Chondrosterin B

Details

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Internal ID be76fecb-97bc-49d1-a283-60f9bd666ec8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Triquinane sesquiterpenoids > Linear triquinanes
IUPAC Name (3R,3aR,3bR)-3b-hydroxy-3,3a,5,5-tetramethyl-3,4-dihydrocyclopenta[a]pentalene-2,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18O3/c1-8-11(16)6-9-5-10-12(17)13(2,3)7-15(10,18)14(8,9)4/h5-6,8,18H,7H2,1-4H3/t8-,14+,15-/m0/s1
InChI Key QGNVEKYDTQENAF-SVGYWBMUSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O3
Molecular Weight 246.30 g/mol
Exact Mass 246.125594432 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEMBL4129664

2D Structure

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2D Structure of Chondrosterin B

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 + 0.8293 82.93%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6344 63.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8777 87.77%
OATP1B3 inhibitior + 0.9644 96.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6929 69.29%
P-glycoprotein inhibitior - 0.9605 96.05%
P-glycoprotein substrate - 0.8479 84.79%
CYP3A4 substrate + 0.5067 50.67%
CYP2C9 substrate - 0.8284 82.84%
CYP2D6 substrate - 0.8927 89.27%
CYP3A4 inhibition - 0.8729 87.29%
CYP2C9 inhibition - 0.8634 86.34%
CYP2C19 inhibition - 0.8957 89.57%
CYP2D6 inhibition - 0.9403 94.03%
CYP1A2 inhibition - 0.8255 82.55%
CYP2C8 inhibition - 0.9247 92.47%
CYP inhibitory promiscuity - 0.9347 93.47%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.4625 46.25%
Eye corrosion - 0.9726 97.26%
Eye irritation - 0.5643 56.43%
Skin irritation + 0.6346 63.46%
Skin corrosion - 0.8720 87.20%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6447 64.47%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.6408 64.08%
skin sensitisation + 0.6020 60.20%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6259 62.59%
Acute Oral Toxicity (c) III 0.3898 38.98%
Estrogen receptor binding - 0.5786 57.86%
Androgen receptor binding + 0.6698 66.98%
Thyroid receptor binding + 0.6384 63.84%
Glucocorticoid receptor binding - 0.7431 74.31%
Aromatase binding - 0.5958 59.58%
PPAR gamma - 0.6306 63.06%
Honey bee toxicity - 0.9262 92.62%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9254 92.54%

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
CHEMBL2581 P07339 Cathepsin D 94.18% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.76% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.76% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.94% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.54% 97.25%
CHEMBL1951 P21397 Monoamine oxidase A 84.15% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.52% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.19% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 81.87% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.22% 86.33%

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 139585750
LOTUS LTS0023528
wikiData Q77490846