deacetylcytochalasin C

Details

Top
Internal ID a6851a52-9752-4ebf-a116-1118212b6897
Taxonomy Organoheterocyclic compounds > Isoindoles and derivatives > Isoindolines > Isoindolones
IUPAC Name (1R,2R,3Z,5R,7S,9Z,11R,12S,15R,16S)-16-benzyl-2,5,12-trihydroxy-5,7,13,14-tetramethyl-17-azatricyclo[9.7.0.01,15]octadeca-3,9,13-triene-6,18-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H35NO5/c1-16-9-8-12-20-24(31)18(3)17(2)23-21(15-19-10-6-5-7-11-19)29-26(33)28(20,23)22(30)13-14-27(4,34)25(16)32/h5-8,10-14,16,20-24,30-31,34H,9,15H2,1-4H3,(H,29,33)/b12-8-,14-13-/t16-,20-,21-,22+,23-,24+,27+,28+/m0/s1
InChI Key AOIKFORBJLUJGZ-DCUUNKSGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H35NO5
Molecular Weight 465.60 g/mol
Exact Mass 465.25152322 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of deacetylcytochalasin C

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9817 98.17%
Caco-2 - 0.7140 71.40%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Plasma membrane 0.6583 65.83%
OATP2B1 inhibitior - 0.7213 72.13%
OATP1B1 inhibitior + 0.8659 86.59%
OATP1B3 inhibitior + 0.9443 94.43%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9545 95.45%
P-glycoprotein inhibitior - 0.8728 87.28%
P-glycoprotein substrate + 0.5532 55.32%
CYP3A4 substrate + 0.6537 65.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8263 82.63%
CYP3A4 inhibition - 0.9240 92.40%
CYP2C9 inhibition - 0.7067 70.67%
CYP2C19 inhibition - 0.7528 75.28%
CYP2D6 inhibition - 0.8931 89.31%
CYP1A2 inhibition - 0.8581 85.81%
CYP2C8 inhibition + 0.4870 48.70%
CYP inhibitory promiscuity + 0.7253 72.53%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Danger 0.4186 41.86%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9624 96.24%
Skin irritation - 0.7492 74.92%
Skin corrosion - 0.9309 93.09%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5257 52.57%
skin sensitisation - 0.8425 84.25%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.8948 89.48%
Acute Oral Toxicity (c) II 0.3187 31.87%
Estrogen receptor binding + 0.6820 68.20%
Androgen receptor binding + 0.6219 62.19%
Thyroid receptor binding + 0.6261 62.61%
Glucocorticoid receptor binding + 0.7730 77.30%
Aromatase binding + 0.6230 62.30%
PPAR gamma + 0.6217 62.17%
Honey bee toxicity - 0.7944 79.44%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.8704 87.04%

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 98.73% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.40% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.12% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.87% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.77% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 89.75% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.15% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.69% 94.45%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.79% 96.25%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 83.76% 97.64%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.24% 90.24%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 82.18% 95.48%
CHEMBL4208 P20618 Proteasome component C5 82.15% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.97% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.82% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.54% 95.89%

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 139587681
LOTUS LTS0021014
wikiData Q105274459