9-Methylfluorene

Details

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Internal ID d5d02930-ee09-4708-8f7e-1dcd66d53f2f
Taxonomy Benzenoids > Fluorenes
IUPAC Name 9-methyl-9H-fluorene
SMILES (Canonical) CC1C2=CC=CC=C2C3=CC=CC=C13
SMILES (Isomeric) CC1C2=CC=CC=C2C3=CC=CC=C13
InChI InChI=1S/C14H12/c1-10-11-6-2-4-8-13(11)14-9-5-3-7-12(10)14/h2-10H,1H3
InChI Key ZVEJRZRAUYJYCO-UHFFFAOYSA-N
Popularity 72 references in papers

Physical and Chemical Properties

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Molecular Formula C14H12
Molecular Weight 180.24 g/mol
Exact Mass 180.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.82
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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9-METHYL-9H-FLUORENE
2523-37-7
9H-Fluorene, 9-methyl-
Fluorene, 9-methyl-
CCRIS 4264
EINECS 219-750-7
NSC 10161
UNII-95M10BKB07
95M10BKB07
MFCD00126475
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 9-Methylfluorene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9016 90.16%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Lysosomes 0.7321 73.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9319 93.19%
OATP1B3 inhibitior + 0.9692 96.92%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7362 73.62%
P-glycoprotein inhibitior - 0.9683 96.83%
P-glycoprotein substrate - 0.9295 92.95%
CYP3A4 substrate - 0.6515 65.15%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.6884 68.84%
CYP3A4 inhibition - 0.7047 70.47%
CYP2C9 inhibition - 0.7213 72.13%
CYP2C19 inhibition - 0.6008 60.08%
CYP2D6 inhibition - 0.7940 79.40%
CYP1A2 inhibition + 0.8312 83.12%
CYP2C8 inhibition - 0.8752 87.52%
CYP inhibitory promiscuity + 0.6388 63.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Danger 0.4006 40.06%
Eye corrosion - 0.6664 66.64%
Eye irritation + 0.9495 94.95%
Skin irritation + 0.8655 86.55%
Skin corrosion - 0.9477 94.77%
Ames mutagenesis + 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4791 47.91%
Micronuclear - 0.6766 67.66%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.8968 89.68%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6101 61.01%
Acute Oral Toxicity (c) III 0.7824 78.24%
Estrogen receptor binding - 0.5397 53.97%
Androgen receptor binding - 0.5313 53.13%
Thyroid receptor binding - 0.5564 55.64%
Glucocorticoid receptor binding - 0.7232 72.32%
Aromatase binding - 0.5433 54.33%
PPAR gamma - 0.7015 70.15%
Honey bee toxicity - 0.9321 93.21%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.9200 92.00%
Fish aquatic toxicity + 0.9847 98.47%

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
CHEMBL2581 P07339 Cathepsin D 92.86% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.98% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.08% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.54% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.05% 86.33%

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.
Illicium verum

Cross-Links

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PubChem 17299
NPASS NPC5640
LOTUS LTS0236376
wikiData Q27271801