(2R,4aalpha)-2beta-Vinyl-2,5,5,8abeta-tetramethyl-6beta-bromooctahydro-2H-1-benzopyran

Details

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Internal ID 60db3850-8b70-4057-bb10-45f03e14bdb1
Taxonomy Organoheterocyclic compounds > Benzopyrans
IUPAC Name (2R,4aS,6S,8aS)-6-bromo-2-ethenyl-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydrochromene
SMILES (Canonical) CC1(C2CCC(OC2(CCC1Br)C)(C)C=C)C
SMILES (Isomeric) C[C@@]1(CC[C@@H]2[C@@](O1)(CC[C@@H](C2(C)C)Br)C)C=C
InChI InChI=1S/C15H25BrO/c1-6-14(4)9-7-11-13(2,3)12(16)8-10-15(11,5)17-14/h6,11-12H,1,7-10H2,2-5H3/t11-,12-,14-,15-/m0/s1
InChI Key HWSCKALJGRRFMK-JURCDPSOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H25BrO
Molecular Weight 301.26 g/mol
Exact Mass 300.10888 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.70
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 (2R,4aalpha)-2beta-Vinyl-2,5,5,8abeta-tetramethyl-6beta-bromooctahydro-2H-1-benzopyran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.6499 64.99%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5565 55.65%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.9350 93.50%
OATP1B3 inhibitior + 0.9223 92.23%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7672 76.72%
P-glycoprotein inhibitior - 0.9220 92.20%
P-glycoprotein substrate - 0.9553 95.53%
CYP3A4 substrate + 0.5814 58.14%
CYP2C9 substrate - 0.7880 78.80%
CYP2D6 substrate - 0.7231 72.31%
CYP3A4 inhibition - 0.7860 78.60%
CYP2C9 inhibition - 0.5653 56.53%
CYP2C19 inhibition - 0.5788 57.88%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition - 0.6841 68.41%
CYP2C8 inhibition - 0.8768 87.68%
CYP inhibitory promiscuity - 0.7437 74.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7723 77.23%
Carcinogenicity (trinary) Non-required 0.6377 63.77%
Eye corrosion - 0.9528 95.28%
Eye irritation - 0.7761 77.61%
Skin irritation - 0.6930 69.30%
Skin corrosion - 0.9361 93.61%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5124 51.24%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5291 52.91%
skin sensitisation + 0.4902 49.02%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.7926 79.26%
Acute Oral Toxicity (c) III 0.6438 64.38%
Estrogen receptor binding - 0.6847 68.47%
Androgen receptor binding - 0.5906 59.06%
Thyroid receptor binding - 0.5719 57.19%
Glucocorticoid receptor binding + 0.6478 64.78%
Aromatase binding + 0.5288 52.88%
PPAR gamma - 0.7126 71.26%
Honey bee toxicity - 0.7019 70.19%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9927 99.27%

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 89.52% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.88% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.55% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.34% 96.09%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.47% 90.24%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.11% 97.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.58% 92.94%
CHEMBL259 P32245 Melanocortin receptor 4 80.44% 95.38%

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.
Anethum graveolens
Cymbidium aloifolium
Delphinium dictyocarpum
Ladeania juncea
Ligularia atroviolacea
Scutellaria glabra
Trifolium pannonicum

Cross-Links

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PubChem 11771060
NPASS NPC26945
LOTUS LTS0011228
wikiData Q105034803