7
Nigelline
2TU4DLG5R3
3-Methoxy-2-(methylamino)benzoic acid methyl ester
DTXSID60197480
RefChem:130836
DTXCID70119971
Benzoic acid, 3-methoxy-2-(methylamino)-, methyl ester
MFCD05663694
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Damascenine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.8739 87.39%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8714 87.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9633 96.33%
OATP1B3 inhibitior + 0.9679 96.79%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8799 87.99%
P-glycoprotein inhibitior - 0.9514 95.14%
P-glycoprotein substrate - 0.8718 87.18%
CYP3A4 substrate - 0.5571 55.71%
CYP2C9 substrate - 0.5986 59.86%
CYP2D6 substrate - 0.7775 77.75%
CYP3A4 inhibition - 0.7829 78.29%
CYP2C9 inhibition - 0.8596 85.96%
CYP2C19 inhibition - 0.6977 69.77%
CYP2D6 inhibition - 0.9463 94.63%
CYP1A2 inhibition + 0.5796 57.96%
CYP2C8 inhibition - 0.6675 66.75%
CYP inhibitory promiscuity - 0.5766 57.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6701 67.01%
Carcinogenicity (trinary) Non-required 0.5330 53.30%
Eye corrosion - 0.9669 96.69%
Eye irritation + 0.9156 91.56%
Skin irritation - 0.8688 86.88%
Skin corrosion - 0.9903 99.03%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4788 47.88%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.5716 57.16%
skin sensitisation - 0.9708 97.08%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6632 66.32%
Acute Oral Toxicity (c) III 0.7452 74.52%
Estrogen receptor binding - 0.8185 81.85%
Androgen receptor binding - 0.6820 68.20%
Thyroid receptor binding - 0.7025 70.25%
Glucocorticoid receptor binding - 0.9266 92.66%
Aromatase binding - 0.8585 85.85%
PPAR gamma - 0.7635 76.35%
Honey bee toxicity - 0.9179 91.79%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.8761 87.61%

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 95.94% 96.09%
CHEMBL2535 P11166 Glucose transporter 92.11% 98.75%
CHEMBL2581 P07339 Cathepsin D 88.82% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 86.93% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.35% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.78% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.39% 86.33%
CHEMBL2321614 Q9NPC2 Potassium channel subfamily K member 9 80.47% 80.00%

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.
Dalbergia odorifera
Dalbergia sissoo

Cross-Links

Top
PubChem 21368
NPASS NPC308694