Cystalgerone

Details

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Internal ID 78793a4a-4458-4911-aa03-aced6c2c9fcd
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name (3aR,7aR)-6-[(E)-4-(2,5-dimethoxy-3-methylphenyl)-2-methylbut-2-enyl]-5-(2-hydroxy-2-methylpropyl)-3a,7a-dimethyl-1,2,3,7-tetrahydroinden-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H42O4/c1-19(10-11-21-16-23(32-7)15-20(2)25(21)33-8)14-22-17-28(5)12-9-13-29(28,6)26(30)24(22)18-27(3,4)31/h10,15-16,31H,9,11-14,17-18H2,1-8H3/b19-10+/t28-,29+/m1/s1
InChI Key JJJJTQJVJRHYKV-UMPJSDBQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H42O4
Molecular Weight 454.60 g/mol
Exact Mass 454.30830982 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.52
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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Cystalgerone
NSC-605981
Cystalgerone from the brown alga Cystoseira algerienss

2D Structure

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2D Structure of Cystalgerone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5265 52.65%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8299 82.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8628 86.28%
OATP1B3 inhibitior + 0.8927 89.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9791 97.91%
P-glycoprotein inhibitior + 0.6498 64.98%
P-glycoprotein substrate - 0.7062 70.62%
CYP3A4 substrate + 0.6423 64.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8147 81.47%
CYP3A4 inhibition - 0.5273 52.73%
CYP2C9 inhibition - 0.6107 61.07%
CYP2C19 inhibition - 0.5861 58.61%
CYP2D6 inhibition - 0.9130 91.30%
CYP1A2 inhibition - 0.5999 59.99%
CYP2C8 inhibition + 0.5406 54.06%
CYP inhibitory promiscuity - 0.6304 63.04%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6769 67.69%
Eye corrosion - 0.9954 99.54%
Eye irritation - 0.8837 88.37%
Skin irritation - 0.6078 60.78%
Skin corrosion - 0.9747 97.47%
Ames mutagenesis - 0.5954 59.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7556 75.56%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6283 62.83%
skin sensitisation - 0.7859 78.59%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.7248 72.48%
Acute Oral Toxicity (c) IV 0.4229 42.29%
Estrogen receptor binding + 0.8749 87.49%
Androgen receptor binding + 0.6482 64.82%
Thyroid receptor binding + 0.7037 70.37%
Glucocorticoid receptor binding + 0.7792 77.92%
Aromatase binding + 0.7493 74.93%
PPAR gamma + 0.7064 70.64%
Honey bee toxicity - 0.8549 85.49%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9973 99.73%

Targets

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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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.20% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.92% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.74% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.16% 85.14%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 92.05% 91.07%
CHEMBL4208 P20618 Proteasome component C5 90.89% 90.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 89.81% 92.68%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.78% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.96% 96.77%
CHEMBL3401 O75469 Pregnane X receptor 88.21% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.97% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.50% 98.95%
CHEMBL2535 P11166 Glucose transporter 86.46% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.29% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.90% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.85% 99.15%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.67% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.55% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.51% 93.00%

Plants that contains it

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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

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PubChem 5459022
LOTUS LTS0187011
wikiData Q104396443