CompoundList

Validamycin A

Also known as Validamycin, Valimon, jinggangmycin

Validamycin A chemical structure, C20H35NO13, CAS 37248-47-8
2D chemical structure

Key facts

What buyers check first

Appearance
Colorless powder
Melting point
130 to 135
Solubility
Very soluble in water, soluble in dimethylformamide, dimethyl sulphoxide, methanol, sparโ€ฆ
HS code
293890
Category
Fungicides
Illustrative photo, 25 kg white woven sacks of powder on a pallet in a warehouse
Typical packagingIllustrative packaging image, not the actual product

What is Validamycin A?

Plain description, key identifiers and synonyms

Validamycin A is a member of the class of validamycins that is (1R,2S,3S,4S,6R)-4-amino-6-(hydroxymethyl)cyclohexane-1,2,3-triol in which the hydroxy group at position 1 has been converted to its beta-D-glucoside and in which one of the hydrogens attached to the nitrogen is replaced by a (1R,4R,5R,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl group. It is the major validamycin produced by Streptomyces hygroscopicus. It has a role as an EC 2.4.1.231 [alpha,alpha-trehalose phosphorylase (configuration-retaining)] inhibitor, an EC 2.4.1.64 (alpha,alpha-trehalose phosphorylase) inhibitor, an EC 3.2.1.28 (alpha,alpha-trehalase) inhibitor and an antifungal agrochemical. It is a polyol, a secondary amino compound, a member of validamycins and an antibiotic fungicide. It is a conjugate base of a validamycin A(1+).

Identifiers

Registry numbers, names and line notations, tap to copy

IUPAC name
(2R,3R,4S,5S,6R)-2-[(1R,2R,3S,4S,6R)-2,3-dihydroxy-6-(hydroxymethyl)-4-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino]cyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
CAS number
37248-47-8 CAS number cross-checkedOther or deprecated CAS: 50642-14-3, 58194-43-7
EC number
609-372-4
Molecular formula
C20H35NO13
UNII
313E9620QS
MDL number
MFCD09028089
InChIKey
JARYYMUOCXVXNK-CSLFJTBJSA-N
InChI
InChI=1S/C20H35NO13/c22-3-6-1-8(12(26)15(29)11(6)25)21-9-2-7(4-23)19(17(31)13(9)27)34-20-18(32)16(30)14(28)10(5-24)33-20/h1,7-32H,2-5H2/t7-,8+,9+,10-,11-,12+,13+,14-,15+,16+,17-,18-,19-,20+/m1/s1
Canonical SMILES
OCC1=CC(NC2CC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C2O)C(O)C(O)C1O
Isomeric SMILES
C1[C@@H]([C@H]([C@@H]([C@H]([C@H]1N[C@H]2C=C([C@H]([C@@H]([C@H]2O)O)O)CO)O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)CO

