Bornyl chloride, (+)-

Details

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Internal ID d594309a-d8b7-436c-bc13-2e4ecbf97585
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (1R,2S,4R)-2-chloro-1,7,7-trimethylbicyclo[2.2.1]heptane
SMILES (Canonical) CC1(C2CCC1(C(C2)Cl)C)C
SMILES (Isomeric) C[C@@]12CC[C@@H](C1(C)C)C[C@@H]2Cl
InChI InChI=1S/C10H17Cl/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8H,4-6H2,1-3H3/t7-,8+,10+/m1/s1
InChI Key XXZAOMJCZBZKPV-WEDXCCLWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H17Cl
Molecular Weight 172.69 g/mol
Exact Mass 172.1018782 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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464-41-5
endo-2-Chlorobornane
2-endo-Bornyl chloride
JXL3Y7EPZB
Bornane, 2-chloro-, endo-(+)-
2-Endo-bornyl chloride, endo-(+)-
UNII-U3GJ0TB404
U3GJ0TB404
30462-53-4
2-Chlorocamphane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Bornyl chloride, (+)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.8228 82.28%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.7360 73.60%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8995 89.95%
OATP1B3 inhibitior + 0.9390 93.90%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9369 93.69%
P-glycoprotein inhibitior - 0.9727 97.27%
P-glycoprotein substrate - 0.9488 94.88%
CYP3A4 substrate + 0.5272 52.72%
CYP2C9 substrate - 0.7759 77.59%
CYP2D6 substrate - 0.7876 78.76%
CYP3A4 inhibition - 0.9169 91.69%
CYP2C9 inhibition - 0.8858 88.58%
CYP2C19 inhibition - 0.8260 82.60%
CYP2D6 inhibition - 0.9400 94.00%
CYP1A2 inhibition - 0.8591 85.91%
CYP2C8 inhibition - 0.8740 87.40%
CYP inhibitory promiscuity - 0.8607 86.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7013 70.13%
Carcinogenicity (trinary) Non-required 0.6242 62.42%
Eye corrosion - 0.8263 82.63%
Eye irritation + 0.9474 94.74%
Skin irritation - 0.6208 62.08%
Skin corrosion - 0.9464 94.64%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7107 71.07%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6321 63.21%
skin sensitisation + 0.7941 79.41%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5405 54.05%
Mitochondrial toxicity - 0.6664 66.64%
Nephrotoxicity + 0.6187 61.87%
Acute Oral Toxicity (c) IV 0.5116 51.16%
Estrogen receptor binding - 0.7722 77.22%
Androgen receptor binding - 0.7963 79.63%
Thyroid receptor binding - 0.7472 74.72%
Glucocorticoid receptor binding - 0.8111 81.11%
Aromatase binding - 0.8737 87.37%
PPAR gamma - 0.7533 75.33%
Honey bee toxicity - 0.5977 59.77%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.76% 97.25%
CHEMBL238 Q01959 Dopamine transporter 89.90% 95.88%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.82% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.23% 97.09%
CHEMBL259 P32245 Melanocortin receptor 4 86.38% 95.38%
CHEMBL2996 Q05655 Protein kinase C delta 86.29% 97.79%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.27% 82.69%
CHEMBL221 P23219 Cyclooxygenase-1 82.21% 90.17%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 82.08% 95.27%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.37% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.12% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.06% 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.
Hansenia forbesii
Hansenia weberbaueriana
Thymus martinezii

Cross-Links

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PubChem 12300207
NPASS NPC4818
LOTUS LTS0073681
wikiData Q76422740