Assamicain C

Details

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Internal ID 90e9ab55-b08d-4144-bb85-faae6c3761cb
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Catechins > Catechin gallates
IUPAC Name [5,7-dihydroxy-6-[2-(3,4,5-trihydroxybenzoyl)oxy-3-(2,4,6-trihydroxyphenyl)-1-(3,4,5-trihydroxyphenyl)propyl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate
SMILES (Canonical) C1C(C(OC2=C1C(=C(C(=C2)O)C(C3=CC(=C(C(=C3)O)O)O)C(CC4=C(C=C(C=C4O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O
SMILES (Isomeric) C1C(C(OC2=C1C(=C(C(=C2)O)C(C3=CC(=C(C(=C3)O)O)O)C(CC4=C(C=C(C=C4O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O
InChI InChI=1S/C44H36O22/c45-18-9-21(46)19(22(47)10-18)11-33(65-43(62)16-5-28(53)40(60)29(54)6-16)35(14-1-24(49)38(58)25(50)2-14)36-23(48)13-32-20(37(36)57)12-34(42(64-32)15-3-26(51)39(59)27(52)4-15)66-44(63)17-7-30(55)41(61)31(56)8-17/h1-10,13,33-35,42,45-61H,11-12H2
InChI Key BQUPFUJDKCDVAE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H36O22
Molecular Weight 916.70 g/mol
Exact Mass 916.16982277 g/mol
Topological Polar Surface Area (TPSA) 406.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 22
H-Bond Donor 17
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Assamicain C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6825 68.25%
Caco-2 - 0.8923 89.23%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.5943 59.43%
OATP2B1 inhibitior - 0.7092 70.92%
OATP1B1 inhibitior + 0.7419 74.19%
OATP1B3 inhibitior + 0.8382 83.82%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8648 86.48%
P-glycoprotein inhibitior + 0.7450 74.50%
P-glycoprotein substrate - 0.5764 57.64%
CYP3A4 substrate + 0.6530 65.30%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.7271 72.71%
CYP3A4 inhibition - 0.8507 85.07%
CYP2C9 inhibition - 0.8488 84.88%
CYP2C19 inhibition - 0.8790 87.90%
CYP2D6 inhibition - 0.9672 96.72%
CYP1A2 inhibition - 0.9190 91.90%
CYP2C8 inhibition + 0.7078 70.78%
CYP inhibitory promiscuity - 0.8600 86.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6785 67.85%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.8832 88.32%
Skin irritation - 0.7271 72.71%
Skin corrosion - 0.9541 95.41%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8135 81.35%
Micronuclear + 0.8318 83.18%
Hepatotoxicity + 0.5657 56.57%
skin sensitisation - 0.8815 88.15%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8857 88.57%
Acute Oral Toxicity (c) II 0.3473 34.73%
Estrogen receptor binding + 0.7802 78.02%
Androgen receptor binding + 0.8080 80.80%
Thyroid receptor binding + 0.5600 56.00%
Glucocorticoid receptor binding - 0.4763 47.63%
Aromatase binding - 0.5434 54.34%
PPAR gamma + 0.7220 72.20%
Honey bee toxicity - 0.7002 70.02%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6250 62.50%
Fish aquatic toxicity + 0.9432 94.32%

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 99.07% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.17% 91.49%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 95.17% 96.37%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.50% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 94.28% 95.17%
CHEMBL2581 P07339 Cathepsin D 93.78% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.38% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.92% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.86% 86.33%
CHEMBL3194 P02766 Transthyretin 91.00% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 89.11% 90.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.07% 89.00%
CHEMBL4302 P08183 P-glycoprotein 1 88.10% 92.98%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.67% 96.95%
CHEMBL2535 P11166 Glucose transporter 87.35% 98.75%
CHEMBL233 P35372 Mu opioid receptor 87.07% 97.93%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 85.59% 98.75%
CHEMBL236 P41143 Delta opioid receptor 84.37% 99.35%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 84.16% 97.53%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.76% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.45% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.94% 99.23%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.88% 90.24%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.85% 92.62%
CHEMBL1993 P26358 DNA (cytosine-5)-methyltransferase 1 80.52% 95.44%

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.
Camellia sinensis

Cross-Links

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PubChem 14284588
LOTUS LTS0194293
wikiData Q104944579