Caloncobic Acid A

Details

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Internal ID b3e32141-ae93-41e4-926e-4b1686e2c98e
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cycloartanols and derivatives
IUPAC Name (1S,3R,8R,11R,12R,15R,16R)-15-[(2R,5S)-5-hydroxy-6-methylhept-6-en-2-yl]-7,7,16-trimethyl-6-oxopentacyclo[9.7.0.01,3.03,8.012,16]octadecane-12-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H46O4/c1-18(2)21(31)8-7-19(3)20-11-14-30(25(33)34)23-10-9-22-26(4,5)24(32)12-13-28(22)17-29(23,28)16-15-27(20,30)6/h19-23,31H,1,7-17H2,2-6H3,(H,33,34)/t19-,20-,21+,22+,23-,27-,28-,29+,30+/m1/s1
InChI Key SYVTXPULSBCSAB-CMWTXFCNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O4
Molecular Weight 470.70 g/mol
Exact Mass 470.33960994 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 6.80
Atomic LogP (AlogP) 6.41
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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Caloncobic acid A
BDBM50384886

2D Structure

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2D Structure of Caloncobic Acid A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 - 0.5223 52.23%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7856 78.56%
OATP2B1 inhibitior - 0.7153 71.53%
OATP1B1 inhibitior + 0.8545 85.45%
OATP1B3 inhibitior - 0.3425 34.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6782 67.82%
BSEP inhibitior - 0.4626 46.26%
P-glycoprotein inhibitior - 0.6059 60.59%
P-glycoprotein substrate - 0.5957 59.57%
CYP3A4 substrate + 0.6466 64.66%
CYP2C9 substrate - 0.8348 83.48%
CYP2D6 substrate - 0.8457 84.57%
CYP3A4 inhibition - 0.7429 74.29%
CYP2C9 inhibition - 0.8055 80.55%
CYP2C19 inhibition - 0.9106 91.06%
CYP2D6 inhibition - 0.9512 95.12%
CYP1A2 inhibition - 0.9047 90.47%
CYP2C8 inhibition - 0.6645 66.45%
CYP inhibitory promiscuity - 0.8757 87.57%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7209 72.09%
Eye corrosion - 0.9937 99.37%
Eye irritation - 0.9339 93.39%
Skin irritation + 0.5929 59.29%
Skin corrosion - 0.9431 94.31%
Ames mutagenesis - 0.7354 73.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6798 67.98%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.6333 63.33%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.6041 60.41%
Acute Oral Toxicity (c) III 0.4124 41.24%
Estrogen receptor binding + 0.7254 72.54%
Androgen receptor binding + 0.7397 73.97%
Thyroid receptor binding + 0.6506 65.06%
Glucocorticoid receptor binding + 0.7708 77.08%
Aromatase binding + 0.7794 77.94%
PPAR gamma - 0.5163 51.63%
Honey bee toxicity - 0.8556 85.56%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL4235 P28845 11-beta-hydroxysteroid dehydrogenase 1 105 nM
IC50
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.67% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.64% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.55% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.06% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.34% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 89.23% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 87.88% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.77% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.81% 89.34%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 83.66% 94.78%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.21% 90.71%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.08% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.93% 99.23%

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.
Caloncoba glauca

Cross-Links

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PubChem 57408764
LOTUS LTS0147838
wikiData Q105263812