Synonyms

  • Validamycin
  • Valimon
  • jinggangmycin
  • 1L-(1,3,4/2,6)-2,3-Dihydroxy-6-hydroxymethyl-4-((1S,4R,5S,6S)-4,5,6-trihydroxy-3-hydroxymethylcyclohex-2-enylamino)cyclohexyl beta-D-glucopyranoside
  • D-1,5,6-Trideoxy-3-O-beta-D-glucopyranosyl-5-(hydroxymethyl)-1-((4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl)amino)-D-chiroinositol
  • (1S-(1a,4a,5B,6a))-1,5,6-Trideoxy-3-O-B-D-glucopyranosyl-5-(hydroxymethyl)-1-((4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl)amino)-d-chiro-inositol
  • 1L-(1,3,4/2,6)-2,3-Dihydroxy-6-hydromethyl-4-((1S,4R,5S,6S)-4,5,6-trihydroxy-3-hydroxymethylcyclohex-2-enylamino)cyclohexyl beta-D-glucopyranoside
  • (1R,2R,3S,4S,6R)-2,3-dihydroxy-6-(hydroxymethyl)-4-{[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino}cyclohexyl beta-D-glucopyranoside
  • (1R,2R,3S,4S,6R)-2,3-dihydroxy-6-(hydroxymethyl)-4-(((1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl)amino)cyclohexyl beta-D-glucopyranoside
  • D-Chiro-inositol, 1,5,6-trideoxy-4-o-beta-d-glucopyranosyl-5-(hydroxymethyl)-1-(((1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl)amino)-
  • Validacin
  • Validamycin A (>70%) Hydrochloride Salt
  • Cepex 10SL, Validacin
  • jinganmycin A
  • D-chiro-Inositol, 1,5,6-trideoxy-4-O-beta-D-glucopyranosyl-5-(hydroxymethyl)-1-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-
  • (+)-validamycin A
  • Validamycin A (Standard)
  • Validamycins validamycin a
  • Validamycin A, PESTANAL(R), analytical standard
  • Validamycin, CE30, JARYYMUOCXVXNK-CSLFJTBJSA-N
  • D-Chiro-inositol, 1,5,6-trideoxy-3-o-beta-d-glucopyranosyl-
  • (1S-(1A,4a,5b,6a))-1,5,6-trideoxy-3-o-b-d-glucopyranosyl-5- (hydroxymethyl)-1-((4,5,6-trihydroxy-3-(hydroxymethyl)-2- cyclohexen-1-yl)amino)-d-chiro-inositol
  • 1,5,6-trideoxy-4-O-beta-D-glucopyranosyl-5-(hydroxymethyl)-1-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-D-chiro-inositol
  • 1l-(1,3,4/2,6)-2,3-Dihydroxy-6-hydromethyl-4-((1S,4R,5S,6S)- 4,5,6-trihydroxy-3-hydroxymethylcyclohex-2- enylamino)cyclohexyl beta-d-glucopyranoside
  • 1l-(1,3,4/2,6)-2,3-Dihydroxy-6-hydroxymethyl-4- ((1S,4R,5S,6S)-4,5,6-trihydroxy-3-hydroxymethylcyclohex-2- enylamino)cyclohexyl beta-d-glucopyranoside
Show all 26 synonyms
  • d-1,5,6-Trideoxy-3-o-beta-d-glucopyranosyl-5- (hydroxymethyl)-1-((4,5,6-trihydroxy-3-(hydroxymethyl)-2- cyclohexen-1-yl)amino)-d-chiroinositol

Physical and chemical properties

Measured values and descriptors computed from the structure

Physical and chemical properties

Measured values, check the supplier specification for your grade

Appearance
Colorless powderexp.
Odour
Odorlessexp.
Melting point
130 to 135exp.
Solubility
Very soluble in water, soluble in dimethylformamide, dimethyl sulphoxide, methanol, sparingly soluble in acetone, ethanol.exp.
Vapour pressure
Negligible at room temperatureexp.

Values vary by grade. Ask suppliers for the COA or TDS of the batch you buy.

Computed descriptors

Calculated from the structure, useful for screening and formulation

Molecular weight
497.49 g/molcalc.
Exact mass
497.2108 Dacalc.
LogP (octanol/water)
-6.75calc.
Topological polar surface area
253 ร…ยฒcalc.
Hydrogen bond donors
12calc.
Hydrogen bond acceptors
14calc.
Rotatable bonds
7calc.
Heavy atoms
34calc.
Rings
3calc.
Aromatic rings
0calc.
Fraction sp3 carbons
0.9calc.
Formal charge
0calc.
Stereocentres
14calc.
Lipinski rule of five
Fails (2 violations)calc.

Calculated for screening. Confirm critical figures with the supplier.

Murcko scaffold

The ring system that remains when every side chain is removed

Murcko scaffold of this chemical, C1=CC(NC2CCC(OC3CCCCO3)CC2)CCC1

C1=CC(NC2CCC(OC3CCCCO3)CC2)CCC1

3 rings, 20 atoms.

3 other chemicals share this scaffold

Safety and hazards

GHS classification summary, not a safety data sheet

GHS signal word
Warning
GHS07: Harmful or irritant
Harmful or irritant

Hazard statements

  • H302Harmful if swallowed.
  • H312Harmful in contact with skin.
  • H332Harmful if inhaled.
Precautionary statements (13)
  • P261Avoid breathing dust, fume, gas, mist, vapours or spray.
  • P264Wash skin thoroughly after handling.
  • P270Do not eat, drink or smoke when using this product.
  • P271Use only outdoors or in a well-ventilated area.
  • P280Wear protective gloves, protective clothing, eye protection and face protection.
  • P301 + P317If swallowed: Get medical help.
  • P302 + P352If on skin: Wash with plenty of water.
  • P304 + P340If inhaled: Remove person to fresh air and keep comfortable for breathing.
  • P317Get medical help.
  • P321Specific treatment (see supplemental first aid instructions on the label).
  • P330Rinse mouth.
  • P362 + P364Take off contaminated clothing. And wash it before reuse.
  • P501Dispose of contents and container in accordance with local regulations.

