Caloncobalactone A

Details

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Internal ID 55169833-2f2f-45a6-b406-2a702515be23
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cycloartanols and derivatives
IUPAC Name (1R,2R,5R,10R,12S,15R,16R,17R,20S,24R)-24-hydroxy-20-(2-hydroxypropan-2-yl)-6,6,15,17-tetramethyl-21-oxahexacyclo[14.6.2.01,15.02,12.05,10.010,12]tetracosane-7,22-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H46O5/c1-17-7-10-22(26(4,5)34)35-24(33)30-15-18(31)23(17)27(30,6)13-14-29-16-28(29)12-11-21(32)25(2,3)19(28)8-9-20(29)30/h17-20,22-23,31,34H,7-16H2,1-6H3/t17-,18-,19+,20-,22+,23+,27-,28-,29+,30+/m1/s1
InChI Key QQKZTKCCQBXMPH-ZNAZFANWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O5
Molecular Weight 486.70 g/mol
Exact Mass 486.33452456 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.06
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL2035570

2D Structure

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2D Structure of Caloncobalactone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9637 96.37%
Caco-2 - 0.5263 52.63%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7468 74.68%
OATP2B1 inhibitior - 0.7197 71.97%
OATP1B1 inhibitior + 0.8773 87.73%
OATP1B3 inhibitior + 0.8816 88.16%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior + 0.7980 79.80%
P-glycoprotein inhibitior - 0.6217 62.17%
P-glycoprotein substrate - 0.6641 66.41%
CYP3A4 substrate + 0.6727 67.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8363 83.63%
CYP3A4 inhibition - 0.6547 65.47%
CYP2C9 inhibition - 0.8105 81.05%
CYP2C19 inhibition - 0.8344 83.44%
CYP2D6 inhibition - 0.9629 96.29%
CYP1A2 inhibition - 0.7349 73.49%
CYP2C8 inhibition + 0.4611 46.11%
CYP inhibitory promiscuity - 0.9768 97.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6851 68.51%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9435 94.35%
Skin irritation + 0.5172 51.72%
Skin corrosion - 0.8961 89.61%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4116 41.16%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8149 81.49%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.8102 81.02%
Acute Oral Toxicity (c) III 0.4956 49.56%
Estrogen receptor binding + 0.7001 70.01%
Androgen receptor binding + 0.7482 74.82%
Thyroid receptor binding + 0.5823 58.23%
Glucocorticoid receptor binding + 0.7671 76.71%
Aromatase binding + 0.7539 75.39%
PPAR gamma + 0.5708 57.08%
Honey bee toxicity - 0.8242 82.42%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9798 97.98%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.37% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.49% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.54% 91.11%
CHEMBL204 P00734 Thrombin 91.87% 96.01%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.86% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.75% 89.34%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.30% 82.69%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 88.20% 83.57%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.98% 92.94%
CHEMBL2581 P07339 Cathepsin D 86.86% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.19% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.16% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.83% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.25% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.57% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.99% 99.23%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.34% 94.78%
CHEMBL5408 Q9UHD2 Serine/threonine-protein kinase TBK1 80.69% 90.48%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.67% 93.04%
CHEMBL259 P32245 Melanocortin receptor 4 80.41% 95.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.38% 95.89%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.21% 85.30%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 80.03% 98.00%

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.
Caloncoba glauca

Cross-Links

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PubChem 70681710
LOTUS LTS0147677
wikiData Q105225911