Lindane

Lindane

SCHEMBL4466086

C[SiH2][SiH3].Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

823298382338688239847Rdl1Rdl2Rdl3

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

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.46
CYP3A4 P08684 1/20 0.46
GABRA1 P14867 1/20 0.46
GABRB1 P18505 1/20 0.46
GABRG2 P18507 1/20 0.46
GABRR1 P24046 1/20 0.46
GABRB3 P28472 1/20 0.46
GABRA6 Q16445 1/20 0.46

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
Lindane SCHEMBL3766691 0.76 LMNA (0.50) LMNACYP3A4GABRA1GABRB1GABRG2
SCHEMBL49256 0.74
Lindane SCHEMBL9208305 0.72 LMNA (0.36) LMNACYP3A4GABRA1GABRB1GABRG2
Lindane SCHEMBL9815928 0.72 LMNA (0.36) LMNACYP3A4GABRA1GABRB1GABRG2
Lindane SCHEMBL3809125 0.72 LMNA (0.36) LMNACYP3A4GABRA1GABRB1GABRG2
Lindane SCHEMBL10767699 0.70 LMNA (0.33) LMNACYP3A4GABRA1GABRB1GABRG2
SCHEMBL28296861 0.68
Fluoride SCHEMBL27257954 0.68
SCHEMBL27744727 0.68
Lindane SCHEMBL75689 0.67 LMNA (1.00) LMNACYP3A4GABRA1GABRB1GABRG2

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0241739-A1 Method of modifying surfaces and application of the method in forming layered structures International Business Machines Corporation (US) 1987-10-21 EP claimed
US-20090012233-A1 Epoxy Resin Molding Material for Sealing and Electronic Component Device HITACHI CHEMICAL CO., LTD. (JP) 2009-01-08 US disclosed
EP-0912473-B1 METHYLATION OF TOLUENE TO PARA-XYLENE EXXONMOBIL CHEM PATENTS INC (US) 2003-04-16 EP disclosed
EP-0914311-B1 PROCESS FOR PRODUCING AROMATIC COMPOUNDS FROM ALIPHATIC HYDROCARBONS EXXONMOBIL CHEM PATENTS INC (US) 2001-07-11 EP disclosed
US-5998686-A AROMATIZATION BY DEHYDROCYCLIZATION, OLIGOMERIZATION USING ZEOLITE CATALYST EXXON CHEMICAL PATENTS INC. (US) 1999-12-07 US disclosed
US-5994603-A CATALYST COMPRISES FIRST ZEOLITE CRYSTALS WHICH ARE BOUND TOGETHER BY SECOND ZEOLITE CRYSTALS. EXXON CHEMICAL PATENTS INC. (US) 1999-11-30 US disclosed
EP-0914311-A1 PROCESS FOR PRODUCING AROMATIC COMPOUNDS FROM ALIPHATIC HYDROCARBONS EXXON CHEMICAL PATENTS INC. (US) 1999-05-12 EP disclosed
EP-0912473-A1 METHYLATION OF TOLUENE TO PARA-XYLENE EXXON CHEMICAL PATENTS INC. (US) 1999-05-06 EP disclosed
WO-1997045387-A1 METHYLATION OF TOLUENE TO PARA-XYLENE EXXON CHEMICAL PATENTS INC. (US) 1997-12-04 WO disclosed
WO-1997045386-A1 PROCESS FOR PRODUCING AROMATIC COMPOUNDS FROM ALIPHATIC HYDROCARBONS EXXON CHEMICAL PATENTS INC. (US) 1997-12-04 WO disclosed
EP-0332042-A1 Aromatic compounds substituted by 4,6-bis-trichloromethyl-s-triazin-2-yl groups, process for their preparation and their use in photosensitive mixtures HOECHST AKTIENGESELLSCHAFT (DE) 1989-09-13 EP disclosed
EP-0332043-A1 Oxadiazole derivatives containing 4,6-bis-trichloromethyl-s-triazin-2-yl groups, process for their preparation and photosensitive mixture containing them HOECHST AKTIENGESELLSCHAFT (DE) 1989-09-13 EP disclosed