d-Camphor

Details

Top
Internal ID 7365b62b-fdd1-441d-88b4-75bace22909a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (1R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
SMILES (Canonical) CC1(C2CCC1(C(=O)C2)C)C
SMILES (Isomeric) C[C@@]12CC[C@H](C1(C)C)CC2=O
InChI InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10-/m0/s1
InChI Key DSSYKIVIOFKYAU-XVKPBYJWSA-N
Popularity 16 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.40
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
(1R)-Camphor
D-(+)-Camphor
Alcanfor
Camphor Powder
Japanese camphor
Camphor USP
d-2-Camphanone
d-2-Bornanone
(-)-Alcanfor
(+)-Camphor
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of d-Camphor

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.8328 83.28%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Mitochondria 0.5569 55.69%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9490 94.90%
OATP1B3 inhibitior + 0.9648 96.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9068 90.68%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.9481 94.81%
CYP3A4 substrate - 0.5505 55.05%
CYP2C9 substrate - 0.7800 78.00%
CYP2D6 substrate - 0.8045 80.45%
CYP3A4 inhibition - 0.9583 95.83%
CYP2C9 inhibition - 0.9088 90.88%
CYP2C19 inhibition - 0.9313 93.13%
CYP2D6 inhibition - 0.9696 96.96%
CYP1A2 inhibition - 0.8876 88.76%
CYP2C8 inhibition - 0.9806 98.06%
CYP inhibitory promiscuity - 0.9780 97.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6307 63.07%
Eye corrosion - 0.8060 80.60%
Eye irritation + 0.9680 96.80%
Skin irritation + 0.8624 86.24%
Skin corrosion - 0.9441 94.41%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7187 71.87%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6613 66.13%
skin sensitisation + 0.9175 91.75%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.7042 70.42%
Acute Oral Toxicity (c) III 0.5502 55.02%
Estrogen receptor binding - 0.8938 89.38%
Androgen receptor binding - 0.6528 65.28%
Thyroid receptor binding - 0.8917 89.17%
Glucocorticoid receptor binding - 0.9215 92.15%
Aromatase binding - 0.8138 81.38%
PPAR gamma - 0.8845 88.45%
Honey bee toxicity - 0.9232 92.32%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9340 93.40%

Targets

Top

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
CHEMBL1937 Q92769 Histone deacetylase 2 91.32% 94.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.41% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.71% 91.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.58% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.87% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.51% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.83% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.57% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.63% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.62% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.61% 100.00%

Cross-Links

Top
PubChem 230921
NPASS NPC222955