Treleasegenin acid

Details

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Internal ID 719766ce-79a8-4f1f-a337-8ca5d987f6c5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (2S,3S,4aR,6aS,6bR,10S,12aR,14bS)-3,10-dihydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
SMILES (Canonical) CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(C(C5)O)(C)CO)C(=O)O)C)C)C
SMILES (Isomeric) C[C@]12CC[C@@H](C(C1CC[C@@]3(C2CC=C4[C@]3(CC[C@@]5([C@H]4C[C@@]([C@H](C5)O)(C)CO)C(=O)O)C)C)(C)C)O
InChI InChI=1S/C30H48O5/c1-25(2)20-9-12-29(6)21(27(20,4)11-10-22(25)32)8-7-18-19-15-26(3,17-31)23(33)16-30(19,24(34)35)14-13-28(18,29)5/h7,19-23,31-33H,8-17H2,1-6H3,(H,34,35)/t19-,20?,21?,22-,23-,26-,27-,28+,29+,30+/m0/s1
InChI Key QXFJACMLXSJEMH-IQQHCVDNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O5
Molecular Weight 488.70 g/mol
Exact Mass 488.35017463 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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MLS000563472
CHEMBL1904698
HMS2270I23
SMR000470877

2D Structure

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2D Structure of Treleasegenin acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 - 0.5938 59.38%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8419 84.19%
OATP2B1 inhibitior - 0.5725 57.25%
OATP1B1 inhibitior + 0.8710 87.10%
OATP1B3 inhibitior - 0.5699 56.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5542 55.42%
BSEP inhibitior + 0.7913 79.13%
P-glycoprotein inhibitior - 0.8507 85.07%
P-glycoprotein substrate - 0.8159 81.59%
CYP3A4 substrate + 0.6552 65.52%
CYP2C9 substrate - 0.6653 66.53%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.8608 86.08%
CYP2C9 inhibition - 0.8469 84.69%
CYP2C19 inhibition - 0.9159 91.59%
CYP2D6 inhibition - 0.9434 94.34%
CYP1A2 inhibition - 0.8926 89.26%
CYP2C8 inhibition - 0.6071 60.71%
CYP inhibitory promiscuity - 0.8884 88.84%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7044 70.44%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9313 93.13%
Skin irritation - 0.5182 51.82%
Skin corrosion - 0.9636 96.36%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5550 55.50%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.7684 76.84%
skin sensitisation - 0.8274 82.74%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7465 74.65%
Acute Oral Toxicity (c) III 0.7595 75.95%
Estrogen receptor binding + 0.7615 76.15%
Androgen receptor binding + 0.6973 69.73%
Thyroid receptor binding + 0.5712 57.12%
Glucocorticoid receptor binding + 0.8200 82.00%
Aromatase binding + 0.6482 64.82%
PPAR gamma + 0.5473 54.73%
Honey bee toxicity - 0.8758 87.58%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9889 98.89%

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 94.98% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.70% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.55% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.77% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 87.44% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.47% 94.45%
CHEMBL2581 P07339 Cathepsin D 84.59% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.41% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.60% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.12% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.32% 82.69%

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.
Stenocereus eruca

Cross-Links

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PubChem 23641097
LOTUS LTS0096260
wikiData Q105229575