Fluorene

Details

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Internal ID 3019b5d2-b2e0-45a3-ab8b-1c7eef3c4be7
Taxonomy Benzenoids > Fluorenes
IUPAC Name 9H-fluorene
SMILES (Canonical) C1C2=CC=CC=C2C3=CC=CC=C31
SMILES (Isomeric) C1C2=CC=CC=C2C3=CC=CC=C31
InChI InChI=1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2
InChI Key NIHNNTQXNPWCJQ-UHFFFAOYSA-N
Popularity 7,708 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10
Molecular Weight 166.22 g/mol
Exact Mass 166.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.26
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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9H-Fluorene
86-73-7
Diphenylenemethane
o-Biphenylenemethane
2,3-Benzindene
2,2'-Methylenebiphenyl
o-Biphenylmethane
Methane, diphenylene-
Fluoren
CCRIS 947
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Fluorene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.9349 93.49%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.7333 73.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9618 96.18%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6130 61.30%
P-glycoprotein inhibitior - 0.9746 97.46%
P-glycoprotein substrate - 0.9722 97.22%
CYP3A4 substrate - 0.7677 76.77%
CYP2C9 substrate - 0.8117 81.17%
CYP2D6 substrate + 0.4387 43.87%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.6504 65.04%
CYP2C19 inhibition - 0.5184 51.84%
CYP2D6 inhibition - 0.7662 76.62%
CYP1A2 inhibition + 0.8047 80.47%
CYP2C8 inhibition - 0.9804 98.04%
CYP inhibitory promiscuity + 0.6841 68.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Warning 0.3871 38.71%
Eye corrosion - 0.6096 60.96%
Eye irritation + 0.9967 99.67%
Skin irritation + 0.9258 92.58%
Skin corrosion - 0.9301 93.01%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6499 64.99%
Micronuclear - 0.6272 62.72%
Hepatotoxicity + 0.7944 79.44%
skin sensitisation + 0.9040 90.40%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4946 49.46%
Acute Oral Toxicity (c) III 0.7918 79.18%
Estrogen receptor binding + 0.7490 74.90%
Androgen receptor binding - 0.8074 80.74%
Thyroid receptor binding - 0.6047 60.47%
Glucocorticoid receptor binding - 0.5711 57.11%
Aromatase binding + 0.5925 59.25%
PPAR gamma - 0.4912 49.12%
Honey bee toxicity - 0.9232 92.32%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.9800 98.00%
Fish aquatic toxicity + 0.9839 98.39%

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 89.03% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.49% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.13% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.69% 95.56%
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 83.92% 92.17%
CHEMBL1951 P21397 Monoamine oxidase A 82.69% 91.49%
CHEMBL221 P23219 Cyclooxygenase-1 81.86% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.45% 96.09%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis
Cornus officinalis
Elsholtzia ciliata
Mosla chinensis
Pinellia ternata
Rehmannia glutinosa
Zea mays

Cross-Links

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PubChem 6853
NPASS NPC263385
LOTUS LTS0020156
wikiData Q417934