Duboscic acid

Details

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Internal ID 8e44b91c-fd4c-481a-897b-aec12a2378d6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,5R,9S,10S,13S,15R,16R,19R,20R,21R)-9,19-dihydroxy-13-methoxy-1,8,8,16,20-pentamethylpentacyclo[13.8.0.02,11.05,10.016,21]tricos-2(11)-ene-5,20-dicarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H48O7/c1-27(2)13-14-31(26(36)37)12-7-19-18(23(31)24(27)33)15-17(38-6)16-21-28(19,3)10-8-20-29(21,4)11-9-22(32)30(20,5)25(34)35/h17,20-24,32-33H,7-16H2,1-6H3,(H,34,35)(H,36,37)/t17-,20-,21+,22-,23-,24+,28+,29+,30-,31-/m1/s1
InChI Key RSQLWSCZCOIUCP-YFSRRQDFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H48O7
Molecular Weight 532.70 g/mol
Exact Mass 532.34000387 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 5.04
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Duboscic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9841 98.41%
Caco-2 - 0.6565 65.65%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8149 81.49%
OATP2B1 inhibitior - 0.5682 56.82%
OATP1B1 inhibitior + 0.8565 85.65%
OATP1B3 inhibitior - 0.4307 43.07%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7071 70.71%
BSEP inhibitior + 0.8395 83.95%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.6244 62.44%
CYP3A4 substrate + 0.7061 70.61%
CYP2C9 substrate - 0.8262 82.62%
CYP2D6 substrate - 0.8513 85.13%
CYP3A4 inhibition - 0.7946 79.46%
CYP2C9 inhibition - 0.5977 59.77%
CYP2C19 inhibition - 0.7944 79.44%
CYP2D6 inhibition - 0.9452 94.52%
CYP1A2 inhibition - 0.7368 73.68%
CYP2C8 inhibition + 0.5336 53.36%
CYP inhibitory promiscuity - 0.9399 93.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9843 98.43%
Carcinogenicity (trinary) Non-required 0.6862 68.62%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9219 92.19%
Skin irritation - 0.5388 53.88%
Skin corrosion - 0.9457 94.57%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4455 44.55%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.6459 64.59%
skin sensitisation - 0.7363 73.63%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6321 63.21%
Acute Oral Toxicity (c) I 0.4563 45.63%
Estrogen receptor binding + 0.6874 68.74%
Androgen receptor binding + 0.7021 70.21%
Thyroid receptor binding + 0.5255 52.55%
Glucocorticoid receptor binding + 0.7457 74.57%
Aromatase binding + 0.7171 71.71%
PPAR gamma + 0.6393 63.93%
Honey bee toxicity - 0.7327 73.27%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9942 99.42%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.55% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 92.42% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.10% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.81% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 89.68% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.16% 91.11%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.68% 94.08%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.57% 94.62%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 84.22% 94.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.75% 100.00%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 83.30% 94.97%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.92% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.76% 95.56%
CHEMBL5028 O14672 ADAM10 82.63% 97.50%
CHEMBL221 P23219 Cyclooxygenase-1 81.73% 90.17%
CHEMBL1902 P62942 FK506-binding protein 1A 81.62% 97.05%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.55% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.52% 95.89%

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.
Duboscia macrocarpa

Cross-Links

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PubChem 50925274
LOTUS LTS0087324
wikiData Q105244826