Photocitral B

Details

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Internal ID d0488d3a-c530-404c-bf72-97189443be5d
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name 1,6,6-trimethylbicyclo[2.1.1]hexane-5-carbaldehyde
SMILES (Canonical) CC1(C2CCC1(C2C=O)C)C
SMILES (Isomeric) CC1(C2CCC1(C2C=O)C)C
InChI InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(7)6-11/h6-8H,4-5H2,1-3H3
InChI Key AGTSNXAZDKAPHU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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6040-45-5
NSC166191
DTXSID80304538
AGTSNXAZDKAPHU-UHFFFAOYSA-N
NSC-166191

2D Structure

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2D Structure of Photocitral B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.7684 76.84%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.7017 70.17%
OATP2B1 inhibitior - 0.8495 84.95%
OATP1B1 inhibitior + 0.8891 88.91%
OATP1B3 inhibitior + 0.9263 92.63%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9214 92.14%
P-glycoprotein inhibitior - 0.9696 96.96%
P-glycoprotein substrate - 0.9731 97.31%
CYP3A4 substrate + 0.5450 54.50%
CYP2C9 substrate - 0.6031 60.31%
CYP2D6 substrate - 0.8016 80.16%
CYP3A4 inhibition - 0.9532 95.32%
CYP2C9 inhibition - 0.8942 89.42%
CYP2C19 inhibition - 0.9146 91.46%
CYP2D6 inhibition - 0.9583 95.83%
CYP1A2 inhibition - 0.8269 82.69%
CYP2C8 inhibition - 0.8686 86.86%
CYP inhibitory promiscuity - 0.9540 95.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5160 51.60%
Eye corrosion + 0.4679 46.79%
Eye irritation + 0.8315 83.15%
Skin irritation + 0.7749 77.49%
Skin corrosion - 0.9085 90.85%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7234 72.34%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5219 52.19%
skin sensitisation + 0.8594 85.94%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7789 77.89%
Nephrotoxicity + 0.5054 50.54%
Acute Oral Toxicity (c) III 0.6713 67.13%
Estrogen receptor binding - 0.7387 73.87%
Androgen receptor binding - 0.7202 72.02%
Thyroid receptor binding - 0.8360 83.60%
Glucocorticoid receptor binding - 0.9202 92.02%
Aromatase binding - 0.8572 85.72%
PPAR gamma - 0.7788 77.88%
Honey bee toxicity - 0.7503 75.03%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.8774 87.74%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.12% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.08% 96.09%
CHEMBL1871 P10275 Androgen Receptor 88.54% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.62% 100.00%
CHEMBL233 P35372 Mu opioid receptor 86.93% 97.93%
CHEMBL221 P23219 Cyclooxygenase-1 84.12% 90.17%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.00% 93.04%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 83.21% 95.27%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.14% 97.09%
CHEMBL259 P32245 Melanocortin receptor 4 82.85% 95.38%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.33% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.08% 82.69%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.69% 95.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.31% 96.61%

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.
Diplotaenia cachrydifolia
Pelargonium citronellum

Cross-Links

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PubChem 296248
LOTUS LTS0023806
wikiData Q82050523