Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4501398

CNCCCOc1cc(F)c(-c2c(Cl)nc3ncnn3c2NCC(F)(F)F)c(F)c1.[Cl-].[H+]

nearest known ligand 0.34

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

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

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
MBOAT4 Q96T53 5/20 0.34
ALDH1A1 P00352 3/20 0.34
TSHR P16473 2/20 0.34
POLB P06746 1/20 0.34
KMT2A Q03164 1/20 0.34
KDM4E B2RXH2 1/20 0.31
GLA P06280 1/20 0.31
GAA P10253 1/20 0.31
NPC1 O15118 1/20 0.30
GALR3 O60755 1/20 0.30
CYP1A2 P05177 1/20 0.30
CYP2D6 P10635 1/20 0.30
CYP2C9 P11712 1/20 0.30
CYP2C19 P33261 1/20 0.30
HTT P42858 1/20 0.30
SMN1; SMN2 Q16637 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
SCHEMBL4483618 0.98 ALDH1A1 (0.35) MBOAT4ALDH1A1TSHRPOLBKMT2A
Hydrochloric Acid SCHEMBL4501402 0.97 ALDH1A1 (0.35) MBOAT4ALDH1A1TSHRPOLBKMT2A
Hydrochloric Acid SCHEMBL4488767 0.89 EGLN2 (0.34) MBOAT4ALDH1A1TSHRPOLBKMT2A
SCHEMBL3220251 0.88 MBOAT4 (0.34) MBOAT4ALDH1A1TSHRPOLBKMT2A
SCHEMBL4492166 0.86 EGLN2 (0.35) MBOAT4ALDH1A1TSHRPOLBKMT2A
Cevipabulin SCHEMBL4488773 0.86 MBOAT4 (0.33) MBOAT4ALDH1A1TSHRPOLBKMT2A
Hydrochloric Acid SCHEMBL4488768 0.86 EGLN2 (0.35) MBOAT4ALDH1A1TSHRPOLBKMT2A
SCHEMBL6186573 0.85 MBOAT4 (0.38) MBOAT4ALDH1A1TSHRPOLBKMT2A
Cevipabulin SCHEMBL4042827 0.84 MBOAT4 (0.34) MBOAT4ALDH1A1TSHRPOLBKMT2A
Cevipabulin SCHEMBL4477222 0.84 MBOAT4 (0.34) MBOAT4ALDH1A1TSHRPOLBKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7507739-B2 6-[(substituted)phenyl]triazolopyrimidines as anticancer agents WYETH (US) 2009-03-24 US disclosed
EP-1680425-B1 6- [(SUBSTITUTED)PHENYL] TRIAZOLOPYRIMIDINES AS ANTICANCER AGENTS WYETH CORP (US) 2007-01-10 EP disclosed
EP-1680425-A1 6- [(SUBSTITUTED)PHENYL] TRIAZOLOPYRIMIDINES AS ANTICANCER AGENTS Wyeth Holdings Corporation (US) 2006-07-19 EP disclosed
US-20050090508-A1 6-[(Substituted)phenyl]triazolopyrimidines as anticancer agents WYETH HOLDINGS CORPORATION (US) 2005-04-28 US disclosed
WO-2005030775-A1 6-[(SUBSTITUTED)PHENYL]TRIAZOLOPYRIMIDINES AS ANTICANCER AGENTS WYETH HOLDINGS CORPORATION (US) 2005-04-07 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-20050090508-A1 6-[(Substituted)phenyl]triazolopyrimidines as anticancer agents ABCC1, ABCB1, TUBB6 MBOAT4 4305/4885ALDH1A1 1838/4885TSHR 3624/4885

“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.