GHS classification summary, not a safety data sheet (SDS). Classifications can differ by supplier, grade and concentration. Always check the supplier's SDS.

Full safety data and first aid

Validamycin A suppliers

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Validamycin A price

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Uses and applications

What the substance is used for, by industry and function

It is fungistatic against a narrow range of fungi and is used to control Pellicularia (Corticium) sasakii of rice at 45-90 g ai/hectare, black scurf of potatoes and damping off of vegetable seedings caused by Thanatephorus cucumeris (Rhizoctonia solani).

Control of Rhizoctonia solani in potatoes, vegetables, rice, tobacco, and other crops, sheath blight of rice, damping off of cotton, etc. Applied as a foliar spray, soil drench, seed dressing, or by soil incorporation.

Nonsystemic antibiotic with fungistatic action.

Roles

  • agrochemical
  • antifungal agent
  • antifungal agrochemical
  • antimicrobial agent
  • enzyme inhibitor
  • fungicide
  • pesticide

How it is made

Produced by Streptomyces variable limoneus.

Regulatory status

Inventories, regulations and trade controls that list this substance

No regulatory list memberships are recorded for this substance yet. Always check the rules of the importing and exporting country before trade.

HS code and trade data

Customs classification and reported world trade statistics

Global trade

World import and export statistics for the HS code Validamycin A is traded under.

HS 2938.90Indicative HS code

Natural or reproduced by synthesis, other than rutoside (rutin) and its derivatives

World exports in 2024
$1.4B
โˆ’8.3% vs 2023, imports $1.35B
2019 to 2024
Top exporters
  1. China49.2%
  2. France * partner reported8.9%
  3. Malaysia6.1%
Top importers
  1. United States22.3%
  2. India * partner reported7.8%
  3. Brazil5.5%

* Partner reported figures, a lower bound.

Reported customs values in USD, not prices.Full trade data

The HS code shown for Validamycin A is indicative (it was assigned by structure rules). Confirm the classification with your customs broker before shipping.

Frequently asked questions

Quick answers about Validamycin A, based on the data on this page

What is Validamycin A?

Validamycin A is a member of the class of validamycins that is (1R,2S,3S,4S,6R)-4-amino-6-(hydroxymethyl)cyclohexane-1,2,3-triol in which the hydroxy group at position 1 has been converted to its beta-D-glucoside and in which one of the hydrogens attached to the nitrogen is replaced by a (1R,4R,5R,6S)-4,5,6-trihydroxyโ€ฆ

What is the CAS number of Validamycin A?

The CAS registry number of Validamycin A is 37248-47-8. Other or deprecated CAS numbers: 50642-14-3, 58194-43-7.

What is the molecular formula and weight of Validamycin A?

The molecular formula of Validamycin A is C20H35NO13 and its molar mass is 497.49 g/mol.

What is Validamycin A used for?

It is fungistatic against a narrow range of fungi and is used to control Pellicularia (Corticium) sasakii of rice at 45-90 g ai/hectare, black scurf of potatoes and damping off of vegetable seedings caused by Thanatephorus cucumeris (Rhizoctonia solani).

Is Validamycin A hazardous?

Validamycin A carries the GHS signal word "Warning". Main hazards: harmful if swallowed, harmful in contact with skin, harmful if inhaled. This summary is not an SDS, always read the supplier safety data sheet.

What is the HS code of Validamycin A?

Validamycin A is usually classified under HS code 293890 (Glycosides, natural or reproduced by synthesis, and their salts, ethers, esters andโ€ฆ). This is indicative, confirm it with your customs broker before shipping.

Where can I buy Validamycin A?

CompoundList lists 19 suppliers of Validamycin A in India, China, Australia, Singapore and 1 more. Send one free request to get and compare quotes. Your contact details stay private until you accept a quote.

Where can I buy Validamycin A in India?

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What is the price of Validamycin A?

Suppliers quote Validamycin A on request because prices depend on grade, purity, quantity and destination. A free request on CompoundList gets you several quotes to compare.

Guides for buyers

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Data last updated 7 Oct 2026. Details may have changed, please confirm them with the supplier. Report an error on this page
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