3-Isopropyl-9a-methyl-1,2,4a,9a-tetrahydroxanthene

Details

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Internal ID 90e720a1-03d1-4b2a-8af0-b82c92ac9268
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthenes
IUPAC Name 9a-methyl-3-propan-2-yl-1,2,4a,9-tetrahydroxanthene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O/c1-12(2)13-8-9-17(3)11-14-6-4-5-7-15(14)18-16(17)10-13/h4-7,10,12,16H,8-9,11H2,1-3H3
InChI Key JCVVMRFAPQPJBD-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O
Molecular Weight 242.36 g/mol
Exact Mass 242.167065321 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.37
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Isopropyl-9a-methyl-1,2,4a,9a-tetrahydroxanthene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.9380 93.80%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.3984 39.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9173 91.73%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7695 76.95%
P-glycoprotein inhibitior - 0.8836 88.36%
P-glycoprotein substrate - 0.8636 86.36%
CYP3A4 substrate + 0.5486 54.86%
CYP2C9 substrate - 0.5856 58.56%
CYP2D6 substrate + 0.4536 45.36%
CYP3A4 inhibition - 0.6585 65.85%
CYP2C9 inhibition - 0.5614 56.14%
CYP2C19 inhibition + 0.8301 83.01%
CYP2D6 inhibition - 0.7129 71.29%
CYP1A2 inhibition + 0.7495 74.95%
CYP2C8 inhibition - 0.9021 90.21%
CYP inhibitory promiscuity + 0.7428 74.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6371 63.71%
Eye corrosion - 0.9757 97.57%
Eye irritation - 0.9541 95.41%
Skin irritation - 0.6200 62.00%
Skin corrosion - 0.9476 94.76%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7568 75.68%
Micronuclear - 0.9641 96.41%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.5858 58.58%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.4547 45.47%
Acute Oral Toxicity (c) III 0.7365 73.65%
Estrogen receptor binding - 0.8783 87.83%
Androgen receptor binding - 0.6562 65.62%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.8127 81.27%
Aromatase binding - 0.5940 59.40%
PPAR gamma - 0.7656 76.56%
Honey bee toxicity - 0.8091 80.91%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9901 99.01%

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 94.63% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.25% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.22% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.37% 95.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.75% 96.47%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.15% 97.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.25% 100.00%
CHEMBL2581 P07339 Cathepsin D 81.21% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.12% 97.09%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.39% 95.71%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.37% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.37% 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.
Indigofera longiracemosa

Cross-Links

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PubChem 15406974
LOTUS LTS0183961
wikiData Q105125165