alpha-Teresantalic acid

Details

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Internal ID a6d814c6-4183-497e-b6d7-742b48a810d2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 2,3-dimethyltricyclo[2.2.1.02,6]heptane-3-carboxylic acid
SMILES (Canonical) CC1(C2CC3C1(C3C2)C)C(=O)O
SMILES (Isomeric) CC1(C2CC3C1(C3C2)C)C(=O)O
InChI InChI=1S/C10H14O2/c1-9(8(11)12)5-3-6-7(4-5)10(6,9)2/h5-7H,3-4H2,1-2H3,(H,11,12)
InChI Key QHDPITNBVDSMQH-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Teresantalic acid
a-Teresantalic acid
.alpha.-Teresantalic acid
Teresantalol 8-carboxylic acid
QHDPITNBVDSMQH-UHFFFAOYSA-N
DTXSID201146497
Q67879685
2,3-dimethyltricyclo[2.2.1.0?,?]heptane-3-carboxylic acid
2,3-Dimethyltricyclo[2.2.1.02,6]heptane-3-carboxylic acid
2,3-dimethyltricyclo[2.2.1.0^{2,6}]heptane-3-carboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of alpha-Teresantalic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.6180 61.80%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6088 60.88%
OATP2B1 inhibitior - 0.8453 84.53%
OATP1B1 inhibitior + 0.9543 95.43%
OATP1B3 inhibitior + 0.9330 93.30%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9316 93.16%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9579 95.79%
CYP3A4 substrate - 0.5398 53.98%
CYP2C9 substrate - 0.5708 57.08%
CYP2D6 substrate - 0.8645 86.45%
CYP3A4 inhibition - 0.8503 85.03%
CYP2C9 inhibition - 0.8315 83.15%
CYP2C19 inhibition - 0.8489 84.89%
CYP2D6 inhibition - 0.9506 95.06%
CYP1A2 inhibition - 0.7845 78.45%
CYP2C8 inhibition - 0.9731 97.31%
CYP inhibitory promiscuity - 0.9318 93.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7213 72.13%
Carcinogenicity (trinary) Non-required 0.6427 64.27%
Eye corrosion - 0.9138 91.38%
Eye irritation + 0.5342 53.42%
Skin irritation + 0.5104 51.04%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6656 66.56%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6845 68.45%
skin sensitisation - 0.5714 57.14%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5039 50.39%
Nephrotoxicity + 0.5968 59.68%
Acute Oral Toxicity (c) III 0.5035 50.35%
Estrogen receptor binding - 0.5694 56.94%
Androgen receptor binding - 0.5557 55.57%
Thyroid receptor binding - 0.7881 78.81%
Glucocorticoid receptor binding - 0.7731 77.31%
Aromatase binding - 0.7763 77.63%
PPAR gamma - 0.6919 69.19%
Honey bee toxicity - 0.9275 92.75%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9919 99.19%

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 92.41% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.06% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 87.45% 91.19%
CHEMBL221 P23219 Cyclooxygenase-1 85.52% 90.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.07% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.21% 95.56%

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.
Phyllanthus emblica
Pterocarpus indicus
Santalum album
Terminalia chebula

Cross-Links

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PubChem 5321816
NPASS NPC57544