CID 75167685

Details

Top
Internal ID e77d866e-2187-4885-9862-a9b040a8bf14
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name
SMILES (Canonical) CN1C(=O)C2(CC3=C(C4(C2C5=CNC6=CC=CC=C65)C(=O)N(C(=N)N4C)C)NC7=CC=CC=C37)N=C1N
SMILES (Isomeric) CN1C(=O)C2(CC3=C(C4(C2C5=CNC6=CC=CC=C65)C(=O)N(C(=N)N4C)C)NC7=CC=CC=C37)N=C1N
InChI InChI=1S/C27H26N8O2/c1-33-22(36)26(32-24(33)28)12-16-14-8-5-7-11-19(14)31-21(16)27(23(37)34(2)25(29)35(27)3)20(26)17-13-30-18-10-6-4-9-15(17)18/h4-11,13,20,29-31H,12H2,1-3H3,(H2,28,32)
InChI Key KJHOCLYVJRTASU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H26N8O2
Molecular Weight 494.50 g/mol
Exact Mass 494.21787210 g/mol
Topological Polar Surface Area (TPSA) 138.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 75167685

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9683 96.83%
Caco-2 - 0.7346 73.46%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5431 54.31%
OATP2B1 inhibitior - 0.7147 71.47%
OATP1B1 inhibitior + 0.8843 88.43%
OATP1B3 inhibitior + 0.9388 93.88%
MATE1 inhibitior - 0.5033 50.33%
OCT2 inhibitior - 0.7529 75.29%
BSEP inhibitior + 0.5885 58.85%
P-glycoprotein inhibitior + 0.7631 76.31%
P-glycoprotein substrate + 0.7106 71.06%
CYP3A4 substrate + 0.6788 67.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7195 71.95%
CYP3A4 inhibition + 0.5225 52.25%
CYP2C9 inhibition - 0.7171 71.71%
CYP2C19 inhibition - 0.6569 65.69%
CYP2D6 inhibition - 0.8584 85.84%
CYP1A2 inhibition - 0.7604 76.04%
CYP2C8 inhibition - 0.5587 55.87%
CYP inhibitory promiscuity - 0.8695 86.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5644 56.44%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.9660 96.60%
Skin irritation - 0.7913 79.13%
Skin corrosion - 0.9365 93.65%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4773 47.73%
Micronuclear + 0.8200 82.00%
Hepatotoxicity - 0.5091 50.91%
skin sensitisation - 0.8645 86.45%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.6024 60.24%
Acute Oral Toxicity (c) III 0.5252 52.52%
Estrogen receptor binding + 0.8497 84.97%
Androgen receptor binding + 0.7636 76.36%
Thyroid receptor binding + 0.6676 66.76%
Glucocorticoid receptor binding + 0.6952 69.52%
Aromatase binding + 0.6423 64.23%
PPAR gamma + 0.7763 77.63%
Honey bee toxicity - 0.8116 81.16%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.6910 69.10%

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
CHEMBL2581 P07339 Cathepsin D 98.34% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.25% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.02% 96.09%
CHEMBL3310 Q96DB2 Histone deacetylase 11 93.82% 88.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.02% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.81% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.80% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.59% 99.23%
CHEMBL2535 P11166 Glucose transporter 87.60% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.25% 91.11%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 85.28% 85.49%
CHEMBL3384 Q16512 Protein kinase N1 84.74% 80.71%
CHEMBL213 P08588 Beta-1 adrenergic receptor 84.72% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.76% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.36% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.81% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.63% 97.09%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.42% 93.65%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.16% 93.40%

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.
Delphinium delavayi
Delphinium dictyocarpum
Delphinium majus
Delphinium umbrosum

Cross-Links

Top
PubChem 75167685
LOTUS LTS0251413
wikiData Q105186912