Hirsutalin A

Details

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Internal ID 6775d2e3-31a5-41c5-a183-360c9df77e12
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Eunicellane and asbestinane diterpenoids
IUPAC Name [(1R,2R,6R,7R,8R,9R,12S)-6-[(2R)-1-butanoyloxypropan-2-yl]-12-hydroxy-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.02,7]pentadec-3-en-9-yl] (2R)-2-hydroxybutanoate
SMILES (Canonical) CCCC(=O)OCC(C)C1CC=C(C2C1C3C(CCC(C(=C)CC2O3)O)(C)OC(=O)C(CC)O)C
SMILES (Isomeric) CCCC(=O)OC[C@H](C)[C@H]1CC=C([C@H]2[C@@H]1[C@@H]3[C@](CC[C@@H](C(=C)C[C@H]2O3)O)(C)OC(=O)[C@@H](CC)O)C
InChI InChI=1S/C28H44O7/c1-7-9-23(31)33-15-18(5)19-11-10-16(3)24-22-14-17(4)21(30)12-13-28(6,26(34-22)25(19)24)35-27(32)20(29)8-2/h10,18-22,24-26,29-30H,4,7-9,11-15H2,1-3,5-6H3/t18-,19+,20+,21-,22+,24+,25+,26+,28+/m0/s1
InChI Key LGCBXJHPKWYGGG-ZEOQMOKSSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H44O7
Molecular Weight 492.60 g/mol
Exact Mass 492.30870374 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.11
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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CHEBI:70340
CHEMBL1631447
Q27138681

2D Structure

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2D Structure of Hirsutalin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 - 0.6709 67.09%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7940 79.40%
OATP2B1 inhibitior - 0.8641 86.41%
OATP1B1 inhibitior + 0.8141 81.41%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7157 71.57%
BSEP inhibitior + 0.7512 75.12%
P-glycoprotein inhibitior + 0.6752 67.52%
P-glycoprotein substrate + 0.6568 65.68%
CYP3A4 substrate + 0.6947 69.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8400 84.00%
CYP3A4 inhibition + 0.6933 69.33%
CYP2C9 inhibition - 0.7560 75.60%
CYP2C19 inhibition - 0.8640 86.40%
CYP2D6 inhibition - 0.9275 92.75%
CYP1A2 inhibition - 0.8317 83.17%
CYP2C8 inhibition + 0.4883 48.83%
CYP inhibitory promiscuity - 0.8576 85.76%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6211 62.11%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9236 92.36%
Skin irritation + 0.5629 56.29%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.6970 69.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7562 75.62%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5502 55.02%
skin sensitisation - 0.8823 88.23%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6088 60.88%
Acute Oral Toxicity (c) III 0.4995 49.95%
Estrogen receptor binding + 0.8128 81.28%
Androgen receptor binding + 0.6508 65.08%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7147 71.47%
Aromatase binding + 0.7145 71.45%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.7736 77.36%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9945 99.45%

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
CHEMBL221 P23219 Cyclooxygenase-1 99.46% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.40% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.26% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.70% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.32% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.07% 98.95%
CHEMBL1871 P10275 Androgen Receptor 91.81% 96.43%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.66% 89.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.25% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.87% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.09% 90.71%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 87.66% 94.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.63% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.16% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.93% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 86.72% 91.19%
CHEMBL220 P22303 Acetylcholinesterase 86.65% 94.45%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.65% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.11% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.93% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.78% 92.62%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.80% 100.00%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 80.58% 97.47%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.42% 93.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.20% 95.56%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.13% 96.90%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 50900038
LOTUS LTS0115405
wikiData Q27138681