Rotundine B

Details

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Internal ID 75804f0a-08fe-4bbb-a624-7c30de007275
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Methylpyridines
IUPAC Name 4-(1,5,5-trimethyl-6,7-dihydrocyclopenta[c]pyridin-6-yl)butan-2-ol
SMILES (Canonical) CC1=NC=CC2=C1CC(C2(C)C)CCC(C)O
SMILES (Isomeric) CC1=NC=CC2=C1CC(C2(C)C)CCC(C)O
InChI InChI=1S/C15H23NO/c1-10(17)5-6-12-9-13-11(2)16-8-7-14(13)15(12,3)4/h7-8,10,12,17H,5-6,9H2,1-4H3
InChI Key IMDXDPUTIISQIM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H23NO
Molecular Weight 233.35 g/mol
Exact Mass 233.177964357 g/mol
Topological Polar Surface Area (TPSA) 33.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.00
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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4-(1,5,5-trimethyl-6,7-dihydrocyclopenta[c]pyridin-6-yl)butan-2-ol
SCHEMBL29710876
CHEBI:173678
4-{1,5,5-trimethyl-5H,6H,7H-cyclopenta[c]pyridin-6-yl}butan-2-ol

2D Structure

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2D Structure of Rotundine B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8698 86.98%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5022 50.22%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9426 94.26%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8310 83.10%
P-glycoprotein inhibitior - 0.9749 97.49%
P-glycoprotein substrate - 0.6961 69.61%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate + 0.3605 36.05%
CYP3A4 inhibition - 0.6615 66.15%
CYP2C9 inhibition - 0.8781 87.81%
CYP2C19 inhibition - 0.7114 71.14%
CYP2D6 inhibition - 0.8842 88.42%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8569 85.69%
CYP inhibitory promiscuity - 0.8024 80.24%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6834 68.34%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.9080 90.80%
Skin irritation - 0.6231 62.31%
Skin corrosion - 0.9029 90.29%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7611 76.11%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5409 54.09%
skin sensitisation + 0.4806 48.06%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8298 82.98%
Acute Oral Toxicity (c) III 0.7071 70.71%
Estrogen receptor binding - 0.8741 87.41%
Androgen receptor binding - 0.8696 86.96%
Thyroid receptor binding + 0.5278 52.78%
Glucocorticoid receptor binding - 0.7440 74.40%
Aromatase binding - 0.6934 69.34%
PPAR gamma - 0.7750 77.50%
Honey bee toxicity - 0.9544 95.44%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.5179 51.79%

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 97.98% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.09% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.81% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.16% 91.11%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.89% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.88% 93.56%
CHEMBL1951 P21397 Monoamine oxidase A 85.38% 91.49%
CHEMBL2094135 Q96BI3 Gamma-secretase 83.77% 98.05%
CHEMBL3401 O75469 Pregnane X receptor 83.29% 94.73%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.91% 90.24%
CHEMBL2535 P11166 Glucose transporter 80.34% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.00% 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.
Cyperus rotundus

Cross-Links

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PubChem 21603505
LOTUS LTS0263515
wikiData Q105115616