Daldinan C

Details

Top
Internal ID f2d3482f-c702-4266-8666-ae9fa63af251
Taxonomy Organoheterocyclic compounds > Isoindoles and derivatives > Isoindolines > Isoindolones
IUPAC Name 4-[6-hydroxy-1-(2-hydroxy-3-methoxy-5-methylphenyl)-4-methoxy-3-oxo-1H-isoindol-2-yl]butanoic acid
SMILES (Canonical) CC1=CC(=C(C(=C1)OC)O)C2C3=C(C(=CC(=C3)O)OC)C(=O)N2CCCC(=O)O
SMILES (Isomeric) CC1=CC(=C(C(=C1)OC)O)C2C3=C(C(=CC(=C3)O)OC)C(=O)N2CCCC(=O)O
InChI InChI=1S/C21H23NO7/c1-11-7-14(20(26)16(8-11)29-3)19-13-9-12(23)10-15(28-2)18(13)21(27)22(19)6-4-5-17(24)25/h7-10,19,23,26H,4-6H2,1-3H3,(H,24,25)
InChI Key LOGFPLSRAOLWIO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C21H23NO7
Molecular Weight 401.40 g/mol
Exact Mass 401.14745207 g/mol
Topological Polar Surface Area (TPSA) 117.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Daldinan C

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8209 82.09%
Caco-2 + 0.5961 59.61%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7170 71.70%
OATP2B1 inhibitior - 0.7218 72.18%
OATP1B1 inhibitior + 0.8580 85.80%
OATP1B3 inhibitior + 0.9090 90.90%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7754 77.54%
BSEP inhibitior + 0.6466 64.66%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.6624 66.24%
CYP3A4 substrate + 0.6047 60.47%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8662 86.62%
CYP3A4 inhibition - 0.5138 51.38%
CYP2C9 inhibition - 0.8957 89.57%
CYP2C19 inhibition - 0.7480 74.80%
CYP2D6 inhibition - 0.9000 90.00%
CYP1A2 inhibition - 0.9096 90.96%
CYP2C8 inhibition + 0.6771 67.71%
CYP inhibitory promiscuity - 0.8186 81.86%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5326 53.26%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.9171 91.71%
Skin irritation - 0.8164 81.64%
Skin corrosion - 0.9511 95.11%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5745 57.45%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.9287 92.87%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8150 81.50%
Acute Oral Toxicity (c) III 0.6333 63.33%
Estrogen receptor binding + 0.7554 75.54%
Androgen receptor binding + 0.6568 65.68%
Thyroid receptor binding + 0.6046 60.46%
Glucocorticoid receptor binding + 0.8695 86.95%
Aromatase binding + 0.6122 61.22%
PPAR gamma + 0.5810 58.10%
Honey bee toxicity - 0.9482 94.82%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.7310 73.10%

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 99.01% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.71% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.27% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.25% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.04% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.22% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.02% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.73% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.25% 89.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.16% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.70% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.24% 90.71%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.04% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.17% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 82.60% 91.19%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.88% 95.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.99% 97.21%
CHEMBL4330 Q9NS75 Cysteinyl leukotriene receptor 2 80.32% 98.00%

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.
There are no matching plants.

Cross-Links

Top
PubChem 139589985
LOTUS LTS0002585
wikiData Q27137525