Tetrahydrofuran

Tetrahydrofuran

SCHEMBL7051923

C1CCOC1.CC(C)=O.CCO

nearest known ligand 0.44

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Tetrahydrofuran. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.44
SMN1; SMN2 Q16637 1/20 0.37
TSHR P16473 4/20 0.35
HTT P42858 1/20 0.35
LMNA P02545 2/20 0.34
POLB P06746 2/20 0.34
L3MBTL1 Q9Y468 2/20 0.33
TDP1 Q9NUW8 1/20 0.33
RECQL P46063 1/20 0.32
GLA P06280 1/20 0.32
RAB9A P51151 1/20 0.32
THPO P40225 1/20 0.32
PIK3CD O00329 1/20 0.31
MEN1 O00255 1/20 0.31
TP53 P04637 1/20 0.31
KMT2A Q03164 1/20 0.31
PAOX Q6QHF9 1/20 0.31

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Acetone SCHEMBL15059718 0.97 ALDH1A1 (0.42) ALDH1A1SMN1; SMN2TSHRHTTLMNA
Tetrahydrofuran SCHEMBL27898407 0.97 ALDH1A1 (0.42) ALDH1A1SMN1; SMN2TSHRHTTLMNA
Tetrahydrofuran SCHEMBL27918528 0.97 ALDH1A1 (0.42) ALDH1A1SMN1; SMN2TSHRHTTLMNA
Dioxane SCHEMBL15059720 0.88 SMN1; SMN2 (0.46) ALDH1A1SMN1; SMN2TSHRHTTLMNA
Tetrahydrofuran SCHEMBL30232 0.88
Tetrahydrofuran SCHEMBL8412489 0.88 ALDH1A1 (0.57) ALDH1A1TSHRHTTLMNAPOLB
Tetrahydrofuran SCHEMBL165529 0.88
Tetrahydrofuran SCHEMBL28302889 0.87 CA1 (0.43) ALDH1A1SMN1; SMN2TSHRHTTLMNA
Tetrahydrofuran SCHEMBL27898672 0.87 ALDH1A1 (0.33) ALDH1A1SMN1; SMN2
Tetrahydrofuran SCHEMBL28295154 0.86 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2TSHRHTTLMNA

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109715616-A Surfactant system for crystallizing organic compounds 诺华股份有限公司 2019-05-03 CN claimed
CN-101041664-B Preparation of cefepime halogen acid salt by calcium salt precipitation process SHENZHEN SALUBRIS PHARM CO LTD 2010-05-26 CN disclosed
CN-100560588-C Preparation of cefepime hydrochlorice by sodium salt precipitation method XINLITAI PHARMACEUTICAL CO LTD (CN) 2009-11-18 CN disclosed
CN-101397304-A Method for preparing high-purity cefpirome sulfate by sodium salt precipitation method SHENZHEN SALUBRIS PHARMACEUTIC (CN) 2009-04-01 CN disclosed
CN-100457759-C Cefepime halogen acid salt preparation method SHENZHEN SALUBRIS PHARMACEUTIC (CN) 2009-02-04 CN disclosed
CN-101104621-A Technique for preparing high-purity cefpirome sulfate SHENZHEN SALUBRIS PHARMACEUTIC (CN) 2008-01-16 CN disclosed
CN-101045734-A Preparation of cefepime hydrochlorice by sodium salt precipitation method XINLITAI PHARMACEUTICAL CO LTD (CN) 2007-10-03 CN disclosed
CN-101041664-A Preparation of cefepime halogen acid salt by calcium salt precipitation process SHENZHEN SALUBRIS PHARMACEUTIC (CN) 2007-09-26 CN disclosed
CN-101007813-A Cefepime halogen acid salt preparation method SHENZHEN SALUBRIS PHARMACEUTIC (CN) 2007-08-01 CN disclosed
EP-0920252-A4 SILVER-BASED ANTIMICROBIAL COMPOSITIONS CAPELLI CHRISTOPHER C (US) 2004-08-18 EP disclosed
EP-0920252-A1 SILVER-BASED ANTIMICROBIAL COMPOSITIONS CAPELLI, Christopher C. (US) 1999-06-09 EP disclosed
WO-1998006260-A1 SILVER-BASED ANTIMICROBIAL COMPOSITIONS CAPELLI CHRISTOPHER C (US) 1998-02-19 WO disclosed
US-4948800-A MUSCLE RELAXANTS; ANTICONVULSANTS; ANXIOLYTIC AGENTS; 3-HYDROXYALKYL-PYRIDO(4,5-B OR-C)IMIDAZOLE COMPOUNDS A. H. ROBINS COMPANY, INCORPORATED (US) 1990-08-14 US disclosed
US-4914109-A ANTICONVULSANTS, ANTIANXIETY AGENTS A. H. ROBINS COMPANY, INCORPORATED (US) 1990-04-03 US disclosed
US-4873251-A MUSCLE RELAXANTS, ANTICONVULSANTS, ANTIANXIETY AGENTS A. H. ROBINS COMPANY, INCORPORATED (US) 1989-10-10 US disclosed
US-4824951-A MUSCLE RELAXANTS, ANTICONVULSANTS, ANXIOLYTIC AGENTS A. H. ROBINS COMPANY, INCORPORATED (US) 1989-04-25 US disclosed
US-4772600-A MUSCLE RELAXANTS, ANTICONVULSANTS, ANXIOLYTIC A. H. ROBINS COMPANY, INC. (US) 1988-09-20 US disclosed
EP-0255217-A1 Fused imidazoheterocyclic compounds A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) (US) 1988-02-03 EP disclosed