Tetrahydrofuran

Tetrahydrofuran

SCHEMBL1704980

C1CCOC1.C1CCOC1.CC(=O)O

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.53
FFAR3 O14843 1/20 0.47
LCK P06239 1/20 0.47
FYN P06241 1/20 0.47
SMN1; SMN2 Q16637 3/20 0.42
GLA P06280 1/20 0.36
MEN1 O00255 1/20 0.35
TP53 P04637 1/20 0.35
KMT2A Q03164 1/20 0.35
HSD17B10 Q99714 1/20 0.33
PKM P14618 1/20 0.33
GAA P10253 1/20 0.32
LMNA P02545 2/20 0.32
SLC15A2 Q16348 1/20 0.32
TTR P02766 1/20 0.31
TSHR P16473 1/20 0.31
CA12 O43570 1/20 0.31
CA1 P00915 1/20 0.31
CA9 Q16790 1/20 0.31
PIK3CD O00329 1/20 0.30

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
Tetrahydrofuran SCHEMBL44945 1.00
Tetrahydrofuran SCHEMBL28650393 1.00 ALDH1A1 (0.53) ALDH1A1FFAR3LCKFYNSMN1; SMN2
Acetic Acid SCHEMBL2354574 0.97 ALDH1A1 (0.50) ALDH1A1FFAR3LCKFYNSMN1; SMN2
Tetrahydrofuran SCHEMBL7457134 0.97 ALDH1A1 (0.50) ALDH1A1FFAR3LCKFYNSMN1; SMN2
Tetrahydrofuran SCHEMBL7645655 0.97 ALDH1A1 (0.50) ALDH1A1FFAR3LCKFYNSMN1; SMN2
Tetrahydrofuran SCHEMBL7175965 0.97 ALDH1A1 (0.50) ALDH1A1FFAR3LCKFYNSMN1; SMN2
Acetic Acid SCHEMBL4868108 0.97 ALDH1A1 (0.50) ALDH1A1FFAR3LCKFYNSMN1; SMN2
Tetrahydrofuran SCHEMBL1056026 0.97 ALDH1A1 (0.50) ALDH1A1FFAR3LCKFYNSMN1; SMN2
Tetrahydrofuran SCHEMBL9359499 0.97 ALDH1A1 (0.50) ALDH1A1FFAR3LCKFYNSMN1; SMN2
Tetrahydrofuran SCHEMBL7613346 0.97 ALDH1A1 (0.50) ALDH1A1FFAR3LCKFYNSMN1; SMN2

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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1720840-B1 METHODS TO MANUFACTURE 1,3-DIOXOLANE NUCLEOSIDES UNIV EMORY (US) 2016-02-03 EP claimed
US-20110130559-A1 Methods to Manufacture 1,3-Dioxolane Nucleosides GILEAD SCIENCES, INC. (US) 2011-06-02 US claimed
US-7785839-B2 Methods to manufacture 1,3-dioxolane nucleosides EMORY UNIVERSITY (US) 2010-08-31 US claimed
EP-1720840-A4 METHODS TO MANUFACTURE 1,3-DIOXOLANE NUCLEOSIDES UNIV EMORY (US) 2009-01-21 EP claimed
EP-1720840-A2 METHODS TO MANUFACTURE 1,3-DIOXOLANE NUCLEOSIDES EMORY UNIVERSITY (US) 2006-11-15 EP claimed
US-20060036092-A1 Methods to manufacture 1,3-dioxolane nucleosides SZNAIDMAN MARCOS 2006-02-16 US claimed
WO-2005074654-A2 METHODS TO MANUFACTURE 1,3-DIOXOLANE NUCLEOSIDES EMORY UNIVERSITY (US) 2005-08-18 WO claimed
US-20230365523-A1 PROCESS FOR PREPARING 3-(CYCLOHEX-1-EN-1-YL)PROPANAL DERIVATIVES FIRMENICH SA (CH) 2023-11-16 US disclosed
CN-116018334-A Process for preparing 3- (cyclohex-1-en-1-yl) propanal derivatives 弗门尼舍有限公司 2023-04-25 CN disclosed
EP-4153552-A2 PROCESS AND INTERMEDIATES FOR PREPARING 3-(CYCLOHEX-1-EN-1-YL) PROPANAL DERIVATIVES Firmenich SA (CH) 2023-03-29 EP disclosed
WO-2022049036-A2 PROCESS FOR PREPARING 3-(CYCLOHEX-1-EN-1-YL)PROPANAL DERIVATIVES FIRMENICH SA (CH) 2022-03-10 WO disclosed
EP-1720840-B1 METHODS TO MANUFACTURE 1,3-DIOXOLANE NUCLEOSIDES UNIV EMORY (US) 2016-02-03 EP disclosed
US-8420354-B2 Methods to manufacture 1,3-dioxolane nucleosides EMORY UNIVERSITY (US) 2013-04-16 US disclosed
EP-0956021-B1 L-BETA-DIOXOLANE URIDINE ANALOGS FOR TREATING AND PREVENTING INFECTIONS BY EBV, VZV AND HV-8 UNIV YALE (US) 2004-11-03 EP disclosed
US-20010018440-A1 L-beta-dioxolane uridine analogs and methods for treating and preventing virus infections YALE UNIVERSITY AND THE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. 2001-08-30 US disclosed
US-6274589-B1 VIRICIDES TO TREAT EPSTEIN-BARR, VARICELLA-ZOSTER, AND/OR HERPES INFECTIONS; KAPOSI'S SARCOMA YALE UNIVERSITY 2001-08-14 US disclosed
US-6022876-A KAPOSI'S SARCOMA; VARICELLA-ZOSTER VIRUS YALE UNIVERSITY (US) 2000-02-08 US disclosed
EP-0956021-A1 L-$g(b)-DIOXOLANE URIDINE ANALOGS AND METHODS FOR TREATING AND PREVENTING VIRUS INFECTIONS YALE UNIVERSITY (US) 1999-11-17 EP disclosed
US-5792773-A L-β-dioxolane uridine analog administration for treating Epstein-Barr virus infection YALE UNIVERSITY (US) 1998-08-11 US disclosed
WO-1998020879-A1 L-β-DIOXOLANE URIDINE ANALOGS AND METHODS FOR TREATING AND PREVENTING VIRUS INFECTIONS YALE UNIVERSITY (US) 1998-05-22 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20060036092-A1 Methods to manufacture 1,3-dioxolane nucleosides DCTD, AMPD1, DAD1 ALDH1A1 163/4885FFAR3 1292/4885LCK 3125/4885
US-20110130559-A1 Methods to Manufacture 1,3-Dioxolane Nucleosides DCTD, AMPD1, DAD1 ALDH1A1 161/4885FFAR3 1239/4885LCK 2949/4885
US-20230365523-A1 PROCESS FOR PREPARING 3-(CYCLOHEX-1-EN-1-YL)PROPANAL DERIVATIVES CYP1A1, CYP51A1, HPD ALDH1A1 125/4885FFAR3 1293/4885LCK 3511/4885
US-20010018440-A1 L-beta-dioxolane uridine analogs and methods for treating and preventing virus infections UNG, DDX18, UMPS ALDH1A1 1027/4885FFAR3 3779/4885LCK 2961/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.