11alpha,12alpha-Epoxy-3beta-hydroxytaraxera-14-ene-28-oic acid

Details

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Internal ID 49079640-37bb-4965-9c61-a9d86d65afbd
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name (1R,2S,4R,5S,6S,11S,15R,18R,20S,23S)-20-hydroxy-5,8,8,15,19,19,23-heptamethyl-3-oxahexacyclo[13.8.0.02,4.05,14.06,11.018,23]tricos-13-ene-11-carboxylic acid
SMILES (Canonical) CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4C6C(C3(C2C1)C)O6)C)O)(C)C)C)C(=O)O)C
SMILES (Isomeric) C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2[C@H]4[C@H](O4)[C@@]5(C3=CC[C@@]6([C@H]5CC(CC6)(C)C)C(=O)O)C)C)(C)C)O
InChI InChI=1S/C30H46O4/c1-25(2)14-15-30(24(32)33)13-9-18-28(6)11-8-17-26(3,4)20(31)10-12-27(17,5)22(28)21-23(34-21)29(18,7)19(30)16-25/h9,17,19-23,31H,8,10-16H2,1-7H3,(H,32,33)/t17-,19-,20-,21-,22+,23-,27-,28-,29+,30+/m0/s1
InChI Key DCSOSRBBKAIOTD-SCORLBCFSA-N
Popularity 1 reference 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) 70.10 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.22
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 11alpha,12alpha-Epoxy-3beta-hydroxytaraxera-14-ene-28-oic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9889 98.89%
Caco-2 + 0.4928 49.28%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7668 76.68%
OATP2B1 inhibitior - 0.7221 72.21%
OATP1B1 inhibitior + 0.8790 87.90%
OATP1B3 inhibitior + 0.9105 91.05%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5821 58.21%
BSEP inhibitior + 0.8406 84.06%
P-glycoprotein inhibitior - 0.5900 59.00%
P-glycoprotein substrate - 0.7573 75.73%
CYP3A4 substrate + 0.6656 66.56%
CYP2C9 substrate - 0.8176 81.76%
CYP2D6 substrate - 0.8474 84.74%
CYP3A4 inhibition - 0.6953 69.53%
CYP2C9 inhibition - 0.7874 78.74%
CYP2C19 inhibition - 0.8295 82.95%
CYP2D6 inhibition - 0.9351 93.51%
CYP1A2 inhibition - 0.6676 66.76%
CYP2C8 inhibition - 0.5897 58.97%
CYP inhibitory promiscuity - 0.9270 92.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6391 63.91%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9300 93.00%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9398 93.98%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5364 53.64%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.6368 63.68%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.5807 58.07%
Acute Oral Toxicity (c) III 0.7057 70.57%
Estrogen receptor binding + 0.7833 78.33%
Androgen receptor binding + 0.6660 66.60%
Thyroid receptor binding + 0.6874 68.74%
Glucocorticoid receptor binding + 0.8241 82.41%
Aromatase binding + 0.7442 74.42%
PPAR gamma + 0.6590 65.90%
Honey bee toxicity - 0.8156 81.56%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9932 99.32%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.12% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.98% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.56% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.79% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.08% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.73% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 85.85% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 84.73% 83.82%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.31% 99.23%
CHEMBL5028 O14672 ADAM10 82.25% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.97% 89.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.57% 100.00%

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.
Gomphrena macrocephala

Cross-Links

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PubChem 11994580
LOTUS LTS0117036
wikiData Q104975891