1-Heptanol

1-Heptanol

SCHEMBL6171012

CCCCCCCO.ClC(Cl)Cl

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.77
TSHR P16473 4/20 0.77
LMNA P02545 3/20 0.77
MEN1 O00255 3/20 0.77
KMT2A Q03164 3/20 0.77
HSD17B10 Q99714 1/20 0.77
SMN1; SMN2 Q16637 1/20 0.71
THRB P10828 2/20 0.47
DNM1 Q05193 3/20 0.42
HTT P42858 1/20 0.42
MAPT P10636 1/20 0.42

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
1-Hexanol SCHEMBL9796428 1.00 ALDH1A1 (0.77) ALDH1A1TSHRLMNAMEN1KMT2A
Dodecanol SCHEMBL27744843 1.00 ALDH1A1 (0.77) ALDH1A1TSHRLMNAMEN1KMT2A
Octacosanol SCHEMBL20477539 1.00 ALDH1A1 (0.77) ALDH1A1TSHRLMNAMEN1KMT2A
Nonanol SCHEMBL12275209 1.00 ALDH1A1 (0.77) ALDH1A1TSHRLMNAMEN1KMT2A
Octanol SCHEMBL467972 1.00 ALDH1A1 (0.77) ALDH1A1TSHRLMNAMEN1KMT2A
1-Hexanol SCHEMBL28327028 0.97 ALDH1A1 (0.72) ALDH1A1TSHRLMNAMEN1KMT2A
1-Pentanol SCHEMBL11280714 0.97 SMN1; SMN2 (0.75) ALDH1A1TSHRLMNAMEN1KMT2A
1-Pentanol SCHEMBL28908456 0.94 SMN1; SMN2 (0.71) ALDH1A1TSHRLMNAMEN1KMT2A
Hexane SCHEMBL28322647 0.91 ALDH1A1 (0.69) ALDH1A1TSHRLMNAMEN1KMT2A
SCHEMBL25421234 0.87 LMNA (1.00) ALDH1A1TSHRLMNAMEN1KMT2A

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
EP-0960121-B1 PEPTIDE NUCLEIC ACIDS HAVING ENHANCED BINDING AFFINITY, SEQUENCE SPECIFICITY AND SOLUBILITY BUCHARDT DORTE (DK) 2005-11-30 EP disclosed
EP-1530472-A1 ISOQUINOLINE DERIVATIVES AS MATRIX METALLOPROTEINASE INHIBITORS Warner-Lambert Company LLC (US) 2005-05-18 EP disclosed
US-6710164-B1 COMPRISING AT LEAST ONE C1-C8 ALKYLAMINE SIDE CHAIN NIELSEN PETER E (DK) 2004-03-23 US disclosed
WO-2004014379-A1 ISOQUINOLINE DERIVATIVES AS MATRIX METALLOPROTEINASE INHIBITORS WARNER-LAMBERT COMPANY LLC (US) 2004-02-19 WO disclosed
EP-0960121-A4 PEPTIDE NUCLEIC ACIDS HAVING ENHANCED BINDING AFFINITY, SEQUENCE SPECIFICITY AND SOLUBILITY BUCHARDT DORTE (DK) 2003-05-28 EP disclosed
US-20030073706-A1 Fused thiophone derivatives and drugs containing the same as the active ingredient KONISHI MIKIO (JP) 2003-04-17 US disclosed
US-6420391-B1 PREVENTION AND/OR TREATMENT OF VARIOUS INFLAMMATORY DISEASES, SEPSIS, MULTIPLE MYELOMA, PLASMA CELL LEUKEMIA, OSTEOPOROSIS, CACHEXIA, PSORIASIS, NEPHRITIS, RENAL CELL CARCINOMA, KAPOSI'S SARCOMA, RHEUMATOID ARTHRITIS, GAMMOPATHY, CASTLEMAN'S ONO PHARMACEUTICAL CO., LTD. (JP) 2002-07-16 US disclosed
EP-1003480-A4 CONJUGATED PEPTIDE NUCLEIC ACIDS HAVING ENHANCED CELLULAR UPTAKE NIELSEN PETER EIGIL (DK) 2002-04-17 EP disclosed
EP-1003480-A1 CONJUGATED PEPTIDE NUCLEIC ACIDS HAVING ENHANCED CELLULAR UPTAKE NIELSEN, Peter Eigil (DK) 2000-05-31 EP disclosed
EP-0960121-A1 PEPTIDE NUCLEIC ACIDS HAVING ENHANCED BINDING AFFINITY, SEQUENCE SPECIFICITY AND SOLUBILITY BUCHARDT, Dorte (DK) 1999-12-01 EP disclosed
WO-1998053801-A1 CONJUGATED PEPTIDE NUCLEIC ACIDS HAVING ENHANCED CELLULAR UPTAKE ISIS PHARMACEUTICALS, INC. (US) 1998-12-03 WO disclosed
US-5766855-A Peptide nucleic acids having enhanced binding affinity and sequence specificity BUCHARDT OLE (DK) 1998-06-16 US disclosed
WO-1998003542-A1 PEPTIDE NUCLEIC ACIDS HAVING ENHANCED BINDING AFFINITY, SEQUENCE SPECIFICITY AND SOLUBILITY BUCHARDT, DORTE (DK) 1998-01-29 WO disclosed
US-5274129-A Hydroxamic acid crown ethers IDAHO RESEARCH FOUNDATION, INC. (US) 1993-12-28 US disclosed
US-5225173-A Chelation, crown ethers IDAHO RESEARCH FOUNDATION, INC. (US) 1993-07-06 US disclosed
US-5162509-A Process for preparing expanded porphyrins: large porphyrin-like tripyrroledimethine-derived macrocycles BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1992-11-10 US disclosed
EP-0462206-A1 EXPANDED PORPHYRINS: LARGE PORPHYRIN-LIKE TRIPYRROLEDIMETHINE-DERIVED MACROCYCLES BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1991-12-27 EP disclosed
WO-1990010633-A1 EXPANDED PORPHYRINS: LARGE PORPHYRIN-LIKE TRIPYRROLEDIMETHINE-DERIVED MACROCYCLES BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1990-09-20 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 (1 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-20030073706-A1 Fused thiophone derivatives and drugs containing the same as the active ingredient TPMT, CD47, THPO ALDH1A1 3159/4885TSHR 662/4885LMNA 2985/4885

“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.