delta9-TETRAHYDROCANNABINOIC ACID B

Details

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Internal ID 6f166980-87d2-48a4-a2ff-3d3586b760e7
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name (6aR,10aR)-1-hydroxy-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydrobenzo[c]chromene-4-carboxylic acid
SMILES (Canonical) CCCCCC1=CC(=C2C3C=C(CCC3C(OC2=C1C(=O)O)(C)C)C)O
SMILES (Isomeric) CCCCCC1=CC(=C2[C@@H]3C=C(CC[C@H]3C(OC2=C1C(=O)O)(C)C)C)O
InChI InChI=1S/C22H30O4/c1-5-6-7-8-14-12-17(23)19-15-11-13(2)9-10-16(15)22(3,4)26-20(19)18(14)21(24)25/h11-12,15-16,23H,5-10H2,1-4H3,(H,24,25)/t15-,16-/m1/s1
InChI Key VITZNDKHSIWPSR-HZPDHXFCSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30O4
Molecular Weight 358.50 g/mol
Exact Mass 358.21440943 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.43
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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Cannabinolic acid B
23978-84-9
Q2682Q3DXB
delta9-Thca-C4 B
Tetrahydrocannabinol acid
delta-9-Tetrahydrocannabinolic acid-C4 B
CHEMBL1086558
delta9-Tetrahydrocannabinoic acid B
delta1-Tetrahydrocannabinolic acid B
1delta9-Tetrahydrocannabinoic acid B
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of delta9-TETRAHYDROCANNABINOIC ACID B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 + 0.7489 74.89%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7121 71.21%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8906 89.06%
OATP1B3 inhibitior + 0.9374 93.74%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5188 51.88%
P-glycoprotein inhibitior - 0.5988 59.88%
P-glycoprotein substrate - 0.6135 61.35%
CYP3A4 substrate + 0.6700 67.00%
CYP2C9 substrate - 0.5894 58.94%
CYP2D6 substrate - 0.8698 86.98%
CYP3A4 inhibition - 0.6176 61.76%
CYP2C9 inhibition + 0.5396 53.96%
CYP2C19 inhibition + 0.6427 64.27%
CYP2D6 inhibition - 0.7840 78.40%
CYP1A2 inhibition + 0.6841 68.41%
CYP2C8 inhibition + 0.8045 80.45%
CYP inhibitory promiscuity + 0.7186 71.86%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6789 67.89%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.8391 83.91%
Skin irritation - 0.6320 63.20%
Skin corrosion - 0.9393 93.93%
Ames mutagenesis - 0.7391 73.91%
Human Ether-a-go-go-Related Gene inhibition - 0.3978 39.78%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.6820 68.20%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6179 61.79%
Acute Oral Toxicity (c) III 0.6217 62.17%
Estrogen receptor binding + 0.7155 71.55%
Androgen receptor binding + 0.7528 75.28%
Thyroid receptor binding + 0.6674 66.74%
Glucocorticoid receptor binding + 0.8910 89.10%
Aromatase binding + 0.7269 72.69%
PPAR gamma + 0.7440 74.40%
Honey bee toxicity - 0.9117 91.17%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5075 50.75%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.89% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.52% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 94.98% 89.63%
CHEMBL2581 P07339 Cathepsin D 94.82% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.27% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.09% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.27% 95.56%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.79% 96.61%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.02% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.74% 89.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 85.24% 96.25%
CHEMBL5255 O00206 Toll-like receptor 4 84.11% 92.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.00% 93.99%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.86% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.58% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.57% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.40% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.74% 99.23%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.56% 100.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.34% 96.38%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.16% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.61% 100.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.18% 90.24%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.99% 95.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.96% 92.94%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 80.49% 95.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.19% 96.95%

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.
Cannabis sativa

Cross-Links

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PubChem 46889976
LOTUS LTS0086064
wikiData Q82599944